Congenital muscular dystrophy with cerebral white matter hypodensity . Correlation of clinical features and merosin deficiency (1996)
- Authors:
- USP affiliated authors: LEVY, JOSE ANTONIO - FM ; REED, UMBERTINA CONTI - FM ; DIAMENT, ARON JUDKA - FM ; ZATZ, MAYANA - IB
- Unidades: FM; IB
- DOI: 10.1016/0387-7604(95)00095-x
- Subjects: GENÉTICA MÉDICA; NEUROLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Brain & Development
- Volume/Número/Paginação/Ano: v.18, p.53-8, 1996
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
REED, Umbertina Conti et al. Congenital muscular dystrophy with cerebral white matter hypodensity . Correlation of clinical features and merosin deficiency. Brain & Development, v. 18, p. 53-8, 1996Tradução . . Disponível em: https://doi.org/10.1016/0387-7604(95)00095-x. Acesso em: 20 abr. 2024. -
APA
Reed, U. C., Marie, S. K. N., Vainzof, M., Salum, P. B., Levy, J. A., Zatz, M., & Diament, A. J. (1996). Congenital muscular dystrophy with cerebral white matter hypodensity . Correlation of clinical features and merosin deficiency. Brain & Development, 18, 53-8. doi:10.1016/0387-7604(95)00095-x -
NLM
Reed UC, Marie SKN, Vainzof M, Salum PB, Levy JA, Zatz M, Diament AJ. Congenital muscular dystrophy with cerebral white matter hypodensity . Correlation of clinical features and merosin deficiency [Internet]. Brain & Development. 1996 ;18 53-8.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1016/0387-7604(95)00095-x -
Vancouver
Reed UC, Marie SKN, Vainzof M, Salum PB, Levy JA, Zatz M, Diament AJ. Congenital muscular dystrophy with cerebral white matter hypodensity . Correlation of clinical features and merosin deficiency [Internet]. Brain & Development. 1996 ;18 53-8.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1016/0387-7604(95)00095-x - Congenital structural myopathies: clinical and pathologic review of 13 patients
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- Congenital structural myopathies: clinical and pathologic review of 13 patients
- Congenital muscular dystrophy: clinical and pathologic review of 24 patients
- Autosomal recessive nondystrophic myotonia
- Distrofia miotonica: estudo da correlacao clinico-genetica em um par familiar (pai-filho)
- Distrofia miotonica: relato de um caso com aspectos clinicos e geneticos inusitados
- Afeccao muscular associada a catarata: relato de dois irmaos
- Miopatia centronuclear (miotubular): relato de caso
- Merosin-positive congenital muscular dystrophy in two siblings with cataract and slight mental retardation
Informações sobre o DOI: 10.1016/0387-7604(95)00095-x (Fonte: oaDOI API)
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