International Journal of Human GeneticsKate SL, Lingojwar DP. Epidemiology of sickle cell disorder in the State of Maharashtra. Int J Hum Genet. 2002;2:161–7.Kate SL, Lingojwar DP (2002). Epidemiology of Sickle cell disorder in the State of Maharashtra. Int J Hum Jenet. 2(3): pp....
Sickle cell disease (SCD) is an autosomal recessive disorder characterized by production of abnormal hemoglobin S and is associated with high morbidity and mortality. Information about the prevalence of SCD in Saudi Arabia is patchy and probably underestimated, but studies have reported that SCD is ...
We conducted a retrospective analysis of 1992 hospital discharge data to determine the incidence of hospitalizations among elementary-school-aged children ... A Chabra,GF Chávez,ES Harris - 《Western Journal of Medicine》 被引量: 200发表: 1999年 Drug resistance prevalence and HIV-1 variant charact...
740 weighted discharges were eligible. The mean age was 10.6 years. The primary insurance was Medicaid in 77.9%. We did not estimate CCI or AMA among pediatric patients. The characteristics of the study population is shown in TableS
et al. Sickle cell trait and the risk of venous thromboembolism among blacks. Blood 110, 908–912 (2007). Article CAS PubMed Google Scholar Merkel, P. A. et al. Brief communication: high incidence of venous thrombotic events among patients with Wegener granulomatosis: the Wegener's Clinical...
Health or disease burden is the distribution of a given disease or health condition among different populations within a given area. In the United States, for instance, the disease burden for cystic fibrosis is borne primarily by White people, that for sickle cell disease overwhelmingly by ...
The fifth pattern of interaction occur when the genotype's effect is reversed depending on the environmental factor's presence (fifth pattern) For example, the sickle cell trait may be advantageous in the presence of malaria but disadvantageous in the absence of this disease....
Epidemiology of stroke in Guadeloupe and the significance of the sickle cell trait.doi:RNE-05-1999-155-5-0000-0000-101019-ART98A. LannuzelV. SalmonG. MévelE. MalpoteR. RabierD. Caparros LefebvreRetour Au Numéro
Thalassemia, hemolytic anemia, polycythemia, and sickle cell disease are all benign disorders with high cell turnover that predispose to uric acid lithiasis [57], [58]. Renal hyperuricosuria Renal wasting of uric acid, hyperuricosuria as well as uric acid nephrolithiasis occur in Fanconi disease...
[195], paroxysmal nocturnal hemoglobinuria [196], rheumatoid arthritis [197,198], obstructive sleep apnea [199,200], thromboangiitis obliterans (Buerger’s disease), thrombotic thrombocytopenic purpura, sickle cell disease [201], systemic lupus erythematosus, and granulomatosis with polyangiitis (Wegener...