Jonathan Strober, MD

  1. 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. Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability. American journal of human genetics 2024. PMID: 39721588


  2. A. Talaga, J. Strober, K. Ishigaki, N. Posner, J. Cappelleri, S. Dukacz, Z. Aslam, E. Morton, H. Iqbal, E. Chatterton, J. DeCourcy. 332P Physician and caregiver concordance in Duchenne muscular dystrophy patients in Europe, Japan, and the USA: a multi-national survey. Neuromuscular Disorders 2024. PMID:


  3. A. Talaga, J. Strober, K. Ishigaki, N. Posner, J. Cappelleri, S. Dukacz, Z. Aslam, E. Morton, H. Iqbal, E. Chatterton, J. DeCourcy. 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. PMID:


  4. 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. Analysis of Gender Discrepancies in Leadership Roles and Recognition Awards in the Child Neurology Society. Neurology 2024. PMID: 39159414


  5. Jiachen Zhou, Sigrid Nilius, Olga Pilipczuk, Anna Scowcroft, Thaïs Tarancón, Frank Tennigkeit, Piotr Zaremba, John Brandsema, Jonathan Strober. Characteristics, Treatment Patterns, and Disease Burden of Juvenile Myasthenia Gravis in the United States (P4-11.017). Neurology 2024. PMID:


  6. J. Strober, K. Ishigaki, V. Merla, N. Posner, J. Cappelleri, S. Xiao, A.K. Talaga, S. Brunner, E. Morton, S. Olsen, J. de Courcy. PCR141 The Impact of Duchenne Muscular Dystrophy on Caregiver Employment: A Survey in Europe, Japan, and the United States. Value in Health 2023. PMID:


  7. J. Strober, K. Ishigaki, V. Merla, N. Posner, J. Cappelleri, S. Xiao, A.K. Talaga, S. Brunner, H. Iqbal, E. Chatterton, N. Hatchell. RWD130 Healthcare Resource Utilization for Pediatric and Adolescent Duchenne Muscular Dystrophy Patients: Analysis of Real-World Data. Value in Health 2023. PMID:


  8. 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. Author Correction: Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population. NPJ genomic medicine 2023. PMID: 37872195


  9. 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. Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population. NPJ genomic medicine 2023. PMID: 37236975


  10. Christy A, Martindale J, Hranilovich J, Orozco-Poore C, Kernan-Schloss F, Anderson CTM, Strober J, Mitchell W, Lerario MP. Sexual and Gender Diversity in Pediatric Neurology: Why We Care. Pediatric neurology 2023. PMID: 37257397


  11. De la Garza-Rodea AS, Moore SA, Zamora-Pineda J, Hoffman EP, Mistry K, Kumar A, Strober JB, Zhao P, Suh JH, Saba JD. 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. PMID: 35886926


  12. Brumback AC, Wilson RB, Augustine EF, Bass NE, Bassuk AG, Cejas DM, Shellhaas RA, Strober JB, Tilton AC, Pearl PL. Introducing the Child Neurology Society Leadership, Diversity, Equity, and Inclusion Task Force. Annals of neurology 2021. PMID: 34288089


  13. 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. 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. PMID: 33909990


  14. Haddad AF, Hofmann JW, Oh T, Jacques L, Yu G, Chiu C, Nolan A, Strober J, Gupta N. Pathologic Findings Associated With a Case of Acute Flaccid Myelitis. Journal of neuropathology and experimental neurology 2021. PMID: 33870421


  15. Fay AJ, Knox R, Neil EE, Strober J. Targeted Treatments for Inherited Neuromuscular Diseases of Childhood. Seminars in neurology 2020. PMID: 32294764


  16. 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. Pathogenic WDFY3 variants cause neurodevelopmental disorders and opposing effects on brain size. Brain : a journal of neurology 2019. PMID: 31327001


  17. 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. Long-Term Safety, Immunologic Response, and Imaging Outcomes following Neural Stem Cell Transplantation for Pelizaeus-Merzbacher Disease. Stem cell reports 2019. PMID: 31378671


  18. 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. Molecular genetics & genomic medicine 2018. PMID: 29441694


  19. Jonathan B. Strober, Carol A. Glaser. 45 Parainfectious and Postinfectious Neurologic Syndromes. Principles and Practice of Pediatric Infectious Diseases 2018. PMID:


  20. 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. PMID: 28583938


  21. Ho ML, Glenn OA, Sherr EH, Strober JB. Serial prenatal and postnatal MRI of dystroglycanopathy in a patient with familial B3GALNT2 mutation. Pediatric radiology 2017. PMID: 28303321


  22. Jahannaz Dastgir, Hernan D. Gonorazky, Jonathan B. Strober, Nicolas Chrestian, James J. Dowling. 148 Congenital Myopathies. Swaiman\u0027s Pediatric Neurology 2017. PMID:


  23. 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. Pediatric neurology 2016. PMID: 27068059


  24. 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. PMID: 26720027


  25. 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. American journal of medical genetics. Part A 2015. PMID: 26174511


