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Annals of Neurology
|
October 1, 2018
NBEA: Developmental disease gene with early generalized epilepsy phenotypes
Maureen S Mulhern, Constance Stumpel, Nicholas Stong, et al.
Clinical Genetics
|
May 26, 2022
Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder
Maria B Christensen, Amanda M Levy, Nazanin A Mohammadi, et al.
Epilepsia
|
February 18, 2022
PIGN encephalopathy: Characterizing the epileptology
Allan Bayat, Guillem de Valles-Ibáñez, Manuela Pendziwiat, et al.
Brain : a Journal of Neurology
|
April 6, 2017
Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders
Markus Wolff, Katrine M Johannesen, Ulrike B S Hedrich, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 13, 2018
IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients
Cyril Mignot, Aoife C McMahon, Claire Bar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 4, 2018
Correction: IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients
Cyril Mignot, Aoife C McMahon, Claire Bar, et al.
Molecular Psychiatry
|
November 17, 2022
Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition
Elizabeth E Palmer, Michael Pusch, Alessandra Picollo, et al.
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of 14
Search research articles
Search
Showing results (131-140 of 137) with videos related to
Sort By:
Page
of 14
You have reached the last page of results.
This site can display upto 137 results.
Annals of Neurology
|
October 1, 2018
NBEA: Developmental disease gene with early generalized epilepsy phenotypes
Maureen S Mulhern, Constance Stumpel, Nicholas Stong, et al.
Clinical Genetics
|
May 26, 2022
Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder
Maria B Christensen, Amanda M Levy, Nazanin A Mohammadi, et al.
Epilepsia
|
February 18, 2022
PIGN encephalopathy: Characterizing the epileptology
Allan Bayat, Guillem de Valles-Ibáñez, Manuela Pendziwiat, et al.
Brain : a Journal of Neurology
|
April 6, 2017
Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders
Markus Wolff, Katrine M Johannesen, Ulrike B S Hedrich, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 13, 2018
IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients
Cyril Mignot, Aoife C McMahon, Claire Bar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 4, 2018
Correction: IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients
Cyril Mignot, Aoife C McMahon, Claire Bar, et al.
Molecular Psychiatry
|
November 17, 2022
Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition
Elizabeth E Palmer, Michael Pusch, Alessandra Picollo, et al.
Page
of 14