FORTHCOMING MEETINGS.
- Published in:
- Acta Myologica, 2019, v. 38, n. 3, p. 190
- Publication type:
- Article
Works matching IS 11282460 AND DT 2019 AND VI 38 AND IP 3
Results: 8
1
2
MSM.
- Published in:
- Acta Myologica, 2019, v. 38, n. 3, p. 189
- Publication type:
- Article
3
AIM.
- Published in:
- Acta Myologica, 2019, v. 38, n. 3, p. 189
- Publication type:
- Article
4
Acute sensorimotor polyneuropathy as an early sign of polyarteritis nodosa. A case report.
- Published in:
- Acta Myologica, 2019, v. 38, n. 3, p. 184
- By:
- Publication type:
- Article
5
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
- By:
- Publication type:
- Article
6
The first Portuguese family with NEFL-related Charcot-Marie-Tooth type 2 disease.
- Published in:
- Acta Myologica, 2019, v. 38, n. 3, p. 180
- By:
- Publication type:
- Article
7
Current and emerging therapies in Becker muscular dystrophy (BMD).
- Published in:
- Acta Myologica, 2019, v. 38, n. 3, p. 172
- By:
- Publication type:
- Article
8
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
- By:
- Publication type:
- Article