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Article

Clinical correlates of steady-state oxyhaemoglobin desaturation in children who have sickle cell disease.

British journal of haematology - 1 Oct 2005

Quinn Charles T, Ahmad Naveed

Abstract excerpt

Individuals with sickle cell disease (SCD) may have oxyhaemoglobin desaturation during the steady-state, the causes of which are incompletely known. We studied a cohort of 585 children who have sickle cell anaemia (SS), sickle beta0-thalassaemia (Sbeta0), sickle-haemoglobin C disease (SC), or sickle beta+-thalassaemia (Sbeta+) to determine the relationships between steady-state oxyhaemoglobin saturation (SpO2)...

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Identifiers

PMID: 16173973
DOI: 10.1111/j.1365-2141.2005.05738.x
PMCID: PMC1866256

Genes

SCD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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