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Andrea Gropman

Showing results (61-70 of 86) with videos related to

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Therapeutic Innovation & Regulatory Science|April 26, 2022
Global Regulatory and Public Health Initiatives to Advance Pediatric Drug Development for Rare DiseasesCarla Epps, Ralph Bax, Alysha Croker, et al.
Pediatric Neurology|November 19, 2020
Developing a New Set of ACGME Milestones for Child Neurology ResidencyDara V F Albert, Nancy Bass, John Bodensteiner, et al.
Telemedicine Journal and E-Health : the Official Journal of the American Telemedicine Association|March 26, 2014
International telemedicine consultations for neurodevelopmental disabilitiesPhillip L Pearl, Craig Sable, Sarah Evans, et al.
American Journal of Human Genetics|January 26, 2016
Mitotic Intragenic Recombination: A Mechanism of Survival for Several Congenital Disorders of GlycosylationMegan S Kane, Mariska Davids, Christopher Adams, et al.
American Journal of Medical Genetics. Part A|April 4, 2020
Musculoskeletal abnormalities in a large international cohort of boys with 49,XXXXYLaura Tosi, Francie Mitchell, Grace F Porter, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 6, 2009
Linear clinical progression, independent of age of onset, in Niemann-Pick disease, type CNicole M Yanjanin, Jorge I Vélez, Andrea Gropman, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 16, 2026
Predicting epistasis across proteins by structural logicMichelle Tang, Gareth A Cromie, Anowarul Kabir, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 3, 2006
Molecular bases of hearing loss in multi-systemic mitochondrial cytopathyFernando Scaglia, Chang-Hung Hsu, Haeyoung Kwon, et al.
Muscle & Nerve|January 3, 2021
Differentiating Moebius syndrome and other congenital facial weakness disorders with electrodiagnostic studiesTanya Lehky, Reversa Joseph, Camilo Toro, et al.
Molecular Genetics and Metabolism|October 18, 2011
Acute management of propionic acidemiaKimberly A Chapman, Andrea Gropman, Erin MacLeod, et al.
Pageof 9

Showing results (61-70 of 86) with videos related to

Sort By:
Pageof 9
Therapeutic Innovation & Regulatory Science|April 26, 2022
Global Regulatory and Public Health Initiatives to Advance Pediatric Drug Development for Rare DiseasesCarla Epps, Ralph Bax, Alysha Croker, et al.
Pediatric Neurology|November 19, 2020
Developing a New Set of ACGME Milestones for Child Neurology ResidencyDara V F Albert, Nancy Bass, John Bodensteiner, et al.
Telemedicine Journal and E-Health : the Official Journal of the American Telemedicine Association|March 26, 2014
International telemedicine consultations for neurodevelopmental disabilitiesPhillip L Pearl, Craig Sable, Sarah Evans, et al.
American Journal of Human Genetics|January 26, 2016
Mitotic Intragenic Recombination: A Mechanism of Survival for Several Congenital Disorders of GlycosylationMegan S Kane, Mariska Davids, Christopher Adams, et al.
American Journal of Medical Genetics. Part A|April 4, 2020
Musculoskeletal abnormalities in a large international cohort of boys with 49,XXXXYLaura Tosi, Francie Mitchell, Grace F Porter, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 6, 2009
Linear clinical progression, independent of age of onset, in Niemann-Pick disease, type CNicole M Yanjanin, Jorge I Vélez, Andrea Gropman, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 16, 2026
Predicting epistasis across proteins by structural logicMichelle Tang, Gareth A Cromie, Anowarul Kabir, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 3, 2006
Molecular bases of hearing loss in multi-systemic mitochondrial cytopathyFernando Scaglia, Chang-Hung Hsu, Haeyoung Kwon, et al.
Muscle & Nerve|January 3, 2021
Differentiating Moebius syndrome and other congenital facial weakness disorders with electrodiagnostic studiesTanya Lehky, Reversa Joseph, Camilo Toro, et al.
Molecular Genetics and Metabolism|October 18, 2011
Acute management of propionic acidemiaKimberly A Chapman, Andrea Gropman, Erin MacLeod, et al.
Pageof 9