نتایج جستجو برای: facioscapulohumeral muscular dystrophy
تعداد نتایج: 52771 فیلتر نتایج به سال:
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...
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...
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...
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.
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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