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Familial cardiomyopathy caused by a novel heterozygous mutation in the gene LMNA (c.1434dupG): a cardiac MRI-augmented segregation study.
- Published in:
- Acta Myologica, 2019, v. 38, n. 3, p. 159
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- Publication type:
- Article
Phenotypic and genetic spectrum of patients with limb-girdle muscular dystrophy type 2A from Serbia.
- Published in:
- Acta Myologica, 2019, v. 38, n. 3, p. 163
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- Publication type:
- Article
Current and emerging therapies in Becker muscular dystrophy (BMD).
- Published in:
- Acta Myologica, 2019, v. 38, n. 3, p. 172
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- Publication type:
- Article
The first Portuguese family with NEFL-related Charcot-Marie-Tooth type 2 disease.
- Published in:
- Acta Myologica, 2019, v. 38, n. 3, p. 180
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- Publication type:
- Article
Acute sensorimotor polyneuropathy as an early sign of polyarteritis nodosa. A case report.
- Published in:
- Acta Myologica, 2019, v. 38, n. 3, p. 184
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- Publication type:
- Article
AIM.
- Published in:
- Acta Myologica, 2019, v. 38, n. 3, p. 189
- Publication type:
- Article
MSM.
- Published in:
- Acta Myologica, 2019, v. 38, n. 3, p. 189
- Publication type:
- Article
FORTHCOMING MEETINGS.
- Published in:
- Acta Myologica, 2019, v. 38, n. 3, p. 190
- Publication type:
- Article