𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Multiple mitochondrial DNA deletions in hereditary inclusion body myopathy

✍ Scribed by Monica Jansson; Niklas Darin; Mårten Kyllerman; Tommy Martinsson; Jan Wahlström; A. Oldfors


Publisher
Springer-Verlag
Year
2000
Tongue
English
Weight
477 KB
Volume
100
Category
Article
ISSN
0001-6322

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Analysis of multiple mitochondrial DNA d
✍ Ali-Reza Moslemi; Christopher Lindberg; Anders Oldfors 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 238 KB 👁 2 views

Inclusion body myositis (IBM) is a sporadic progressive myopathy, which is morphologically characterized by inflammatory cell infiltrates and rimmed vacuoles in muscle fibers. Mitochondrial changes are regularly present with ragged-red fibers showing deficiency of cytochrome c oxidase. In these musc

Multiple mitochondrial DNA deletions in
✍ F. M. Santorelli; M. Sciacco; K. Tanji; S. Shanske; T. H. Vu; V. Golzi; R. C. Gr 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 795 KB

## Abstract Inclusion body myositis, a chronic inflammatory disorder, is the most common cause of myopathy in adults over the age of 50. Diagnosis is based on clinical features and distinctive morphological findings by both light and electron microscopy. The causes of inclusion body myositis are st