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A case of inclusion body myositis with systemic sclerosis

โœ Scribed by M. Kusaoi; T. Fukazawa; M. Hirashima; Y. Morita; C. Yamaji; S. Takai; Y. Takasaki; H. Hashimoto

Publisher
Springer
Year
2003
Tongue
English
Weight
250 KB
Volume
13
Category
Article
ISSN
1439-7595

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๐Ÿ“œ SIMILAR VOLUMES

Inclusion body myositis with cricopharyn
Inclusion body myositis with cricopharyngeus muscle involvement and severe dysphagia
โœ Dr.; MD A. Verma; Dr.; DM; FRCP Walter Bradley; Dr.; MD A. M. Adesina; Dr.; MD R ๐Ÿ“‚ Article ๐Ÿ“… 1991 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 432 KB

A patient with inclusion body myositis (IBM) is presented. Unusual aspects of this case include a myopathy of 36 years duration, severe dysphagia due to cricopharyngeus muscle dysfunction, improvement with cricopharyngeus myotomy, and a diagnostic cricopharyngeus muscle biopsy.

Prevalence of sporadic inclusion body my
Prevalence of sporadic inclusion body myositis in Western Australia
โœ Beverley A. Phillips; Paul J. Zilko; Frank L. Mastaglia ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 114 KB ๐Ÿ‘ 2 views

A 10-year retrospective review was conducted to ascertain the prevalence of inclusion body myositis (IBM) in Western Australia. Seventeen patients with sporadic IBM aged 45-90 years were identified and the prevalence of IBM was calculated to be 9.3 ร— 10 -6 . The prevalence was higher in men (10.9 ร—