Evans Sarah H - Physical Medicine, Children's National Medical Center Washington DC

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论文共 14 篇作者统计合作学者相似作者

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A Multi-Disciplinary Clinic for SCN8A-related Epilepsy

John M. Schreiber,Laura Tochen,Mackenzie Brown,Sarah Evans, Laura J. Ball,Adrian Bumbut,Rapeepat Thewamit,Matthew T. Whitehead,Chelsea Black,Emanuel Boutzoukas,Eleanor Fanto,William Suslovic,Madison Berl,Michael Hammer,William D. Gaillard

Epilepsy Research (2020)

引用19浏览0WOS引用

Absence of Axoglial Paranodal Junctions in a Child With CNTNAP1 Mutations, Hypomyelination, and Arthrogryposis

Alexander Conant,Julian Curiel,Amy Pizzino,Parisa Sabetrasekh,Jennifer Murphy,Miriam Bloom,Sarah H Evans,Guy Helman,Ryan J Taft,Cas Simons,Matthew T Whitehead,Steven A Moore,Adeline Vanderver

JOURNAL OF CHILD NEUROLOGY（2018）

引用12浏览0WOS引用

Mutations in SZT2 result in early-onset epileptic encephalopathy and leukoencephalopathy

Amy Pizzino,Matthew Whitehead,Parisa Sabet Rasekh,Jennifer Murphy,Guy Helman,Miriam Bloom,Sarah H Evans, John G Murnick,Joan Conry,Ryan J Taft,Cas Simons,Adeline Vanderver,Laura A Adang

AMERICAN JOURNAL OF MEDICAL GENETICS PART A（2018）

引用13浏览0WOS引用

Revised Consensus Statement on the Preventive and Symptomatic Care of Patients with Leukodystrophies

Molecular genetics and metabolismno. 1-2 (2017): 18-32

引用39浏览0WOS引用

Poster 139: PedBOT: Robotically Assisted Rehabilitation for Children with Cerebral Palsy

Sarah H. Evans

PM&R（2017）

引用0浏览0引用

Gjc2 Promoter Mutations Causing Pelizaeus-Merzbacher-Like Disease (Vol 111, Pg 393, 2014)

Leo Gotoh,Ken Inoue,Guy Heiman,Sara Mora,Kiran Maski,Janet S. Soul,Miriam Bloom,Sarah H. Evans,Yu-Ichi Goto,Ljubica Caldovic,Grace M. Hobson,Adeline Vanderver

MOLECULAR GENETICS AND METABOLISMno. 3 (2016)

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Corrigendum to "GJC2 Promoter Mutations Causing Pelizaeus-Merzbacher-like Disease" [mol. Genet. Metab. 111 (2014) 393-398]

Leo Gotoh,Ken Inoue,Guy Helman,Sara Mora,Kiran Maski,Janet S Soul,Miriam Bloom,Sarah H Evans,Yu-Ichi Goto,Ljubica Caldovic,Grace M Hobson,Adeline Vanderver

Molecular genetics and metabolism（2016）

引用0浏览0WOS引用

Loss-of-function Alanyl-Trna Synthetase Mutations Cause an Autosomal-Recessive Early-Onset Epileptic Encephalopathy with Persistent Myelination Defect

American journal of human geneticsno. 4 (2015): 675-81

引用85浏览0WOS引用

International telemedicine consultations for neurodevelopmental disabilities

Phillip L Pearl,Craig Sable,Sarah Evans,Joseph Knight,Parker Cunningham,Gaetano R Lotrecchiano,Andrea Gropman,Sheela Stuart,Penny Glass,Anne Conway,Issam Ramadan,Tania Paiva,Mark L Batshaw,Roger J Packer

TELEMEDICINE AND E-HEALTH（2014）

引用24浏览0WOS引用

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