  26. 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. Annals of clinical and translational neurology 2015. PMID: 26125038


  27. 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. PMID: 25663223


  28. Rosow LK, Strober JB. Infant botulism: review and clinical update. Pediatric neurology 2015. PMID: 25882077


  29. Poonam Patel, Carol Glaser, Michael Samuel, Jonathan Strober, Heidi Flori. 488. Critical care medicine 2014. PMID:


  30. 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. Quantitative MRI analysis in children with multiple sclerosis: a multicenter feasibility pilot study. BMC neurology 2013. PMID: 24225378


  31. 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. Science translational medicine 2012. PMID: 23052294


  32. 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. Journal of neurology 2012. PMID: 22752062


  33. J. Graves, L. Krupp, B. Weinstock-Guttman, J. Strober, A. Belman, E. A. Yeh, J. Ness, M. Gorman, M. Rodriguez, T. Chitnis, E. Waubant. EBV, CMV, and HSV IgG Titers Are Not Predictive of Subsequent Relapse Risk in Pediatric Multiple Sclerosis (P02.096). Neurology 2012. PMID:


  34. Carol Glaser, Jonathan B. Strober. 45 Para- and Postinfectious Neurologic Syndromes. 2012. PMID:


  35. Jonathan B. Strober. Chapter 93 Congenital Myopathies. 2012. PMID:


  36. Fay AJ, Mowry EM, Strober J, Waubant E. Relapse severity and recovery in early pediatric multiple sclerosis. Multiple sclerosis (Houndmills, Basingstoke, England) 2011. PMID: 22183939


  37. 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. Common viruses associated with lower pediatric multiple sclerosis risk. Neurology 2011. PMID: 21646624


  38. 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. Neurologic clinics 2011. PMID: 21439455


  39. Johnson EC, West TW, Ko NU, Strober JB. A 41-year-old man with new headache and altered mental status. 2011. PMID: 23983837


  40. Nancy L. Kuntz, Jonathan Strober. Differential diagnosis of multiple sclerosis and acquired central nervous system demyelinating disorders in children and adolescents. 2011. PMID:


  41. Fiore DM, Strober JB. Treatment of hypokalemic periodic paralysis with topiramate. Muscle & nerve 2011. PMID: 21171065


  42. 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. Pediatric neurology 2010. PMID: 20610119


  43. 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. 2010. PMID: 20579074


  44. 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. Annals of neurology 2010. PMID: 20437559


  45. Marco EJ, Anderson JE, Neilson DE, Strober JB. Acute necrotizing encephalopathy in 3 brothers. 2010. PMID: 20142283


  46. 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. Younger children with MS have a distinct CSF inflammatory profile at disease onset. Neurology 2010. PMID: 20124205


  47. 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. Archives of neurology 2009. PMID: 19667217


  48. Strober J, Cowan MJ, Horn BN. Allogeneic hematopoietic cell transplantation for refractory myasthenia gravis. Archives of neurology 2009. PMID: 19433668


  49. Chabas D, Castillo-Trivino T, Mowry EM, Strober JB, Glenn OA, Waubant E. Vanishing MS T2-bright lesions before puberty: a distinct MRI phenotype? Neurology 2008. PMID: 18824673


  50. Chabas D, Strober J, Waubant E. Pediatric multiple sclerosis. Current neurology and neuroscience reports 2008. PMID: 18713581


  51. Smith AB, Gupta N, Strober J, Chin C. Magnetic resonance neurography in children with birth-related brachial plexus injury. 2007. PMID: 18034234


  52. 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.4.15 CAPN3 mutations in patients with idiopathic eosinophilic myositis: A predystrophic stage of LGMD2A?. 2007. PMID:


  53. J. Strober, T. Rando. G.P.6.07 Mycophenolate mofetil’s beneficial effects on skeletal muscle in the mdx mouse. 2007. PMID:


  54. Strober JB. Do all patients with Duchenne muscular dystrophy require surgery for the correction of scoliosis? 2007. PMID: 17205069


  55. Strober JB. Therapeutics in duchenne muscular dystrophy. 2006. PMID: 16554260


  56. 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. 2006. PMID: 16410107


  57. 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. 2005. PMID: 15730901


  58. Fox CK, Keet CA, Strober JB. Recent advances in infant botulism. 2005. PMID: 15730893


  59. Strober JB. Genetics of pediatric neuromuscular disease. 2000. PMID: 11106273


  60. Strober JB, Tennekoon GI. Progressive spinal muscular atrophies. 1999. PMID: 10593543


  61. Strober JB, Zuppa A, Brooks-Kayal AR. A 15-year-old with back pain, fever, and leg numbness. 1999. PMID: 10522338


  62. Strober JB, Bienkowski RS, Maytal J. The incidence of acute and remote seizures in children with intraventricular hemorrhage. 1997. PMID: 9391738


  63. Jonathan B. Strober, Joseph Maytal. Incidence of acute and chronic seizure disorder in infants with intraventricular hemorrhage. 1994. PMID: