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dc.typeArtigo de periódicopt_BR
dc.titleMulticore Disease: Histochemical Analysis Of A Family [miopatia Do Multicore: Análise Histoquímica De Uma Família]pt_BR
dc.contributor.authorDe Lima Resende L.A.pt_BR
dc.contributor.authorKimaid P.A.T.pt_BR
dc.contributor.authorDe Lima Castro H.A.pt_BR
dc.contributor.authorFonseca R.G.pt_BR
dc.contributor.authorDal Pai V.pt_BR
dc.contributor.authorUeda A.K.pt_BR
dc.contributor.authorMontenegro M.R.G.pt_BR
unicamp.authorDe Lima Castro, H.A., FOP, UNICAMP, Brazilpt_BR Lima Resende, L.A., Faculdade de Medicina de Botucatu, UNESP, Brazilpt, P.A.T., Faculdade de Medicina de Botucatu, UNESP, Brazilpt, R.G., Faculdade de Medicina de Botucatu, UNESP, Brazilpt Pai, V., Instituto de Biocièncias, UNESP, Brazilpt, A.K., Faculdade de Medicina de Botucatu, UNESP, Brazilpt, M.R.G., Faculdade de Medicina de Botucatu, UNESP, Brazilpt
dc.description.abstractIn this paper the authors describe three cases of multicore myopathy in the same family. Case J was a white 77-year-old patient with proximal muscular atrophy and weakness, global hypotonia and global hypoactive deep tendon reflexes. Motor and sensory conduction studies were normal in all limbs. EMG examination showed a myopathic pattern with frequent spontaneous activity consisting of fibrillations and positive sharp waves. Histochemical reactions showed typical oxidative alterations of multicore myopathy. Cases 2 and 3 were the son and the daughter of case 1 respectively. They were both non-symptomatic patients with minimal EMG and histochemical alterations. These three patients illustrated the great clinical variability of this condition.en
dc.relation.ispartofRevista Brasileira de Neurologiapt_BR
dc.identifier.citationRevista Brasileira De Neurologia. , v. 34, n. 2, p. 55 - 58, 1998.pt_BR
dc.description.provenanceMade available in DSpace on 2015-06-30T15:04:48Z (GMT). No. of bitstreams: 0 Previous issue date: 1998en
dc.description.provenanceMade available in DSpace on 2015-11-26T15:12:51Z (GMT). No. of bitstreams: 0 Previous issue date: 1998en
dc.description.referenceEngel, A.G., Gomez, M.R., Groover, R.B., Multicore disease. A recently recognized congenital myopathy associated with multifocal degeneration of muscle fibres (1971) Mayo Clin Proc, 46, pp. 666-681pt_BR
dc.description.referenceRicoy, J.R., Cabello, A., Goizueta, G., Myopathy with multiple minicore. Report of two siblings (1980) J Neurol Sci, 48, pp. 81-92pt_BR
dc.description.referenceBertini, E., Bosman, C., Bevilacqua, M., Ricci, E., Gagliardi, G.M., Parisi, F., Servidei, S., Ballerini, L., Cardiomyopathy and multicore myopathy with accumulation of intermediate filaments (1990) Eur J Pediatr, 149, pp. 856-858pt_BR
dc.description.referenceChudley, A.D., Rozdilsky, B., Houston, C.S., Becker, L.E., Knoll, J.H., Multicore disease in sibs with severe mental retardation, short stature, facial anomalies, hypoplasia of the pituitary fossa, and hypogonadotrophic hypogonadism (1985) Am J Med Genet, 20, pp. 145-158pt_BR
dc.description.referenceEdstrom, L., Mair, W.P.G., Wroblewski, R., Hovmoller, M., Malm, G., Type distribution of muscle fibres and their ultrastructure related to intracellular elemental composition as revealed by energy dispersive X-ray microanalysis (1986) J Neurol Sci, 76, pp. 31-48pt_BR
dc.description.referenceGordon, C.P., Litz, S., Multicore myopathy in a patient with anhidrotic ectodermal dysplasia (1992) Can J Anaesth, 39, pp. 966-968pt_BR
dc.description.referenceKim, J.J., Armstrong, D.D., Fishman, M.A., Multicore myopathy, microcephaly aganglionosis, and short stature (1994) J Child Neurol, 9, pp. 275-277. , Abstractpt_BR
dc.description.referenceKumano, K., Congenital non-progressive myopathy, associated with scoliosis. Clinical, histological. histochemical and electron microscopic studies of seven cases (1980) J Jpn Orthop Ass, 54, pp. 381-402pt_BR
