Merosin-positive congenital muscular dystrophy with cerebellar hypoplasia and mental retardation: report of three cases (2002)
- Authors:
- USP affiliated authors: REED, UMBERTINA CONTI - FM ; MARIE, SUELY KAZUE NAGAHASHI - FM
- Unidade: FM
- Subjects: DISTROFIA MUSCULAR; NEUROLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título: Neuromuscular Disorders
- ISSN: 0960-8966
- Volume/Número/Paginação/Ano: v. 12, n. 7-8, p. 765, res. D.P.5.7, October 2002
- Conference titles: International Congress of the World Muscle Society
-
ABNT
REED, Umbertina Conti et al. Merosin-positive congenital muscular dystrophy with cerebellar hypoplasia and mental retardation: report of three cases. Neuromuscular Disorders. Oxford: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 30 dez. 2025. , 2002 -
APA
Reed, U. C., Gurgel-Giannetti, J., Resende, M. B. D., Ferreira, L. G., Carvalho, M. S., & Marie, S. K. N. (2002). Merosin-positive congenital muscular dystrophy with cerebellar hypoplasia and mental retardation: report of three cases. Neuromuscular Disorders. Oxford: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Reed UC, Gurgel-Giannetti J, Resende MBD, Ferreira LG, Carvalho MS, Marie SKN. Merosin-positive congenital muscular dystrophy with cerebellar hypoplasia and mental retardation: report of three cases. Neuromuscular Disorders. 2002 ; 12( 7-8): 765.[citado 2025 dez. 30 ] -
Vancouver
Reed UC, Gurgel-Giannetti J, Resende MBD, Ferreira LG, Carvalho MS, Marie SKN. Merosin-positive congenital muscular dystrophy with cerebellar hypoplasia and mental retardation: report of three cases. Neuromuscular Disorders. 2002 ; 12( 7-8): 765.[citado 2025 dez. 30 ] - MHC class 1 as an additional marker to the course of juvenille dermatomyositis
- Síndrome de Russel; apresentação clássica e atípica: relato de 2 casos
- Horizontal gaze palsy with progressive scoliosis: clinical and neuroimage aspects
- Deletions of study of dystrophin gene in Duchenne and Becker muscular dystrophy
- Quantification of muscle strength and motor ability in patients with Duchenne muscular dystrophy on steroid therapy
- Distrofia Muscular Congênita Como Causa de Fraqueza Cervical
- Miosite Eosinofílica Idiopática: Estágio Inicial de Distrofia de Cinturas Por Deficiência de Calpaína?: Relato de Um Caso
- Yoga breathing exercises improve the respiratory function in Duchenne dystrophy
- Avaliação funcional de pacientes em cadeira de rodas com distrofia muscular de Duchenne
- Relevance of the A8344G and T8356C mtDNA mutation analyses in the approach of progressive myoclonic epilepsy
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas