Literature DB >> 8364702

Clinical and genetic aspects of myotonic dystrophy.

P R Barnes1.   

Abstract

Myotonic dystrophy is the commonest inherited muscle disease of adults. It causes significant clinical features in many organ systems and requires a broad-based approach for optimum management. Recent genetic advances promise to provide exciting new insights into the pathophysiology of the disease and may allow rational treatments to be developed.

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Year:  1993        PMID: 8364702

Source DB:  PubMed          Journal:  Br J Hosp Med        ISSN: 0007-1064


  2 in total

1.  Incorrect diagnosis of myotonic dystrophy and its potential consequences revealed by subsequent direct genetic analysis.

Authors:  P R Barnes; D Hilton-Jones; G Norbury; A Roberts; S M Huson
Journal:  J Neurol Neurosurg Psychiatry       Date:  1994-05       Impact factor: 10.154

2.  Clinical characteristics of pregnancies complicated by congenital myotonic dystrophy.

Authors:  Cheonga Yee; Suk-Joo Choi; Soo-Young Oh; Chang-Seok Ki; Cheong-Rae Roh; Jong-Hwa Kim
Journal:  Obstet Gynecol Sci       Date:  2017-07-14
  2 in total

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