Jonathan Strober, MD

Title(s)Professor, Neurology
SchoolSchool of Medicine
Address550 16th Street, #5104
San Francisco CA 94158
Phone415-353-3652
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    Other Positions
    Title(s)UCSF Weill Institute for Neurosciences


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    University of California, San Francisco, CA2017Diversity, Equity, and Inclusion Champion Training

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    PEDIATRIC CLINICAL RESEARCH CENTER
    NIH M01RR001271Dec 1, 1981 - Mar 31, 2007
    Role: Co-Investigator

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    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. Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability. Am J Hum Genet. 2025 Jan 02; 112(1):75-86. Sabeh P, Dumas SA, Maios C, Daghar H, Korzeniowski M, Rousseau J, Lines M, Guerin A, Millichap JJ, Landsverk M, Grebe T, Lindstrom K, Strober J, Ait Mouhoub T, Zweier C, Steinraths M, Hebebrand M, Callewaert B, Abou Jamra R, Kautza-Lucht M, Wegler M, Kruszka P, Kumps C, Banne E, Waberski MB, Dieux A, Raible S, Krantz I, Medne L, Pechter K, Villard L, Guerrini R, Bianchini C, Barba C, Mei D, Blanc X, Kallay C, Ranza E, Yang XR, O'Heir E, Donald KA, Murugasen S, Bruwer Z, Calikoglu M, Mathews JM, Lesieur-Sebellin M, Baujat G, Derive N, Pierson TM, Murrell JR, Shillington A, Ormieres C, Rondeau S, Reis A, Fernandez-Jaen A, Au PYB, Sweetser DA, Briere LC, Couque N, Perrin L, Schymick J, Gueguen P, Lefebvre M, Van Andel M, Juusola J, Antonarakis SE, Parker JA, Burnett BG, Campeau PM. PMID: 39721588; PMCID: PMC11739880.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimalsCells
    2. 333P Real-World symptom progression in Duchenne muscular dystrophy patients in Europe, Japan, and the USA: results from a multi-national survey. Neuromuscular Disorders. 2024 Oct 1; 43:104441.664. Talaga TA, Strober SJ, Ishigaki IK, Posner PN, Cappelleri CJ, Dukacz DS, Aslam AZ, Morton ME, Iqbal IH, Chatterton CE, DeCourcy DJ. .
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    3. 332P Physician and caregiver concordance in Duchenne muscular dystrophy patients in Europe, Japan, and the USA: a multi-national survey. Neuromuscular Disorders. 2024 Oct 1; 43:104441.663. Talaga TA, Strober SJ, Ishigaki IK, Posner PN, Cappelleri CJ, Dukacz DS, Aslam AZ, Morton ME, Iqbal IH, Chatterton CE, DeCourcy DJ. .
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    4. Analysis of Gender Discrepancies in Leadership Roles and Recognition Awards in the Child Neurology Society. Neurology. 2024 Sep 10; 103(5):e209746. Martindale JM, Christy AL, Gombolay GY, Aravamuthan BR, Jansen L, Joshi S, Strober JB, Terrell M, Tilton AH, Pearl PL, Silver JK, Mink JW, Khakoo Y. PMID: 39159414; PMCID: PMC11338498.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    5. Characteristics, Treatment Patterns, and Disease Burden of Juvenile Myasthenia Gravis in the United States (P4-11.017). Neurology. 2024 Apr 9; 102(17_supplement_1). Zhou ZJ, Nilius NS, Pilipczuk PO, Scowcroft SA, Tarancón TT, Tennigkeit TF, Zaremba ZP, Brandsema BJ, Strober SJ. .
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    6. RWD130 Healthcare Resource Utilization for Pediatric and Adolescent Duchenne Muscular Dystrophy Patients: Analysis of Real-World Data. Value in Health. 2023 Dec 1; 26(12):s529. Strober SJ, Ishigaki IK, Merla MV, Posner PN, Cappelleri CJ, Xiao XS, Talaga TA, Brunner BS, Iqbal IH, Chatterton CE, Hatchell HN. .
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    7. PCR141 The Impact of Duchenne Muscular Dystrophy on Caregiver Employment: A Survey in Europe, Japan, and the United States. Value in Health. 2023 Dec 1; 26(12):s476. Strober SJ, Ishigaki IK, Merla MV, Posner PN, Cappelleri CJ, Xiao XS, Talaga TA, Brunner BS, Morton ME, Olsen OS, de Courcy dJ. .
