𝔖 Bobbio Scriptorium
✦   LIBER   ✦

McArdle disease and sporadic inclusion body myositis

✍ Scribed by M. Scarpelli; G. Vattemi; M. Filosto; S. Krause; M. Marini; G. Tomelleri; P. Tonin

Book ID
110852656
Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
382 KB
Volume
35
Category
Article
ISSN
0305-1846

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Sporadic inclusion body myositis: Pathog
Sporadic inclusion body myositis: Pathogenic considerations
✍ George Karpati; Erin K. O'Ferrall πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 124 KB πŸ‘ 1 views

## Abstract Sporadic inclusion body myositis is the commonest acquired disease of skeletal muscles after 50 years of age, and as such it has commanded a great deal of attention of investigators over the past 25 years. As a result, a large amount of information has accumulated concerning its clinica

Quantitative electrophysiologic studies
Quantitative electrophysiologic studies in sporadic inclusion body myositis
✍ Paul E. Barkhaus; M. Isabel Periquet; Sanjeev D. Nandedkar πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 235 KB πŸ‘ 2 views

Sporadic inclusion body myositis (S-IBM) is a progressive, acquired disease of unknown etiology. Prior studies have suggested neurogenic involvement based on electrophysiologic data, although the biopsy is compatible with a myopathic process. Quantitative electrophysiologic studies were performed in

49. Sporadic inclusion body myositis: A
49. Sporadic inclusion body myositis: A case cohort
✍ M.M. Dimachkie; B.K. Estephan Dajdaj; R.J. Barohn; L.L. Herbelin; M. Pasnoor; A. πŸ“‚ Article πŸ“… 2012 πŸ› Elsevier Science 🌐 English βš– 44 KB