Duchenne Muscular Dystrophy - A Medical Dictionary, by Icon Health Publications

By Icon Health Publications

This can be a 3-in-1 reference publication. It offers a whole scientific dictionary overlaying thousands of phrases and expressions in terms of Duchenne muscular dystrophy. It additionally supplies wide lists of bibliographic citations. ultimately, it offers details to clients on easy methods to replace their wisdom utilizing quite a few web assets. The publication is designed for physicians, clinical scholars getting ready for Board examinations, clinical researchers, and sufferers who are looking to get to grips with study devoted to Duchenne muscular dystrophy. in the event that your time is effective, this booklet is for you. First, you won't waste time looking the web whereas lacking loads of suitable info. moment, the publication additionally saves you time indexing and defining entries. eventually, you won't waste time and cash printing hundreds and hundreds of web content.

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Extra resources for Duchenne Muscular Dystrophy - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References

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Source: Free Radical Biology & Medicine. 1994 June; 16(6): 851-3. cmd=Retrieve&db=PubMed&list_ uids=8070691&dopt=Abstract • ERG phenotype of a dystrophin mutation in heterozygous female carriers of Duchenne muscular dystrophy. Author(s): Fitzgerald KM, Cibis GW, Gettel AH, Rinaldi R, Harris DJ, White RA. Source: Journal of Medical Genetics. 1999 April; 36(4): 316-22. cmd=Retrieve&db=PubMed&list_ uids=10227401&dopt=Abstract • Establishment of long-term myogenic cultures from patients with Duchenne muscular dystrophy by retroviral transduction of a temperature-sensitive SV40 large T antigen.

Collectively, these findings can provide the basis for design of immune interventions to reduce the pathology of dystrophin deficient muscle. ; Associate Professor; Neurology; University of Utah Salt Lake City, Ut 84102 Timing: Fiscal Year 2002; Project Start 20-SEP-2002; Project End 31-JUL-2005 Summary: (provided by applicant): Duchenne Muscular Dystrophy (DMD) and Becker Muscular Dystrophy (BMD) are devastating disorders. 4 million bases of genomic sequence. Deletions of large portions of the gene account for around 60% of all dystrophin mutations.

2001 July 15; 534(Pt. 2): 343-55. cmd=Retrieve&db=PubMed&list_ uids=11454955&dopt=Abstract 36 Duchenne Muscular Dystrophy • Cardiac involvement of female carrier of Duchenne muscular dystrophy. Author(s): Kamakura K. Source: Intern Med. 2000 January; 39(1): 2-3. No Abstract Available. cmd=Retrieve&db=PubMed&list_ uids=10674837&dopt=Abstract • Cardiac transplantation in a Duchenne muscular dystrophy carrier. Author(s): Melacini P, Fanin M, Angelini A, Pegoraro E, Livi U, Danieli GA, Hoffman EP, Thiene G, Dalla Volta S, Angelini C.

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