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European Journal of Obstetrics, Gynecology, and Reproductive Biology|May 29, 2016
Pregnancy in sickle cell-haemoglobin C (SC) disease. A retrospective study of birth size and maternal weight gainMinerva M Thame, Indira Singh-Minott, Clive Osmond, et al.Hemoglobin|September 6, 2017
A Plea for the Newborn Diagnosis of Hb S-Hereditary Persistence of Fetal HemoglobinGraham R Serjeant, Beryl E Serjeant, Ian R Hambleton, et al.American Journal of Hematology|February 9, 2002
Patterns of low-affinity immunoglobulin receptor polymorphisms in stroke and homozygous sickle cell diseaseJames G Taylor, Delia Tang, Charles B Foster, et al.Ophthalmology|September 21, 2005
Incidence and natural history of proliferative sickle cell retinopathy: observations from a cohort studySusan M Downes, Ian R Hambleton, Elaine L Chuang, et al.Disease Markers|June 8, 2012
Elevated IL-1α and CXCL10 serum levels occur in patients with homozygous sickle cell disease and a history of acute splenic sequestrationAdel Driss, Nana O Wilson, Karlene Mason, et al.Hemoglobin|January 22, 2011
Hb S-β-thalassemia: molecular, hematological and clinical comparisonsGraham R Serjeant, Beryl E Serjeant, Raphael A Fraser, et al.Plos One|March 2, 2018
Causes of death and early life determinants of survival in homozygous sickle cell disease: The Jamaican cohort study from birthGraham R Serjeant, Nicki Chin, Monika R Asnani, et al.Blood|October 24, 2002
Variants in the VCAM1 gene and risk for symptomatic stroke in sickle cell diseaseJames G Taylor, Delia C Tang, Sharon A Savage, et al.Journal of Medical Screening|August 8, 2022
Newborn screening for abnormal haemoglobins in Jamaica: Practical issues in an island programmeGraham R Serjeant, Beryl E Serjeant, Karlene P Mason, et al.Pageof 3