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    8. Author Correction: Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population. NPJ Genom Med. 2023 Oct 23; 8(1):34. Slavotinek A, Rego S, Sahin-Hodoglugil N, Kvale M, Lianoglou B, Yip T, Hoban H, Outram S, Anguiano B, Chen F, Michelson J, Cilio RM, Curry C, Gallagher RC, Gardner M, Kuperman R, Mendelsohn B, Sherr E, Shieh J, Strober J, Tam A, Tenney J, Weiss W, Whittle A, Chin G, Faubel A, Prasad H, Mavura Y, Van Ziffle J, Devine WP, Hodoglugil U, Martin PM, Sparks TN, Koenig B, Ackerman S, Risch N, Kwok PY, Norton ME. PMID: 37872195; PMCID: PMC10593851.
      View in: PubMed   Mentions:
    9. Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population. NPJ Genom Med. 2023 May 26; 8(1):10. Slavotinek A, Rego S, Sahin-Hodoglugil N, Kvale M, Lianoglou B, Yip T, Hoban H, Outram S, Anguiano B, Chen F, Michelson J, Cilio RM, Curry C, Gallagher RC, Gardner M, Kuperman R, Mendelsohn B, Sherr E, Shieh J, Strober J, Tam A, Tenney J, Weiss W, Whittle A, Chin G, Faubel A, Prasad H, Mavura Y, Van Ziffle J, Devine WP, Hodoglugil U, Martin PM, Sparks TN, Koenig B, Ackerman S, Risch N, Kwok PY, Norton ME. PMID: 37236975; PMCID: PMC10220040.
      View in: PubMed   Mentions: 16  
    10. Sexual and Gender Diversity in Pediatric Neurology: Why We Care. Pediatr Neurol. 2023 Aug; 145:28-29. Christy A, Martindale J, Hranilovich J, Orozco-Poore C, Kernan-Schloss F, Anderson CTM, Strober J, Mitchell W, Lerario MP. PMID: 37257397.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    11. Sphingosine Phosphate Lyase Is Upregulated in Duchenne Muscular Dystrophy, and Its Inhibition Early in Life Attenuates Inflammation and Dystrophy in Mdx Mice. Int J Mol Sci. 2022 Jul 08; 23(14). De la Garza-Rodea AS, Moore SA, Zamora-Pineda J, Hoffman EP, Mistry K, Kumar A, Strober JB, Zhao P, Suh JH, Saba JD. PMID: 35886926; PMCID: PMC9316262.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimals
    12. Introducing the Child Neurology Society Leadership, Diversity, Equity, and Inclusion Task Force. Ann Neurol. 2021 10; 90(4):537-538. Brumback AC, Wilson RB, Augustine EF, Bass NE, Bassuk AG, Cejas DM, Shellhaas RA, Strober JB, Tilton AC, Pearl PL. PMID: 34288089.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    13. Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature. Am J Hum Genet. 2021 06 03; 108(6):1053-1068. Rots D, Chater-Diehl E, Dingemans AJM, Goodman SJ, Siu MT, Cytrynbaum C, Choufani S, Hoang N, Walker S, Awamleh Z, Charkow J, Meyn S, Pfundt R, Rinne T, Gardeitchik T, de Vries BBA, Deden AC, Leenders E, Kwint M, Stumpel CTRM, Stevens SJC, Vermeulen JR, van Harssel JVT, Bosch DGM, van Gassen KLI, van Binsbergen E, de Geus CM, Brackel H, Hempel M, Lessel D, Denecke J, Slavotinek A, Strober J, Crunk A, Folk L, Wentzensen IM, Yang H, Zou F, Millan F, Person R, Xie Y, Liu S, Ousager LB, Larsen M, Schultz-Rogers L, Morava E, Klee EW, Berry IR, Campbell J, Lindstrom K, Pruniski B, Neumeyer AM, Radley JA, Phornphutkul C, Schmidt B, Wilson WG, Õunap K, Reinson K, Pajusalu S, van Haeringen A, Ruivenkamp C, Cuperus R, Santos-Simarro F, Palomares-Bralo M, Pacio-Míguez M, Ritter A, Bhoj E, Tønne E, Tveten K, Cappuccio G, Brunetti-Pierri N, Rowe L, Bunn J, Saenz M, Platzer K, Mertens M, Caluseriu O, Nowaczyk MJM, Cohn RD, Kannu P, Alkhunaizi E, Chitayat D, Scherer SW, Brunner HG, Vissers LELM, Kleefstra T, Koolen DA, Weksberg R. PMID: 33909990; PMCID: PMC8206150.
