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Wendy Mitchell

Showing results (21-30 of 25) with videos related to

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Autism Research : Official Journal of the International Society for Autism Research|October 19, 2016
Research needs and priorities for transition and employment in autism: Considerations reflected in a "Special Interest Group" at the International Meeting for Autism ResearchDavid B Nicholas, Sandra Hodgetts, Lonnie Zwaigenbaum, et al.
Epilepsia|July 21, 2021
Long-term safety and efficacy of add-on cannabidiol in patients with Lennox-Gastaut syndrome: Results of a long-term open-label extension trialAnup D Patel, Maria Mazurkiewicz-Bełdzińska, Richard F Chin, et al.
Frontiers in Genetics|May 28, 2021
Deep-Phenotyping the Less Severe Spectrum of <i>PIGT</i> Deficiency and Linking the Gene to Myoclonic Atonic SeizuresAllan Bayat, Manuela Pendziwiat, Ewa Obersztyn, 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.
Human Mutation|March 1, 2019
SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported IndividualsBobby G Ng, Paulina Sosicka, Satish Agadi, et al.
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Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Autism Research : Official Journal of the International Society for Autism Research|October 19, 2016
Research needs and priorities for transition and employment in autism: Considerations reflected in a "Special Interest Group" at the International Meeting for Autism ResearchDavid B Nicholas, Sandra Hodgetts, Lonnie Zwaigenbaum, et al.
Epilepsia|July 21, 2021
Long-term safety and efficacy of add-on cannabidiol in patients with Lennox-Gastaut syndrome: Results of a long-term open-label extension trialAnup D Patel, Maria Mazurkiewicz-Bełdzińska, Richard F Chin, et al.
Frontiers in Genetics|May 28, 2021
Deep-Phenotyping the Less Severe Spectrum of <i>PIGT</i> Deficiency and Linking the Gene to Myoclonic Atonic SeizuresAllan Bayat, Manuela Pendziwiat, Ewa Obersztyn, 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.
Human Mutation|March 1, 2019
SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported IndividualsBobby G Ng, Paulina Sosicka, Satish Agadi, et al.
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