Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0 [Carta] (2019)
- Authors:
- USP affiliated authors: REED, UMBERTINA CONTI - FM ; ZANOTELI, EDMAR - FM
- Unidade: FM
- DOI: 10.1002/ana.25597
- Subjects: ATROFIA MUSCULAR; DOENÇAS DA MEDULA ESPINHAL; DOENÇAS DO SISTEMA NERVOSO CENTRAL; CONVULSÕES; PROTEÍNAS DE TRANSPORTE; APOPTOSE; PROTEÍNAS DO TECIDO NERVOSO; GENES REGULADORES; FENÓTIPOS
- Language: Inglês
- Imprenta:
- Source:
- Título: Annals of neurology
- ISSN: 0364-5134
- Volume/Número/Paginação/Ano: v. 86, n. 5, p. 803-803, 2019
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
MENDONCA, Rodrigo H et al. Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0 [Carta]. Annals of neurology. Hoboken: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1002/ana.25597. Acesso em: 15 fev. 2026. , 2019 -
APA
Mendonca, R. H., Rocha, A. J., Lozano-Arango, A., Diaz, A. B., Castiglioni, C., Silva, A. M. S., et al. (2019). Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0 [Carta]. Annals of neurology. Hoboken: Faculdade de Medicina, Universidade de São Paulo. doi:10.1002/ana.25597 -
NLM
Mendonca RH, Rocha AJ, Lozano-Arango A, Diaz AB, Castiglioni C, Silva AMS, Reed UC, Kulikowski L, Paramonov I, Zanoteli E. Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0 [Carta] [Internet]. Annals of neurology. 2019 ; 86( 5): 803-803.[citado 2026 fev. 15 ] Available from: https://doi.org/10.1002/ana.25597 -
Vancouver
Mendonca RH, Rocha AJ, Lozano-Arango A, Diaz AB, Castiglioni C, Silva AMS, Reed UC, Kulikowski L, Paramonov I, Zanoteli E. Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0 [Carta] [Internet]. Annals of neurology. 2019 ; 86( 5): 803-803.[citado 2026 fev. 15 ] Available from: https://doi.org/10.1002/ana.25597 - Common and variable clinical, histological, and imaging findings of recessive RYR1-related centronuclear myopathy patients
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Informações sobre o DOI: 10.1002/ana.25597 (Fonte: oaDOI API)
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