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kw.\*:("Distrofia muscular progresiva Becker")

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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

Cardiac manifestations and their management in Becker's muscular dystrophyORLOV, Y. S. K; BRODSKY, M. A; ALLEN, B. J et al.The American heart journal. 1994, Vol 128, Num 1, pp 193-196, issn 0002-8703Article

Becker Muscular Dystrophy With r(X) Carrying an Out-of-Frame DMD DeletionLEE, Kyung A; SUNG HEE HAN; JONG RAK CHOI et al.Pediatric neurology. 2008, Vol 39, Num 2, pp 129-132, issn 0887-8994, 4 p.Article

Delayed expression of dystrophin on renegerating muscle from two siblings with Becker muscular dystrophyTACHI, N; WAKAI, S; WATANABE, Y et al.Journal of the neurological sciences. 1992, Vol 110, Num 1-2, pp 165-168, issn 0022-510XArticle

Les syndromes myotoniques = Myotonic syndromesPOUGET, J; DESNUELLE, C.La Revue du praticien (Paris). 1988, Num 22, pp 1546-1551, issn 0035-2640Article

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

The application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophyHODGSON, S; WALKER, A; COLE, C et al.Journal of medical genetics. 1987, Vol 24, Num 3, pp 152-159, 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

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

Cardiac Involvement in Patients With Limb-Girdle Muscular Dystrophy Type 2 and Becker Muscular DystrophySVEEN, Marie-Louise; THUNE, Jens Jakob; KØBER, Lars et al.Archives of neurology (Chicago). 2008, Vol 65, Num 9, pp 1196-1201, issn 0003-9942, 6 p.Article

Measurement of the clinical utility of a combined mutation detection protocol in carriers of Duchenne and Becker muscular dystrophyTAYLOR, Peter J; MAROULIS, Sarah; BELL, Christopher G et al.Journal of medical genetics. 2007, Vol 44, Num 6, pp 368-372, issn 0022-2593, 5 p.Article

Evolution of gastric electrical features and gastric emptying in children with duchenne and becker muscular dystrophyBORRELLI, Osvaldo; SALVIA, Gennaro; MANCINI, Valentina et al.The American journal of gastroenterology. 2005, Vol 100, Num 3, pp 695-702, issn 0002-9270, 8 p.Article

Interleaved MRI/MRS study of muscle perfusion, oxygenation and high energy phosphate metabolism in normal subjects and Becker's myopathic patientsTOUSSAINT, J. F; BRILLAULT-SALVAT, C; GIACOMINI, E et al.Journal de chimie physique. 1998, Vol 95, Num 2, pp 250-255, issn 0021-7689Conference Paper

Characterization of genetic deletions in Becker muscular dystrophy using monoclonal antibodies against a deletion-prone region of dystrophinLE THIET THANH; NGUYEN THI MAN; HORI, S et al.American journal of medical genetics. 1995, Vol 58, Num 2, pp 177-186, issn 0148-7299Article

Immunostaining of dystrophin and utrophin in skeletal muscle of dystrophinopathiesSAHASHI, K; IBI, T; SUOH, H et al.Internal medicine (Tokyo. 1992). 1994, Vol 33, Num 5, pp 277-283, issn 0918-2918Article

Becker muscular dystrophy with onset after 60 yearsHEALD, A; ANDERSON, L. V. B; BUSHBY, K. M. D et al.Neurology. 1994, Vol 44, Num 12, pp 2388-2390, issn 0028-3878Article

Steroid-responsive myalgia in a patient with Becker muscular dystrophyHIGUCHI, I; NAKAMURA, K; NAKAGAWA, M et al.Journal of the neurological sciences. 1993, Vol 115, Num 2, pp 219-222, issn 0022-510XArticle

A 3' consensus splice mutation in the human dystrophin gene detected by a screening for intra-exonic deletionsSAAD, F. A; VITIELLO, L; MERLINI, L et al.Human molecular genetics (Print). 1992, Vol 1, Num 5, pp 345-346, issn 0964-6906Article

Two distinct mutations in a single dystrophin gene : chance occurence or premutation ?LAING, N. G; LAYTON, M. G; JOHNSEN, R. D et al.American journal of medical genetics. 1992, Vol 42, Num 5, pp 688-692, issn 0148-7299Article

Predicted and observed sizes of dystrophin in some patients with gene deletions that disrupt the open reading frameNICHOLSON, L. V. B; BUSHBY, K. M. D; JOHNSON, M. A et al.Journal of medical genetics. 1992, Vol 29, Num 12, pp 892-896, issn 0022-2593Article

Prevalence and incidence of Becker muscular dystrophyDUSHBY, K. M. D; THAMBYAYAH, M; GARDNER-MEDWIN, D et al.Lancet (British edition). 1991, Vol 337, Num 8748, pp 1022-1024, issn 0140-6736, 3 p.Article

Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphismsCLEMENS, P. R; FENWICK, R. G; CHAMBERLAIN, J. S et al.American journal of human genetics. 1991, Vol 49, Num 5, pp 951-960, issn 0002-9297Article

Is dystrophin labelling always discontinuous in Becker muscular dystrophy ?SLATER, C. R; NICHOLSON, L. V. B.Journal of the neurological sciences. 1991, Vol 101, Num 2, pp 187-192, issn 0022-510XArticle

The correlation between electrical after-activity and slowed relaxation in myotoniaIAIZZO, P. A; LEHMANN-HORN, F.Muscle & nerve. 1990, Vol 13, Num 3, pp 240-246, issn 0148-639XArticle

Ultrastructural localization of dystrophin in human muscle by using gold immunolabellingCULLEN, M. J; WALSH, J; NICHOLSON, L. V. B et al.Proceedings of the Royal society of London. Series B. Biological sciences. 1990, Vol 239, Num 1297, pp 197-210, issn 0080-4649Article

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