dc.description.referenceLee, Y.S., Yip, W.C.L., A fatal congenital myopathy with severe type 1 fibre atrophy, central nuclei and multicores (1981) J Neurol Sci, 50, pp. 277-290pt_BR
dc.description.referenceMarolda, M., Filla, A., Pellegrini, G., Esposito, V., Maiuri, F., Zotti, G., "Central core" and "Multicore" disease. Clinical, histochemical and ultrastructural study of two cases with unusual hereditary transmission (1985) Acta Neurol, 7, pp. 473-481. , (Napoli), citados por Martin et al (1986)pt_BR
dc.description.referenceMartin, J.J., Bruyland, M., Busch, H.F.M., Farriaux, J.P., Krivosic, I., Ceuterick, C., Pleocore disease. Multi-minicore disease and focal loss of cross striations (1986) Acta Neuropathol, 72, pp. 142-149. , Berlinpt_BR
dc.description.referenceMyong, N.H., Kang, Y.K., Chi, J.G., Suk, S.I., Multicore myopathy: A case report (1993) J Korean Med Sci, 8, pp. 312-317. , Abstractpt_BR
dc.description.referenceOhkubo, M., Ino, T., Shimazaki, S., Yabuto, K., Okada, R., Sato, T., Multicore myopathy associated with multiple pterygium syndrome and hypertrophic cardiomyopathy (1996) Pediatr Cardiol, 17, pp. 53-56pt_BR
dc.description.referencePagès, M., Echenne, B., Pagès, A.M., Dimeglio, A., Sires, A., Multicore disease and Marfan's syndrome: A case report (1985) Eur Neurol, 24, pp. 170-175pt_BR
dc.description.referencePenegyres, P.K., Kakulas, B.A., The natural history of minicore - Multicore myopathy (1991) Muscle & Nerve, 14, pp. 411-415pt_BR
dc.description.referenceRimmer, K.P., Withelaw, W.A., The respiratory muscles in multicore myopathy (1993) Am Rev Respir Dis, 148, pp. 227-231pt_BR
dc.description.referenceSwash, M., Schwartz, M.S., Familial multicore disease with focal loss of cross-stations and ophthalmoplegia (1981) J Neurol Sci, 52, pp. 1-10pt_BR
dc.description.referenceVallat, J.M., Lumley, L., Loubet, A., Corvisier, N., Umdenstock, R., Coexistence of minicores, cores, and rods in the same muscle biopsy. A new example of mixed congenital myopathy (1982) Acta Neuropathol, 58, pp. 229-232. , Berlinpt_BR
dc.description.referenceWerneck, L.C., Correlaçào entre a incapacidade funcional, idade e enzimas sėricas nas doenças neuromusculares (1995) Arq Neuro-psiquiatr, 53, pp. 60-68pt_BR
dc.description.referenceNewsholme, S.J., Gaskell, C.J., Myopathy with core-like structures in a dog (1987) J Comp Path, 97, pp. 597-600pt_BR
dc.description.referenceWalton, J., (1981) Disorders of Voluntary Muscle, , Churchill-Livingstone, Edinburghpt_BR
dc.description.referenceDubowitz, V., Brooke, M., (1973) Muscle Biopsy: A Modem Approach, , W.B. Saunders, Philadelphiapt_BR
dc.description.referenceTaratuto, A.L., Spaello, Z.M., Fezzonico, C., Morales, R.C., Multicore disease - Report of a case with lack of fibre type differentiation (1978) Neuropediat, 9, pp. 285-297pt_BR
dc.description.referenceKorényi-Both, A., Korényi-Both, I., Congenital myopathies with "diagnostic" pathological features (1987) J Med, 18, pp. 93-107pt_BR
dc.description.referencePagès, A., Pagès, M., La myopathie à axe central. Etude optique, histoenzymologique et ultrastructurale de 2 cas avec revue de la littérature (1981) Ann Pathol, 1, pp. 38-47pt_BR
dc.description.referenceByrne, E., Blumbergs, P.C., Hallpike, J.F., Central core disease. Study of a family with five affected generations (1982) J Neurol Sci, 53, pp. 77-83pt_BR
dc.description.referencePatterson, V.H., Hill, T.R.G., Fletcher, P.J.H., Heron, J.R., Central core disease. Clinical and pathological evidence of progression within a family (1979) Brain, 102, pp. 581-594pt_BR
dc.description.referenceRamsey, P.L., Heinsinger, R.N., Congenital dislocation of the hip associated with central core disease (1975) J Bone J Surg, 57 A, pp. 648-651pt_BR
dc.description.referenceKar, N.C., Pearson, C.M., Verity, M.A., Muscle fructose 1,6 diphosphatase deficiency associated with an atypical central core disease (1980) J Neurol Sci, 48, pp. 243-256pt_BR
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