Maya Lodish, MD

Title(s)Professor, Pediatrics
SchoolSchool of Medicine
Address550 16th Street, #4803
San Francisco CA 94158
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    Collapse Biography 
    Collapse Education and Training
    University of California, San Francisco, CA2019Diversity, Equity, and Inclusion Champion Training
    Yale University School of Medicine, New Haven, CTMD2003
    Johns Hopkins Hospital, Baltimore MD2006Residency in Pediatrics
    National Institutes of Health, Bethesda MD2009Fellowship in Pediatric Endocrinology
    Dartmouth College, Hanover, NHBA1998Biochemistry and molecular biology
    Duke UniversityMHSc2012Clinical Research
    Collapse Awards and Honors
    UCSF2023Exceptional Teaching Award

    Collapse Overview 
    Collapse Overview
    Maya Lodish, MD, MHSc, Selna L. Kaplan Chair, Distinguished Professorship in Pediatric Endocrinology/Diabetes, Professor of Pediatrics, Division Chief of Pediatric Endocrinology

    Dr. Lodish completed her undergraduate degree at Dartmouth College, Hanover NH and she went on to Yale University School of Medicine. She completed her Internship & Residency in Pediatrics at the Johns Hopkins Hospital, Baltimore, MD. She pursued her Fellowship in Pediatric Endocrinology at the National Institutes of Health, Bethesda, MD. She completed a masters in clinical research at Duke University, Durham NC. While at the NIH, she served as Associate Research Physician and Director of the Fellowship in Pediatric Endocrinology. She led clinical research on endocrine tumors bridging collaborative endeavors between the National Cancer Institute (NCI), the National Institute of Neurological Disorders and Stroke (NINDS) and the National Institute of Child Health and Human Development (NICHD). She was the Primary Investigator for the protocol “A Clinical and genetic investigation of pituitary tumors and related hypothalamic disorders.” In 2018, Dr. Lodish joined the faculty at the University of California, San Francisco as the Selna L. Kaplan Chair, Distinguished Professorship in Pediatric Endocrinology/Diabetes, Professor of Pediatrics. Dr. Lodish’s role in the division is to mentor fellows, residents, and medical students in the intricacies of clinical research and quality improvement. She is working towards creating an interdisciplinary pediatric thyroid & endocrine oncology center at UCSF. Her research interests are in the endocrine-related complications faced by survivors of pediatric cancers, as well as in the genetic etiologies of pediatric neuroendocrine tumors. She plays a leading role in a number of studies to understand the pathophysiology and to improve the clinical care for pediatric patients with endocrine tumors including pheochromocytoma, Cushing syndrome, and thyroid cancer. At UCSF, Dr. Lodish is building a dynamic clinical research team in the field of endocrine oncology, fostering collaborations across campus including the neuro-oncology clinic, the cancer survivor multidisciplinary clinic, and the Pediatric Hereditary Cancer Clinic through the UCSF Cancer Genetics and Prevention Program. She has served as primary research mentor for a number of clinical fellows in pediatric endocrinology and is an active member of the scholarship oversight committee and program oversight committee at UCSF. Nationally, Dr. Lodish is a leader in the field of medical education as a member of the Clinical Education Committee of the Endocrine society from 2015-2018 and serves on the Pediatric Endocrine Society Education Committee.

    Collapse Research 
    Collapse Research Activities and Funding
    Detection and Treatment of Endocrine Abnormalities in Childhood Cancer Survivors
    NIH ZIAHD008894
    Role: Principal Investigator
    Pediatric Endocrinology Training Program
    NIH ZIEHD008944
    Role: Principal Investigator

    Collapse Bibliographic 
    Collapse Publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Anthropometric measurements of children with neurofibromatosis type I: impact of plexiform neurofibroma volume and treatment. Pediatr Res. 2024 Aug 28. Lemberg KM, Gross AM, Sproule LM, Liewehr DJ, Dombi E, Baldwin A, Steinberg SM, Bornhorst M, Lodish M, Blakeley JO, Widemann BC. PMID: 39198589.
      View in: PubMed   Mentions:    Fields:    
    2. Phase 3 Trial of Crinecerfont in Pediatric Congenital Adrenal Hyperplasia. N Engl J Med. 2024 08 08; 391(6):493-503. Sarafoglou K, Kim MS, Lodish M, Felner EI, Martinerie L, Nokoff NJ, Clemente M, Fechner PY, Vogiatzi MG, Speiser PW, Auchus RJ, Rosales GBG, Roberts E, Jeha GS, Farber RH, Chan JL, CAHtalyst Pediatric Trial Investigators. PMID: 38828945.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCTClinical Trials
    3. Author Correction: Diagnosis and management of prolactin-secreting pituitary adenomas: a Pituitary Society international Consensus Statement. Nat Rev Endocrinol. 2024 Jan; 20(1):62. Petersenn S, Fleseriu M, Casanueva FF, Giustina A, Biermasz N, Biller BMK, Bronstein M, Chanson P, Fukuoka H, Gadelha M, Greenman Y, Gurnell M, Ho KKY, Honegger J, Ioachimescu AG, Kaiser UB, Karavitaki N, Katznelson L, Lodish M, Maiter D, Marcus HJ, McCormack A, Molitch M, Muir CA, Neggers S, Pereira AM, Pivonello R, Post K, Raverot G, Salvatori R, Samson SL, Shimon I, Spencer-Segal J, Vila G, Wass J, Melmed S. PMID: 37848631.
      View in: PubMed   Mentions:    Fields:    
    4. Diagnosis and management of prolactin-secreting pituitary adenomas: a Pituitary Society international Consensus Statement. Nat Rev Endocrinol. 2023 Dec; 19(12):722-740. Petersenn S, Fleseriu M, Casanueva FF, Giustina A, Biermasz N, Biller BMK, Bronstein M, Chanson P, Fukuoka H, Gadelha M, Greenman Y, Gurnell M, Ho KKY, Honegger J, Ioachimescu AG, Kaiser UB, Karavitaki N, Katznelson L, Lodish M, Maiter D, Marcus HJ, McCormack A, Molitch M, Muir CA, Neggers S, Pereira AM, Pivonello R, Post K, Raverot G, Salvatori R, Samson SL, Shimon I, Spencer-Segal J, Vila G, Wass J, Melmed S. PMID: 37670148.
      View in: PubMed   Mentions: 43     Fields:    Translation:Humans
    5. Prevalence of nonalcoholic fatty liver disease increased with type 2 diabetes mellitus in overweight/obese youth with polycystic ovary syndrome. J Pediatr Endocrinol Metab. 2023 May 25; 36(5):441-446. Patel-Sanchez N, Perito E, Tsai P, Raymond-Flesch M, Lodish M, Sarkar M. PMID: 37060356; PMCID: PMC10214017.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    6. Utility of genetic work-up for 46, XY patients with severe hypospadias. J Pediatr Urol. 2023 06; 19(3):261-272. Srivastava P, Tenney J, Lodish M, Slavotinek A, Baskin L. PMID: 36496321.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    7. Safety of growth hormone replacement in survivors of cancer and intracranial and pituitary tumours: a consensus statement. Eur J Endocrinol. 2022 04 21; 186(6):P35-P52. Boguszewski MCS, Boguszewski CL, Chemaitilly W, Cohen LE, Gebauer J, Higham C, Hoffman AR, Polak M, Yuen KCJ, Alos N, Antal Z, Bidlingmaier M, Biller BMK, Brabant G, Choong CSY, Cianfarani S, Clayton PE, Coutant R, Cardoso-Demartini AA, Fernandez A, Grimberg A, Guðmundsson K, Guevara-Aguirre J, Ho KKY, Horikawa R, Isidori AM, Jørgensen JOL, Kamenicky P, Karavitaki N, Kopchick JJ, Lodish M, Luo X, McCormack AI, Meacham L, Melmed S, Mostoufi Moab S, Müller HL, Neggers SJCMM, Aguiar Oliveira MH, Ozono K, Pennisi PA, Popovic V, Radovick S, Savendahl L, Touraine P, van Santen HM, Johannsson G. PMID: 35319491; PMCID: PMC9066587.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
    8. Neurofibromatosis Type 1 Has a Wide Spectrum of Growth Hormone Excess. J Clin Med. 2022 Apr 13; 11(8). Hannah-Shmouni F, Trivellin G, Beckers P, Karaviti LP, Lodish M, Tatsi C, Adesina AM, Adamidou F, Mintziori G, Josefson JL, Quezado M, Stratakis CA. PMID: 35456261; PMCID: PMC9029762.