      View in: PubMed   Mentions: 29     Fields:    Translation:HumansCells
    14. Pathologic Findings Associated With a Case of Acute Flaccid Myelitis. J Neuropathol Exp Neurol. 2021 Apr 16; 80(5):484-487. Haddad AF, Hofmann JW, Oh T, Jacques L, Yu G, Chiu C, Nolan A, Strober J, Gupta N. PMID: 33870421.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    15. Targeted Treatments for Inherited Neuromuscular Diseases of Childhood. Semin Neurol. 2020 Jun; 40(3):335-341. Fay AJ, Knox R, Neil EE, Strober J. PMID: 32294764.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    16. Pathogenic WDFY3 variants cause neurodevelopmental disorders and opposing effects on brain size. Brain. 2019 09 01; 142(9):2617-2630. Le Duc D, Giulivi C, Hiatt SM, Napoli E, Panoutsopoulos A, Harlan De Crescenzo A, Kotzaeridou U, Syrbe S, Anagnostou E, Azage M, Bend R, Begtrup A, Brown NJ, Büttner B, Cho MT, Cooper GM, Doering JH, Dubourg C, Everman DB, Hildebrand MS, Santos FJR, Kellam B, Keller-Ramey J, Lemke JR, Liu S, Niyazov D, Payne K, Person R, Quélin C, Schnur RE, Smith BT, Strober J, Walker S, Wallis M, Walsh L, Yang S, Yuen RKC, Ziegler A, Sticht H, Pride MC, Orosco L, Martínez-Cerdeño V, Silverman JL, Crawley JN, Scherer SW, Zarbalis KS, Jamra R. PMID: 31327001; PMCID: PMC6736092.
      View in: PubMed   Mentions: 23     Fields:    Translation:HumansAnimalsCells
    17. Long-Term Safety, Immunologic Response, and Imaging Outcomes following Neural Stem Cell Transplantation for Pelizaeus-Merzbacher Disease. Stem Cell Reports. 2019 08 13; 13(2):254-261. Gupta N, Henry RG, Kang SM, Strober J, Lim DA, Ryan T, Perry R, Farrell J, Ulman M, Rajalingam R, Gage A, Huhn SL, Barkovich AJ, Rowitch DH. PMID: 31378671; PMCID: PMC6700500.
      View in: PubMed   Mentions: 26     Fields:    
    18. Presynaptic congenital myasthenic syndrome with altered synaptic vesicle homeostasis linked to compound heterozygous sequence variants in RPH3A. Mol Genet Genomic Med. 2018 05; 6(3):434-440. Maselli RA, Vázquez J, Schrumpf L, Arredondo J, Lara M, Strober JB, Pytel P, Wollmann RL, Ferns M. PMID: 29441694; PMCID: PMC6014458.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    19. 45 Parainfectious and Postinfectious Neurologic Syndromes. Principles and Practice of Pediatric Infectious Diseases. 2018 Jan 1; (MMWR Morb Mortal Wkly Rep632014):323-328.e1. Strober SJ, Glaser GC. .
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    20. Clinical Reasoning: A 16-year-old girl with subacute weakness and sensory loss. Neurology. 2017 06 06; 88(23):e225-e229. Quintanilla-Bordás C, Nourbakhsh B, Strober J, Raffel C, Waubant E. PMID: 28583938.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    21. Serial prenatal and postnatal MRI of dystroglycanopathy in a patient with familial B3GALNT2 mutation. Pediatr Radiol. 2017 Jun; 47(7):884-888. Ho ML, Glenn OA, Sherr EH, Strober JB. PMID: 28303321.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    22. 148 Congenital Myopathies. Swaiman\u0027s Pediatric Neurology. 2017 Jan 1; 1123-1130. Dastgir DJ, Gonorazky GH, Strober SJ, Chrestian CN, Dowling DJ. .
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    23. Clinical Course of Six Children With GNAO1 Mutations Causing a Severe and Distinctive Movement Disorder. Pediatr Neurol. 2016 06; 59:81-4. Ananth AL, Robichaux-Viehoever A, Kim YM, Hanson-Kahn A, Cox R, Enns GM, Strober J, Willing M, Schlaggar BL, Wu YW, Bernstein JA. PMID: 27068059.
