Congenital muscular dystrophy in two siblings with cataracts and slight cerebral involvement (1994)
- Authors:
- USP affiliated authors: LEVY, JOSE ANTONIO - FM ; REED, UMBERTINA CONTI - FM ; DIAMENT, ARON JUDKA - FM ; TSANACLIS, ANA MARIA CROUS - FM
- Unidade: FM
- Assunto: NEUROLOGIA
- Language: Inglês
- Imprenta:
- Publisher: Ana
- Publisher place: San Francisco
- Date published: 1994
- Source:
- Título do periódico: Abstracts
- Conference titles: Cong Child Intern Child Neur Assoc
-
ABNT
REED, Umbertina Conti et al. Congenital muscular dystrophy in two siblings with cataracts and slight cerebral involvement. 1994, Anais.. San Francisco: Ana, 1994. . Acesso em: 23 abr. 2024. -
APA
Reed, U. C., Marie, S. K. N., Tsanaclis, A. M. C., Carvalho, M. S., Roinzenblat, J., Pedreira, C. C., et al. (1994). Congenital muscular dystrophy in two siblings with cataracts and slight cerebral involvement. In Abstracts. San Francisco: Ana. -
NLM
Reed UC, Marie SKN, Tsanaclis AMC, Carvalho MS, Roinzenblat J, Pedreira CC, Diament AJ, Levy JA. Congenital muscular dystrophy in two siblings with cataracts and slight cerebral involvement. Abstracts. 1994 ;[citado 2024 abr. 23 ] -
Vancouver
Reed UC, Marie SKN, Tsanaclis AMC, Carvalho MS, Roinzenblat J, Pedreira CC, Diament AJ, Levy JA. Congenital muscular dystrophy in two siblings with cataracts and slight cerebral involvement. Abstracts. 1994 ;[citado 2024 abr. 23 ] - 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
- Congenital muscular dystrophy in two seblings with cataracts and slight cerebral involvement
- Congenital structural myopathies: clinical and pathologic review of 13 patients
- Congenital muscular dystrophy: clinical and pathologic review of 24 patients
- Congenital structural myopathies: clinical and pathologic review of 13 patients
- Congenital muscular dystrophy: clinical and pathologic review of 24 patients
- Autosomal recessive nondystrophic myotonia
- Miopatia miotubular: relato de caso
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