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Article

Paroxysmal nocturnal hemoglobinuria cells in patients with bone marrow failure syndromes.

Annals of internal medicine - 21 Sept 1999

Dunn D E, Tanawattanacharoen P, Boccuni P, Nagakura S, Green S W, Kirby M R, Kumar M S, Rosenfeld S, Young N S

Abstract excerpt

BACKGROUND: Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired hematopoietic stem-cell disorder in which the affected cells are deficient in glycosylphosphatidylinositol (GPI)-anchored proteins. Paroxysmal nocturnal hemoglobinuria is frequently associated with aplastic anemia, although the basis of this relation is unknown. OBJECTIVE: To assess the PNH status of patients with diverse marrow failure...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 10498555
DOI: 10.7326/0003-4819-131-6-199909210-00002

Genes

GPI

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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