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Antibodies to motor nerve terminals: an electrophysiological study of a human myasthenic syndrome transferred to mouse.

Immunoglobulin G(IgG) prepared from the plasma of patients with a presynaptic disorder of neuromuscular transmission (Lambert-Eaton myasthenic syndrome, l.e.m.s.), or from normal pooled control human plasma, was injected into mice (10 mg daily) for up to 99 days. Micro-electrodes were used to record...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Lang, B, Newsom-Davis, J, Prior, C, Wray, D
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 1983
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1193844/
https://ncbi.nlm.nih.gov/pubmed/6655585
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