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Caregiver burden in Duchenne muscular dystrophy in Europe, Japan, and the United States - a real-world study. BMC Neurol. 2026 Jan 10; 26(1):79. Strober J, Ishigaki K, Posner N, Cappelleri JC, Xiao S, Talaga A, Dukacz S, Iqbal H, Chatterton E, Morton E, Weatherby S, de Courcy J. PMID: 41519700; PMCID: PMC12882272.
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Safety and effectiveness of nipocalimab in adolescent participants in the open label phase 2/3 Vibrance-MG clinical study. Clinical Neurophysiology. 2025 Aug 1; 176:2110868. Strober SJ, Black BS, Ramchandren RS, Bernes BS, Uzawa UA, Kimoto KY, Ishigaki IK, Vu VT, Huang HD, Zhu ZY, Sun SH, Möller MS. .
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Treatment Patterns and Disease Burden of Juvenile Myasthenia Gravis in the United States: A Cohort Study Using Health Care Claims Databases. Neurology. 2025 Jul 08; 105(1):e213736. Zhou J, Nilius S, Pilipczuk O, Scowcroft A, Tarancón T, Tennigkeit F, Zaremba P, Chandra N, Kuntz N, Strober J, Brandsema J. PMID: 40489715; PMCID: PMC12151331.
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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 Jun 1; 52(s1):s32-s32. Strober SJ, Black BS, Ramchandren RS, Ait-Tihyaty AM, Sattin SB, Bernes BS, Uzawa UA, Kimoto KY, Ishigaki IK, Vu VT, Huang HD, Zhu ZY, Sun SH. .
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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.
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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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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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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.
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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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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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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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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.
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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.
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Sexual and Gender Diversity in Pediatric Neurology: Why We Care. Pediatr Neurol. 2023 08; 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.
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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.
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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.
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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.
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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.
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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.
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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.
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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.
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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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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.
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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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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.
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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.
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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.
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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.
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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.
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Infant botulism: review and clinical update. Pediatr Neurol. 2015 May; 52(5):487-92. Rosow LK, Strober JB. PMID: 25882077.
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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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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.
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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.
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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.
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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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Chapter 93 Congenital Myopathies. Swaiman\u0027s Pediatric Neurology. 2012 Jan 1; 1607-1612. Strober SJ. .
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45 Para- and Postinfectious Neurologic Syndromes. . 2012 Jan 1; 314-319.e1. Glaser GC, Strober SJ. .
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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.
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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.
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Treatment of hypokalemic periodic paralysis with topiramate. Muscle Nerve. 2011 Jan; 43(1):127-9. Fiore DM, Strober JB. PMID: 21171065.
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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.
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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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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.
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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.
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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.
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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.
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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.
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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.
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Allogeneic hematopoietic cell transplantation for refractory myasthenia gravis. Arch Neurol. 2009 May; 66(5):659-61. Strober J, Cowan MJ, Horn BN. PMID: 19433668.
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Pediatric multiple sclerosis. Curr Neurol Neurosci Rep. 2008 Sep; 8(5):434-41. Chabas D, Strober J, Waubant E. PMID: 18713581.
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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.
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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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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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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.
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Therapeutics in duchenne muscular dystrophy. NeuroRx. 2006 Apr; 3(2):225-34. Strober JB. PMID: 16554260; PMCID: PMC3593432.
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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.
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Recent advances in infant botulism. Pediatr Neurol. 2005 Mar; 32(3):149-54. Fox CK, Keet CA, Strober JB. PMID: 15730893.
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Genetics of pediatric neuromuscular disease. Curr Opin Pediatr. 2000 Dec; 12(6):549-53. Strober JB. PMID: 11106273.
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Progressive spinal muscular atrophies. J Child Neurol. 1999 Nov; 14(11):691-5. Strober JB, Tennekoon GI. PMID: 10593543.
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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.
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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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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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