Therapeutic Approaches in Facioscapulohumeral Muscular Dystrophy
Author:
Funder
Friends of FSH Research
FSH Society
Publisher
Elsevier BV
Subject
Molecular Biology,Molecular Medicine
Reference127 articles.
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4. A pediatric review of facioscapulohumeral muscular dystrophy;Mah;J. Pediatr. Neurol.,2018
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2. An open-label pilot study of losmapimod to evaluate the safety, tolerability, and changes in biomarker and clinical outcome assessments in participants with facioscapulohumeral muscular dystrophy type 1;Journal of the Neurological Sciences;2024-07
3. First‐trimester noninvasive prenatal diagnosis of seven facioscapulohumeral muscular dystrophy type 1 families using SNP‐based amplicon sequencing: An earlier, rapid and safer way;American Journal of Medical Genetics Part A;2024-02-08
4. A Targeted Approach for Evaluating DUX4-Regulated Proteins as Potential Serum Biomarkers for Facioscapulohumeral Muscular Dystrophy Using Immunoassay Proteomics;Journal of Neuromuscular Diseases;2023-11-07
5. Deciphering D4Z4 CpG methylation gradients in fascioscapulohumeral muscular dystrophy using nanopore sequencing;Genome Research;2023-09
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