      View in: PubMed   Mentions: 27     Fields:    Translation:Humans
    24. Acute Flaccid Myelitis of Unknown Etiology in California, 2012-2015. JAMA. 2015 Dec 22-29; 314(24):2663-71. Van Haren K, Ayscue P, Waubant E, Clayton A, Sheriff H, Yagi S, Glenn-Finer R, Padilla T, Strober JB, Aldrovandi G, Wadford DA, Chiu CY, Xia D, Harriman K, Watt JP, Glaser CA. PMID: 26720027.
      View in: PubMed   Mentions: 52     Fields:    Translation:HumansCells
    25. Novel KIF7 missense substitutions in two patients presenting with multiple malformations and features of acrocallosal syndrome. Am J Med Genet A. 2015 Nov; 167A(11):2767-76. Tunovic S, Barañano KW, Barkovich JA, Strober JB, Jamal L, Slavotinek AM. PMID: 26174511.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    26. De novo mutations in KIF1A cause progressive encephalopathy and brain atrophy. Ann Clin Transl Neurol. 2015 Jun; 2(6):623-35. Esmaeeli Nieh S, Madou MR, Sirajuddin M, Fregeau B, McKnight D, Lexa K, Strober J, Spaeth C, Hallinan BE, Smaoui N, Pappas JG, Burrow TA, McDonald MT, Latibashvili M, Leshinsky-Silver E, Lev D, Blumkin L, Vale RD, Barkovich AJ, Sherr EH. PMID: 26125038; PMCID: PMC4479523.
      View in: PubMed   Mentions: 48     Fields:    
    27. Measuring quality of life in muscular dystrophy. Neurology. 2015 Mar 10; 84(10):1034-42. Bann CM, Abresch RT, Biesecker B, Conway KC, Heatwole C, Peay H, Scal P, Strober J, Uzark K, Wolff J, Margolis M, Blackwell A, Street N, Montesanti A, Bolen J. PMID: 25663223; PMCID: PMC4352095.
      View in: PubMed   Mentions: 11     Fields:    
    28. Infant botulism: review and clinical update. Pediatr Neurol. 2015 May; 52(5):487-92. Rosow LK, Strober JB. PMID: 25882077.
      View in: PubMed   Mentions: 32     Fields:    Translation:Humans
    29. 488. Critical Care Medicine. 2014 Dec 1; 42(12):a1477-a1478. Patel PP, Glaser GC, Samuel SM, Strober SJ, Flori FH. .
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    30. Quantitative MRI analysis in children with multiple sclerosis: a multicenter feasibility pilot study. BMC Neurol. 2013 Nov 13; 13:173. Chitnis T, Guttmann CR, Zaitsev A, Musallam A, Weinstock-Guttman B, Yeh A, Rodriguez M, Ness J, Gorman MP, Healy BC, Kuntz N, Chabas D, Strober JB, Waubant E, Krupp L, Pelletier D, Erickson B, Bergsland N, Zivadinov R, U.S. Network of Pediatric MS Centers of Excellence. PMID: 24225378; PMCID: PMC3832402.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    31. Neural stem cell engraftment and myelination in the human brain. Sci Transl Med. 2012 Oct 10; 4(155):155ra137. Gupta N, Henry RG, Strober J, Kang SM, Lim DA, Bucci M, Caverzasi E, Gaetano L, Mandelli ML, Ryan T, Perry R, Farrell J, Jeremy RJ, Ulman M, Huhn SL, Barkovich AJ, Rowitch DH. PMID: 23052294; PMCID: PMC3893824.
      View in: PubMed   Mentions: 119     Fields:    Translation:HumansCellsCTClinical Trials
    32. Neurological symptoms in individuals with fibrodysplasia ossificans progressiva. J Neurol. 2012 Dec; 259(12):2636-43. Kitterman JA, Strober JB, Kan L, Rocke DM, Cali A, Peeper J, Snow J, Delai PL, Morhart R, Pignolo RJ, Shore EM, Kaplan FS. PMID: 22752062; PMCID: PMC3523705.
      View in: PubMed   Mentions: 27     Fields:    Translation:Humans
    33. EBV, CMV, and HSV IgG Titers Are Not Predictive of Subsequent Relapse Risk in Pediatric Multiple Sclerosis (P02.096). Neurology. 2012 Apr 24; 78(Meeting Abstracts 1):p02.096-p02.096. Graves GJ, Krupp KL, Weinstock-Guttman WB, Strober SJ, Belman BA, Yeh YE, Ness NJ, Gorman GM, Rodriguez RM, Chitnis CT, Waubant WE. .
