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

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

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

Scansione densitometrica come supporto nella ricerca dello stato di portatrice di distrofia muscolare di Duchenne o di BeckerRIGO, A; PINCELLI, S; SOLERO, G. P et al.Giornale italiano di chimica clinica. 1991, Vol 16, Num 1, pp 51-53, issn 0392-2227Article

Scoliosis associated with Duchenne muscular dystrophyLORD, J; BEHRMAN, B; VARZOS, N et al.Archives of physical medicine and rehabilitation. 1990, Vol 71, Num 1, pp 13-17, issn 0003-9993Article

Clinical investigation of Duchenne muscular dystrophy: a methodology for therapeutic trials based on natural history controlsMENDELL, J. R; PROVINCE, M. A; SIGNORE, L et al.Archives of neurology (Chicago). 1987, Vol 44, Num 8, pp 808-811, issn 0003-9942Article

Ventilation mécanique dans la dystrophie musculaire de Duchenne = Mechanical ventilation in Duchenne's muscular dystrophyGRANATA, C; CAPELLI, T; SCHIAVINA, M et al.La Semaine des hôpitaux de Paris. 1989, Vol 65, Num 17, pp 1037-1041, issn 0037-1777Article

Early diagnosis and secondary prevention of Duchenne muscular dystrophySMITH, R. A; SIBERT, J. R; WALLACE, S. J et al.Archives of disease in childhood. 1989, Vol 64, Num 6, pp 787-790, issn 0003-9888, 4 p.Article

Essai thérapeutique du mazindol contre placebo dans la dystrophie musculaire de Duchenne: suivi de l'évolution pendant 1 an chez 14 enfants = Therapeutic trial of mazindol versus placebo in Duchenne muscular dystrophyDESNUELLE, C; SERRATRICE, G; VAN KHAN N'GUYEN et al.Archives françaises de pédiatrie. 1989, Vol 46, Num 10, pp 759-765, issn 0003-9764, 7 p.Article

Platelet intracellular calcium in patients with Duchenne muscular dystrophyLECHI, C; SINIGAGLIA, D; GUZZO, P et al.Clinica chimica acta. 1988, Vol 177, Num 1, pp 119-121, issn 0009-8981Article

Development of Duchenne-type cardiomyopathy: morphologic studies in a canine modelVALENTINE, B. A; CUMMINGS, J. F; COOPER, B. J et al.The American journal of pathology. 1989, Vol 135, Num 4, pp 671-678, issn 0002-9440, 8 p.Article

Duchenne's muscular dystrophy : review and recent scientific findingsEVANS, B. K; GOYNE, C.The American journal of the medical sciences. 1991, Vol 302, Num 2, pp 118-123, issn 0002-9629Article

Implications psychologiques des études familiales en biologie moléculaire. Un exemple: la myopathie de Duchenne = Muscular dystrophy as an example of psychological implications of genetic counselling after DNA analysisHAYEZ, J. Y; VERELLEN-DUMOULIN, C.Journal de génétique humaine. 1989, Vol 37, Num 1, pp 29-38, issn 0021-7743, 10 p.Article

Genetic epidemiology of Duchenne muscular dystrophy in Japan : classical segregation analysisKANAMORI, M; MORTON, N. E; FUJIKI, K et al.Genetic epidemiology. 1987, Vol 4, Num 6, pp 425-432, issn 0741-0395Article

The missing link in DMD?BONATTI, E.Nature (London). 1987, Vol 330, Num 6150, pp 692-693, issn 0028-0836Article

Isolation of a random cosmid clone, cX5, which defines a new polymorphic locus DXS148 near the locus for Duchenne muscular dystrophyHOFKER, M. H; BERGEN, A. A. B; SKRAASTAD, M. I et al.Human genetics. 1986, Vol 74, Num 3, pp 275-279, issn 0340-6717Article

Detection of molecular deletions in the chinese DMD patients using two amplified dystrophin sequencesZENG YI-TAO; CHEN MEI-JUUE; REN ZHAO-RUI et al.Biochemical medicine and metabolic biology. 1992, Vol 47, Num 2, pp 195-197, issn 0885-4505Article

Duchenne muscular dystrophy quantification : a multivariate analysis of surface EMGPRIEZ, A; DUCHENE, J; GOUBEL, F et al.Medical & biological engineering & computing. 1992, Vol 30, Num 3, pp 283-291, issn 0140-0118Article

The complete sequence of dystrophin predicts a rod-shaped cytoskeletal proteinKOENIG, M; MONACO, A. P; KUNKEL, L. M et al.Cell (Cambridge). 1988, Vol 53, Num 2, pp 219-228, issn 0092-8674Article

Mutants in duchenne muscular dystrophy: implications for preventionROSES, A. D.Archives of neurology (Chicago). 1988, Vol 45, Num 1, pp 84-85, issn 0003-9942Article

Mutations in Duchenne muscular dystrophyHACHINSKI, V.Archives of neurology (Chicago). 1988, Vol 45, Num 1, issn 0003-9942, 87Article

Etude en double aveugle de l'efficacité d'un antisérotoninergique, le pizotifène, dans la myopathie de Duchenne de Boulogne = Double-blind study of a Serotonin antagonist, pizotifen, in Duchenne muscular dystrophySTERU, D; PACLET, J. P; THEILLAC, A et al.Archives françaises de pédiatrie. 1987, Vol 44, Num 6, pp 461-465, issn 0003-9764Article

Isolation of a conserved sequence deleted in Duchenne muscular dystrophy patientsSMITH, T. J; WILSON, L; KENWRICK, S. J et al.Nucleic acids research. 1987, Vol 15, Num 5, pp 2167-2174, issn 0305-1048Article

On the power to detect differences between male and female mutation rates for Duchenne muscular dystrophy, using classical segregation analysis and restriction fragment length polymorphismsKAREL, E. R; TE MEERMAN, G. J; TEN KATE, L. P et al.American journal of human genetics. 1986, Vol 38, Num 6, pp 827-840, issn 0002-9297Article