Sickle cell anemia: iron availability and nocturnal oximetry.

Sickle cell anemia: iron availability and nocturnal oximetry.

STUDY OBJECTIVE: To test the hypothesis that low iron availability, measured as transferrin saturation, is associated with low nocturnal hemoglobin oxygen saturation (SpO(2)) in children with homozygous sickle cell anemia (SCA; hemoglobin SS). METHODS: This was a cross-sectional study of Tanzanian c...

Podrobná bibliografie
Hlavní autoři:	Cox, SE, L'Esperance, V, Makani, J, Soka, D, Prentice, A, Hill, C, Kirkham, F
Médium:	Journal article
Jazyk:	English
Vydáno:	2012

Podobné jednotky

Nocturnal haemoglobin oxygen saturation variability is associated with vitamin C deficiency in Tanzanian children with sickle cell anaemia
Autor: L'Esperance, V, a další
Vydáno: (2010)

Nocturnal haemoglobin oxygen desaturation in urban and rural East African paediatric cohorts with and without sickle cell anaemia: a cross-sectional study
Autor: L'Esperance, VS, a další
Vydáno: (2015)

Tricuspid regurgitant jet velocity and hospitalization in Tanzanian children with sickle cell anemia.
Autor: Cox, SE, a další
Vydáno: (2014)

Tricuspid regurgitant jet velocity and hospitalization in Tanzanian children with sickle cell anemia
Autor: Sharon E. Cox, a další
Vydáno: (2014-01-01)

Nutritional status, hospitalization and mortality among patients with sickle cell anemia in Tanzania.
Autor: Cox, SE, a další
Vydáno: (2011)

Global arginine bioavailability in Tanzanian sickle cell anaemia patients at steady-state: a nested case control study of deaths versus survivors.
Autor: Cox, SE, a další
Vydáno: (2011)

Global arginine bioavailability in Tanzanian sickle cell anaemia patients at steady-state: A nested case control study of deaths versus survivors
Autor: Cox, SE, a další
Vydáno: (2011)

Nutritional status, hospitalization and mortality among patients with sickle cell anaemia in Tanzania
Autor: Cox, SE, a další
Vydáno: (2011)

Nutritional status, hospitalization and mortality among patients with sickle cell anemia in Tanzania
Autor: Sharon E. Cox, a další
Vydáno: (2011-07-01)

Genetics of fetal hemoglobin in Tanzanian and British patients with sickle cell anemia.
Autor: Makani, J, a další
Vydáno: (2011)

Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania
Autor: Mtatiro, SN, a další
Vydáno: (2014)

Mortality in sickle cell anemia in Africa: a prospective cohort study in Tanzania.
Autor: Makani, J, a další
Vydáno: (2011)

Haptoglobin, alpha-thalassaemia and glucose-6-phosphate dehydrogenase polymorphisms and risk of abnormal transcranial Doppler among patients with sickle cell anaemia in Tanzania.
Autor: Cox, SE, a další
Vydáno: (2014)

Haptoglobin, alpha-thalassaemia and glucose-6-phosphate dehydrogenase polymorphisms and risk of abnormal transcranial Doppler among patients with sickle cell anaemia in Tanzania
Autor: Cox, SE, a další
Vydáno: (2014)

Association between morphometric variables and nocturnal desaturation in sickle-cell anemia
Autor: Cristina Salles, a další
Vydáno: (2014-07-01)

Association between morphometric variables and nocturnal desaturation in sickle‐cell anemia
Autor: Cristina Salles, a další
Vydáno: (2014-07-01)

Association between morphometric variables and nocturnal desaturation in sickle-cell anemia
Autor: Cristina Salles, a další
Vydáno: (2014-07-01)

Ready-to-use food supplement, with or without arginine and citrulline, with daily chloroquine in Tanzanian children with sickle-cell disease: a double-blind, random order crossover trial
Autor: Cox, SE, a další
Vydáno: (2018)

Mortality in sickle cell anemia in Africa: a prospective cohort study in Tanzania.
Autor: Julie Makani, a další
Vydáno: (2011-02-01)

Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania.
Autor: Siana Nkya Mtatiro, a další
Vydáno: (2014-01-01)

High prevalence of individuals with low concentration of fetal hemoglobin in F-cells in sickle cell anemia in Tanzania.
Autor: Urio, F, a další
Vydáno: (2016)

Health policy for sickle cell disease in Africa: experience from Tanzania on interventions to reduce under-five mortality.
Autor: Makani, J, a další
Vydáno: (2015)

Nocturnal enuresis and K+ transport in red blood cells from patients with sickle cell anemia
Autor: Sanjay Tewari, a další
Vydáno: (2016-12-01)

Effectiveness of nocturnal oximetry in predicting obstructive sleep apnea hypopnea syndrome: value of nocturnal oximetry in prediction of obstructive sleep apnea hypopnea syndrome
Autor: Lucy A. Suliman, a další
Vydáno: (2016-11-01)

Mortality in sickle cell anaemia in Africa: rates and risk factors from a prospective cohort study in Tanzania
Autor: Makani, J, a další
Vydáno: (2011)

Pulse oximetry in a cohort study of sickle cell disease
Autor: Homi, J, a další
Vydáno: (1997)

Health education for sickle cell disease: Strategies to support families and health care workers in Tanzania
Autor: G.P. Venner, a další
Vydáno: (2014-09-01)

Comparison of pulse oximetry and earlobe blood gas with CO-oximetry in children with sickle cell disease: a retrospective review
Autor: Subarna Chakravorty, a další
Vydáno: (2020-02-01)

Iron Chelation Reduces DNA Damage in Sickle Cell Anemia
Autor: Rawan S. Al-Khateeb, a další
Vydáno: (2021-10-01)

Hydroxyurea mobile directly observed therapy versus standard monitoring in patients with sickle cell anemia: a phase 2 randomized trial
Autor: Philip Sasi, a další
Vydáno: (2024-08-01)

Novel Indices to Improve the Diagnostic Ability of Nocturnal Oximetry in Children with OSAS
Autor: Panagiota Pappa, a další
Vydáno: (2023-02-01)

Transcranial doppler and magnetic resonance in Tanzanian children with sickle cell disease
Autor: Kija, EN, a další
Vydáno: (2019)

Fetal hemoglobin is associated with peripheral oxygen saturation in sickle cell disease in Tanzania.
Autor: Nkya, S, a další
Vydáno: (2017)

Transcranial doppler in sickle cell disease in Africa
Autor: Ajala-Agbo, T, a další
Vydáno: (2007)

Executive Function and Processing Speed in Children Living with Sickle Cell Anemia
Autor: Stephanie C. Kelleher, a další
Vydáno: (2023-09-01)

Decreased hepcidin levels are associated with low steady-state hemoglobin in children with sickle cell disease in Tanzania
Autor: Lee, N, a další
Vydáno: (2018)

Bacteraemia in sickle cell anaemia is associated with low haemoglobin: a report of 890 admissions to a tertiary hospital in Tanzania
Autor: Makani, J, a další
Vydáno: (2015)

Iron deficiency decreases hemolysis in sickle cell anemia Anemia ferropriva diminui hemólise em anemia falciforme
Autor: Oswaldo Castro, a další
Vydáno: (2009-02-01)

Nocturnal pulse oximetry for the detection and prediction of acute mountain sickness: An observational study
Autor: Kelsey E. Joyce, a další
Vydáno: (2024-11-01)

A ten year review of the sickle cell program in Muhimbili National Hospital, Tanzania
Autor: Makani, J, a další
Vydáno: (2018)