      View in: PubMed   Mentions: 6  
    9. How do clinicians integrate oral octreotide into their treatment plan for acromegaly? Lancet Diabetes Endocrinol. 2022 02; 10(2):86-87. Lodish MB. PMID: 34953532.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    10. Trend of Diabetes-Related Hospital Admissions During the Transition Period From Adolescence to Adulthood in the State of California. Diabetes Care. 2021 12; 44(12):2723-2728. Nip ASY, Lodish M. PMID: 34675057.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    11. Pheochromocytomas and paragangliomas. Curr Opin Pediatr. 2021 08 01; 33(4):430-435. Yen K, Lodish M. PMID: 34039901; PMCID: PMC10122989.
      View in: PubMed   Mentions: 3  Translation:Humans
    12. Cushing syndrome and glucocorticoids: T-cell lymphopenia, apoptosis, and rescue by IL-21. J Allergy Clin Immunol. 2022 01; 149(1):302-314. Hwang S, Tatsi C, Kuehn HS, Niemela JE, Stoddard J, Su Y, Lodish M, Uzel G, Spolski R, Leonard WJ, Holland SM, Fleisher TA, Stratakis CA, Rosenzweig SD. PMID: 34089750; PMCID: PMC8636539.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    13. Pediatric Cushing's syndrome: greater risk of being overweight or obese after long-term remission and its predictive factors. Eur J Endocrinol. 2021 Jan; 184(1):179-187. Valdés N, Tirosh A, Keil M, Stratakis CA, Lodish M. PMID: 33112275.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    14. The Association of ARMC5 with the Renin-Angiotensin-Aldosterone System, Blood Pressure, and Glycemia in African Americans. J Clin Endocrinol Metab. 2020 08 01; 105(8). Joseph JJ, Zhou X, Zilbermint M, Stratakis CA, Faucz FR, Lodish MB, Berthon A, Wilson JG, Hsueh WA, Golden SH, Lin S. PMID: 32436940; PMCID: PMC7308077.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    15. Rare Germline DICER1 Variants in Pediatric Patients With Cushing's Disease: What Is Their Role? Front Endocrinol (Lausanne). 2020; 11:433. Martínez de LaPiscina I, Hernández-Ramírez LC, Portillo N, Gómez-Gila AL, Urrutia I, Martínez-Salazar R, García-Castaño A, Aguayo A, Rica I, Gaztambide S, Faucz FR, Keil MF, Lodish MB, Quezado M, Pankratz N, Chittiboina P, Lane J, Kay DM, Mills JL, Castaño L, Stratakis CA. PMID: 32714280; PMCID: PMC7351020.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    16. Computerized Analysis of Brain MRI Parameter Dynamics in Young Patients With Cushing Syndrome-A Case-Control Study. J Clin Endocrinol Metab. 2020 05 01; 105(5). Tirosh A, RaviPrakash H, Papadakis GZ, Tatsi C, Belyavskaya E, Charalampos L, Lodish MB, Bagci U, Stratakis CA. PMID: 31875913; PMCID: PMC7089850.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    17. Germline USP8 Mutation Associated With Pediatric Cushing Disease and Other Clinical Features: A New Syndrome. J Clin Endocrinol Metab. 2019 10 01; 104(10):4676-4682. Cohen M, Persky R, Stegemann R, Hernández-Ramírez LC, Zeltser D, Lodish MB, Chen A, Keil MF, Tatsi C, Faucz FR, Buchner DA, Stratakis CA, Tiosano D. PMID: 31162547; PMCID: PMC6736211.
      View in: PubMed   Mentions: 26     Fields:    Translation:Humans
    18. Cushing disease in a patient with nonbullous congenital ichthyosiform erythroderma: lessons in avoiding glucocorticoids in ichthyosis. J Pediatr Endocrinol Metab. 2019 Aug 27; 32(8):911-914. Hartley IR, Costa Beber Nunes J, Lodish M, Stratakis CA. PMID: 31256066; PMCID: PMC7427504.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    19. ARMC 5 Variants and Risk of Hypertension in Blacks: MH- GRID Study. J Am Heart Assoc. 2019 07 16; 8(14):e012508. Zilbermint M, Gaye A, Berthon A, Hannah-Shmouni F, Faucz FR, Lodish MB, Davis AR, Gibbons GH, Stratakis CA. PMID: 31266387; PMCID: PMC6662143.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    20. Lipoprotein particles in patients with pediatric Cushing disease and possible cardiovascular risks. Pediatr Res. 2019 09; 86(3):375-381. Makri A, Cheung A, Sinaii N, Remaley AT, Sampson M, Keil M, Belyavskaya E, Lyssikatos C, De La Luz Sierra M, Stratakis CA, Lodish M. PMID: 31112990; PMCID: PMC6702083.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    21. CRH stimulation improves 18F-FDG-PET detection of pituitary adenomas in Cushing's disease. Endocrine. 2019 07; 65(1):155-165. Boyle J, Patronas NJ, Smirniotopoulos J, Herscovitch P, Dieckman W, Millo C, Maric D, Chatain GP, Hayes CP, Benzo S, Scott G, Edwards N, Ray Chaudhury A, Lodish MB, Sharma S, Nieman LK, Stratakis CA, Lonser RR, Chittiboina P. PMID: 31062234.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCTClinical Trials
    22. SGPL1 Deficiency: A Rare Cause of Primary Adrenal Insufficiency. J Clin Endocrinol Metab. 2019 05 01; 104(5):1484-1490. Settas N, Persky R, Faucz FR, Sheanon N, Voutetakis A, Lodish M, Metherell LA, Stratakis CA. PMID: 30517686; PMCID: PMC6435096.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    23. Large Genomic Aberrations in Corticotropinomas Are Associated With Greater Aggressiveness. J Clin Endocrinol Metab. 2019 05 01; 104(5):1792-1801. Tatsi C, Pankratz N, Lane J, Faucz FR, Hernández-Ramírez LC, Keil M, Trivellin G, Chittiboina P, Mills JL, Stratakis CA, Lodish MB. PMID: 30597087; PMCID: PMC6452317.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    24. Genetic Tumor Syndromes with Endocrine Involvement: A Compendium and an Update. Pediatr Endocrinol Rev. 2019 Mar; 16(3):311-334. Kushchayeva Y, Lightbourne M, Lodish M, Stratakis CA. PMID: 30888124.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    25. Careful investigation of a rare disease: insights into multiple endocrine neoplasia type 2B. Lancet Diabetes Endocrinol. 2019 03; 7(3):167-168. Lodish MB. PMID: 30660596.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    26. Aortic pulse wave velocity in children with Cushing syndrome: A window into a marker of early cardiovascular disease. Endocrinol Diabetes Metab. 2019 Apr; 2(2):e00054. Blain H, Sinaii N, Zeltser D, Lyssikatos C, Belyavskaya E, Keil M, Bluemke DA, Stratakis C, Bandettini WP, Lodish M. PMID: 31008362; PMCID: PMC6458483.
      View in: PubMed   Mentions: 2     Fields:    
    27. Correction: Optical Imaging Technology: A Useful Tool to Identify Remission in Cushing Disease After Surgery. Horm Metab Res. 2019 Feb; 51(2):e1. Afshari A, Keil M, Lyssikatos C, Belyavskaya E, Valdés N, Chowdhry FA, Parsa K, Ardeshirpour Y, Pursley R, Khare S, Kainerstorfer JM, Chittiboina P, Lodish MB, Mazzuchi TA, Gandjbakhche AH, Stratakis CA. PMID: 30641579; PMCID: PMC7299089.
