Found: 7
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Mild limb girdle muscular dystrophy R9 phenotype caused by novel compound heterozygous FKRP gene mutation.
- Published in:
- Acta Myologica, 2023, v. 42, n. 4, p. 106, doi. 10.36185/2532-1900-391
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- Publication type:
- Article
Skeletal muscle involvement in biallelic SORD mutations: case report and review of the literature.
- Published in:
- Acta Myologica, 2023, v. 42, n. 4, p. 113, doi. 10.36185/2532-1900-323
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- Publication type:
- Article
Continuitiy of care with ataluren in Duchenne Muscular Dystrophy patients with nonsense mutations after loss of ambulation. Personal experience.
- Published in:
- Acta Myologica, 2023, v. 42, n. 4, p. 118, doi. 10.36185/2532-1900-396
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- Publication type:
- Article
Long-read sequencing improves diagnostic rate in neuromuscular disorders.
- Published in:
- Acta Myologica, 2023, v. 42, n. 4, p. 123, doi. 10.36185/2532-1900-394
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- Publication type:
- Article
Efficacy of N-163 beta-glucan in beneficially improving biomarkers of relevance to muscle function in patients with muscular dystrophies in a pilot clinical study.
- Published in:
- Acta Myologica, 2023, v. 42, n. 4, p. 129, doi. 10.36185/2532-1900-312
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- Publication type:
- Article
NEWS FROM AROUND THE WORLD.
- Published in:
- Acta Myologica, 2023, v. 42, n. 4, p. 135
- Publication type:
- Article
FORTHCOMING MEETINGS.
- Published in:
- Acta Myologica, 2023, v. 42, n. 4, p. 137
- Publication type:
- Article