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2020
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The FSHD2 gene SMCHD1 is a modifier of disease severity in families affected by FSHD1.
Not available
S-EPMC3791262
|
biostudies-literature
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Circulating protein biomarkers identified in two independent clinical trial cohorts of glucocorticoid-naive Duchenne muscular dystrophy patients.
Not available
S-EPMC12618936
|
biostudies-literature
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Developing standardized corticosteroid treatment for Duchenne muscular dystrophy.
Not available
S-EPMC6279424
|
biostudies-literature
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A checklist for clinical trials in rare disease: obstacles and anticipatory actions-lessons learned from the FOR-DMD trial.
Not available
S-EPMC5968578
|
biostudies-literature
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Effect of Different Corticosteroid Dosing Regimens on Clinical Outcomes in Boys With Duchenne Muscular Dystrophy: A Randomized Clinical Trial.
Not available
S-EPMC8984930
|
biostudies-literature
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Height, weight, and body mass index trajectories and their correlation with functional outcome assessments in boys with Duchenne muscular dystrophy.
Not available
S-EPMC12875185
|
biostudies-literature
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Suitability of external controls for drug evaluation in Duchenne muscular dystrophy.
Not available
S-EPMC7538219
|
biostudies-literature
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Efficacy and Safety of Bimagrumab in Sporadic Inclusion Body Myositis: Long-term Extension of RESILIENT.
Not available
S-EPMC8032371
|
biostudies-literature
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Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy.
Not available
S-EPMC7818383
|
biostudies-literature
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Measurement of the differential cross section for top quark pair production in pp collisions at [Formula: see text].
Not available
S-EPMC4657759
|
biostudies-literature
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