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    34. Chapter 93 Congenital Myopathies. Swaiman\u0027s Pediatric Neurology. 2012 Jan 1; 1607-1612. Strober SJ. .
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    35. 45 Para- and Postinfectious Neurologic Syndromes. . 2012 Jan 1; 314-319.e1. Glaser GC, Strober SJ. .
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    36. Relapse severity and recovery in early pediatric multiple sclerosis. Mult Scler. 2012 Jul; 18(7):1008-12. Fay AJ, Mowry EM, Strober J, Waubant E. PMID: 22183939.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    37. Common viruses associated with lower pediatric multiple sclerosis risk. Neurology. 2011 Jun 07; 76(23):1989-95. Waubant E, Mowry EM, Krupp L, Chitnis T, Yeh EA, Kuntz N, Ness J, Chabas D, Strober J, McDonald J, Belman A, Milazzo M, Gorman M, Weinstock-Guttman B, Rodriguez M, Oksenberg JR, James JA, US Pediatric MS Network. PMID: 21646624; PMCID: PMC3109881.
      View in: PubMed   Mentions: 50     Fields:    Translation:Humans
    38. Pediatric multiple sclerosis. Neurol Clin. 2011 May; 29(2):481-505. Chitnis T, Krupp L, Yeh A, Rubin J, Kuntz N, Strober JB, Chabas D, Weinstock-Guttmann B, Ness J, Rodriguez M, Waubant E. PMID: 21439455.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    39. Treatment of hypokalemic periodic paralysis with topiramate. Muscle Nerve. 2011 Jan; 43(1):127-9. Fiore DM, Strober JB. PMID: 21171065.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    40. A 41-year-old man with new headache and altered mental status. Neurohospitalist. 2011 Jan; 1(1):48-54. Johnson EC, West TW, Ko NU, Strober JB. PMID: 23983837; PMCID: PMC3726099.
      View in: PubMed   Mentions: 4  
    41. Differential diagnosis of multiple sclerosis and acquired central nervous system demyelinating disorders in children and adolescents. Demyelinating Disorders of the Central Nervous System in Childhood. 2011 Jan 1; 58-74. Kuntz KN, Strober SJ. .
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    42. Health-related quality of life is reduced in pediatric multiple sclerosis. Pediatr Neurol. 2010 Aug; 43(2):97-102. Mowry EM, Julian LJ, Im-Wang S, Chabas D, Galvin AJ, Strober JB, Waubant E. PMID: 20610119.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    43. Extensive FUS-immunoreactive pathology in juvenile amyotrophic lateral sclerosis with basophilic inclusions. Brain Pathol. 2010 Nov; 20(6):1069-76. Huang EJ, Zhang J, Geser F, Trojanowski JQ, Strober JB, Dickson DW, Brown RH, Shapiro BE, Lomen-Hoerth C. PMID: 20579074; PMCID: PMC2951498.
      View in: PubMed   Mentions: 68     Fields:    Translation:HumansCells
    44. Vitamin D status is associated with relapse rate in pediatric-onset multiple sclerosis. Ann Neurol. 2010 May; 67(5):618-24. Mowry EM, Krupp LB, Milazzo M, Chabas D, Strober JB, Belman AL, McDonald JC, Oksenberg JR, Bacchetti P, Waubant E. PMID: 20437559.
      View in: PubMed   Mentions: 118     Fields:    Translation:Humans
    45. Acute necrotizing encephalopathy in 3 brothers. Pediatrics. 2010 Mar; 125(3):e693-8. Marco EJ, Anderson JE, Neilson DE, Strober JB. PMID: 20142283; PMCID: PMC3207236.
      View in: PubMed   Mentions: 20     Fields:    Translation:Humans
    46. Younger children with MS have a distinct CSF inflammatory profile at disease onset. Neurology. 2010 Feb 02; 74(5):399-405. Chabas D, Ness J, Belman A, Yeh EA, Kuntz N, Gorman MP, Strober JB, De Kouchkovsky I, McCulloch C, Chitnis T, Rodriguez M, Weinstock-Guttman B, Krupp LB, Waubant E, US Network of Pediatric MS Centers of Excellence. PMID: 20124205; PMCID: PMC2816008.
