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Annals of Clinical and Translational Neurology
|
September 11, 2023
Propensity matched comparison of omaveloxolone treatment to Friedreich ataxia natural history data
David R Lynch, Angie Goldsberry, Christian Rummey, et al.
Annals of Neurology
|
October 17, 2020
Safety and Efficacy of Omaveloxolone in Friedreich Ataxia (MOXIe Study)
David R Lynch, Melanie P Chin, Martin B Delatycki, et al.
International Journal of Epidemiology
|
June 23, 2023
Variance of age-specific log incidence decomposition (VALID): a unifying model of measured and unmeasured genetic and non-genetic risks
John L Hopper, James G Dowty, Tuong L Nguyen, et al.
Neurology
|
December 30, 2004
Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteria
M K Bruno, M Hallett, K Gwinn-Hardy, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
October 13, 2006
The muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet): surveillance methodology
Lisa A Miller, Paul A Romitti, Christopher Cunniff, et al.
Muscle & Nerve
|
April 25, 2020
The care of patients with Duchenne, Becker, and other muscular dystrophies in the COVID-19 pandemic
Aravindhan Veerapandiyan, Kathryn R Wagner, Susan Apkon, et al.
Journal of Child Neurology
|
April 3, 2018
Impact of Mobility Device Use on Quality of Life in Children With Friedreich Ataxia
Resham Ejaz, Shiyi Chen, Charles J Isaacs, et al.
Journal of Neuromuscular Diseases
|
April 12, 2024
Management of Select Adverse Events Following Delandistrogene Moxeparvovec Gene Therapy for Patients With Duchenne Muscular Dystrophy
Craig M Zaidman, Natalie L Goedeker, Amal A Aqul, et al.
Annals of Clinical and Translational Neurology
|
March 27, 2019
Randomized, double-blind, placebo-controlled study of interferon-<i>γ</i> 1b in Friedreich Ataxia
David R Lynch, Lauren Hauser, Ashley McCormick, et al.
Annals of Neurology
|
October 1, 2008
Collagen VI glycine mutations: perturbed assembly and a spectrum of clinical severity
Rishika A Pace, Rachel A Peat, Naomi L Baker, et al.
Page
of 45
Search research articles
Search
Showing results (401-410 of 450) with videos related to
Sort By:
Page
of 45
Annals of Clinical and Translational Neurology
|
September 11, 2023
Propensity matched comparison of omaveloxolone treatment to Friedreich ataxia natural history data
David R Lynch, Angie Goldsberry, Christian Rummey, et al.
Annals of Neurology
|
October 17, 2020
Safety and Efficacy of Omaveloxolone in Friedreich Ataxia (MOXIe Study)
David R Lynch, Melanie P Chin, Martin B Delatycki, et al.
International Journal of Epidemiology
|
June 23, 2023
Variance of age-specific log incidence decomposition (VALID): a unifying model of measured and unmeasured genetic and non-genetic risks
John L Hopper, James G Dowty, Tuong L Nguyen, et al.
Neurology
|
December 30, 2004
Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteria
M K Bruno, M Hallett, K Gwinn-Hardy, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
October 13, 2006
The muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet): surveillance methodology
Lisa A Miller, Paul A Romitti, Christopher Cunniff, et al.
Muscle & Nerve
|
April 25, 2020
The care of patients with Duchenne, Becker, and other muscular dystrophies in the COVID-19 pandemic
Aravindhan Veerapandiyan, Kathryn R Wagner, Susan Apkon, et al.
Journal of Child Neurology
|
April 3, 2018
Impact of Mobility Device Use on Quality of Life in Children With Friedreich Ataxia
Resham Ejaz, Shiyi Chen, Charles J Isaacs, et al.
Journal of Neuromuscular Diseases
|
April 12, 2024
Management of Select Adverse Events Following Delandistrogene Moxeparvovec Gene Therapy for Patients With Duchenne Muscular Dystrophy
Craig M Zaidman, Natalie L Goedeker, Amal A Aqul, et al.
Annals of Clinical and Translational Neurology
|
March 27, 2019
Randomized, double-blind, placebo-controlled study of interferon-<i>γ</i> 1b in Friedreich Ataxia
David R Lynch, Lauren Hauser, Ashley McCormick, et al.
Annals of Neurology
|
October 1, 2008
Collagen VI glycine mutations: perturbed assembly and a spectrum of clinical severity
Rishika A Pace, Rachel A Peat, Naomi L Baker, et al.
Page
of 45