Jonathan Strober, MD

Title(s)Professor, Neurology
SchoolSchool of Medicine
Address350 Parnassus
San Francisco CA 94117
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. 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 Apr 19. 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.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    2. 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:    
    3. 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
    4. 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.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansCells
    5. 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.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    6. 45 Parainfectious and Postinfectious Neurologic Syndromes. Principles and Practice of Pediatric Infectious Diseases. 2018 Jan 1; (MMWR Morb Mortal Wkly Rep632014):323-328.e1. Jonathan B. Strober, Carol A. Glaser. .
      View in: Publisher Site   Mentions:
    7. 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
    8. 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:    Fields:    Translation:Humans
    9. 148 Congenital Myopathies. Swaiman\u0027s Pediatric Neurology. 2017 Jan 1; 1123-1130. Jahannaz Dastgir, Hernan D. Gonorazky, Jonathan B. Strober, Nicolas Chrestian, James J. Dowling. .
      View in: Publisher Site   Mentions:
    10. 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: 16     Fields:    Translation:Humans
    11. 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: 35     Fields:    Translation:HumansCells
    12. Novel KIF7 missense substitutions in two patients presenting with multiple malformations and features of acrocallosal syndrome. . 2015 Nov; 167A(11):2767-76. Tunovic S, Barañano KW, Barkovich JA, Strober JB, Jamal L, Slavotinek AM. PMID: 26174511.
      View in: PubMed   Mentions:
    13. 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.
      View in: PubMed   Mentions: 36     Fields:    
    14. 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.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    15. Infant botulism: review and clinical update. Pediatr Neurol. 2015 May; 52(5):487-92. Rosow LK, Strober JB. PMID: 25882077.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    16. 488. Critical Care Medicine. 2014 Dec 1; 42(12):a1477-a1478. Poonam Patel, Carol Glaser, Michael Samuel, Jonathan Strober, Heidi Flori. .
      View in: Publisher Site   Mentions:
    17. 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.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    18. 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.
      View in: PubMed   Mentions: 105     Fields:    Translation:HumansCellsCTClinical Trials
    19. 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.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    20. 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. J. Graves, L. Krupp, B. Weinstock-Guttman, J. Strober, A. Belman, E. A. Yeh, J. Ness, M. Gorman, M. Rodriguez, T. Chitnis, E. Waubant. .
      View in: Publisher Site   Mentions:
    21. Chapter 93 Congenital Myopathies. Swaiman\u0027s Pediatric Neurology. 2012 Jan 1; 1607-1612. Jonathan B. Strober. .
      View in: Publisher Site   Mentions:
    22. 45 Para- and Postinfectious Neurologic Syndromes. . 2012 Jan 1; 314-319.e1. Carol Glaser, Jonathan B. Strober. .
      View in: Publisher Site   Mentions:
    23. 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: 15     Fields:    Translation:Humans
    24. 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: 13     Fields:    Translation:Humans
    25. 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
    26. 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.
      View in: PubMed   Mentions:
    27. 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. Nancy L. Kuntz, Jonathan Strober. .
      View in: Publisher Site   Mentions:
    28. 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: 6     Fields:    Translation:Humans
    29. 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.
      View in: PubMed   Mentions: 66     Fields:    Translation:HumansCells
    30. 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: 97     Fields:    Translation:Humans
    31. Acute necrotizing encephalopathy in 3 brothers. Pediatrics. 2010 Mar; 125(3):e693-8. Marco EJ, Anderson JE, Neilson DE, Strober JB. PMID: 20142283.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    32. 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.
      View in: PubMed   Mentions: 26     Fields:    Translation:Humans
    33. 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: 39     Fields:    Translation:Humans
    34. 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: 11     Fields:    Translation:HumansCells
    35. 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: 27     Fields:    Translation:HumansCells
    36. 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: 7     Fields:    Translation:Humans
    37. 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: 12     Fields:    Translation:Humans
    38. 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. M. Krahn, F. Hanisch, M. Goicoechea, E. Groen, C. Pécheux, F. Garcia-Bragado, R. Layzer, F. Leturcq, J. Strober, J.A. Urtizberea, A. Sáenz, K. Bushby, N. Lévy, A. Lopez de Munain. .
      View in: Publisher Site   Mentions:
    39. 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. J. Strober, T. Rando. .
      View in: Publisher Site   Mentions:
    40. 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:    
    41. Therapeutics in duchenne muscular dystrophy. NeuroRx. 2006 Apr; 3(2):225-34. Strober JB. PMID: 16554260.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansAnimals
    42. 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: 10     Fields:    Translation:Humans
    43. 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: 13     Fields:    Translation:HumansCells
    44. 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: 6     Fields:    Translation:HumansCells
    45. Genetics of pediatric neuromuscular disease. Curr Opin Pediatr. 2000 Dec; 12(6):549-53. Strober JB. PMID: 11106273.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    46. 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.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    47. Incidence of acute and chronic seizure disorder in infants with intraventricular hemorrhage. Pediatric Neurology. 1994 Sep 1; 11(2):157-158. Jonathan B. Strober, Joseph Maytal. .
      View in: Publisher Site   Mentions:
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