      View in: PubMed   Mentions: 32     Fields:    Translation:Humans
    47. Difference in disease burden and activity in pediatric patients on brain magnetic resonance imaging at time of multiple sclerosis onset vs adults. Arch Neurol. 2009 Aug; 66(8):967-71. Waubant E, Chabas D, Okuda DT, Glenn O, Mowry E, Henry RG, Strober JB, Soares B, Wintermark M, Pelletier D. PMID: 19667217.
      View in: PubMed   Mentions: 53     Fields:    Translation:Humans
    48. Allogeneic hematopoietic cell transplantation for refractory myasthenia gravis. Arch Neurol. 2009 May; 66(5):659-61. Strober J, Cowan MJ, Horn BN. PMID: 19433668.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansCells
    49. Vanishing MS T2-bright lesions before puberty: a distinct MRI phenotype? Neurology. 2008 Sep 30; 71(14):1090-3. Chabas D, Castillo-Trivino T, Mowry EM, Strober JB, Glenn OA, Waubant E. PMID: 18824673.
      View in: PubMed   Mentions: 31     Fields:    Translation:HumansCells
    50. Pediatric multiple sclerosis. Curr Neurol Neurosci Rep. 2008 Sep; 8(5):434-41. Chabas D, Strober J, Waubant E. PMID: 18713581.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    51. Magnetic resonance neurography in children with birth-related brachial plexus injury. Pediatr Radiol. 2008 Feb; 38(2):159-63. Smith AB, Gupta N, Strober J, Chin C. PMID: 18034234.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    52. G.P.4.15 CAPN3 mutations in patients with idiopathic eosinophilic myositis: A predystrophic stage of LGMD2A?. Neuromuscular Disorders. 2007 Oct 1; 17(9-10):791-792. Krahn KM, Hanisch HF, Goicoechea GM, Groen GE, Pécheux PC, Garcia-Bragado GF, Layzer LR, Leturcq LF, Strober SJ, Urtizberea UJ, Sáenz SA, Bushby BK, Lévy LN, de Munain dA. .
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    53. G.P.6.07 Mycophenolate mofetil’s beneficial effects on skeletal muscle in the mdx mouse. Neuromuscular Disorders. 2007 Oct 1; 17(9-10):803. Strober SJ, Rando RT. .
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    54. Do all patients with Duchenne muscular dystrophy require surgery for the correction of scoliosis? Nat Clin Pract Neurol. 2007 Jan; 3(1):18-9. Strober JB. PMID: 17205069.
      View in: PubMed   Mentions:    Fields:    
    55. Therapeutics in duchenne muscular dystrophy. NeuroRx. 2006 Apr; 3(2):225-34. Strober JB. PMID: 16554260; PMCID: PMC3593432.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansAnimals
    56. Long-term follow-up after thymectomy for myasthenia gravis: thoracoscopic vs open. J Pediatr Surg. 2006 Jan; 41(1):50-4; discussion 50-4. Wagner AJ, Cortes RA, Strober J, Grethel EJ, Clifton MS, Harrison MR, Farmer DL, Nobuhara KK, Lee H. PMID: 16410107.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    57. Recent advances in infant botulism. Pediatr Neurol. 2005 Mar; 32(3):149-54. Fox CK, Keet CA, Strober JB. PMID: 15730893.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCells
    58. Infant botulism, type F, presenting at 54 hours of life. Pediatr Neurol. 2005 Mar; 32(3):193-6. Keet CA, Fox CK, Margeta M, Marco E, Shane AL, Dearmond SJ, Strober JB, Miller SP. PMID: 15730901.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    59. Genetics of pediatric neuromuscular disease. Curr Opin Pediatr. 2000 Dec; 12(6):549-53. Strober JB. PMID: 11106273.
      View in: PubMed   Mentions: 1  Translation:Humans
    60. Progressive spinal muscular atrophies. J Child Neurol. 1999 Nov; 14(11):691-5. Strober JB, Tennekoon GI. PMID: 10593543.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    61. A 15-year-old with back pain, fever, and leg numbness. Semin Pediatr Neurol. 1999 Sep; 6(3):190-4; discussion 194-5. Strober JB, Zuppa A, Brooks-Kayal AR. PMID: 10522338.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    62. The incidence of acute and remote seizures in children with intraventricular hemorrhage. Clin Pediatr (Phila). 1997 Nov; 36(11):643-7. Strober JB, Bienkowski RS, Maytal J. PMID: 9391738.
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    63. Incidence of acute and chronic seizure disorder in infants with intraventricular hemorrhage. Pediatric Neurology. 1994 Sep 1; 11(2):157-158. Strober SJ, Maytal MJ. .
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