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Scott Demarest

Showing results (51-60 of 61) with videos related to

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Epilepsia|April 28, 2023
Epileptic spasms in CDKL5 deficiency disorder: Delayed treatment and poor response to first-line therapiesHeather E Olson, Scott Demarest, Elia Pestana-Knight, et al.
Brain Communications|November 26, 2020
Current knowledge of SLC6A1-related neurodevelopmental disordersKimberly Goodspeed, Eduardo Pérez-Palma, Sumaiya Iqbal, et al.
American Journal of Medical Genetics. Part A|August 29, 2024
Deletions in the CDKL5 5' untranslated region lead to CDKL5 deficiency disorderIsabel Haviland, Ralph D Hector, Lindsay C Swanson, et al.
Pediatric Neurology|June 1, 2019
Severity Assessment in CDKL5 Deficiency DisorderScott Demarest, Elia M Pestana-Knight, Heather E Olson, et al.
Annals of Neurology|April 29, 2020
Randomized Clinical Trial of First-Line Genome Sequencing in Pediatric White Matter DisordersAdeline Vanderver, Geneviève Bernard, Guy Helman, et al.
Medrxiv : the Preprint Server for Health Sciences|February 12, 2026
A Prospective Natural History Study Protocol for Clinical Trial Readiness in Synaptic DisordersJillian L McKee, Sarah M Ruggiero, Kristin Cunningham, et al.
Brain : a Journal of Neurology|July 28, 2025
Variants in DENND2B are associated with vulnerability for neurodevelopmental impairment, psychosis and catatoniaHarsha Murthy, Ny Hoang, Jamie C Stark, et al.
Brain : a Journal of Neurology|August 12, 2021
De novo DHDDS variants cause a neurodevelopmental and neurodegenerative disorder with myoclonusSerena Galosi, Ban H Edani, Simone Martinelli, et al.
Brain : a Journal of Neurology|February 22, 2022
Assessing the landscape of STXBP1-related disorders in 534 individualsJulie Xian, Shridhar Parthasarathy, Sarah M Ruggiero, et al.
Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
The natural history of CDKL5 deficiency disorder into adulthoodAngel Aledo-Serrano, David Lewis-Smith, Helen Leonard, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
Epilepsia|April 28, 2023
Epileptic spasms in CDKL5 deficiency disorder: Delayed treatment and poor response to first-line therapiesHeather E Olson, Scott Demarest, Elia Pestana-Knight, et al.
Brain Communications|November 26, 2020
Current knowledge of SLC6A1-related neurodevelopmental disordersKimberly Goodspeed, Eduardo Pérez-Palma, Sumaiya Iqbal, et al.
American Journal of Medical Genetics. Part A|August 29, 2024
Deletions in the CDKL5 5' untranslated region lead to CDKL5 deficiency disorderIsabel Haviland, Ralph D Hector, Lindsay C Swanson, et al.
Pediatric Neurology|June 1, 2019
Severity Assessment in CDKL5 Deficiency DisorderScott Demarest, Elia M Pestana-Knight, Heather E Olson, et al.
Annals of Neurology|April 29, 2020
Randomized Clinical Trial of First-Line Genome Sequencing in Pediatric White Matter DisordersAdeline Vanderver, Geneviève Bernard, Guy Helman, et al.
Medrxiv : the Preprint Server for Health Sciences|February 12, 2026
A Prospective Natural History Study Protocol for Clinical Trial Readiness in Synaptic DisordersJillian L McKee, Sarah M Ruggiero, Kristin Cunningham, et al.
Brain : a Journal of Neurology|July 28, 2025
Variants in DENND2B are associated with vulnerability for neurodevelopmental impairment, psychosis and catatoniaHarsha Murthy, Ny Hoang, Jamie C Stark, et al.
Brain : a Journal of Neurology|August 12, 2021
De novo DHDDS variants cause a neurodevelopmental and neurodegenerative disorder with myoclonusSerena Galosi, Ban H Edani, Simone Martinelli, et al.
Brain : a Journal of Neurology|February 22, 2022
Assessing the landscape of STXBP1-related disorders in 534 individualsJulie Xian, Shridhar Parthasarathy, Sarah M Ruggiero, et al.
Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
The natural history of CDKL5 deficiency disorder into adulthoodAngel Aledo-Serrano, David Lewis-Smith, Helen Leonard, et al.
Pageof 7