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Article

Defective Natural Killer Cell Function in Patients with Hemophagocytic Lymphohistiocytosis and in First Degree Relatives

1 Oct 1998

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Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9773832
DOI: 10.1203/00006450-199810000-00001

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Defective Natural Killer Cell Function in Patients with Hemophagocytic Lymphohistiocytosis and in First Degree RelativesPMID 9773832Read ↗

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Clinical Significance of Cytotoxic Lymphocyte Subsets and the Expression of Perforin in Cytotoxic Lymphocytes in Secondary Hemophagocytic Lymphohistiocytosis PatientsSemantic proximity Read ↗

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Familial haemophagocytic lymphohistiocytosis in patients who are heterozygous for the A91V perforin variation is often associated with other genetic defects.Semantic proximity Read ↗

Familial hemophagocytic lymphohistiocytosis: an entity leading to early death.Semantic proximity Read ↗

Natural killer cell activity and dysfunction in Hermansky-Pudlak syndrome.Semantic proximity Read ↗

Perforin expression in cytotoxic lymphocytes from patients with hemophagocytic lymphohistiocytosis and their family members.Semantic proximity Read ↗

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