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S Verhoeven

Showing results (51-60 of 60) with videos related to

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Brain Communications|September 6, 2024
Quality of life in <i>SCN1A</i>-related seizure disorders across the lifespanCrista A Minderhoud, Amber Postma, Floor E Jansen, et al.
Annals of Clinical and Translational Neurology|March 25, 2020
Cardiac arrhythmias in Dravet syndrome: an observational multicenter studySharon Shmuely, Rainer Surges, Robert M Helling, et al.
Cerebral Cortex (New York, N.Y. : 1991)|November 4, 2011
Is there a common neuroanatomical substrate of language deficit between autism spectrum disorder and specific language impairment?Judith S Verhoeven, Nathalie Rommel, Elena Prodi, et al.
BMC Health Services Research|March 26, 2022
Identifying client characteristics to predict homecare use more accurately: a Delphi-study involving nurses and homecare purchasing specialistsAnne O E van den Bulck, Arianne M J Elissen, Silke F Metzelthin, et al.
Epilepsia|December 8, 2018
Diagnostic exome sequencing in 100 consecutive patients with both epilepsy and intellectual disabilityFrancesca M Snoeijen-Schouwenaars, Jans S van Ool, Judith S Verhoeven, et al.
Journal of Neurophysiology|May 18, 2022
Human <i>KCNQ5</i> de novo mutations underlie epilepsy and intellectual disabilityAguan D Wei, Paul Wakenight, Theresa A Zwingman, et al.
Molecular Psychiatry|June 19, 2013
The autism brain imaging data exchange: towards a large-scale evaluation of the intrinsic brain architecture in autismA Di Martino, C-G Yan, Q Li, et al.
Epilepsia|January 10, 2018
Defining the phenotypic spectrum of SLC6A1 mutationsKatrine M Johannesen, Elena Gardella, Tarja Linnankivi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 4, 2020
NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patternsHannah Stamberger, Trine B Hammer, Elena Gardella, et al.
Brain : a Journal of Neurology|August 25, 2021
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implicationsKatrine M Johannesen, Yuanyuan Liu, Mahmoud Koko, et al.
Pageof 6

Showing results (51-60 of 60) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 60 results.
Brain Communications|September 6, 2024
Quality of life in <i>SCN1A</i>-related seizure disorders across the lifespanCrista A Minderhoud, Amber Postma, Floor E Jansen, et al.
Annals of Clinical and Translational Neurology|March 25, 2020
Cardiac arrhythmias in Dravet syndrome: an observational multicenter studySharon Shmuely, Rainer Surges, Robert M Helling, et al.
Cerebral Cortex (New York, N.Y. : 1991)|November 4, 2011
Is there a common neuroanatomical substrate of language deficit between autism spectrum disorder and specific language impairment?Judith S Verhoeven, Nathalie Rommel, Elena Prodi, et al.
BMC Health Services Research|March 26, 2022
Identifying client characteristics to predict homecare use more accurately: a Delphi-study involving nurses and homecare purchasing specialistsAnne O E van den Bulck, Arianne M J Elissen, Silke F Metzelthin, et al.
Epilepsia|December 8, 2018
Diagnostic exome sequencing in 100 consecutive patients with both epilepsy and intellectual disabilityFrancesca M Snoeijen-Schouwenaars, Jans S van Ool, Judith S Verhoeven, et al.
Journal of Neurophysiology|May 18, 2022
Human <i>KCNQ5</i> de novo mutations underlie epilepsy and intellectual disabilityAguan D Wei, Paul Wakenight, Theresa A Zwingman, et al.
Molecular Psychiatry|June 19, 2013
The autism brain imaging data exchange: towards a large-scale evaluation of the intrinsic brain architecture in autismA Di Martino, C-G Yan, Q Li, et al.
Epilepsia|January 10, 2018
Defining the phenotypic spectrum of SLC6A1 mutationsKatrine M Johannesen, Elena Gardella, Tarja Linnankivi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 4, 2020
NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patternsHannah Stamberger, Trine B Hammer, Elena Gardella, et al.
Brain : a Journal of Neurology|August 25, 2021
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implicationsKatrine M Johannesen, Yuanyuan Liu, Mahmoud Koko, et al.
Pageof 6