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

British Journal of Haematology

Volumn 131, Issue 1, 2005, Pages 129-134

  Quinn, Charles T ^a,b,c,d   Ahmad, Naveed ^c  

^a UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

^b Southwestern Comprehensive Sickle Cell Center   (United States)

^c CHILDREN S MEDICAL CENTER   (United States)

^d UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

Author keywords

Children; Hypoxaemia; Pulse oximetry; Sickle cell disease

Indexed keywords

OXYHEMOGLOBIN; HEMOGLOBIN;

ACUTE CHEST SYNDROME; AGING; ANEMIA; ARTICLE; BETA THALASSEMIA; CHILD; COHORT ANALYSIS; CORRELATION ANALYSIS; FEMALE; GENOTYPE; HEMOGLOBIN DETERMINATION; HEMOGLOBIN SC DISEASE; HUMAN; HYPOXEMIA; MAJOR CLINICAL STUDY; MALE; MULTIVARIATE ANALYSIS; OXYGEN DISSOCIATION CURVE; PRIORITY JOURNAL; RETICULOCYTE COUNT; SEX DIFFERENCE; SICKLE CELL ANEMIA; STEADY STATE; ADOLESCENT; AGE; BLOOD; METABOLISM; OXIMETRY; PRESCHOOL CHILD; RETROSPECTIVE STUDY;

ADOLESCENT; AGE FACTORS; ANEMIA, SICKLE CELL; CHILD; CHILD, PRESCHOOL; FEMALE; GENOTYPE; HEMOGLOBINS; HUMANS; MALE; OXIMETRY; OXYHEMOGLOBINS; RETICULOCYTE COUNT; RETROSPECTIVE STUDIES; SEX FACTORS;

EID: 27744562780     PISSN: 00071048     EISSN: 13652141     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2005.05738.x     Document Type: Article

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