Mortality in sickle cell anaemia in Africa: rates and risk factors from a prospective cohort study in Tanzania

Mortality in sickle cell anaemia in Africa: rates and risk factors from a prospective cohort study in Tanzania

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς:	Makani, J, Cox, SE, Soka, D, Komba, A, Magesa, P, Rwezaula, S, Meda, E, Mgaya, J, Fegan, G, Kirkham, F, Marsh, K, Newton, C, Roberts, D
Μορφή:	Conference item
Έκδοση:	2011

Παρόμοια τεκμήρια

Mortality in sickle cell anemia in Africa: a prospective cohort study in Tanzania.
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Bacteraemia in sickle cell anaemia is associated with low haemoglobin: a report of 890 admissions to a tertiary hospital in Tanzania
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Mortality in sickle cell anemia in Africa: a prospective cohort study in Tanzania.
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Nutritional status, hospitalization and mortality among patients with sickle cell anaemia in Tanzania
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Neurological events and abnormalities in SCD cohort in Tanzania
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Nutritional status, hospitalization and mortality among patients with sickle cell anemia in Tanzania.
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Health policy for sickle cell disease in Africa: experience from Tanzania on interventions to reduce under-five mortality.
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Global arginine bioavailability in Tanzanian sickle cell anaemia patients at steady-state: a nested case control study of deaths versus survivors.
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Global arginine bioavailability in Tanzanian sickle cell anaemia patients at steady-state: A nested case control study of deaths versus survivors
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Sickle cell anaemia in East Africa: Preliminary results from a cohort study.
ανά: Makani, J, κ.ά.
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Malaria in patients with sickle cell anemia: burden, risk factors, and outcome at the outpatient clinic and during hospitalization.
ανά: Makani, J, κ.ά.
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Nocturnal haemoglobin oxygen desaturation in urban and rural East African paediatric cohorts with and without sickle cell anaemia: a cross-sectional study
ανά: L'Esperance, VS, κ.ά.
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A ten year review of the sickle cell program in Muhimbili National Hospital, Tanzania
ανά: Makani, J, κ.ά.
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Nutritional status, hospitalization and mortality among patients with sickle cell anemia in Tanzania
ανά: Sharon E. Cox, κ.ά.
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Haptoglobin, alpha-thalassaemia and glucose-6-phosphate dehydrogenase polymorphisms and risk of abnormal transcranial Doppler among patients with sickle cell anaemia in Tanzania.
ανά: Cox, SE, κ.ά.
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Haptoglobin, alpha-thalassaemia and glucose-6-phosphate dehydrogenase polymorphisms and risk of abnormal transcranial Doppler among patients with sickle cell anaemia in Tanzania
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Nocturnal haemoglobin oxygen saturation variability is associated with vitamin C deficiency in Tanzanian children with sickle cell anaemia
ανά: L'Esperance, V, κ.ά.
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ανά: Makani, J, κ.ά.
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ανά: Makani, J, κ.ά.
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Genetics of fetal hemoglobin in Tanzanian and British patients with sickle cell anemia.
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Fetal hemoglobin is associated with peripheral oxygen saturation in sickle cell disease in Tanzania.
ανά: Nkya, S, κ.ά.
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Rates and risk factors of hypertension in adolescents and adults with sickle cell anaemia in Tanzania: 10 years' experience.
ανά: Makubi, A, κ.ά.
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Transcranial doppler in sickle cell disease in Africa
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The role of malaria infection in morbidity and mortality in sickle cell disease in east africa: Preliminary evidence from a cohort study [MIM-JM-1200]
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ανά: Mtatiro, SN, κ.ά.
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Tricuspid regurgitant jet velocity and hospitalization in Tanzanian children with sickle cell anemia.
ανά: Cox, SE, κ.ά.
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Spectrum of cerebral blood flow velocities measured by transcranial Doppler ultrasonography in children with sickle cell disease in Africa
ανά: Ajala-Agbo, T, κ.ά.
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Sickle cell anemia: iron availability and nocturnal oximetry.
ανά: Cox, SE, κ.ά.
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Associations between oxyhaemoglobin desaturation and haematology in African children with sickle cell anaemia
ανά: Ajala-Agbo, T, κ.ά.
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Frequency of red cell antibody alloimmunization in patients with sickle cell disease at Muhimbili National Hospital, Dar-es-Salaam, Tanzania
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Fetal Hemoglobin is Associated with Peripheral Oxygen Saturation in Sickle Cell Disease in Tanzania
ανά: Siana Nkya, κ.ά.
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Newborn screening for hemoglobinopathies at Muhimbili National Hospital, Dar es Salaam - Tanzania
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Negative Epistasis between Sickle and Foetal Haemoglobin Suggests a Reduction in Protection against Malaria.
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Malaria as a cause of morbidity and mortality in children with homozygous sickle cell disease on the coast of Kenya
ανά: Komba, A, κ.ά.
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Cerebral blood flow velocities measured by transcranial Doppler ultrasonography in children with sickle cell disease in Africa.
ανά: Makani, J, κ.ά.
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Hematological and Biochemical Reference Ranges for the Population with Sickle Cell Disease at Steady State in Tanzania
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