Works matching IS 11282460 AND DT 2020 AND VI 39 AND IP 1
Results: 8
Neuromuscular tetanic hyperexcitability syndrome associated to a heterozygous Kv1.1 N255D mutation with normal serum magnesium levels.
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- Acta Myologica, 2020, v. 39, n. 1, p. 36, doi. 10.36185/2532-1900-007
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- Article
Myotonic dystrophy type 1 and high ventricular vulnerability at the electrophysiological evaluation: ICD yes or not?
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- Acta Myologica, 2020, v. 39, n. 1, p. 32, doi. 10.36185/2532-1900-006
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- Article
Facioscapulohumeral muscular dystrophy (FSHD) and multiple sclerosis: a case report.
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- Acta Myologica, 2020, v. 39, n. 1, p. 29, doi. 10.36185/2532-1900-005
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- Article
Laing early-onset distal myopathy with subsarcolemmal hyaline bodies caused by a novel variant in the MYH7 gene.
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- Acta Myologica, 2020, v. 39, n. 1, p. 24, doi. 10.36185/2532-1900-004
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- Article
Late-onset MADD: a rare cause of cirrhosis and acute liver failure?
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- Acta Myologica, 2020, v. 39, n. 1, p. 19, doi. 10.36185/2532-1900-003
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- Article
Coagulation disorders in Duchenne muscular dystrophy? Results of a registry-based online survey.
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- Acta Myologica, 2020, v. 39, n. 1, p. 2, doi. 10.36185/2532-1900-001
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- Article
New graphic for Acta Myologica.
- Published in:
- Acta Myologica, 2020, v. 39, n. 1, p. 1
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- Article
Identification, molecular characterization and segregation analysis of a variant DMPK pre-mutation allele in a three-generation Italian family.
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- Acta Myologica, 2020, v. 39, n. 1, p. 13, doi. 10.36185/2532-1900-002
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- Article