نتایج جستجو برای: facioscapulohumeral muscular dystrophy

تعداد نتایج: 52771  

Journal: :Neuroepidemiology 2014
Alice Theadom Miriam Rodrigues Richard Roxburgh Shiavnthi Balalla Chris Higgins Rohit Bhattacharjee Kelly Jones Rita Krishnamurthi Valery Feigin

BACKGROUND Determining the prevalence of neuromuscular disorders for the general population is important to identify the scope of burden on society and enable comparisons with other health conditions. This systematic review aims to identify and collate the findings of studies published between 1960 and 2013 on the prevalence of all types of muscular dystrophies. SUMMARY Relevant articles were...

Journal: :Annals of neurology 2008
Kathryn R Wagner James L Fleckenstein Anthony A Amato Richard J Barohn Katharine Bushby Diana M Escolar Kevin M Flanigan Alan Pestronk Rabi Tawil Gil I Wolfe Michelle Eagle Julaine M Florence Wendy M King Shree Pandya Volker Straub Paul Juneau Kathleen Meyers Cristina Csimma Tracey Araujo Robert Allen Stephanie A Parsons John M Wozney Edward R Lavallie Jerry R Mendell

OBJECTIVE Myostatin is an endogenous negative regulator of muscle growth and a novel target for muscle diseases. We conducted a safety trial of a neutralizing antibody to myostatin, MYO-029, in adult muscular dystrophies (Becker muscular dystrophy, facioscapulohumeral dystrophy, and limb-girdle muscular dystrophy). METHODS This double-blind, placebo-controlled, multinational, randomized study...

Journal: :The Veterinary record 2002
R W Blowey

The last confirmed case of FMD in the UK was recorded on 30 September 2001. Since then, all counties in Great Britain have been classed as FMD free for the purposes of licensed movements of animals, following an absence of outbreaks of disease for at least 3 months and extensive serological surveillance of sheep and goat flocks. On 22 January 2002, the OIE (World Animal Health Organisation) res...

Journal: :Turkish journal of anaesthesiology and reanimation 2014
Gamze Sarkılar Aydın Mermer Melike Yücekul Bedia Mine Çeken Celalettin Altun Şeref Otelcioğlu

Limb-girdle muscular dystrophies are a group of disorders with wide genetic and clinical heterogeneity. These disorders may lead to an increase in life-threatening complications related to surgery and anaesthesia. In this case, the anaesthetic management of a child with limb-girdle muscular dystrophy is presented.

Journal: :American journal of human genetics 1995
M Zatz S K Marie M R Passos-Bueno M Vainzof S Campiotto A Cerqueira C Wijmenga G Padberg R Frants

A gene responsible for facioscapulohumeral muscular dystrophy (FSHD) has been localized at 4q35. Subsequently, it was found that probe p13E-11 detects a polymorphic EcoRI fragment, usually > 28 kb, in normal individuals, whereas in sporadic and familial FSHD cases, an EcoRI fragment, usually < 28 kb, was found. Although these findings have been amply confirmed, several aspects are as yet either...

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