Jonathan Strober, MD
Professor
Neurology
School of Medicine

Education & Training

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• Diversity, Equity, and Inclusion Champion Training University of California 2017

Websites

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• Clinical Profile at UCSF Benioff Children's Hospital (ucsfbenioffchildrens.org)

Grants and Projects

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• Pediatric Clinical Research Center, NIH, 1981-2007

Publications (66)

Top publication keywords:
Carbonic Anhydrase InhibitorsImmunologic FactorsMuscular DystrophiesImmunoglobulinsMuscular Dystrophy, DuchenneCarbonic AnhydrasesNeurologyHypokalemic Periodic ParalysisBotulismMyelitisNeurodevelopmental DisordersGenetic TherapyNeuromuscular DiseasesMyasthenia GravisN-Acetylgalactosaminyltransferases

• Safety and effectiveness of nipocalimab in adolescent participants in the open label phase 2/3 Vibrance-MG clinical study.
  Clinical Neurophysiology 2025 Jonathan Strober, Shawn Black, Sindhu Ramchandren, Saunder Bernes, Akiyuki Uzawa, Yasuhiro Kimoto, Keiko Ishigaki, Tuan Vu, Dan Huang, Yaowei Zhu, Hong Sun, Sebastian Möller
• Treatment Patterns and Disease Burden of Juvenile Myasthenia Gravis in the United States: A Cohort Study Using Health Care Claims Databases.
  Neurology 2025 Zhou J, Nilius S, Pilipczuk O, Scowcroft A, Tarancón T, Tennigkeit F, Zaremba P, Chandra N, Kuntz N, Strober J, Brandsema J
• P.072 Safety and effectiveness of Nipocalimab in adolescent participants in the open label phase 2/3 Vibrance-mg clinical study.
  Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 2025 J Strober, S Black, S Ramchandren, M Ait-Tihyaty, B Sattin, S Bernes, A Uzawa, Y Kimoto, K Ishigaki, T Vu, D Huang, Y Zhu, H Sun
• Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability.
  American journal of human genetics 2024 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, …
• 332P Physician and caregiver concordance in Duchenne muscular dystrophy patients in Europe, Japan, and the USA: a multi-national survey.
  Neuromuscular Disorders 2024 A. Talaga, J. Strober, K. Ishigaki, N. Posner, J. Cappelleri, S. Dukacz, Z. Aslam, E. Morton, H. Iqbal, E. Chatterton, J. DeCourcy

