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Volumn 88, Issue 2, 1991, Pages 647-651
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Immunoglobulins from animal models of motor neuron disease and from human amyotrophic lateral sclerosis patients passively transfer physiological abnormalities to the neuromuscular junction
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Author keywords
[No Author keywords available]
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Indexed keywords
ANIMALIA;
CAVIA PORCELLUS;
SUS SCROFA;
IMMUNOGLOBULIN;
AMYOTROPHIC LATERAL SCLEROSIS;
ANIMAL EXPERIMENT;
ANIMAL MODEL;
ARTICLE;
CLINICAL ARTICLE;
GUINEA PIG;
HUMAN;
MOTOR NEURON DISEASE;
NEUROMUSCULAR SYNAPSE;
NONHUMAN;
PRIORITY JOURNAL;
ADULT;
AMYOTROPHIC LATERAL SCLEROSIS;
ANIMAL;
AUTOIMMUNE DISEASES;
ELECTROPHYSIOLOGY;
FEMALE;
HUMAN;
IMMUNOGLOBULINS;
IMMUNOTHERAPY, ADOPTIVE;
MALE;
MEMBRANE POTENTIALS;
MICE;
MICE, INBRED BALB C;
MIDDLE AGE;
MOTOR ENDPLATE;
MOTOR NEURONS;
NEUROMUSCULAR DISEASES;
NEUROMUSCULAR JUNCTION;
REFERENCE VALUES;
SUPPORT, NON-U.S. GOV'T;
SUPPORT, U.S. GOV'T, P.H.S.;
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EID: 0026098442
PISSN: 00278424
EISSN: None
Source Type: Journal
DOI: 10.1073/pnas.88.2.647 Document Type: Article |
Times cited : (109)
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References (27)
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