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Impaired lymphocyte transformation in intestinal lymphangiectasia: evidence for at least two functionally distinct lymphocyte populations in man

Intestinal lymphangiectasia is a disease characterized by hypoproteinemia and edema resulting from protein-losing gastroenteropathy secondary to abnormal intestinal lymphatics. Immunologic abnormalities associated with this disease include hypogammaglobulinemia, lymphocytopenia, skin anergy, and imp...

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Bibliografiske detaljer
Udgivet i:J Clin Invest
Main Authors: Weiden, Paul L., Blaese, R. Michael, Strober, Warren, Block, Jerome B., Waldmann, Thomas A.
Format: Artigo
Sprog:Inglês
Udgivet: American Society for Clinical Investigation 1972
Fag:
Online adgang:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC292269/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/4554185/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI106928
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