Loading...

Jonathan Strober, MD

TitleProfessor
InstitutionUniversity of California San Francisco
DepartmentNeurology
Address350 Parnassus
San Francisco CA 94117
Phone415-353-3651
vCardDownload vCard

    Collapse Research 
    Collapse Research Activities and Funding
    PEDIATRIC CLINICAL RESEARCH CENTER
    NIH/NCRR M01RR001271Dec 1, 1981 - Mar 31, 2007
    Role: Co-Investigator

    Collapse ORNG Applications 
    Collapse Clinical Trials
    Collapse Websites
    Collapse In The News

    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.
    List All   |   Timeline
    1. Maselli RA, Vázquez J, Schrumpf L, Arredondo J, Lara M, Strober JB, Pytel P, Wollmann RL, Ferns M. Presynaptic congenital myasthenic syndrome with altered synaptic vesicle homeostasis linked to compound heterozygous sequence variants in RPH3A. Mol Genet Genomic Med. 2018 Feb 14. PMID: 29441694.
      View in: PubMed
    2. Quintanilla-Bordás C, Nourbakhsh B, Strober J, Raffel C, Waubant E. Clinical Reasoning: A 16-year-old girl with subacute weakness and sensory loss. Neurology. 2017 Jun 06; 88(23):e225-e229. PMID: 28583938.
      View in: PubMed
    3. Ho ML, Glenn OA, Sherr EH, Strober JB. Serial prenatal and postnatal MRI of dystroglycanopathy in a patient with familial B3GALNT2 mutation. Pediatr Radiol. 2017 Jun; 47(7):884-888. PMID: 28303321.
      View in: PubMed
    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. Clinical Course of Six Children With GNAO1 Mutations Causing a Severe and Distinctive Movement Disorder. Pediatr Neurol. 2016 06; 59:81-4. PMID: 27068059.
      View in: PubMed
    5. 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. Acute Flaccid Myelitis of Unknown Etiology in California, 2012-2015. JAMA. 2015 Dec 22-29; 314(24):2663-71. PMID: 26720027.
      View in: PubMed
    6. Tunovic S, Barañano KW, Barkovich JA, Strober JB, Jamal L, Slavotinek AM. 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. PMID: 26174511.
      View in: PubMed
    7. 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. De novo mutations in KIF1A cause progressive encephalopathy and brain atrophy. Ann Clin Transl Neurol. 2015 Jun; 2(6):623-35. PMID: 26125038; PMCID: PMC4479523.
      View in: PubMed, PubMed Central
    8. 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. Measuring quality of life in muscular dystrophy. Neurology. 2015 Mar 10; 84(10):1034-42. PMID: 25663223; PMCID: PMC4352095.
      View in: PubMed, PubMed Central
    9. Rosow LK, Strober JB. Infant botulism: review and clinical update. Pediatr Neurol. 2015 May; 52(5):487-92. PMID: 25882077.
      View in: PubMed
    10. 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. Quantitative MRI analysis in children with multiple sclerosis: a multicenter feasibility pilot study. BMC Neurol. 2013 Nov 13; 13:173. PMID: 24225378; PMCID: PMC3832402.
      View in: PubMed, PubMed Central
    11. 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. Neural stem cell engraftment and myelination in the human brain. Sci Transl Med. 2012 Oct 10; 4(155):155ra137. PMID: 23052294; PMCID: PMC3893824.
      View in: PubMed, PubMed Central
    12. Kitterman JA, Strober JB, Kan L, Rocke DM, Cali A, Peeper J, Snow J, Delai PL, Morhart R, Pignolo RJ, Shore EM, Kaplan FS. Neurological symptoms in individuals with fibrodysplasia ossificans progressiva. J Neurol. 2012 Dec; 259(12):2636-43. PMID: 22752062; PMCID: PMC3523705.
      View in: PubMed, PubMed Central
    13. Fay AJ, Mowry EM, Strober J, Waubant E. Relapse severity and recovery in early pediatric multiple sclerosis. Mult Scler. 2012 Jul; 18(7):1008-12. PMID: 22183939.
      View in: PubMed
