Literature DB >> 426473

Emery-Dreifuss muscular dystrophy.

L P Rowland, M Fetell, M Olarte, A Hays, N Singh, F E Wanat.   

Abstract

A man had weakness of humeroperoneal distribution associated with limited range of motion of the cervical spine and elbows. At age 25 he developed permanent atrial paralysis, and a cardiac pacemaker was inserted. Although this case was sporadic, most others have been transmitted as an X-linked recessive trait. Mixed patterns in electromyography and muscle histology have caused nosological confusion, but the unique clinical signs seem to define a distinct form of muscular dystrophy, warranting the designation "emery-Dreifuss" type.

Entities:  

Mesh:

Year:  1979        PMID: 426473     DOI: 10.1002/ana.410050203

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  33 in total

1.  Cardiac transplantation in female Emery-Dreifuss muscular dystrophy.

Authors:  M P Merchut; D Zdonczyk; M Gujrati
Journal:  J Neurol       Date:  1990-08       Impact factor: 4.849

2.  Emery-Dreifuss muscular dystrophy in the evaluation of decreased spinal mobility and joint contractures.

Authors:  Kamil Goncu; Rengin Guzel; Fusun Guler-Uysal
Journal:  Clin Rheumatol       Date:  2003-10-21       Impact factor: 2.980

Review 3.  Emery-Dreifuss muscular dystrophy.

Authors:  Antoine Muchir; Howard J Worman
Journal:  Curr Neurol Neurosci Rep       Date:  2007-01       Impact factor: 5.081

4.  Identification of a new locus for a peculiar form of congenital muscular dystrophy with early rigidity of the spine, on chromosome 1p35-36.

Authors:  B Moghadaszadeh; I Desguerre; H Topaloglu; F Muntoni; S Pavek; C Sewry; M Mayer; M Fardeau; F M Tomé; P Guicheney
Journal:  Am J Hum Genet       Date:  1998-06       Impact factor: 11.025

5.  A novel emerin mutation in a Japanese patient with Emery-Dreifuss muscular dystrophy.

Authors:  T Yamada; T Kobayashi
Journal:  Hum Genet       Date:  1996-05       Impact factor: 4.132

6.  Familial myopathy with scapulohumeral distribution, rigid spine, cardiopathy and mitochondrial abnormality.

Authors:  K Tanaka; T Yoshimura; H Muratani; J Kira; Y Itoyama; I Goto
Journal:  J Neurol       Date:  1989-01       Impact factor: 4.849

Review 7.  The nuclear envelope: an intriguing focal point for neurogenetic disease.

Authors:  Howard J Worman; William T Dauer
Journal:  Neurotherapeutics       Date:  2014-10       Impact factor: 7.620

8.  The rigid spine syndrome--a myopathy of uncertain nosological position.

Authors:  W Poewe; H Willeit; E Sluga; U Mayr
Journal:  J Neurol Neurosurg Psychiatry       Date:  1985-09       Impact factor: 10.154

9.  [Dominant autosomal humeroperoneal syndrome with early contractures and cardiomyopathy (Emery-Dreifuss syndrome)].

Authors:  X Baur; T N Witt; D Pongratz; M Gokel; P Rosenbeiger; G Steinbeck
Journal:  Klin Wochenschr       Date:  1987-08-03

10.  Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy.

Authors:  Lucie Gueneau; Anne T Bertrand; Jean-Philippe Jais; Mustafa A Salih; Tanya Stojkovic; Manfred Wehnert; Maria Hoeltzenbein; Simone Spuler; Shinji Saitoh; Annie Verschueren; Christine Tranchant; Maud Beuvin; Emmanuelle Lacene; Norma B Romero; Simon Heath; Diana Zelenika; Thomas Voit; Bruno Eymard; Rabah Ben Yaou; Gisèle Bonne
Journal:  Am J Hum Genet       Date:  2009-08-27       Impact factor: 11.025

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.