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• 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 A. Talaga, J. Strober, K. Ishigaki, N. Posner, J. Cappelleri, S. Dukacz, Z. Aslam, E. Morton, H. Iqbal, E. Chatterton, J. DeCourcy
• Analysis of Gender Discrepancies in Leadership Roles and Recognition Awards in the Child Neurology Society.
  Neurology 2024 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
• Characteristics, Treatment Patterns, and Disease Burden of Juvenile Myasthenia Gravis in the United States (P4-11.017).
  Neurology 2024 Jiachen Zhou, Sigrid Nilius, Olga Pilipczuk, Anna Scowcroft, Thaïs Tarancón, Frank Tennigkeit, Piotr Zaremba, John Brandsema, Jonathan Strober
• PCR141 The Impact of Duchenne Muscular Dystrophy on Caregiver Employment: A Survey in Europe, Japan, and the United States.
  Value in Health 2023 J. Strober, K. Ishigaki, V. Merla, N. Posner, J. Cappelleri, S. Xiao, A.K. Talaga, S. Brunner, E. Morton, S. Olsen, J. de Courcy
• RWD130 Healthcare Resource Utilization for Pediatric and Adolescent Duchenne Muscular Dystrophy Patients: Analysis of Real-World Data.
  Value in Health 2023 J. Strober, K. Ishigaki, V. Merla, N. Posner, J. Cappelleri, S. Xiao, A.K. Talaga, S. Brunner, H. Iqbal, E. Chatterton, N. Hatchell
• Author Correction: Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population.
  NPJ genomic medicine 2023 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…
• Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population.
  NPJ genomic medicine 2023 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…
• Sexual and Gender Diversity in Pediatric Neurology: Why We Care.
  Pediatric neurology 2023 Christy A, Martindale J, Hranilovich J, Orozco-Poore C, Kernan-Schloss F, Anderson CTM, Strober J, Mitchell W, Lerario MP
• Sphingosine Phosphate Lyase Is Upregulated in Duchenne Muscular Dystrophy, and Its Inhibition Early in Life Attenuates Inflammation and Dystrophy in Mdx Mice.
  International journal of molecular sciences 2022 De la Garza-Rodea AS, Moore SA, Zamora-Pineda J, Hoffman EP, Mistry K, Kumar A, Strober JB, Zhao P, Suh JH, Saba JD
• Introducing the Child Neurology Society Leadership, Diversity, Equity, and Inclusion Task Force.
  Annals of neurology 2021 Brumback AC, Wilson RB, Augustine EF, Bass NE, Bassuk AG, Cejas DM, Shellhaas RA, Strober JB, Tilton AC, Pearl PL
• Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature.
  American journal of human genetics 2021 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…
• Pathologic Findings Associated With a Case of Acute Flaccid Myelitis.
  Journal of neuropathology and experimental neurology 2021 Haddad AF, Hofmann JW, Oh T, Jacques L, Yu G, Chiu C, Nolan A, Strober J, Gupta N
• Targeted Treatments for Inherited Neuromuscular Diseases of Childhood.
  Seminars in neurology 2020 Fay AJ, Knox R, Neil EE, Strober J
• Pathogenic WDFY3 variants cause neurodevelopmental disorders and opposing effects on brain size.
  Brain : a journal of neurology 2019 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, …
• Long-Term Safety, Immunologic Response, and Imaging Outcomes following Neural Stem Cell Transplantation for Pelizaeus-Merzbacher Disease.
  Stem cell reports 2019 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
• Presynaptic congenital myasthenic syndrome with altered synaptic vesicle homeostasis linked to compound heterozygous sequence variants in RPH3A.
  Molecular genetics & genomic medicine 2018 Maselli RA, Vázquez J, Schrumpf L, Arredondo J, Lara M, Strober JB, Pytel P, Wollmann RL, Ferns M
• 45 Parainfectious and Postinfectious Neurologic Syndromes.
  Principles and Practice of Pediatric Infectious Diseases 2018 Jonathan B. Strober, Carol A. Glaser
• Clinical Reasoning: A 16-year-old girl with subacute weakness and sensory loss.
  Neurology 2017 Quintanilla-Bordás C, Nourbakhsh B, Strober J, Raffel C, Waubant E
• Serial prenatal and postnatal MRI of dystroglycanopathy in a patient with familial B3GALNT2 mutation.
  Pediatric radiology 2017 Ho ML, Glenn OA, Sherr EH, Strober JB
• 148 Congenital Myopathies.
  Swaiman\u0027s Pediatric Neurology 2017 Jahannaz Dastgir, Hernan D. Gonorazky, Jonathan B. Strober, Nicolas Chrestian, James J. Dowling
• Clinical Course of Six Children With GNAO1 Mutations Causing a Severe and Distinctive Movement Disorder.
  Pediatric neurology 2016 Ananth AL, Robichaux-Viehoever A, Kim YM, Hanson-Kahn A, Cox R, Enns GM, Strober J, Willing M, Schlaggar BL, Wu YW, Bernstein JA
• Acute Flaccid Myelitis of Unknown Etiology in California, 2012-2015.
  JAMA 2015 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
• Novel KIF7 missense substitutions in two patients presenting with multiple malformations and features of acrocallosal syndrome.
  American journal of medical genetics. Part A 2015 Tunovic S, Barañano KW, Barkovich JA, Strober JB, Jamal L, Slavotinek AM
• De novo mutations in KIF1A cause progressive encephalopathy and brain atrophy.
  Annals of clinical and translational neurology 2015 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, …
• Measuring quality of life in muscular dystrophy.
  Neurology 2015 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
• Infant botulism: review and clinical update.
  Pediatric neurology 2015 Rosow LK, Strober JB
• 488.
  Critical Care Medicine 2014 Poonam Patel, Carol Glaser, Michael Samuel, Jonathan Strober, Heidi Flori
