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Journal of Medical Genetics|February 1, 2020
Whole genome sequence-based haplotypes reveal a single origin of the 1393 bp HBB deletionXunde Wang, Julia Z Xu, Anna Conrey, et al.
Cytokine|June 14, 2017
Association of plasma CD40L with acute chest syndrome in sickle cell anemiaVanessa Tonin Garrido, Laura Sonzogni, Siana Nkya Mtatiro, 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.
European Journal of Pediatrics|December 16, 2004
Exhaled carbon monoxide levels in children with sickle cell diseaseKarl P Sylvester, Richard A Patey, Gerrard F Rafferty, et al.
British Journal of Haematology|November 18, 2003
Lamin B-receptor mutations in Pelger-Huët anomalySteve Best, Filippo Salvati, Juraj Kallo, et al.
British Journal of Haematology|February 1, 2011
Blood transfusion usage among adults with sickle cell disease - a single institution experience over ten yearsEmma Drasar, Norris Igbineweka, Nisha Vasavda, et al.
The British Journal of Ophthalmology|January 18, 2015
Spectral domain optical coherence tomography in patients with sickle cell diseaseRaeba Mathew, Rinoza Bafiq, Jayashree Ramu, et al.
BMC Nephrology|September 23, 2017
Increased prevalence of renal cysts in patients with sickle cell diseaseDaveena Meeks, Arunraj Navaratnarajah, Emma Drasar, et al.
Case Reports in Hematology|May 1, 2020
Two Consecutive Episodes of Severe Delayed Hemolytic Transfusion Reaction in a Sickle Cell Disease PatientClarisse Mpinganzima, Alf Haaland, Anne Guro Vreim Holm, et al.
Haematologica|March 10, 2015
The clinical significance of K-Cl cotransport activity in red cells of patients with HbSC diseaseDavid C Rees, Swee Lay Thein, Anna Osei, et al.
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