𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Lambert-Eaton Myasthenic syndrome in a child with an autoimmune phenotype

✍ Scribed by Hoffman, William H. ;Helman, Sandra W. ;Sekul, Elizabeth ;Carroll, James E. ;Vega, Roger A.


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
62 KB
Volume
119A
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Single-fiber electromyography improvemen
✍ Dae S. Kim; Gwendolyn C. Claussen; Shin J. Oh πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 72 KB πŸ‘ 1 views

The high incidence of elevated immunoglobulin (Ig)G anti-GQ1b antibody in sera from patients with acute phase Miller-Fisher syndrome (MFS) was first reported by Chiba et al. 1 and later confirmed by two other groups. 3,4 Chiba et al. 2 pointed out that anti-GQ1b IgG antibody is associated specifical

Specificity of autoantibodies react with
✍ Akihito Suenaga; Susumu Shirabe; Tatsufumi Nakamura; Masakatsu Motomura; Mitsuhi πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 250 KB πŸ‘ 1 views

Lambert-Eaton myasthenic syndrome (LEMS) is a neurological disorder characterized by reduced presynaptic release of acetylcholine.' Antibodies measured with o-conotoxin GVIA (GVIA), a long-lasting N-type calcium channel blocker, have been detected in 44-90% of patients with LEMS and in 10-42% of pat