全部文献期刊学位论文会议报纸专利标准年鉴图书|学者科研项目
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作者:T. Voit , M. A. Kroos ...
来源:[J].Orphanet Journal of Rare Diseases(IF 4.315), 2016, Vol.11 (1)Springer
摘要:Abstract(#br) Background(#br)As little information is available on children with non-classic presentations of Pompe disease, we wished to gain knowledge of specific clinical characteristics and genotypes. We included all patients younger than 18 years, who had been evaluated...
作者:... L. Debernard , C. Themar-Noel , T. Voit
来源:[J].IRBM(IF 0.398), 2015, Vol.36 (1), pp.4-9Elsevier
摘要:Abstract(#br)Objectives: Increasing fibrosis of skeletal muscle is a hallmark of the dystrophic process in Duchenne muscular dystrophy (DMD) and is a hindrance to functional muscle regeneration. We sought to evaluate the capacity of magnetic resonance elastography (MRE) to c...
作者:T. Voit , Y. Barnouin ...
来源:[J].AGE(IF 4.084), 2014, Vol.36 (1), pp.275-285Springer
摘要:Abstract(#br)Relative and absolute muscle mass and muscle strength are used as diagnostic criteria for sarcopenia. We aimed to assess which diagnostic criteria are most associated with physical performance in 180 young (18–30 years) and 281 healthy old participants (69–81 ye...
作者:T. Voit
来源:[J].Neuromuscular Disorders(IF 3.464), 2014, Vol.24 (9-10), pp.918-919Elsevier
摘要:Therapies are finally under way for neuromuscular disorders (NMDs) such as spinal muscular atrophies or muscular dystrophies. However, two pivotal trials for Duchenne muscular dystrophy failed to show significant results and have raised questions of feasibility in this field. Thi...
作者:T. Voit , F. Pietri-Rouxel
来源:[J].Neuromuscular Disorders(IF 3.464), 2014, Vol.24 (9-10), pp.822-823Elsevier
摘要:Adeno Associated virus serotype 8 (AAV8) is of particular interest as a vector for pre-clinical and clinical trial for Duchenne Muscular Dystrophy (DMD). In several cell lines, this vector has been shown to enter cells through clathrin-mediated endocytosis followed by a trafficki...

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