      View in: PubMed   Mentions:    Fields:    
    28. Optical Imaging Technology: A Useful Tool to Identify Remission in Cushing Disease After Surgery. Horm Metab Res. 2019 Feb; 51(2):120-126. Afshari A, Keil M, Lyssikatos C, Belyavskaya E, Valdés N, Chowdhry FA, Parsa K, Ardeshirpour Y, Pursley R, Khare S, Kainerstorfer JM, Chittiboina P, Lodish MB, Mazzuchi TA, Gandjbakhche AH, Stratakis CA. PMID: 30602178; PMCID: PMC6753582.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    29. Pheochromocytoma in Children and Adolescents With Multiple Endocrine Neoplasia Type 2B. J Clin Endocrinol Metab. 2019 01 01; 104(1):7-12. Makri A, Akshintala S, Derse-Anthony C, Del Rivero J, Widemann B, Stratakis CA, Glod J, Lodish M. PMID: 30113649; PMCID: PMC6240163.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansPHPublic Health
    30. Multiple Endocrine Neoplasia Type 2B Presents Early in Childhood but Often Is Undiagnosed for Years. J Pediatr. 2018 12; 203:447-449. Makri A, Akshintala S, Derse-Anthony C, Widemann B, Stratakis CA, Glod J, Lodish M. PMID: 30314660; PMCID: PMC6707507.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    31. Mini-review of hair cortisol concentration for evaluation of Cushing syndrome. Expert Rev Endocrinol Metab. 2018 09; 13(5):225-231. Hodes A, Meyer J, Lodish MB, Stratakis CA, Zilbermint M. PMID: 30234410; PMCID: PMC6378952.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    32. Xq26.3 Duplication in a Boy With Motor Delay and Low Muscle Tone Refines the X-Linked Acrogigantism Genetic Locus. J Endocr Soc. 2018 Oct 01; 2(10):1100-1108. Trivellin G, Sharwood E, Hijazi H, Carvalho CMB, Yuan B, Tatton-Brown K, Coman D, Lupski JR, Cotterill AM, Lodish MB, Stratakis CA. PMID: 30525125; PMCID: PMC6137279.
      View in: PubMed   Mentions: 4  
    33. Children with MEN1 gene mutations may present first (and at a young age) with Cushing disease. Clin Endocrinol (Oxf). 2018 10; 89(4):437-443. Makri A, Bonella MB, Keil MF, Hernandez-Ramirez L, Paluch G, Tirosh A, Saldarriaga C, Chittiboina P, Marx SJ, Stratakis CA, Lodish M. PMID: 29927501; PMCID: PMC6341462.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    34. Cushing's Syndrome in Pediatrics: An Update. Endocrinol Metab Clin North Am. 2018 06; 47(2):451-462. Lodish MB, Keil MF, Stratakis CA. PMID: 29754644; PMCID: PMC5962291.
      View in: PubMed   Mentions: 28     Fields:    Translation:Humans
    35. Irreversible Primary Amenorrhea Secondary to Uterine Damage and Premature Ovarian Failure in 2 Patients with Ewing Sarcoma. J Pediatr Adolesc Gynecol. 2018 Dec; 31(6):648-650. Makri A, Boyce AM, Stratakis CA, Lodish M. PMID: 29857112; PMCID: PMC6341470.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    36. Impaired Bone Mineral Density in Pediatric Patients with Chronic Graft-versus-Host Disease. Biol Blood Marrow Transplant. 2018 07; 24(7):1415-1423. Buxbaum NP, Robinson C, Sinaii N, Ling A, Curtis LM, Pavletic SZ, Baird K, Lodish MB. PMID: 29496562; PMCID: PMC6045967.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    37. Incidence of Autoimmune and Related Disorders After Resolution of Endogenous Cushing Syndrome in Children. Horm Metab Res. 2018 Apr; 50(4):290-295. Tatsi C, Keil M, Lyssikatos C, Belyavskaya E, Stratakis CA, Lodish MB. PMID: 29458220; PMCID: PMC6341463.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    38. Postoperative Diabetes Insipidus and Hyponatremia in Children after Transsphenoidal Surgery for Adrenocorticotropin Hormone and Growth Hormone Secreting Adenomas. J Pediatr. 2018 04; 195:169-174.e1. Saldarriaga C, Lyssikatos C, Belyavskaya E, Keil M, Chittiboina P, Sinaii N, Stratakis CA, Lodish M. PMID: 29395172; PMCID: PMC5869073.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    39. Earlier post-operative hypocortisolemia may predict durable remission from Cushing's disease. Eur J Endocrinol. 2018 Mar; 178(3):255-263. Ironside N, Chatain G, Asuzu D, Benzo S, Lodish M, Sharma S, Nieman L, Stratakis CA, Lonser RR, Chittiboina P. PMID: 29330227; PMCID: PMC5812811.
      View in: PubMed   Mentions: 20     Fields:    Translation:Humans
    40. Decreased lymphocytes and increased risk for infection are common in endogenous pediatric Cushing syndrome. Pediatr Res. 2018 02; 83(2):431-437. Tatsi C, Boden R, Sinaii N, Keil M, Lyssikatos C, Belyavskaya E, Rosenzweig SD, Stratakis CA, Lodish MB. PMID: 29211058; PMCID: PMC5866174.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCells
    41. Superiority of 68Ga-DOTATATE over 18F-FDG and anatomic imaging in the detection of succinate dehydrogenase mutation (SDHx )-related pheochromocytoma and paraganglioma in the pediatric population. Eur J Nucl Med Mol Imaging. 2018 05; 45(5):787-797. Jha A, Ling A, Millo C, Gupta G, Viana B, Lin FI, Herscovitch P, Adams KT, Taïeb D, Metwalli AR, Linehan WM, Brofferio A, Stratakis CA, Kebebew E, Lodish M, Civelek AC, Pacak K. PMID: 29204718; PMCID: PMC6707509.
      View in: PubMed   Mentions: 31     Fields:    Translation:Humans
    42. Outcomes of Children and Adolescents with Advanced Hereditary Medullary Thyroid Carcinoma Treated with Vandetanib. Clin Cancer Res. 2018 02 15; 24(4):753-765. Kraft IL, Akshintala S, Zhu Y, Lei H, Derse-Anthony C, Dombi E, Steinberg SM, Lodish M, Waguespack SG, Kapustina O, Fox E, Balis FM, Merino MJ, Meltzer PS, Glod JW, Shern JF, Widemann BC. PMID: 29187393; PMCID: PMC5815946.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    43. Failure to Thrive in the Context of Carney Complex. Horm Res Paediatr. 2018; 89(1):38-46. Tirosh A, Auerbach A, Bonella B, Zavras PD, Belyavskaya E, Lyssikatos C, Meir K, Weiss R, Daum H, Lodish MB, Gillis D, Stratakis CA. PMID: 29161691.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    44. Large pituitary gland with an expanding lesion in the context of neurofibromatosis 1. BMJ Case Rep. 2017 Oct 25; 2017. Hannah-Shmouni F, Demidowich AP, Rowell J, Lodish M, Stratakis CA. PMID: 29070623; PMCID: PMC5665192.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    45. Potential utility of FLAIR in MRI-negative Cushing's disease. J Neurosurg. 2018 09; 129(3):620-628. Chatain GP, Patronas N, Smirniotopoulos JG, Piazza M, Benzo S, Ray-Chaudhury A, Sharma S, Lodish M, Nieman L, Stratakis CA, Chittiboina P. PMID: 29027863; PMCID: PMC6398169.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansCTClinical Trials
    46. Harvey Cushing Treated the First Known Patient With Carney Complex. J Endocr Soc. 2017 Oct 01; 1(10):1312-1321. Tsay CJ, Stratakis CA, Faucz FR, London E, Stathopoulou C, Allgauer M, Quezado M, Dagradi T, Spencer DD, Lodish M. PMID: 29264456; PMCID: PMC5686675.
      View in: PubMed   Mentions: 4  
    47. Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing Disease. J Clin Endocrinol Metab. 2017 08 01; 102(8):2836-2843. Faucz FR, Tirosh A, Tatsi C, Berthon A, Hernández-Ramírez LC, Settas N, Angelousi A, Correa R, Papadakis GZ, Chittiboina P, Quezado M, Pankratz N, Lane J, Dimopoulos A, Mills JL, Lodish M, Stratakis CA. PMID: 28505279; PMCID: PMC5546857.
      View in: PubMed   Mentions: 47     Fields:    Translation:Humans
    48. Normalized Early Postoperative Cortisol and ACTH Values Predict Nonremission After Surgery for Cushing Disease. J Clin Endocrinol Metab. 2017 07 01; 102(7):2179-2187. Asuzu D, Chatain GP, Hayes C, Benzo S, McGlotten R, Keil M, Beri A, Sharma ST, Nieman L, Lodish M, Stratakis C, Lonser RR, Oldfield EH, Chittiboina P. PMID: 28323961; PMCID: PMC6283430.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    49. The Pediatric Medical Student Research Forum: Fostering Interest in Pediatric Research. J Pediatr. 2017 09; 188:3-4. Rivkees SA, Kelly M, Lodish M, Weiner D. PMID: 28645440.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    50. Obesity and the diagnostic accuracy for primary aldosteronism. J Clin Hypertens (Greenwich). 2017 Aug; 19(8):790-797. Tirosh A, Hannah-Shmouni F, Lyssikatos C, Belyavskaya E, Zilbermint M, Abraham SB, Lodish MB, Stratakis CA. PMID: 28612447; PMCID: PMC5602533.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCTClinical Trials
    51. Cushing Disease in a patient with Multiple Endocrine Neoplasia type 2B. J Clin Transl Endocrinol Case Rep. 2017 Jun; 4:1-4. Kasturi K, Fernandes L, Quezado M, Eid M, Marcus L, Chittiboina P, Rappaport M, Stratakis CA, Widemann B, Lodish M. PMID: 28435794; PMCID: PMC5395709.
