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Danielle M Andrade

Showing results (81-90 of 122) with videos related to

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Neurology. Genetics|November 27, 2024
Adult Phenotype of <i>CHD2</i>-Associated DisordersMarlene Rong, Quratulain Zulfiqar Ali, Angel Aledo-Serrano, et al.
American Journal of Medical Genetics. Part A|February 17, 2015
Movement disorders and other motor abnormalities in adults with 22q11.2 deletion syndromeErik Boot, Nancy J Butcher, Thérèse A M J van Amelsvoort, et al.
Psychiatric Genetics|November 4, 2015
Identification of a homozygous missense mutation in LRP2 and a hemizygous missense mutation in TSPYL2 in a family with mild intellectual disabilityNasim Vasli, Iltaf Ahmed, Kirti Mittal, et al.
Epilepsia Open|June 12, 2020
Daily listening to Mozart reduces seizures in individuals with epilepsy: A randomized control studyMarjan Rafiee, Kramay Patel, David M Groppe, et al.
Epilepsy & Behavior : E&B|January 18, 2019
STXBP1 encephalopathy is associated with awake bruxismArezoo Rezazadeh, Mohammed Uddin, O Carter Snead, et al.
Neurology. Genetics|December 4, 2023
Adult Phenotype of <i>SYNGAP1</i>-DEEMarlene Rong, Tim Benke, Quratulain Zulfiqar Ali, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 1, 2014
Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literatureChelsea Lowther, Gregory Costain, Dimitri J Stavropoulos, et al.
Epilepsy Research|October 8, 2021
Dravet syndrome: A quick transition guide for the adult neurologistDanielle M Andrade, Anne T Berg, Veronica Hood, et al.
Epilepsia|December 30, 2021
Adults with tuberous sclerosis complex: A distinct patient populationKenan Bachour, Andrew A House, Danielle M Andrade, et al.
Epilepsy Research|April 30, 2023
A comprehensive narrative review of epilepsy with eyelid myocloniaKelsey M Smith, Elaine C Wirrell, Danielle M Andrade, et al.
Pageof 13

Showing results (81-90 of 122) with videos related to

Sort By:
Pageof 13
Neurology. Genetics|November 27, 2024
Adult Phenotype of <i>CHD2</i>-Associated DisordersMarlene Rong, Quratulain Zulfiqar Ali, Angel Aledo-Serrano, et al.
American Journal of Medical Genetics. Part A|February 17, 2015
Movement disorders and other motor abnormalities in adults with 22q11.2 deletion syndromeErik Boot, Nancy J Butcher, Thérèse A M J van Amelsvoort, et al.
Psychiatric Genetics|November 4, 2015
Identification of a homozygous missense mutation in LRP2 and a hemizygous missense mutation in TSPYL2 in a family with mild intellectual disabilityNasim Vasli, Iltaf Ahmed, Kirti Mittal, et al.
Epilepsia Open|June 12, 2020
Daily listening to Mozart reduces seizures in individuals with epilepsy: A randomized control studyMarjan Rafiee, Kramay Patel, David M Groppe, et al.
Epilepsy & Behavior : E&B|January 18, 2019
STXBP1 encephalopathy is associated with awake bruxismArezoo Rezazadeh, Mohammed Uddin, O Carter Snead, et al.
Neurology. Genetics|December 4, 2023
Adult Phenotype of <i>SYNGAP1</i>-DEEMarlene Rong, Tim Benke, Quratulain Zulfiqar Ali, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 1, 2014
Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literatureChelsea Lowther, Gregory Costain, Dimitri J Stavropoulos, et al.
Epilepsy Research|October 8, 2021
Dravet syndrome: A quick transition guide for the adult neurologistDanielle M Andrade, Anne T Berg, Veronica Hood, et al.
Epilepsia|December 30, 2021
Adults with tuberous sclerosis complex: A distinct patient populationKenan Bachour, Andrew A House, Danielle M Andrade, et al.
Epilepsy Research|April 30, 2023
A comprehensive narrative review of epilepsy with eyelid myocloniaKelsey M Smith, Elaine C Wirrell, Danielle M Andrade, et al.
Pageof 13