    14. Chitnis T, Krupp L, Yeh A, Rubin J, Kuntz N, Strober JB, Chabas D, Weinstock-Guttmann B, Ness J, Rodriguez M, Waubant E. Pediatric multiple sclerosis. Neurol Clin. 2011 May; 29(2):481-505. PMID: 21439455.
      View in: PubMed
    15. Johnson EC, West TW, Ko NU, Strober JB. A 41-year-old man with new headache and altered mental status. Neurohospitalist. 2011 Jan; 1(1):48-54. PMID: 23983837; PMCID: PMC3726099.
      View in: PubMed, PubMed Central
    16. Fiore DM, Strober JB. Treatment of hypokalemic periodic paralysis with topiramate. Muscle Nerve. 2011 Jan; 43(1):127-9. PMID: 21171065.
      View in: PubMed
    17. Mowry EM, Julian LJ, Im-Wang S, Chabas D, Galvin AJ, Strober JB, Waubant E. Health-related quality of life is reduced in pediatric multiple sclerosis. Pediatr Neurol. 2010 Aug; 43(2):97-102. PMID: 20610119.
      View in: PubMed
    18. Huang EJ, Zhang J, Geser F, Trojanowski JQ, Strober JB, Dickson DW, Brown RH, Shapiro BE, Lomen-Hoerth C. Extensive FUS-immunoreactive pathology in juvenile amyotrophic lateral sclerosis with basophilic inclusions. Brain Pathol. 2010 Nov; 20(6):1069-76. PMID: 20579074; PMCID: PMC2951498.
      View in: PubMed, PubMed Central
    19. Mowry EM, Krupp LB, Milazzo M, Chabas D, Strober JB, Belman AL, McDonald JC, Oksenberg JR, Bacchetti P, Waubant E. Vitamin D status is associated with relapse rate in pediatric-onset multiple sclerosis. Ann Neurol. 2010 May; 67(5):618-24. PMID: 20437559.
      View in: PubMed
    20. Marco EJ, Anderson JE, Neilson DE, Strober JB. Acute necrotizing encephalopathy in 3 brothers. Pediatrics. 2010 Mar; 125(3):e693-8. PMID: 20142283; PMCID: PMC3207236.
      View in: PubMed, PubMed Central
    21. Waubant E, Chabas D, Okuda DT, Glenn O, Mowry E, Henry RG, Strober JB, Soares B, Wintermark M, Pelletier D. 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. PMID: 19667217.
      View in: PubMed
    22. Strober J, Cowan MJ, Horn BN. Allogeneic hematopoietic cell transplantation for refractory myasthenia gravis. Arch Neurol. 2009 May; 66(5):659-61. PMID: 19433668.
      View in: PubMed
    23. Chabas D, Strober J, Waubant E. Pediatric multiple sclerosis. Curr Neurol Neurosci Rep. 2008 Sep; 8(5):434-41. PMID: 18713581.
      View in: PubMed
    24. Smith AB, Gupta N, Strober J, Chin C. Magnetic resonance neurography in children with birth-related brachial plexus injury. Pediatr Radiol. 2008 Feb; 38(2):159-63. PMID: 18034234.
      View in: PubMed
    25. Strober JB. Do all patients with Duchenne muscular dystrophy require surgery for the correction of scoliosis? Nat Clin Pract Neurol. 2007 Jan; 3(1):18-9. PMID: 17205069.
      View in: PubMed
    26. Strober JB. Therapeutics in duchenne muscular dystrophy. NeuroRx. 2006 Apr; 3(2):225-34. PMID: 16554260; PMCID: PMC3593432.
      View in: PubMed, PubMed Central
    27. Wagner AJ, Cortes RA, Strober J, Grethel EJ, Clifton MS, Harrison MR, Farmer DL, Nobuhara KK, Lee H. Long-term follow-up after thymectomy for myasthenia gravis: thoracoscopic vs open. J Pediatr Surg. 2006 Jan; 41(1):50-4; discussion 50-4. PMID: 16410107.
      View in: PubMed
    28. Fox CK, Keet CA, Strober JB. Recent advances in infant botulism. Pediatr Neurol. 2005 Mar; 32(3):149-54. PMID: 15730893.
      View in: PubMed
    29. Keet CA, Fox CK, Margeta M, Marco E, Shane AL, Dearmond SJ, Strober JB, Miller SP. Infant botulism, type F, presenting at 54 hours of life. Pediatr Neurol. 2005 Mar; 32(3):193-6. PMID: 15730901.
      View in: PubMed
    Jonathan's Networks
    Concepts
    Derived automatically from this person's publications.
    See all (152) concept(s)
    _
    Co-Authors
    People in Profiles who have published with this person.
    See all (38) people
    _
    Related Authors
    People who share related concepts with this person.
    See all (60) people
    _
    ↑