      View in: PubMed   Mentions: 9  
    52. Bone mineral density in patients with inherited bone marrow failure syndromes. Pediatr Res. 2017 Sep; 82(3):458-464. Shankar RK, Giri N, Lodish MB, Sinaii N, Reynolds JC, Savage SA, Stratakis CA, Alter BP. PMID: 28486441; PMCID: PMC5570650.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    53. Corticotropinoma as a Component of Carney Complex. J Endocr Soc. 2017 Jul 01; 1(7):918-925. Hernández-Ramírez LC, Tatsi C, Lodish MB, Faucz FR, Pankratz N, Chittiboina P, Lane J, Kay DM, Valdés N, Dimopoulos A, Mills JL, Stratakis CA. PMID: 29264542; PMCID: PMC5686778.
      View in: PubMed   Mentions: 23  
    54. Loss-of-function mutations in the CABLES1 gene are a novel cause of Cushing's disease. Endocr Relat Cancer. 2017 08; 24(8):379-392. Hernández-Ramírez LC, Gam R, Valdés N, Lodish MB, Pankratz N, Balsalobre A, Gauthier Y, Faucz FR, Trivellin G, Chittiboina P, Lane J, Kay DM, Dimopoulos A, Gaillard S, Neou M, Bertherat J, Assié G, Villa C, Mills JL, Drouin J, Stratakis CA. PMID: 28533356; PMCID: PMC5510591.
      View in: PubMed   Mentions: 30     Fields:    Translation:HumansAnimalsCells
    55. Pediatric Cushing disease: disparities in disease severity and outcomes in the Hispanic and African-American populations. Pediatr Res. 2017 Aug; 82(2):272-277. Gkourogianni A, Sinaii N, Jackson SH, Karageorgiadis AS, Lyssikatos C, Belyavskaya E, Keil MF, Zilbermint M, Chittiboina P, Stratakis CA, Lodish MB. PMID: 28422946; PMCID: PMC5552413.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    56. 3D Volumetric Measurements of GH Secreting Adenomas Correlate with Baseline Pituitary Function, Initial Surgery Success Rate, and Disease Control. Horm Metab Res. 2017 Jun; 49(6):440-445. Tirosh A, Papadakis GZ, Chittiboina P, Lyssikatos C, Belyavskaya E, Keil M, Lodish MB, Stratakis CA. PMID: 28472827; PMCID: PMC6309337.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    57. Quantification of Thyroid Cancer and Multinodular Goiter Risk in the DICER1 Syndrome: A Family-Based Cohort Study. J Clin Endocrinol Metab. 2017 05 01; 102(5):1614-1622. Khan NE, Bauer AJ, Schultz KAP, Doros L, Decastro RM, Ling A, Lodish MB, Harney LA, Kase RG, Carr AG, Rossi CT, Field A, Harris AK, Williams GM, Dehner LP, Messinger YH, Hill DA, Stewart DR. PMID: 28323992; PMCID: PMC5443331.
      View in: PubMed   Mentions: 59     Fields:    Translation:Humans
    58. Circadian Plasma Cortisol Measurements Reflect Severity of Hypercortisolemia in Children with Different Etiologies of Endogenous Cushing Syndrome. Horm Res Paediatr. 2017; 87(5):295-300. Tirosh A, Lodish MB, Lyssikatos C, Belyavskaya E, Papadakis GZ, Stratakis CA. PMID: 28433999; PMCID: PMC5506540.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCTClinical Trials
    59. Characteristics of Pediatric vs Adult Pheochromocytomas and Paragangliomas. J Clin Endocrinol Metab. 2017 Apr 01; 102(4):1122-1132. Pamporaki C, Hamplova B, Peitzsch M, Prejbisz A, Beuschlein F, Timmers HJLM, Fassnacht M, Klink B, Lodish M, Stratakis CA, Huebner A, Fliedner S, Robledo M, Sinnott RO, Januszewicz A, Pacak K, Eisenhofer G. PMID: 28324046; PMCID: PMC5460722.
      View in: PubMed   Mentions: 48     Fields:    Translation:Humans
    60. Genetics of Adrenocortical Development and Tumors. Endocrinol Metab Clin North Am. 2017 06; 46(2):419-433. Lodish M. PMID: 28476230; PMCID: PMC5424622.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansCells
    61. Coagulation Profile in Patients with Different Etiologies for Cushing Syndrome: A Prospective Observational Study. Horm Metab Res. 2017 May; 49(5):365-371. Tirosh A, Lodish M, Lyssikatos C, Belyavskaya E, Feelders RA, Stratakis CA. PMID: 28226363; PMCID: PMC6533628.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    62. Hair cortisol in the evaluation of Cushing syndrome. Endocrine. 2017 Apr; 56(1):164-174. Hodes A, Lodish MB, Tirosh A, Meyer J, Belyavskaya E, Lyssikatos C, Rosenberg K, Demidowich A, Swan J, Jonas N, Stratakis CA, Zilbermint M. PMID: 28194652; PMCID: PMC5437744.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    63. Case 1: Poor Growth With Presence of a Pituitary Lesion in an 11-year-old Boy. Pediatr Rev. 2017 Jan; 38(1):44-45. Karageorgiadis AS, Lyssikatos C, Belyavskaya E, Papadakis GZ, Patronas NJ, Lodish MB, Stratakis CA. PMID: 28044033; PMCID: PMC6343498.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    64. Delayed Diagnosis of Cushing's Disease in a Pediatric Patient due to Apparent Remission from Spontaneous Apoplexy. J Clin Transl Endocrinol Case Rep. 2016 Dec; 2:30-34. Rahman SH, Chittibonia P, Quezado M, Patronas N, Stratakis CA, Lodish MB. PMID: 28848696; PMCID: PMC5571867.
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    65. Effects of Glucocorticoids on Bone: What we can Learn from Pediatric Endogenous Cushing's Syndrome. Horm Metab Res. 2016 Nov; 48(11):764-770. Tack LJ, Tatsi C, Stratakis CA, Lodish MB. PMID: 27728929.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    66. Diurnal Plasma Cortisol Measurements Utility in Differentiating Various Etiologies of Endogenous Cushing Syndrome. Horm Metab Res. 2016 Sep; 48(10):677-681. Tirosh A, Lodish MB, Papadakis GZ, Lyssikatos C, Belyavskaya E, Stratakis CA. PMID: 27643448; PMCID: PMC6341983.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    67. Spontaneously Resolving Hyperreninemic Hypertension Caused by Accessory Renal Artery Stenosis in a 13-Year-Old Girl: A Case Report. J Clin Hypertens (Greenwich). 2017 01; 19(1):100-102. Akbeyaz IH, Tirosh A, Robinson C, Broadney MM, Papadakis GZ, Belyavskaya E, Lyssikatos C, Lodish MB, Stratakis CA. PMID: 27528003; PMCID: PMC6341473.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    68. Coagulation Profile Dynamics in Pediatric Patients with Cushing Syndrome: A Prospective, Observational Comparative Study. J Pediatr. 2016 10; 177:227-231. Birdwell L, Lodish M, Tirosh A, Chittiboina P, Keil M, Lyssikatos C, Belyavskaya E, Feelders RA, Stratakis CA. PMID: 27496264; PMCID: PMC5298225.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    69. Growth hormone and risk for cardiac tumors in Carney complex. Endocr Relat Cancer. 2016 09; 23(9):739-46. Bandettini WP, Karageorgiadis AS, Sinaii N, Rosing DR, Sachdev V, Schernthaner-Reiter MH, Gourgari E, Papadakis GZ, Keil MF, Lyssikatos C, Carney JA, Arai AE, Lodish M, Stratakis CA. PMID: 27535175; PMCID: PMC4991637.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    70. Bilateral Adrenal Hyperplasia as a Possible Mechanism for Hyperandrogenism in Women With Polycystic Ovary Syndrome. J Clin Endocrinol Metab. 2016 09; 101(9):3353-60. Gourgari E, Lodish M, Keil M, Sinaii N, Turkbey E, Lyssikatos C, Nesterova M, de la Luz Sierra M, Xekouki P, Khurana D, Ten S, Dobs A, Stratakis CA. PMID: 27336356; PMCID: PMC5010568.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    71. Screening for GPR101 defects in pediatric pituitary corticotropinomas. Endocr Relat Cancer. 2016 06 01; 23(5):357-365. Trivellin G, Correa RR, Batsis M, Faucz FR, Chittiboina P, Bjelobaba I, Larco DO, Quezado M, Daly AF, Stojilkovic SS, Wu TJ, Beckers A, Lodish M, Stratakis CA. PMID: 26962002; PMCID: PMC5017905.
