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Elliott H Sherr

Showing results (1-10 of 119) with videos related to

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Current Opinion in Pediatrics|November 25, 2003
The ARX story (epilepsy, mental retardation, autism, and cerebral malformations): one gene leads to many phenotypesElliott H Sherr
Seminars in Pediatric Neurology|September 26, 2009
IntroductionElliott H Sherr
Neurology|November 20, 2015
Neuroimaging in Aicardi-Goutières syndrome: Biomarkers for a progressive encephalopathyBesim Uzgil, Elliott H Sherr
Nature Clinical Practice. Neurology|January 24, 2008
Hematopoietic stem cell transplantation for the treatment of childhood cerebral X-linked adrenoleukodystrophyLuigi Maccotta, Elliott H Sherr
Annals of Neurology|August 30, 2008
The importance of metabolic testing in the evaluation of intellectual disabilitySabine Mueller, Elliott H Sherr
Journal of Neurogenetics|January 5, 2016
A de novo mutation in PRICKLE1 in fetal agenesis of the corpus callosum and polymicrogyriaAlexander G Bassuk, Elliott H Sherr
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|October 1, 2014
Epileptic encephalopathies: new genes and new pathwaysSahar Esmaeeli Nieh, Elliott H Sherr
Trends in Molecular Medicine|July 8, 2023
The variant landscape and function of DDX3X in cancer and neurodevelopmental disordersMargaret Gadek, Elliott H Sherr, Stephen N Floor
Pediatric Neurology|April 16, 2008
Dilated perivascular spaces: an informative radiologic finding in Sanfilippo syndrome type ASimay Kara, Elliott H Sherr, A James Barkovich
Pediatric Neurology|April 18, 2022
De Novo GLI3 Pathogenic Variants May Cause Hypotonia and a Range of Brain Malformations Without Skeletal AbnormalitiesLyna Siafa, Emanuela Argilli, Elliott H Sherr, et al.
Pageof 12

Showing results (1-10 of 119) with videos related to

Sort By:
Pageof 12
Current Opinion in Pediatrics|November 25, 2003
The ARX story (epilepsy, mental retardation, autism, and cerebral malformations): one gene leads to many phenotypesElliott H Sherr
Seminars in Pediatric Neurology|September 26, 2009
IntroductionElliott H Sherr
Neurology|November 20, 2015
Neuroimaging in Aicardi-Goutières syndrome: Biomarkers for a progressive encephalopathyBesim Uzgil, Elliott H Sherr
Nature Clinical Practice. Neurology|January 24, 2008
Hematopoietic stem cell transplantation for the treatment of childhood cerebral X-linked adrenoleukodystrophyLuigi Maccotta, Elliott H Sherr
Annals of Neurology|August 30, 2008
The importance of metabolic testing in the evaluation of intellectual disabilitySabine Mueller, Elliott H Sherr
Journal of Neurogenetics|January 5, 2016
A de novo mutation in PRICKLE1 in fetal agenesis of the corpus callosum and polymicrogyriaAlexander G Bassuk, Elliott H Sherr
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|October 1, 2014
Epileptic encephalopathies: new genes and new pathwaysSahar Esmaeeli Nieh, Elliott H Sherr
Trends in Molecular Medicine|July 8, 2023
The variant landscape and function of DDX3X in cancer and neurodevelopmental disordersMargaret Gadek, Elliott H Sherr, Stephen N Floor
Pediatric Neurology|April 16, 2008
Dilated perivascular spaces: an informative radiologic finding in Sanfilippo syndrome type ASimay Kara, Elliott H Sherr, A James Barkovich
Pediatric Neurology|April 18, 2022
De Novo GLI3 Pathogenic Variants May Cause Hypotonia and a Range of Brain Malformations Without Skeletal AbnormalitiesLyna Siafa, Emanuela Argilli, Elliott H Sherr, et al.
Pageof 12