Limb girdle muscle dystrophy: a Brazilian cohort on ICGNMD study (2022)
- Authors:
- USP affiliated authors: TOMASELLI, PEDRO JOSÉ - FMRP ; MARQUES JÚNIOR, WILSON - FMRP ; SOBREIRA, CLAUDIA FERREIRA DA ROSA - FMRP ; FREZATTI, RODRIGO SIQUEIRA SOARES - FMRP
- Unidade: FMRP
- DOI: 10.1016/j.nmd.2022.07.319
- Subjects: DOENÇAS MUSCULOSQUELÉTICAS; DISTROFIA MUSCULAR; ESTUDOS DE COORTES
- Language: Inglês
- Imprenta:
- Publisher place: Kidlington
- Date published: 2022
- Source:
- Título: Neuromuscular Disorders
- ISSN: 0960-8966
- Volume/Número/Paginação/Ano: v. 32, n. suppl. 1, p. S119, res. P.181, 2022
- Conference titles: International Congress of the World Muscle Society Halifax
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
TOMASELLI, Pedro José et al. Limb girdle muscle dystrophy: a Brazilian cohort on ICGNMD study. Neuromuscular Disorders. Kidlington: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.nmd.2022.07.319. Acesso em: 24 fev. 2026. , 2022 -
APA
Tomaselli, P. J., Frezatti, R. S. S., Record, C., Pitceathly, R., Houlden, H., Hanna, M., et al. (2022). Limb girdle muscle dystrophy: a Brazilian cohort on ICGNMD study. Neuromuscular Disorders. Kidlington: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1016/j.nmd.2022.07.319 -
NLM
Tomaselli PJ, Frezatti RSS, Record C, Pitceathly R, Houlden H, Hanna M, Reilly M, Marques Júnior W, Sobreira CF da R. Limb girdle muscle dystrophy: a Brazilian cohort on ICGNMD study [Internet]. Neuromuscular Disorders. 2022 ; 32( suppl. 1): S119.[citado 2026 fev. 24 ] Available from: https://doi.org/10.1016/j.nmd.2022.07.319 -
Vancouver
Tomaselli PJ, Frezatti RSS, Record C, Pitceathly R, Houlden H, Hanna M, Reilly M, Marques Júnior W, Sobreira CF da R. Limb girdle muscle dystrophy: a Brazilian cohort on ICGNMD study [Internet]. Neuromuscular Disorders. 2022 ; 32( suppl. 1): S119.[citado 2026 fev. 24 ] Available from: https://doi.org/10.1016/j.nmd.2022.07.319 - P.215 Non 5Q SMA: a Brazilian cohort study
- Distal hereditary motor neuropathy: a brazilian cohort study
- Conduction block and temporal dispersion in a SIGMAR1-related neuropathy
- Misdiagnoses in a Brazilian population with amyotrophic lateral sclerosis
- Small‑expanded allele spinocerebellar ataxia type 17 leading to broad movement disorder phenotype in a brazilian patient [Carta]
- Autosomal recessive cerebellar ataxias in South America [Carta]: a multicenter study of 1338 patients
- Monoclonal gammopathy-associated peripheral neuropathies: uncovering pearls and challenges
- Clinical phenotipes of primary coenzyme Q10 deficiency
- Brain structural signature of of RFC1-related disorder
- Increasing the differential diagnosis of the inherited demyelinating neuropathies with non-uniform nerve conduction(NCS): Andermann syndrome
Informações sobre o DOI: 10.1016/j.nmd.2022.07.319 (Fonte: oaDOI API)
Download do texto completo
| Tipo | Nome | Link | |
|---|---|---|---|
 |
003265782.pdf |
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