      View in: PubMed   Mentions: 11     Fields:    
    72. Attention Deficit Hyperactivity Disorder in Pediatric Patients with Pheochromocytoma and Paraganglioma. Horm Metab Res. 2016 Aug; 48(8):509-13. Batsis M, Dagalakis U, Stratakis CA, Prodanov T, Papadakis GZ, Adams K, Lodish M, Pacak K. PMID: 27171833; PMCID: PMC7441823.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    73. Use of 3-Dimensional Volumetric Modeling of Adrenal Gland Size in Patients with Primary Pigmented Nodular Adrenocortical Disease. Horm Metab Res. 2016 Apr; 48(4):242-6. Chrysostomou PP, Lodish MB, Turkbey EB, Papadakis GZ, Stratakis CA. PMID: 27065461; PMCID: PMC6300994.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    74. Cases of Psychiatric Morbidity in Pediatric Patients After Remission of Cushing Syndrome. Pediatrics. 2016 Apr; 137(4). Keil MF, Zametkin A, Ryder C, Lodish M, Stratakis CA. PMID: 27025959; PMCID: PMC4811308.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCTClinical Trials
    75. A genetic and molecular update on adrenocortical causes of Cushing syndrome. Nat Rev Endocrinol. 2016 May; 12(5):255-62. Lodish M, Stratakis CA. PMID: 26965378.
      View in: PubMed   Mentions: 30     Fields:    Translation:HumansAnimals
    76. Somatic mosaicism underlies X-linked acrogigantism syndrome in sporadic male subjects. Endocr Relat Cancer. 2016 04; 23(4):221-33. Daly AF, Yuan B, Fina F, Caberg JH, Trivellin G, Rostomyan L, de Herder WW, Naves LA, Metzger D, Cuny T, Rabl W, Shah N, Jaffrain-Rea ML, Zatelli MC, Faucz FR, Castermans E, Nanni-Metellus I, Lodish M, Muhammad A, Palmeira L, Potorac I, Mantovani G, Neggers SJ, Klein M, Barlier A, Liu P, Ouafik L, Bours V, Lupski JR, Stratakis CA, Beckers A. PMID: 26935837; PMCID: PMC4877443.
      View in: PubMed   Mentions: 26     Fields:    Translation:Humans
    77. Pituitary gigantism: update on molecular biology and management. Curr Opin Endocrinol Diabetes Obes. 2016 Feb; 23(1):72-80. Lodish MB, Trivellin G, Stratakis CA. PMID: 26574647; PMCID: PMC4727441.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    78. A novel AVPR2 splice site mutation leads to partial X-linked nephrogenic diabetes insipidus in two brothers. Eur J Pediatr. 2016 May; 175(5):727-33. Schernthaner-Reiter MH, Adams D, Trivellin G, Ramnitz MS, Raygada M, Golas G, Faucz FR, Nilsson O, Nella AA, Dileepan K, Lodish M, Lee P, Tifft C, Markello T, Gahl W, Stratakis CA. PMID: 26795631; PMCID: PMC6561467.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    79. Pseudohypoaldosteronism type 1 due to novel variants of SCNN1B gene. Endocrinol Diabetes Metab Case Rep. 2016; 2016:150104. Nobel YR, Lodish MB, Raygada M, Rivero JD, Faucz FR, Abraham SB, Lyssikatos C, Belyavskaya E, Stratakis CA, Zilbermint M. PMID: 26807262; PMCID: PMC4722246.
      View in: PubMed   Mentions: 8  
    80. Kidney Stones as an Underrecognized Clinical Sign in Pediatric Cushing Disease. J Pediatr. 2016 Mar; 170:273-7.e1. Rahman SH, Papadakis GZ, Keil MF, Faucz FR, Lodish MB, Stratakis CA. PMID: 26703870; PMCID: PMC4769940.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    81. Phase I Clinical Trial of Ipilimumab in Pediatric Patients with Advanced Solid Tumors. Clin Cancer Res. 2016 Mar 15; 22(6):1364-70. Merchant MS, Wright M, Baird K, Wexler LH, Rodriguez-Galindo C, Bernstein D, Delbrook C, Lodish M, Bishop R, Wolchok JD, Streicher H, Mackall CL. PMID: 26534966; PMCID: PMC5027962.
      View in: PubMed   Mentions: 142     Fields:    Translation:HumansCTClinical Trials
    82. Pituitary abnormalities in patients with Fanconi anaemia. Clin Endocrinol (Oxf). 2016 Feb; 84(2):307-309. Kanakatti Shankar R, Giri N, Lodish MB, Butman JA, Patronas NJ, Sinaii N, Keil M, Alter BP, Stratakis CA. PMID: 26300308.
      View in: PubMed   Mentions: 1     Fields:    
    83. Lipoprotein Particles in Adolescents and Young Women With PCOS Provide Insights Into Their Cardiovascular Risk. J Clin Endocrinol Metab. 2015 Nov; 100(11):4291-8. Gourgari E, Lodish M, Shamburek R, Keil M, Wesley R, Walter M, Sampson M, Bernstein S, Khurana D, Lyssikatos C, Ten S, Dobs A, Remaley AT, Stratakis CA. PMID: 26371381; PMCID: PMC4702461.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    84. Residual manifestations of hypercortisolemia following surgical treatment in a patient with Cushing syndrome. Int J Pediatr Endocrinol. 2015; 2015(1):19. Bartz SK, Karaviti LP, Brandt ML, Lopez ME, Masand P, Devaraj S, Hicks J, Anderson L, Lodish M, Keil M, Stratakis CA. PMID: 26322079; PMCID: PMC4551381.
      View in: PubMed   Mentions: 4  
    85. Facial Plethora: Modern Technology for Quantifying an Ancient Clinical Sign and Its Use in Cushing Syndrome. J Clin Endocrinol Metab. 2015 Oct; 100(10):3928-33. Afshari A, Ardeshirpour Y, Lodish MB, Gourgari E, Sinaii N, Keil M, Belyavskaya E, Lyssikatos C, Chowdhry FA, Chernomordik V, Anderson AA, Mazzuchi TA, Gandjbakhche A, Stratakis CA. PMID: 26301943; PMCID: PMC4596033.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    86. The ARMC5 gene shows extensive genetic variance in primary macronodular adrenocortical hyperplasia. Eur J Endocrinol. 2015 Oct; 173(4):435-40. Correa R, Zilbermint M, Berthon A, Espiard S, Batsis M, Papadakis GZ, Xekouki P, Lodish MB, Bertherat J, Faucz FR, Stratakis CA. PMID: 26162405; PMCID: PMC4572515.
      View in: PubMed   Mentions: 22     Fields:    Translation:Humans
    87. Germline PRKACA amplification causes variable phenotypes that may depend on the extent of the genomic defect: molecular mechanisms and clinical presentations. Eur J Endocrinol. 2015 06; 172(6):803-11. Lodish MB, Yuan B, Levy I, Braunstein GD, Lyssikatos C, Salpea P, Szarek E, Karageorgiadis AS, Belyavskaya E, Raygada M, Faucz FR, Izzat L, Brain C, Gardner J, Quezado M, Carney JA, Lupski JR, Stratakis CA. PMID: 25924874; PMCID: PMC4428149.
      View in: PubMed   Mentions: 23     Fields:    Translation:Humans
    88. Expanding the clinical and molecular characteristics of PIGT-CDG, a disorder of glycosylphosphatidylinositol anchors. Mol Genet Metab. 2015 Jun-Jul; 115(2-3):128-140. Lam C, Golas GA, Davids M, Huizing M, Kane MS, Krasnewich DM, Malicdan MCV, Adams DR, Markello TC, Zein WM, Gropman AL, Lodish MB, Stratakis CA, Maric I, Rosenzweig SD, Baker EH, Ferreira CR, Danylchuk NR, Kahler S, Garnica AD, Bradley Schaefer G, Boerkoel CF, Gahl WA, Wolfe LA. PMID: 25943031; PMCID: PMC6341466.
