Pathological Findings in Human Autoimmune Lymphoproliferative Syndrome

The defects in lymphocyte apoptosis that underlie the autoimmune lymphoproliferative syndrome (ALPS) are usually attributable to inherited mutations of the CD95 (Fas) gene. In this report, we present the histopathological and immunophenotypic features seen in the lymph nodes (n = 16), peripheral blo...

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Main Authors: Lim, Megan S., Straus, Stephen E., Dale, Janet K., Fleisher, Thomas A., Stetler-Stevenson, Maryalice, Strober, Warren, Sneller, Michael C., Puck, Jennifer M., Lenardo, Michael J., Elenitoba-Johnson, Kojo S. J., Lin, Albert Y., Raffeld, Mark, Jaffe, Elaine S.
Formato: Artigo
Idioma:Inglês
Publicado: American Society for Investigative Pathology 1998
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Regular Articles
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC1853411/
https://ncbi.nlm.nih.gov/pubmed/9811346
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