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Article

Diagnosing XLP1 in patients with hemophagocytic lymphohistiocytosis.

The Journal of allergy and clinical immunology - 1 Dec 2014

Meazza Raffaella, Tuberosa Claudia, Cetica Valentina, Falco Michela, Parolini Silvia, Grieve Sam, Griffiths Gillian M, Sieni Elena, Marcenaro Stefania, Micalizzi Concetta, Montin Davide, Fagioli Franca, Moretta Alessandro, Mingari Maria C, Moretta Lorenzo, Notarangelo Luigi D, Bottino Cristina, Aricò Maurizio, Pende Daniela

Abstract excerpt

BACKGROUND: Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening, heterogeneous, hyperinflammmatory disorder. Prompt identification of inherited forms resulting from mutation in genes involved in cellular cytotoxicity can be crucial. X-linked lymphoproliferative disease 1 (XLP1), due to...

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Share to Antigens, CD
Share to Intracellular Signaling Peptides and Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Killer Cells, Natural

Share to Leukocytes, Mononuclear

Share to Lymphohistiocytosis, Hemophagocytic

Share to Lymphoproliferative Disorders

Share to Receptors, Immunologic

Share to Signaling Lymphocytic Activation Molecule Associated Protein

Source

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Identifiers

PMID: 24985396
DOI: 10.1016/j.jaci.2014.04.043
PMCID: PMC7611500

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24985396-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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