Serial assessment of myocardial T2 in Duchenne muscular dystrophy
โ Scribed by Janaka Wansapura; Kan Hor; Wojciech Mazur; Robert Fleck; Michael Taylor; D Woodrow Benson; William Gottliebson
- Book ID
- 104498855
- Publisher
- BioMed Central
- Year
- 2011
- Tongue
- English
- Weight
- 183 KB
- Volume
- 13
- Category
- Article
- ISSN
- 1097-6647
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๐ SIMILAR VOLUMES
Erythrocytes from patients with Duchenne muscular dystrophy (DMD) were studied in relation to the extracellular calcium ion concentration. The shape of fresh erythrocytes in DMD was normal and not affected by Ca++. When DMD erythrocytes were stored in buffer solution with Ca++, however, the rate of
A 42-year-old so-called manifesting carrier of Duchenne muscular dystrophy (DMD), whose first complaints were severe myocardial symptoms, is described. Immunohistochemical study using anti-dystrophin anti-serum and analysis of cloned segments of X chromosome DNA were performed. Her two sons and one
The series elastic component (SEC) of Hill's muscle model is sensitive to a modification in muscle functional demand. In this study, SEC stiffness was quantified from quick-released movements in knee extensors of Duchenne muscular dystrophy (DMD) boys to look for possible modifications with the stag