      View in: PubMed   Mentions: 29     Fields:    Translation:HumansCells
    89. Primary Aldosteronism and ARMC5 Variants. J Clin Endocrinol Metab. 2015 Jun; 100(6):E900-9. Zilbermint M, Xekouki P, Faucz FR, Berthon A, Gkourogianni A, Schernthaner-Reiter MH, Batsis M, Sinaii N, Quezado MM, Merino M, Hodes A, Abraham SB, Libé R, Assié G, Espiard S, Drougat L, Ragazzon B, Davis A, Gebreab SY, Neff R, Kebebew E, Bertherat J, Lodish MB, Stratakis CA. PMID: 25822102; PMCID: PMC4454793.
      View in: PubMed   Mentions: 45     Fields:    Translation:HumansCells
    90. X-linked acrogigantism syndrome: clinical profile and therapeutic responses. Endocr Relat Cancer. 2015 Jun; 22(3):353-67. Beckers A, Lodish MB, Trivellin G, Rostomyan L, Lee M, Faucz FR, Yuan B, Choong CS, Caberg JH, Verrua E, Naves LA, Cheetham TD, Young J, Lysy PA, Petrossians P, Cotterill A, Shah NS, Metzger D, Castermans E, Ambrosio MR, Villa C, Strebkova N, Mazerkina N, Gaillard S, Barra GB, Casulari LA, Neggers SJ, Salvatori R, Jaffrain-Rea ML, Zacharin M, Santamaria BL, Zacharieva S, Lim EM, Mantovani G, Zatelli MC, Collins MT, Bonneville JF, Quezado M, Chittiboina P, Oldfield EH, Bours V, Liu P, W de Herder W, Pellegata N, Lupski JR, Daly AF, Stratakis CA. PMID: 25712922; PMCID: PMC4433400.
      View in: PubMed   Mentions: 65     Fields:    Translation:HumansCells
    91. Pituitary adenoma with paraganglioma/pheochromocytoma (3PAs) and succinate dehydrogenase defects in humans and mice. J Clin Endocrinol Metab. 2015 May; 100(5):E710-9. Xekouki P, Szarek E, Bullova P, Giubellino A, Quezado M, Mastroyannis SA, Mastorakos P, Wassif CA, Raygada M, Rentia N, Dye L, Cougnoux A, Koziol D, Sierra Mde L, Lyssikatos C, Belyavskaya E, Malchoff C, Moline J, Eng C, Maher LJ, Pacak K, Lodish M, Stratakis CA. PMID: 25695889; PMCID: PMC4422891.
      View in: PubMed   Mentions: 60     Fields:    Translation:HumansAnimals
    92. Patterns of thyroid hormone levels in pediatric medullary thyroid carcinoma patients on vandetanib therapy. Int J Pediatr Endocrinol. 2015; 2015(1):3. Lodish M, Gkourogianni A, Bornstein E, Sinaii N, Fox E, Chuk M, Marcus L, Akshintala S, Balis F, Widemann B, Stratakis CA. PMID: 25972901; PMCID: PMC4429462.
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    93. A gender-dependent analysis of Cushing's disease in childhood: pre- and postoperative follow-up. Clin Endocrinol (Oxf). 2015 Jul; 83(1):72-7. Libuit LG, Karageorgiadis AS, Sinaii N, Nguyen May NM, Keil MF, Lodish MB, Stratakis CA. PMID: 25388128; PMCID: PMC6342464.
      View in: PubMed   Mentions: 20     Fields:    Translation:HumansCTClinical Trials
    94. Cushing's syndrome in childhood: update on genetics, treatment, and outcomes. Curr Opin Endocrinol Diabetes Obes. 2015 Feb; 22(1):48-54. Lodish M. PMID: 25517021; PMCID: PMC4415092.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    95. Endocrine disorders in Fanconi anemia: recommendations for screening and treatment. J Clin Endocrinol Metab. 2015 Mar; 100(3):803-11. Petryk A, Kanakatti Shankar R, Giri N, Hollenberg AN, Rutter MM, Nathan B, Lodish M, Alter BP, Stratakis CA, Rose SR. PMID: 25575015; PMCID: PMC4333044.
      View in: PubMed   Mentions: 33     Fields:    Translation:HumansPHPublic Health
    96. Ectopic adrenocorticotropic hormone and corticotropin-releasing hormone co-secreting tumors in children and adolescents causing cushing syndrome: a diagnostic dilemma and how to solve it. J Clin Endocrinol Metab. 2015 Jan; 100(1):141-8. Karageorgiadis AS, Papadakis GZ, Biro J, Keil MF, Lyssikatos C, Quezado MM, Merino M, Schrump DS, Kebebew E, Patronas NJ, Hunter MK, Alwazeer MR, Karaviti LP, Balazs AE, Lodish MB, Stratakis CA. PMID: 25291050; PMCID: PMC4283025.
      View in: PubMed   Mentions: 32     Fields:    Translation:Humans
    97. Is IGSF1 involved in human pituitary tumor formation? Endocr Relat Cancer. 2015 Feb; 22(1):47-54. Faucz FR, Horvath AD, Azevedo MF, Levy I, Bak B, Wang Y, Xekouki P, Szarek E, Gourgari E, Manning AD, de Alexandre RB, Saloustros E, Trivellin G, Lodish M, Hofman P, Anderson YC, Holdaway I, Oldfield E, Chittiboina P, Nesterova M, Biermasz NR, Wit JM, Bernard DJ, Stratakis CA. PMID: 25527509; PMCID: PMC4272759.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansAnimalsCells
    98. Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutation. N Engl J Med. 2014 Dec 18; 371(25):2363-74. Trivellin G, Daly AF, Faucz FR, Yuan B, Rostomyan L, Larco DO, Schernthaner-Reiter MH, Szarek E, Leal LF, Caberg JH, Castermans E, Villa C, Dimopoulos A, Chittiboina P, Xekouki P, Shah N, Metzger D, Lysy PA, Ferrante E, Strebkova N, Mazerkina N, Zatelli MC, Lodish M, Horvath A, de Alexandre RB, Manning AD, Levy I, Keil MF, Sierra Mde L, Palmeira L, Coppieters W, Georges M, Naves LA, Jamar M, Bours V, Wu TJ, Choong CS, Bertherat J, Chanson P, Kamenický P, Farrell WE, Barlier A, Quezado M, Bjelobaba I, Stojilkovic SS, Wess J, Costanzi S, Liu P, Lupski JR, Beckers A, Stratakis CA. PMID: 25470569; PMCID: PMC4291174.
      View in: PubMed   Mentions: 118     Fields:    Translation:HumansCells
    99. Use of aromatase inhibitors in large cell calcifying sertoli cell tumors: effects on gynecomastia, growth velocity, and bone age. J Clin Endocrinol Metab. 2014 Dec; 99(12):E2673-80. Crocker MK, Gourgari E, Lodish M, Stratakis CA. PMID: 25226294; PMCID: PMC4255117.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    100. Not all glucocorticoid-induced obesity is the same: differences in adiposity among various diagnostic groups of Cushing syndrome. Horm Metab Res. 2014 Nov; 46(12):897-903. London E, Lodish M, Keil M, Lyssikatos C, de la Luz Sierra M, Nesterova M, Stratakis CA. PMID: 25295416.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    101. Germline PRKACA amplification leads to Cushing syndrome caused by 3 adrenocortical pathologic phenotypes. Hum Pathol. 2015 Jan; 46(1):40-9. Carney JA, Lyssikatos C, Lodish MB, Stratakis CA. PMID: 25449630; PMCID: PMC6309372.
      View in: PubMed   Mentions: 25     Fields:    Translation:Humans
    102. Post-operative growth is different in various forms of pediatric Cushing's syndrome. Endocr Relat Cancer. 2014; 21(6):L27-31. Gourgari E, Lodish M, Keil M, Wesley R, Hill S, Xekouki P, Lyssikatos C, Belyavskaya E, De La Luz SM, Stratakis CA. PMID: 25258026; PMCID: PMC4209309.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    103. Death in pediatric Cushing syndrome is uncommon but still occurs. Eur J Pediatr. 2015 Apr; 174(4):501-7. Gkourogianni A, Lodish MB, Zilbermint M, Lyssikatos C, Belyavskaya E, Keil MF, Stratakis CA. PMID: 25241829; PMCID: PMC4370787.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    104. Vitamin B12 deficiency in an adolescent girl with polycystic ovarian syndrome. Eur J Obstet Gynecol Reprod Biol. 2014 Aug; 179:254. Gourgari E, Nella AA, Lodish M, Stratakis CA, Yanovski JA. PMID: 24933126; PMCID: PMC4160304.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    105. Vandetanib successfully controls medullary thyroid cancer-related Cushing syndrome in an adolescent patient. J Clin Endocrinol Metab. 2014 Sep; 99(9):3055-9. Nella AA, Lodish MB, Fox E, Balis FM, Quezado MM, Whitcomb PO, Derdak J, Kebebew E, Widemann BC, Stratakis CA. PMID: 24617713; PMCID: PMC4154103.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    106. Macronodular adrenal hyperplasia due to mutations in an armadillo repeat containing 5 (ARMC5) gene: a clinical and genetic investigation. J Clin Endocrinol Metab. 2014 Jun; 99(6):E1113-9. Faucz FR, Zilbermint M, Lodish MB, Szarek E, Trivellin G, Sinaii N, Berthon A, Libé R, Assié G, Espiard S, Drougat L, Ragazzon B, Bertherat J, Stratakis CA. PMID: 24601692; PMCID: PMC4037724.
