Home Contact Sitemap

PedAM

Pediatric Disease Annotations & Medicines




Disease muscular dystrophy
Phenotype C0026848|myopathy
Sentences 7
PubMedID- 25364719 Even though broad spectrum mmp inhibitory compounds appear to improve myopathy in animal models of muscular dystrophy, it is noteworthy that so far no clinical trial using mmpis has been considered as truly successful in cancer or other disease states because of deleterious side effects (parsons et al., 1997; nemunaitis et al., 1998; macaulay et al., 1999; bramhall et al., 2001, 2002a,b; fingleton, 2007).
PubMedID- 21798082 Like raptor knockouts, mtor-deficient muscles develop a myopathy reminiscent of muscular dystrophy, together with impaired oxidative metabolism.
PubMedID- 24600397 Given the skeletal myopathy that develops with muscular dystrophy, it is logical to suggest that the function of this reflex might also be abnormal with the pathogenesis of disease.
PubMedID- 21424749 Furthermore, facioscapulohumeral muscular dystrophy with isolated axial myopathy has also been reported [19].
PubMedID- 24706943 The family was counselled that their condition was likely a form of autosomal dominant muscular dystrophy, with bethlem myopathy and emery-dreifuss muscular dystrophy included in the differential diagnosis.
PubMedID- 23050857 According to its clinical and histopathological presentation, mm has been categorized as distal myopathy with typical findings of muscular dystrophy [3,4].
PubMedID- 20658601 Facioscapulohumeral muscular dystrophy presenting with isolated axial myopathy and bent spine syndrome.

Page: 1