• Quantitative MRI analysis in children with multiple sclerosis: a multicenter feasibility pilot study.
  BMC neurology 2013 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, …
• Neural stem cell engraftment and myelination in the human brain.
  Science translational medicine 2012 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
• Neurological symptoms in individuals with fibrodysplasia ossificans progressiva.
  Journal of neurology 2012 Kitterman JA, Strober JB, Kan L, Rocke DM, Cali A, Peeper J, Snow J, Delai PL, Morhart R, Pignolo RJ, Shore EM, Kaplan FS
• EBV, CMV, and HSV IgG Titers Are Not Predictive of Subsequent Relapse Risk in Pediatric Multiple Sclerosis (P02.096).
  Neurology 2012 J. Graves, L. Krupp, B. Weinstock-Guttman, J. Strober, A. Belman, E. A. Yeh, J. Ness, M. Gorman, M. Rodriguez, T. Chitnis, E. Waubant
• 45 Para- and Postinfectious Neurologic Syndromes.
  2012 Carol Glaser, Jonathan B. Strober
• Chapter 93 Congenital Myopathies.
  Swaiman\u0027s Pediatric Neurology 2012 Jonathan B. Strober
• Relapse severity and recovery in early pediatric multiple sclerosis.
  Multiple sclerosis (Houndmills, Basingstoke, England) 2011 Fay AJ, Mowry EM, Strober J, Waubant E
• Common viruses associated with lower pediatric multiple sclerosis risk.
  Neurology 2011 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…
• Pediatric multiple sclerosis.
  Neurologic clinics 2011 Chitnis T, Krupp L, Yeh A, Rubin J, Kuntz N, Strober JB, Chabas D, Weinstock-Guttmann B, Ness J, Rodriguez M, Waubant E
• A 41-year-old man with new headache and altered mental status.
  The Neurohospitalist 2011 Johnson EC, West TW, Ko NU, Strober JB
• 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 Nancy L. Kuntz, Jonathan Strober
• Treatment of hypokalemic periodic paralysis with topiramate.
  Muscle & nerve 2011 Fiore DM, Strober JB
• Health-related quality of life is reduced in pediatric multiple sclerosis.
  Pediatric neurology 2010 Mowry EM, Julian LJ, Im-Wang S, Chabas D, Galvin AJ, Strober JB, Waubant E
• Extensive FUS-immunoreactive pathology in juvenile amyotrophic lateral sclerosis with basophilic inclusions.
  Brain pathology (Zurich, Switzerland) 2010 Huang EJ, Zhang J, Geser F, Trojanowski JQ, Strober JB, Dickson DW, Brown RH, Shapiro BE, Lomen-Hoerth C
• Vitamin D status is associated with relapse rate in pediatric-onset multiple sclerosis.
  Annals of neurology 2010 Mowry EM, Krupp LB, Milazzo M, Chabas D, Strober JB, Belman AL, McDonald JC, Oksenberg JR, Bacchetti P, Waubant E
• Acute necrotizing encephalopathy in 3 brothers.
  Pediatrics 2010 Marco EJ, Anderson JE, Neilson DE, Strober JB
• Younger children with MS have a distinct CSF inflammatory profile at disease onset.
  Neurology 2010 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 …
• Difference in disease burden and activity in pediatric patients on brain magnetic resonance imaging at time of multiple sclerosis onset vs adults.
  Archives of neurology 2009 Waubant E, Chabas D, Okuda DT, Glenn O, Mowry E, Henry RG, Strober JB, Soares B, Wintermark M, Pelletier D
• Allogeneic hematopoietic cell transplantation for refractory myasthenia gravis.
  Archives of neurology 2009 Strober J, Cowan MJ, Horn BN
• Vanishing MS T2-bright lesions before puberty: a distinct MRI phenotype?
  Neurology 2008 Chabas D, Castillo-Trivino T, Mowry EM, Strober JB, Glenn OA, Waubant E
• Pediatric multiple sclerosis.
  Current neurology and neuroscience reports 2008 Chabas D, Strober J, Waubant E
• Magnetic resonance neurography in children with birth-related brachial plexus injury.
  Pediatric radiology 2007 Smith AB, Gupta N, Strober J, Chin C
• G.P.4.15 CAPN3 mutations in patients with idiopathic eosinophilic myositis: A predystrophic stage of LGMD2A?.
  Neuromuscular Disorders 2007 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
• G.P.6.07 Mycophenolate mofetil’s beneficial effects on skeletal muscle in the mdx mouse.
  Neuromuscular Disorders 2007 J. Strober, T. Rando
• Do all patients with Duchenne muscular dystrophy require surgery for the correction of scoliosis?
  Nature clinical practice. Neurology 2007 Strober JB
• Therapeutics in duchenne muscular dystrophy.
  NeuroRx : the journal of the American Society for Experimental NeuroTherapeutics 2006 Strober JB
• Long-term follow-up after thymectomy for myasthenia gravis: thoracoscopic vs open.
  Journal of pediatric surgery 2006 Wagner AJ, Cortes RA, Strober J, Grethel EJ, Clifton MS, Harrison MR, Farmer DL, Nobuhara KK, Lee H
• Infant botulism, type F, presenting at 54 hours of life.
  Pediatric neurology 2005 Keet CA, Fox CK, Margeta M, Marco E, Shane AL, Dearmond SJ, Strober JB, Miller SP
• Recent advances in infant botulism.
  Pediatric neurology 2005 Fox CK, Keet CA, Strober JB
• Genetics of pediatric neuromuscular disease.
  Current opinion in pediatrics 2000 Strober JB
• Progressive spinal muscular atrophies.
  Journal of child neurology 1999 Strober JB, Tennekoon GI
• A 15-year-old with back pain, fever, and leg numbness.
  Seminars in pediatric neurology 1999 Strober JB, Zuppa A, Brooks-Kayal AR
• The incidence of acute and remote seizures in children with intraventricular hemorrhage.
  Clinical pediatrics 1997 Strober JB, Bienkowski RS, Maytal J
• Incidence of acute and chronic seizure disorder in infants with intraventricular hemorrhage.
  Pediatric Neurology 1994 Jonathan B. Strober, Joseph Maytal