kw.\*:("Distrofia muscular")
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Muscular dystrophy overview: genetics and diagnosisMATHEWS, Katherine D.Neurologic clinics. 2003, Vol 21, Num 4, issn 0733-8619, vi, 795-816 [23 p.]Article
An examination of some factors influencing creatine Kinase in the blood of parients with muscular dystrophyJACKSON, M. J; ROUND, J. M; NEWHAM, D. J et al.Muscle & nerve. 1987, Vol 10, Num 1, pp 15-21, issn 0148-639XArticle
The genetics of muscular dystrophiesHARPER, P. S.Progress in medical genetics. 1985, Vol 6, pp 53-90, issn 0079-6441Article
Duchenne and Becker muscular dystrophy and DNA deletionsMORTON, R. G.Biomedicine & pharmacotherapy. 1990, Vol 44, Num 4, pp 239-239, issn 0753-3322, 1 p.Article
Respiratory load-compensating mechanisms in muscular dystrophyAXEN, K; BISHOP, M; HAAS, F et al.Journal of applied physiology (1985). 1987, Vol 62, Num 4, pp 1647-1654, issn 8750-7587Article
Molecular deletion patterns in families from southern France with Duchenne/Becker muscular dystrophiesCLAUSTRES, M; TUFFERY, S; CHEVRON, M.-P et al.Human genetics. 1991, Vol 88, Num 2, pp 179-184, issn 0340-6717Article
DNA deletions and recombinations in the gene locus of X-linked muscular dystrophiesSHIMMOTO, M; TSUJI, A; YANG, R.-C et al.Journal of inherited metabolic disease. 1988, Vol 11, Num 3, pp 324-328, issn 0141-8955Article
Detection of Duchenne/Becker muscular dystrophy carriers by densitometric scanningPRIOR, T. W; FRIEDMAN, K. J; SILVERMAN, L. M et al.Clinical chemistry (Baltimore, Md.). 1989, Vol 35, Num 6, pp 1256-1257, issn 0009-9147, 2 p.Article
Future prospectsLACHMANN, P. J.British medical bulletin. 1989, Vol 45, Num 3, pp 819-824, issn 0007-1420Article
Linkage studies in Duchenne and Becker muscular dystrophiesWALKER, A; HART, K; COLE, C et al.Journal of medical genetics. 1986, Vol 23, Num 6, pp 538-547, issn 0022-2593Article
Diagnosis of Duchenne and Becker muscular dystrophies by polymerase chain reaction : a multicenter studyJAMA, the journal of the American Medical Association. 1992, Vol 267, Num 19, pp 2609-2615, issn 0098-7484Article
Dystrophin diagnosis: comparison of dystrophin abnormalities by immunofluorescence and immunoblot analysesARAHATA, K; HOFFMAN, E. P; KUNKEL, L. M et al.Proceedings of the National Academy of Sciences of the United States of America. 1989, Vol 86, Num 18, pp 7154-7158, issn 0027-8424, 5 p.Article
Intrarater reliability of manual muscle test (Medical research concil scale) grades in Duchenne's muscular dystrophyFLORENCE, J.M; PANDYA, S; KING, W.M et al.Physical therapy. 1992, Vol 72, Num 0002, pp 00115-00121, issn 0031-9023Article
Resultats de l'instrumentation rachidienne de Luque dans la dystrophie musculaire de BoulogneBONNET, I; BONNARD, C; GLORION, B et al.Revue de chirurgie orthopédique et réparatrice de l'appareil moteur. 1992, Vol 78, Num 0001, issn 0035-1040, 00146, supplementArticle
Fetal dystrophin to diagnose carrier statusGINJAAR, I. B; SOFFERS, S; MOORMAN, A. F. M et al.Lancet (British edition). 1991, Vol 338, Num 8761, pp 258-259, issn 0140-6736, 2 p.Article
Carrier status diagnosis in Duchenne muscular dystrophy with conformtional DNA polymorphismZIETKWICZ, E; SIMARD, L. R; MELANCON, S. B et al.MELANCON, S. B et al.Lancet (British edition). 1992, Vol 339, Num 8785, issn 0140-6736, p. 134Article
Behandlungskronzepte der physikalischen medizin bei myopathienWEIMANN, G; ARNOLD, C.R; KEMPER, M et al.Kranken Gymnastik. 1991, Vol 43, Num 1, pp 5-7, issn 0023-4494Article
Becker muscular dystrophy (BMD) and Klinefelter's syndrome: a possible cause of variable expression of BMD within a pedigreeSUTHERS, G. K; MANSON, J. I; STERN, L. M et al.Journal of medical genetics. 1989, Vol 26, Num 4, pp 251-254, issn 0022-2593, 4 p.Article
Childhood muscular dystrophy: an african reviewSALIH, M. A. M.Annals of tropical paediatrics. 1985, Vol 5, Num 4, pp 167-173, issn 0272-4936Article
Clinical and genetic studies of muscular dystrophy in young girlsYOSHIOKA, M; ITAGAKI, Y; SAIDA, K et al.Clinical genetics. 1986, Vol 29, Num 2, pp 137-142, issn 0009-9163Article
Myopathie de Duchenne le bout du tunnel? = Duchenne's myopathy: the end of the tunnel?PLOIN, M.Gazette médicale de France (1969). 1987, Vol 94, Num 26, pp 20-21, issn 0016-5557Article
Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) geneGILLARD, E. F; CHAMBERLAIN, J. S; KLAMUT, H. J et al.American journal of human genetics. 1989, Vol 45, Num 4, pp 507-520, issn 0002-9297Article
The frequency of patients with dystrophin abnormalities in a limb-girdle patient populationARIKAWA, E; HOFFMAN, E. P; KAIDO, M et al.Neurology. 1991, Vol 41, Num 9, pp 1491-1496, issn 0028-3878Article
Rapid carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophyROBERTS, R. G; COLE, C. G; HART, K. A et al.Nucleic acids research. 1989, Vol 17, Num 2, issn 0305-1048, 811Article