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Michael Shevell

Showing results (161-170 of 168) with videos related to

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Brain : a Journal of Neurology|April 19, 2007
Phenotypical spectrum of DOK7 mutations in congenital myasthenic syndromesJuliane S Müller, Agnes Herczegfalvi, Juan J Vilchez, et al.
Pediatric Neurology|March 4, 2017
Epidemiology and Outcomes of Arterial Ischemic Stroke in Children: The Canadian Pediatric Ischemic Stroke RegistryGabrielle A deVeber, Adam Kirton, Frances A Booth, et al.
Epilepsia|May 19, 2015
Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcomeBronwyn E Grinton, Sarah E Heron, James T Pelekanos, et al.
Pediatric Neurology|June 4, 2018
Health-Related Quality of Life for Patients With Genetically Determined LeukoencephalopathyAmytice Mirchi, Félixe Pelletier, Luan T Tran, et al.
Health Care Transitions|June 19, 2026
An e-health transition intervention for youth with brain-based disabilities: Pilot and feasibility results from a Randomized Controlled TrialJan Willem Gorter, Ronen Rozenblum, Adrienne H Kovacs, et al.
American Journal of Human Genetics|March 8, 2011
Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disabilityFadi F Hamdan, Julie Gauthier, Yoichi Araki, et al.
European Journal of Human Genetics : EJHG|October 7, 2018
Heterozygous loss-of-function variants of MEIS2 cause a triad of palatal defects, congenital heart defects, and intellectual disabilityRosalind Verheije, Gabriel S Kupchik, Bertrand Isidor, et al.
Nature Genetics|March 30, 2024
Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsyDarcy L Fehlings, Mehdi Zarrei, Worrawat Engchuan, et al.
Pageof 17

Showing results (161-170 of 168) with videos related to

Sort By:
Pageof 17
You have reached the last page of results.This site can display upto 168 results.
Brain : a Journal of Neurology|April 19, 2007
Phenotypical spectrum of DOK7 mutations in congenital myasthenic syndromesJuliane S Müller, Agnes Herczegfalvi, Juan J Vilchez, et al.
Pediatric Neurology|March 4, 2017
Epidemiology and Outcomes of Arterial Ischemic Stroke in Children: The Canadian Pediatric Ischemic Stroke RegistryGabrielle A deVeber, Adam Kirton, Frances A Booth, et al.
Epilepsia|May 19, 2015
Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcomeBronwyn E Grinton, Sarah E Heron, James T Pelekanos, et al.
Pediatric Neurology|June 4, 2018
Health-Related Quality of Life for Patients With Genetically Determined LeukoencephalopathyAmytice Mirchi, Félixe Pelletier, Luan T Tran, et al.
Health Care Transitions|June 19, 2026
An e-health transition intervention for youth with brain-based disabilities: Pilot and feasibility results from a Randomized Controlled TrialJan Willem Gorter, Ronen Rozenblum, Adrienne H Kovacs, et al.
American Journal of Human Genetics|March 8, 2011
Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disabilityFadi F Hamdan, Julie Gauthier, Yoichi Araki, et al.
European Journal of Human Genetics : EJHG|October 7, 2018
Heterozygous loss-of-function variants of MEIS2 cause a triad of palatal defects, congenital heart defects, and intellectual disabilityRosalind Verheije, Gabriel S Kupchik, Bertrand Isidor, et al.
Nature Genetics|March 30, 2024
Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsyDarcy L Fehlings, Mehdi Zarrei, Worrawat Engchuan, et al.
Pageof 17