Publications by authors named "Jonathan Strober"

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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.
Jiachen Zhou, Sigrid Nilius, Olga Pilipczuk, Anna Scowcroft, Thaïs Tarancón, Jonathan Strober

Neurology· July 2025

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Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability.
Pascale Sabeh, Samantha A Dumas, Claudia Maios, Hiba Daghar, Marek Korzeniowski, Jonathan Strober

Am J Hum Genet· January 2025

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Analysis of Gender Discrepancies in Leadership Roles and Recognition Awards in the Child Neurology Society.
Jaclyn M Martindale, Alison L Christy, Grace Y Gombolay, Bhooma R Aravamuthan, Laura Jansen, Jonathan B Strober

Neurology· September 2024

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Author Correction: Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population.
Anne Slavotinek, Shannon Rego, Nuriye Sahin-Hodoglugil, Mark Kvale, Billie Lianoglou, Jonathan Strober

NPJ Genom Med· October 2023

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Sexual and Gender Diversity in Pediatric Neurology: Why We Care.
Alison Christy, Jaclyn Martindale, Jennifer Hranilovich, Casey Orozco-Poore, Finley Kernan-Schloss, Jonathan Strober

Pediatr Neurol· August 2023

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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.
Anabel S De la Garza-Rodea, Steven A Moore, Jesus Zamora-Pineda, Eric P Hoffman, Karishma Mistry, Jonathan B Strober

Int J Mol Sci· July 2022

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Introducing the Child Neurology Society Leadership, Diversity, Equity, and Inclusion Task Force.
Audrey C Brumback, Rujuta B Wilson, Erika F Augustine, Nancy E Bass, Alexander G Bassuk, Jonathan B Strober

Ann Neurol· October 2021

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Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature.
Dmitrijs Rots, Eric Chater-Diehl, Alexander J M Dingemans, Sarah J Goodman, Michelle T Siu, Jonathan Strober

Am J Hum Genet· June 2021

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Pathologic Findings Associated With a Case of Acute Flaccid Myelitis.
Alexander F Haddad, Jeffrey W Hofmann, Taemin Oh, Line Jacques, Guixia Yu, Jonathan Strober

J Neuropathol Exp Neurol· April 2021

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Targeted Treatments for Inherited Neuromuscular Diseases of Childhood.
Alex J Fay, Renatta Knox, Erin E Neil, Jonathan Strober

Semin Neurol· June 2020

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Pathogenic WDFY3 variants cause neurodevelopmental disorders and opposing effects on brain size.
Diana Le Duc, Cecilia Giulivi, Susan M Hiatt, Eleonora Napoli, Alexios Panoutsopoulos, Jonathan Strober

Brain· September 2019

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Long-Term Safety, Immunologic Response, and Imaging Outcomes following Neural Stem Cell Transplantation for Pelizaeus-Merzbacher Disease.
Nalin Gupta, Roland G Henry, Sang-Mo Kang, Jonathan Strober, Daniel A Lim

Stem Cell Reports· August 2019

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Presynaptic congenital myasthenic syndrome with altered synaptic vesicle homeostasis linked to compound heterozygous sequence variants in RPH3A.
Ricardo A Maselli, Jessica Vázquez, Leah Schrumpf, Juan Arredondo, Marian Lara, Jonathan B Strober

Mol Genet Genomic Med· May 2018

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Serial prenatal and postnatal MRI of dystroglycanopathy in a patient with familial B3GALNT2 mutation.
Mai-Lan Ho, Orit A Glenn, Eliott H Sherr, Jonathan B Strober

Pediatr Radiol· June 2017

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Clinical Reasoning: A 16-year-old girl with subacute weakness and sensory loss.
Carlos Quintanilla-Bordás, Bardia Nourbakhsh, Jonathan Strober, Corey Raffel, Emmanuelle Waubant

Neurology· June 2017

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Clinical Course of Six Children With GNAO1 Mutations Causing a Severe and Distinctive Movement Disorder.
Amitha L Ananth, Amy Robichaux-Viehoever, Young-Min Kim, Andrea Hanson-Kahn, Rachel Cox, Jonathan Strober

Pediatr Neurol· June 2016

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Acute Flaccid Myelitis of Unknown Etiology in California, 2012-2015.
Keith Van Haren, Patrick Ayscue, Emmanuelle Waubant, Anna Clayton, Heather Sheriff, Jonathan B Strober

JAMA· February 2016

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Novel KIF7 missense substitutions in two patients presenting with multiple malformations and features of acrocallosal syndrome.
Sanjin Tunovic, Kristin W Barañano, James A Barkovich, Jonathan B Strober, Leila Jamal

Am J Med Genet A· November 2015

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De novo mutations in KIF1A cause progressive encephalopathy and brain atrophy.
Sahar Esmaeeli Nieh, Maura R Z Madou, Minhajuddin Sirajuddin, Brieana Fregeau, Dianalee McKnight, Jonathan Strober

Ann Clin Transl Neurol· June 2015

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Infant botulism: review and clinical update.
Laura K Rosow, Jonathan B Strober

Pediatr Neurol· May 2015

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Measuring quality of life in muscular dystrophy.
Carla M Bann, Richard T Abresch, Barbara Biesecker, Kristin Caspers Conway, Chad Heatwole, Jonathan Strober

Neurology· March 2015

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Quantitative MRI analysis in children with multiple sclerosis: a multicenter feasibility pilot study.
Tanuja Chitnis, Charles R Guttmann, Alexander Zaitsev, Alexander Musallam, Bianca Weinstock-Guttman, Jonathan B Strober

BMC Neurol· November 2013

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Neural stem cell engraftment and myelination in the human brain.
Nalin Gupta, Roland G Henry, Jonathan Strober, Sang-Mo Kang, Daniel A Lim

Sci Transl Med· October 2012

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