✦ LIBER ✦

Clinical, pathological, and genetic mutation analysis of sporadic inclusion body myositis in Japanese people

✍ Scribed by Cai, Huaying; Yabe, Ichiro; Sato, Kazunori; Kano, Takahiro; Nakamura, Masakazu; Hozen, Hideki; Sasaki, Hidenao

Book ID: 118784322
Publisher: Springer
Year: 2012
Tongue: English
Weight: 613 KB
Volume: 259
Category: Article
ISSN: 0340-5354
DOI: 10.1007/s00415-012-6439-0

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Analysis of HLA class I and II alleles i

Analysis of HLA class I and II alleles in sporadic inclusion-body myositis

✍ JohannesB. Lampe; Gudrun Gossrau; Andrea Kempe; Monika Füssel; Katja Schwurack; 📂 Article 📅 2003 🏛 Springer 🌐 English ⚖ 195 KB

Four-year longitudinal study of clinical

Four-year longitudinal study of clinical and functional endpoints in sporadic inclusion body myositis: Implications for therapeutic trials

✍ Hogrel, Jean-Yves; Allenbach, Yves; Canal, Aurélie; Leroux, Gaëlle; Ollivier, Gw 📂 Article 📅 2014 🏛 Elsevier Science 🌐 English ⚖ 841 KB

Analysis of HLA-DRB3 alleles and superty

Analysis of HLA-DRB3 alleles and supertypical genotypes in the MHC Class II region in sporadic inclusion body myositis

✍ Rojana-udomsart, Arada; Mitrpant, Chalermchai; James, Ian; Witt, Campbell; Needh 📂 Article 📅 2013 🏛 Elsevier Science 🌐 English ⚖ 205 KB

Familial amyotrophic lateral sclerosis w

Familial amyotrophic lateral sclerosis with onset in bulbar sign, benign clinical course, and Bunina bodies: a clinical, genetic, and pathological study of a Japanese family

✍ K. Tsuchiya; S. Shintani; H. Nakabayashi; K. Kikugawa; R. Nakano; C. Haga; I. Na 📂 Article 📅 2000 🏛 Springer-Verlag 🌐 English ⚖ 126 KB

Aceruloplasminemia in a Japanese woman w

Aceruloplasminemia in a Japanese woman with a novel mutation of CP gene: Clinical presentations and analysis of genetic and molecular pathogenesis

✍ Ayumi Hida; Hisatomo Kowa; Atsushi Iwata; Masaki Tanaka; Shin Kwak; Shoji Tsuji 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 552 KB

Clinical, pathological, and genetic feat

Clinical, pathological, and genetic features of limb-girdle muscular dystrophy type 2A with new calpain 3 gene mutations in seven patients from three Japanese families

✍ Hisaomi Kawai; Masashi Akaike; Makoto Kunishige; Toshio Inui; Katsuhito Adachi; 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 469 KB 👁 3 views

We report on the clinical, pathological, and genetic features of 7 patients with limb-girdle muscular dystrophy type 2A (LGMD2A) from three Japanese families. The mean age of onset was 9.7 ± 3.1 years (mean ± SD), and loss of ambulance occurred at 38.5 ± 2.1 years. Muscle atrophy was predominant in