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Blood|February 26, 2014
How we treat sickle hepatopathy and liver transplantation in adultsKate Gardner, Abid Suddle, Pauline Kane, et al.American Journal of Hematology|September 30, 2014
Genetic variants at HbF-modifier loci moderate anemia and leukocytosis in sickle cell disease in TanzaniaSiana Nkya Mtatiro, Julie Makani, Bruno Mmbando, et al.Blood|June 19, 2004
Quantitative trait locus on chromosome 8q influences the switch from fetal to adult hemoglobinChad Garner, Nicholas Silver, Steve Best, et al.Pediatric Pulmonology|January 31, 2007
Airway hyperresponsiveness and acute chest syndrome in children with sickle cell anemiaKarl P Sylvester, Richard A Patey, Gerrard F Rafferty, et al.Heart (British Cardiac Society)|December 14, 2006
Adult patients with Eisenmenger syndrome report flying safely on commercial airlinesCraig S Broberg, Anselm Uebing, Linda Cuomo, et al.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.Pageof 18