      View in: PubMed   Mentions: 69     Fields:    Translation:Humans
    107. Pituitary stalk lesion in a 13-year-old female. J Pediatr Endocrinol Metab. 2014 Mar; 27(3-4):359-62. Zilbermint M, Ramnitz MS, Lodish MB, Kanaka-Gantenbein C, Kattamis A, Lyssikatos C, Patronas NJ, Quezado MM, Stratakis CA. PMID: 24129100; PMCID: PMC4727445.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    108. Skeletal maturation in children with Cushing syndrome is not consistently delayed: the role of corticotropin, obesity, and steroid hormones, and the effect of surgical cure. J Pediatr. 2014 Apr; 164(4):801-6. Lodish MB, Gourgari E, Sinaii N, Hill S, Libuit L, Mastroyannis S, Keil M, Batista DL, Stratakis CA. PMID: 24412141; PMCID: PMC3963265.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    109. Puberty and plexiform neurofibroma tumor growth in patients with neurofibromatosis type I. J Pediatr. 2014 Mar; 164(3):620-4. Dagalakis U, Lodish M, Dombi E, Sinaii N, Sabo J, Baldwin A, Steinberg SM, Stratakis CA, Widemann BC. PMID: 24321536; PMCID: PMC3943976.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    110. Differences in adiposity in Cushing syndrome caused by PRKAR1A mutations: clues for the role of cyclic AMP signaling in obesity and diagnostic implications. J Clin Endocrinol Metab. 2014 Feb; 99(2):E303-10. London E, Rothenbuhler A, Lodish M, Gourgari E, Keil M, Lyssikatos C, de la Luz Sierra M, Patronas N, Nesterova M, Stratakis CA. PMID: 24248186; PMCID: PMC3913816.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    111. Racial disparities in pubertal development. Semin Reprod Med. 2013 Sep; 31(5):333-9. Ramnitz MS, Lodish MB. PMID: 23934693.
      View in: PubMed   Mentions: 28     Fields:    Translation:Humans
    112. Vandetanib in children and adolescents with multiple endocrine neoplasia type 2B associated medullary thyroid carcinoma. Clin Cancer Res. 2013 Aug 01; 19(15):4239-48. Fox E, Widemann BC, Chuk MK, Marcus L, Aikin A, Whitcomb PO, Merino MJ, Lodish M, Dombi E, Steinberg SM, Wells SA, Balis FM. PMID: 23766359; PMCID: PMC4274128.
      View in: PubMed   Mentions: 49     Fields:    Translation:HumansCTClinical Trials
    113. Multiple endocrine neoplasia type 2. Front Horm Res. 2013; 41:16-29. Lodish M. PMID: 23652668.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    114. Clinical review: kinase inhibitors: adverse effects related to the endocrine system. J Clin Endocrinol Metab. 2013 Apr; 98(4):1333-42. Lodish MB. PMID: 23450053; PMCID: PMC3615204.
      View in: PubMed   Mentions: 34     Fields:    Translation:Humans
    115. Bone mineral density in children and young adults with neurofibromatosis type 1. Endocr Relat Cancer. 2012 Dec; 19(6):817-25. Lodish MB, Dagalakis U, Sinaii N, Bornstein E, Kim A, Lokie KB, Baldwin AM, Reynolds JC, Dombi E, Stratakis CA, Widemann BC. PMID: 23089139; PMCID: PMC4132947.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    116. Identification of novel genetic variants in phosphodiesterase 8B (PDE8B), a cAMP-specific phosphodiesterase highly expressed in the adrenal cortex, in a cohort of patients with adrenal tumours. Clin Endocrinol (Oxf). 2012 Aug; 77(2):195-9. Rothenbuhler A, Horvath A, Libé R, Faucz FR, Fratticci A, Raffin Sanson ML, Vezzosi D, Azevedo M, Levy I, Almeida MQ, Lodish M, Nesterova M, Bertherat J, Stratakis CA. PMID: 22335482; PMCID: PMC3360985.
      View in: PubMed   Mentions: 36     Fields:    Translation:Humans
    117. Recovery of the hypothalamic-pituitary-adrenal axis in children and adolescents after surgical cure of Cushing's disease. J Clin Endocrinol Metab. 2012 May; 97(5):1483-91. Lodish M, Dunn SV, Sinaii N, Keil MF, Stratakis CA. PMID: 22399509; PMCID: PMC3339895.
      View in: PubMed   Mentions: 23     Fields:    Translation:Humans
    118. Lack of mutations in the gene coding for the hGR (NR3C1) in a pediatric patient with ACTH-secreting pituitary adenoma, absence of stigmata of Cushing's syndrome and unusual histologic features. J Pediatr Endocrinol Metab. 2012; 25(1-2):213-9. Briassoulis G, Horvath A, Christoforou P, Lodish M, Xekouki P, Quezado M, Patronas N, Keil MF, Stratakis CA. PMID: 22570980; PMCID: PMC5590677.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    119. Known VDR polymorphisms are not associated with bone mineral density measures in pediatric Cushing disease. J Pediatr Endocrinol Metab. 2012; 25(1-2):221-3. Lodish MB, Mastroyannis SA, Sinaii N, Boikos SA, Stratakis CA. PMID: 22570981; PMCID: PMC4034061.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    120. (111)In-octreotide scintigraphy for identification of metastatic medullary thyroid carcinoma in children and adolescents. J Clin Endocrinol Metab. 2012 Feb; 97(2):E207-12. Lodish M, Dagalakis U, Chen CC, Sinaii N, Whitcomb P, Aikin A, Dombi E, Marcus L, Widemann B, Fox E, Chuk M, Balis F, Wells S, Stratakis CA. PMID: 22162469; PMCID: PMC3275365.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCTClinical Trials
    121. Metastatic pheochromocytoma/paraganglioma related to primary tumor development in childhood or adolescence: significant link to SDHB mutations. J Clin Oncol. 2011 Nov 01; 29(31):4137-42. King KS, Prodanov T, Kantorovich V, Fojo T, Hewitt JK, Zacharin M, Wesley R, Lodish M, Raygada M, Gimenez-Roqueplo AP, McCormack S, Eisenhofer G, Milosevic D, Kebebew E, Stratakis CA, Pacak K. PMID: 21969497; PMCID: PMC3208535.
      View in: PubMed   Mentions: 80     Fields:    Translation:Humans
    122. The differential diagnosis of familial lentiginosis syndromes. Fam Cancer. 2011 Sep; 10(3):481-90. Lodish MB, Stratakis CA. PMID: 21538076; PMCID: PMC3417307.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    123. Defects in succinate dehydrogenase in gastrointestinal stromal tumors lacking KIT and PDGFRA mutations. Proc Natl Acad Sci U S A. 2011 Jan 04; 108(1):314-8. Janeway KA, Kim SY, Lodish M, Nosé V, Rustin P, Gaal J, Dahia PL, Liegl B, Ball ER, Raygada M, Lai AH, Kelly L, Hornick JL, NIH Pediatric and Wild-Type GIST Clinic, O'Sullivan M, de Krijger RR, Dinjens WN, Demetri GD, Antonescu CR, Fletcher JA, Helman L, Stratakis CA. PMID: 21173220; PMCID: PMC3017134.
