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Jonathan Strober

Showing results (11-20 of 22) with videos related to

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BMC Neurology|January 10, 2026
Caregiver burden in Duchenne muscular dystrophy in Europe, Japan, and the United States - a real-world studyJonathan Strober, Keiko Ishigaki, Nate Posner, et al.
Pediatric Neurology|April 13, 2016
Clinical Course of Six Children With GNAO1 Mutations Causing a Severe and Distinctive Movement DisorderAmitha L Ananth, Amy Robichaux-Viehoever, Young-Min Kim, et al.
Neurology|February 10, 2015
Measuring quality of life in muscular dystrophyCarla M Bann, Richard T Abresch, Barbara Biesecker, et al.
Stem Cell Reports|August 6, 2019
Long-Term Safety, Immunologic Response, and Imaging Outcomes following Neural Stem Cell Transplantation for Pelizaeus-Merzbacher DiseaseNalin Gupta, Roland G Henry, Sang-Mo Kang, et al.
Science Translational Medicine|October 12, 2012
Neural stem cell engraftment and myelination in the human brainNalin Gupta, Roland G Henry, Jonathan Strober, et al.
Annals of Clinical and Translational Neurology|July 1, 2015
De novo mutations in KIF1A cause progressive encephalopathy and brain atrophySahar Esmaeeli Nieh, Maura R Z Madou, Minhajuddin Sirajuddin, et al.
Muscle & Nerve|June 16, 2026
Electrodiagnostic Studies as a Diagnostic and Prognostic Tool in Acute Flaccid MyelitisJelte Helfferich, Judith M Vonk, Melodie Aubart, et al.
NPJ Genomic Medicine|May 26, 2023
Diagnostic yield of pediatric and prenatal exome sequencing in a diverse populationAnne Slavotinek, Shannon Rego, Nuriye Sahin-Hodoglugil, et al.
NPJ Genomic Medicine|October 23, 2023
Author Correction: Diagnostic yield of pediatric and prenatal exome sequencing in a diverse populationAnne Slavotinek, Shannon Rego, Nuriye Sahin-Hodoglugil, et al.
Brain : a Journal of Neurology|July 22, 2019
Pathogenic WDFY3 variants cause neurodevelopmental disorders and opposing effects on brain sizeDiana Le Duc, Cecilia Giulivi, Susan M Hiatt, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
BMC Neurology|January 10, 2026
Caregiver burden in Duchenne muscular dystrophy in Europe, Japan, and the United States - a real-world studyJonathan Strober, Keiko Ishigaki, Nate Posner, et al.
Pediatric Neurology|April 13, 2016
Clinical Course of Six Children With GNAO1 Mutations Causing a Severe and Distinctive Movement DisorderAmitha L Ananth, Amy Robichaux-Viehoever, Young-Min Kim, et al.
Neurology|February 10, 2015
Measuring quality of life in muscular dystrophyCarla M Bann, Richard T Abresch, Barbara Biesecker, et al.
Stem Cell Reports|August 6, 2019
Long-Term Safety, Immunologic Response, and Imaging Outcomes following Neural Stem Cell Transplantation for Pelizaeus-Merzbacher DiseaseNalin Gupta, Roland G Henry, Sang-Mo Kang, et al.
Science Translational Medicine|October 12, 2012
Neural stem cell engraftment and myelination in the human brainNalin Gupta, Roland G Henry, Jonathan Strober, et al.
Annals of Clinical and Translational Neurology|July 1, 2015
De novo mutations in KIF1A cause progressive encephalopathy and brain atrophySahar Esmaeeli Nieh, Maura R Z Madou, Minhajuddin Sirajuddin, et al.
Muscle & Nerve|June 16, 2026
Electrodiagnostic Studies as a Diagnostic and Prognostic Tool in Acute Flaccid MyelitisJelte Helfferich, Judith M Vonk, Melodie Aubart, et al.
NPJ Genomic Medicine|May 26, 2023
Diagnostic yield of pediatric and prenatal exome sequencing in a diverse populationAnne Slavotinek, Shannon Rego, Nuriye Sahin-Hodoglugil, et al.
NPJ Genomic Medicine|October 23, 2023
Author Correction: Diagnostic yield of pediatric and prenatal exome sequencing in a diverse populationAnne Slavotinek, Shannon Rego, Nuriye Sahin-Hodoglugil, et al.
Brain : a Journal of Neurology|July 22, 2019
Pathogenic WDFY3 variants cause neurodevelopmental disorders and opposing effects on brain sizeDiana Le Duc, Cecilia Giulivi, Susan M Hiatt, et al.
Pageof 3