Literature DB >> 15249635

Ventilatory support in facioscapulohumeral muscular dystrophy.

M Wohlgemuth1, E L van der Kooi, R G van Kesteren, S M van der Maarel, G W Padberg.   

Abstract

Respiratory insufficiency due to respiratory muscle weakness is a common complication of many neuromuscular diseases. The prevalence of respiratory failure in facioscapulohumeral muscular dystrophy (FSHD) is unknown. The authors identified 10 FSHD patients on nocturnal ventilatory support at home, representing approximately 1% of the Dutch FSHD population. Severe muscle disease, wheelchair dependency, and kyphoscoliosis appeared to be risk factors for respiratory failure.

Entities:  

Mesh:

Year:  2004        PMID: 15249635     DOI: 10.1212/01.wnl.0000133126.86377.e8

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  29 in total

1.  Orthognathic surgery in a case of infantile facioscapulohumeral muscular dystrophy with macroglossia.

Authors:  Marcus Stephan Kriwalsky; Marcus Deschauer; Alexander Walter Eckert; Johannes Schubert; Stephan Zierz
Journal:  Oral Maxillofac Surg       Date:  2008-12

2.  [Facioscapulohumeral muscular dystrophy. Clinical picture, atypical forms, diagnostics, genetics].

Authors:  B Jordan; C Müller-Reible; S Zierz
Journal:  Nervenarzt       Date:  2011-06       Impact factor: 1.214

Review 3.  Facioscapulohumeral Muscular Dystrophy.

Authors:  Jeffrey M Statland; Rabi Tawil
Journal:  Continuum (Minneap Minn)       Date:  2016-12

4.  Restrictive lung involvement in facioscapulohumeral muscular dystrophy.

Authors:  Michele A Scully; Katy J Eichinger; Colleen M Donlin-Smith; Rabi Tawil; Jeffery M Statland
Journal:  Muscle Nerve       Date:  2014-09-29       Impact factor: 3.217

Review 5.  Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled?

Authors:  Mark Richards; Frédérique Coppée; Nick Thomas; Alexandra Belayew; Meena Upadhyaya
Journal:  Hum Genet       Date:  2011-10-09       Impact factor: 4.132

Review 6.  Facioscapulohumeral Dystrophy.

Authors:  Leo H Wang; Rabi Tawil
Journal:  Curr Neurol Neurosci Rep       Date:  2016-07       Impact factor: 5.081

Review 7.  Respiratory involvement in inherited primary muscle conditions.

Authors:  N Shahrizaila; W J M Kinnear; A J Wills
Journal:  J Neurol Neurosurg Psychiatry       Date:  2006-10       Impact factor: 10.154

8.  Facioscapulohumeral dystrophy myoblasts efficiently repair moderate levels of oxidative DNA damage.

Authors:  Yara Bou Saada; Carla Dib; Petr Dmitriev; Aline Hamade; Gilles Carnac; Dalila Laoudj-Chenivesse; Marc Lipinski; Yegor S Vassetzky
Journal:  Histochem Cell Biol       Date:  2016-02-09       Impact factor: 4.304

Review 9.  Deciphering transcription dysregulation in FSH muscular dystrophy.

Authors:  Melanie Ehrlich; Michelle Lacey
Journal:  J Hum Genet       Date:  2012-06-21       Impact factor: 3.172

10.  Evidence-based guideline summary: Evaluation, diagnosis, and management of facioscapulohumeral muscular dystrophy: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology and the Practice Issues Review Panel of the American Association of Neuromuscular & Electrodiagnostic Medicine.

Authors:  Rabi Tawil; John T Kissel; Chad Heatwole; Shree Pandya; Gary Gronseth; Michael Benatar
Journal:  Neurology       Date:  2015-07-28       Impact factor: 9.910

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.