Study of 4q dna markers in brazilian fascioscapulohumeral muscular dystrophy (fshd) families (1993)
- Authors:
- USP affiliated authors: LEVY, JOSE ANTONIO - FM ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB ; AKIYAMA, JEANNE YUKIE - FM
- Unidades: FM; IB
- Assunto: NEUROLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Canadian Journal of Neurological Sciences
- Volume/Número/Paginação/Ano: v.20, n.suppl.4, p.s30, aug. 1993
- Conference titles: World Congress of Neurology
-
ABNT
PASSOS-BUENO, Maria Rita et al. Study of 4q dna markers in brazilian fascioscapulohumeral muscular dystrophy (fshd) families. Canadian Journal of Neurological Sciences. Calgary: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 24 abr. 2024. , 1993 -
APA
Passos-Bueno, M. R., Wijmenga, C., Takata, R. I., Marie, S. K. N., Vainzof, M., Pavanello, R. C. M., et al. (1993). Study of 4q dna markers in brazilian fascioscapulohumeral muscular dystrophy (fshd) families. Canadian Journal of Neurological Sciences. Calgary: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Passos-Bueno MR, Wijmenga C, Takata RI, Marie SKN, Vainzof M, Pavanello RCM, Hewitt JE, Bakker E, Carvalho AAS, Akiyama J, Frants RR. Study of 4q dna markers in brazilian fascioscapulohumeral muscular dystrophy (fshd) families. Canadian Journal of Neurological Sciences. 1993 ;20( suppl.4): s30.[citado 2024 abr. 24 ] -
Vancouver
Passos-Bueno MR, Wijmenga C, Takata RI, Marie SKN, Vainzof M, Pavanello RCM, Hewitt JE, Bakker E, Carvalho AAS, Akiyama J, Frants RR. Study of 4q dna markers in brazilian fascioscapulohumeral muscular dystrophy (fshd) families. Canadian Journal of Neurological Sciences. 1993 ;20( suppl.4): s30.[citado 2024 abr. 24 ] - Brazilian family with 3271 mutation in mitochondrial dna
- Correlation between ctg trinucleotide repeat length and clinical picture in brazilian patients affected with myotonic dystrophy
- Caucasian family with the 3271 mutation in mitochondrial dna
- Becker-type muscular dystrophy in a mother of three boys affected by duchenne muscular dystrophy: a follow-up study
- Em busca de alivio e cura para uma doenca cruel: o instituto de biociencias da usp pesquisa mecanismos das distrofias musculares progressivas, enquanto uma associacao e o hc dao apoio a assistencia aos atingidos. [Depoimento]
- Dystrophin immunofluorescence pattern in manifesting and asymptomatic carriers of duchenne's and becker muscular dystrophies of different ages
- Estudo imunohistoquimico da distrofina em musculo de afetados por distrofias musculares progressivas
- Distrofina nas distrofias musculares progressivas
- Variacao do quadro clinico da distrofia fascio-escapulo-umeral em 31 familias brasileiras (resumo)
- Why is the reproductive performance lower in becker (bmd) as compared to limb girdle (lgmd) muscular dystrophy male patients?
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