Autoantibody to dihydropyridine receptor in myasthenia gravis
β Scribed by Takahiro Maruta; Hiroaki Yoshikawa; Shuichi Fukasawa; Sho Umeshita; Yoshihiro Inaoka; Shigeki Edahiro; Hirotsugu Kado; Yuko Motozaki; Kazuo Iwasa; Masahito Yamada
- Book ID
- 113730426
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- English
- Weight
- 406 KB
- Volume
- 208
- Category
- Article
- ISSN
- 0165-5728
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
To improve the sensitivity of the radioimmunoassay method for anti-AChR-antibody, large amounts of sera from patients with myasthenia gravis, and higher concentrations of antigens and rabbit anti-human-IgG-antiserum, were used. These procedures enabled measurement of the titre value of over 0.04 pmo
Myasthenia gravis (MG) is an autoimmune disease amyotrophic lateral sclerosis, 3 with polymyositis, and 2 with Lambert-Eaton syndrome) were used for con-of the neuromuscular junction caused by circulating antibodies to acetylcholine receptor (AChR). In addi-trol; none had antihuman AChR antibodies.