      View in: PubMed   Mentions: 260     Fields:    Translation:Humans
    124. Rare and unusual endocrine cancer syndromes with mutated genes. Semin Oncol. 2010 Dec; 37(6):680-90. Lodish MB, Stratakis CA. PMID: 21167385; PMCID: PMC3053053.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    125. Frequent phosphodiesterase 11A gene (PDE11A) defects in patients with Carney complex (CNC) caused by PRKAR1A mutations: PDE11A may contribute to adrenal and testicular tumors in CNC as a modifier of the phenotype. J Clin Endocrinol Metab. 2011 Jan; 96(1):E208-14. Libé R, Horvath A, Vezzosi D, Fratticci A, Coste J, Perlemoine K, Ragazzon B, Guillaud-Bataille M, Groussin L, Clauser E, Raffin-Sanson ML, Siegel J, Moran J, Drori-Herishanu L, Faucz FR, Lodish M, Nesterova M, Bertagna X, Bertherat J, Stratakis CA. PMID: 21047926; PMCID: PMC3038483.
      View in: PubMed   Mentions: 48     Fields:    Translation:HumansCells
    126. The role of germline AIP, MEN1, PRKAR1A, CDKN1B and CDKN2C mutations in causing pituitary adenomas in a large cohort of children, adolescents, and patients with genetic syndromes. Clin Genet. 2010 Nov; 78(5):457-63. Stratakis CA, Tichomirowa MA, Boikos S, Azevedo MF, Lodish M, Martari M, Verma S, Daly AF, Raygada M, Keil MF, Papademetriou J, Drori-Herishanu L, Horvath A, Tsang KM, Nesterova M, Franklin S, Vanbellinghen JF, Bours V, Salvatori R, Beckers A. PMID: 20507346; PMCID: PMC3050035.
      View in: PubMed   Mentions: 81     Fields:    Translation:Humans
    127. SDHB immunohistochemistry: a useful tool in the diagnosis of Carney-Stratakis and Carney triad gastrointestinal stromal tumors. Mod Pathol. 2011 Jan; 24(1):147-51. Gaal J, Stratakis CA, Carney JA, Ball ER, Korpershoek E, Lodish MB, Levy I, Xekouki P, van Nederveen FH, den Bakker MA, O'Sullivan M, Dinjens WN, de Krijger RR. PMID: 20890271; PMCID: PMC3415983.
      View in: PubMed   Mentions: 63     Fields:    Translation:HumansCells
    128. Endocrine side effects of broad-acting kinase inhibitors. Endocr Relat Cancer. 2010 Sep; 17(3):R233-44. Lodish MB, Stratakis CA. PMID: 20603395; PMCID: PMC3039175.
      View in: PubMed   Mentions: 25     Fields:    Translation:HumansAnimals
    129. Succinate dehydrogenase gene mutations are strongly associated with paraganglioma of the organ of Zuckerkandl. Endocr Relat Cancer. 2010 Sep; 17(3):581-8. Lodish MB, Adams KT, Huynh TT, Prodanov T, Ling A, Chen C, Shusterman S, Jimenez C, Merino M, Hughes M, Cradic KW, Milosevic D, Singh RJ, Stratakis CA, Pacak K. PMID: 20418362; PMCID: PMC3417306.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    130. Endocrine tumours in neurofibromatosis type 1, tuberous sclerosis and related syndromes. Best Pract Res Clin Endocrinol Metab. 2010 Jun; 24(3):439-49. Lodish MB, Stratakis CA. PMID: 20833335; PMCID: PMC2939061.
      View in: PubMed   Mentions: 34     Fields:    Translation:Humans
    131. Intrauterine growth retardation associated with precocious puberty and sertoli cell hyperplasia. Horm Metab Res. 2010 Aug; 42(9):682-8. Lodish MB, Gartner LA, Albini P, Sabnis G, Brodie A, Meck JM, Meloni-Ehrig AM, Hill S, Tsilou E, Valera VA, Walter BA, Merino MJ, Stratakis CA. PMID: 20411478; PMCID: PMC3412584.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    132. Effects of Cushing disease on bone mineral density in a pediatric population. J Pediatr. 2010 Jun; 156(6):1001-1005. Lodish MB, Hsiao HP, Serbis A, Sinaii N, Rothenbuhler A, Keil MF, Boikos SA, Reynolds JC, Stratakis CA. PMID: 20223476; PMCID: PMC2875346.
      View in: PubMed   Mentions: 21     Fields:    Translation:Humans
    133. Pseudotumor cerebri after surgical remission of Cushing's disease. J Clin Endocrinol Metab. 2010 Apr; 95(4):1528-32. Kiehna EN, Keil M, Lodish M, Stratakis C, Oldfield EH. PMID: 20164289; PMCID: PMC2853987.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    134. The growth hormone receptor (GHR) polymorphism in growth-retarded children with Cushing disease: lack of association with growth and measures of the somatotropic axis. Horm Metab Res. 2010 Mar; 42(3):194-7. Drori-Herishanu L, Lodish M, Verma S, Bimpaki E, Keil MF, Horvath A, Stratakis CA. PMID: 20013551; PMCID: PMC3412355.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    135. Reversible posterior encephalopathy syndrome associated with micronodular adrenocortical disease and Cushing syndrome. Eur J Pediatr. 2010 Jan; 169(1):125-6. Lodish M, Patronas NJ, Stratakis CA. PMID: 19415327; PMCID: PMC3124700.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    136. An Intronic mutation is associated with prolactinoma in a young boy, decreased penetrance in his large family, and variable effects on MEN1 mRNA and protein. Horm Metab Res. 2009 Aug; 41(8):630-4. Drori-Herishanu L, Horvath A, Nesterova M, Patronas Y, Lodish M, Bimpaki E, Patronas N, Agarwal S, Salvatori R, Martari M, Mericq V, Stratakis CA. PMID: 19391077; PMCID: PMC3124761.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    137. Blood pressure in pediatric patients with Cushing syndrome. J Clin Endocrinol Metab. 2009 Jun; 94(6):2002-8. Lodish MB, Sinaii N, Patronas N, Batista DL, Keil M, Samuel J, Moran J, Verma S, Popovic J, Stratakis CA. PMID: 19293264; PMCID: PMC2690429.
      View in: PubMed   Mentions: 28     Fields:    Translation:Humans
    138. Extensive and largely reversible ischemic cerebral infarctions in a prepubertal child with hypertension and Cushing disease. J Clin Endocrinol Metab. 2009 Jan; 94(1):1-2. Nguyen JH, Lodish MB, Patronas NJ, Ugrasbul F, Keil MF, Roberts MD, Popovic J, Stratakis CA. PMID: 19126630; PMCID: PMC2630863.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    139. RET oncogene in MEN2, MEN2B, MTC and other forms of thyroid cancer. Expert Rev Anticancer Ther. 2008 Apr; 8(4):625-32. Lodish MB, Stratakis CA. PMID: 18402529; PMCID: PMC2670186.
      View in: PubMed   Mentions: 37     Fields:    Translation:Humans
    140. Insulinoma and gastrinoma syndromes from a single intrapancreatic neuroendocrine tumor. J Clin Endocrinol Metab. 2008 Apr; 93(4):1123-8. Lodish MB, Powell AC, Abu-Asab M, Cochran C, Lenz P, Libutti SK, Pingpank JF, Tsokos M, Gorden P. PMID: 18252785; PMCID: PMC2291484.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    141. GATA-factor dependence of the multitype zinc-finger protein FOG-1 for its essential role in megakaryopoiesis. Proc Natl Acad Sci U S A. 2002 Jul 09; 99(14):9237-42. Chang AN, Cantor AB, Fujiwara Y, Lodish MB, Droho S, Crispino JD, Orkin SH. PMID: 12077323; PMCID: PMC123124.
      View in: PubMed   Mentions: 69     Fields:    Translation:AnimalsCells
    142. Proper coronary vascular development and heart morphogenesis depend on interaction of GATA-4 with FOG cofactors. Genes Dev. 2001 Apr 01; 15(7):839-44. Crispino JD, Lodish MB, Thurberg BL, Litovsky SH, Collins T, Molkentin JD, Orkin SH. PMID: 11297508; PMCID: PMC312667.
      View in: PubMed   Mentions: 101     Fields:    Translation:AnimalsCells
    143. Use of altered specificity mutants to probe a specific protein-protein interaction in differentiation: the GATA-1:FOG complex. Mol Cell. 1999 Feb; 3(2):219-28. Crispino JD, Lodish MB, MacKay JP, Orkin SH. PMID: 10078204.
      View in: PubMed   Mentions: 121     Fields:    Translation:AnimalsCells
    144. Autotransplantation of pancreatic islet cell fragments into the renal capsule prepared without collagenase. Am Surg. 1984 Dec; 50(12):679-81. Toledo-Pereyra LH, Rowlett AL, Lodish M. PMID: 6095710.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
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