ライフサイエンスコーパス: sickle cell trait

1 ia, despite a newborn-screening diagnosis of sickle cell trait.

2 Among 26 siblings screened, 21 children had sickle cell trait.

3 The prevalence of both the sickle cell trait (10/218 [4.6%]) and homozygous alpha+t

4 Among 5002 patients (10.3% sickle cell trait and 2.4% hemoglobin C trait) receiving

5 Prevalence of sickle cell trait and disease were high in Uganda, with

6 of the study was to calculate prevalence of sickle cell trait and disease.

7 Our findings suggest that the presence of sickle cell trait and hemoglobin C trait may explain, at

8 lysis to manage anemia, but the influence of sickle cell trait and other hemoglobinopathy traits on a

9 Heterozygous hemoglobin (Hb) AS (sickle-cell trait) and HbAC are hypothesized to protect

10 -American patients, 542 (10.2%) patients had sickle cell trait, and 129 (2.4%) patients had hemoglobi

11 cells in normal blood donors, patients with sickle cell trait, and patients with hemolytic anemias n

12 Sudden death in military recruits with sickle cell trait appears to be related to hyperthermia

13 (+) thalassemia (S beta(+)-thal), and 4 were sickle cell trait (AS).

14 nce in the risk of death among soldiers with sickle cell trait, as compared with those without the tr

15 th sickle cell trait except for the cases of sickle cell trait associated with systemic arterial hype

16 in status (healthy control subjects, n = 10; sickle cell trait carriers, n = 10; and SCA patients, n

17 eased approximately 2-fold among blacks with sickle cell trait compared with those with the wild-type

18 he mechanisms by which alpha-thalassemia and sickle cell traits confer protection from severe Plasmod

19 These data suggest that sickle-cell trait does not reduce the risk of malaria by

20 Studies have suggested that sickle cell trait elevates the risks of exertional rhabd

21 an uncommon complication in individuals with sickle cell trait except for the cases of sickle cell tr

22 ian genetics wherein a patient who inherited sickle cell trait has mild SCD resulting from postzygoti

23 , and occurred at the following frequencies: sickle cell trait (HbAS) 220 (14%), HbC heterozygosity (

24 Sickle cell trait (HbAS) associates with impaired urinar

25 Sickle cell trait (HbAS) is known to be protective again

26 des of genetic epidemiological research, the sickle cell trait (HbAS) sickle cell polymorphism, ABO b

27 gic responses in pregnant Gambian women with sickle cell trait (HbAS) than in similar women with the

28 Among children aged 2-10 years, sickle cell trait (HbAS) was associated with a 34-day de

29 Sickle cell trait (HbAS) was present in 17.7% of the chi

30 OL1 alleles that were directly genotyped and sickle cell trait (hemoglobin subunit beta gene [HBB] va

31 Although his father has sickle cell trait, his mother has no abnormal hemoglobin

32 We conducted a study of sickle cell trait in relation to these outcomes, control

33 e with normal hemoglobin or with nondisease, sickle-cell trait in under 12 min.

34 high-transmission season, and absence of the sickle cell trait increased severe-malaria risk and para

35 We conclude that sickle cell trait is a risk factor for venous thromboemb

36 ology of renal abnormalities associated with sickle cell trait is described.

37 No correlation with sickle cell trait or glucose-6-phosphate-dehydrogenase d

38 s states of hemoglobin (Hb) A and HbS (HbAS, sickle-cell trait) or HbC (HbAC) protect against Plasmod

39 s significantly more common in children with sickle cell trait (P =.014).

40 Within subgroups, sickle cell trait patients received 13.2% (P=0.003) high

41 Among children with sickle cell trait, percentage of hemoglobin S was signif

42 Although sickle cell trait protects against severe disease due to

43 Sickle cell trait (relative risk [RR], 0.68 [95% confide

44 The association between sickle cell trait (SCT) and chronic kidney disease (CKD)

45 sk genotypes, hemoglobin variants, including sickle cell trait (SCT) and hemoglobin C trait, have a r

46 s relationship may differ between those with sickle cell trait (SCT) and those without it.

47 f stem cell mobilization in individuals with sickle cell trait (SCT) has not been documented.

48 The contribution of sickle cell trait (SCT) to racial disparities in cardiop

49 um malaria in its heterozygous state, called sickle cell trait (SCT).

50 aining are the most serious complications of sickle cell trait (SCT).

51 rhabdomyolysis and death varied according to sickle cell trait status among 47,944 black soldiers who

52 -matched control (n = 11) volunteers without sickle cell trait to assess whole-brain oxygen extractio

53 rst reported case of conversion of inherited sickle cell trait to SCD by uniparental disomy (UPD) res

54 The overall number of children with sickle cell trait was 12,979 (13.3%) and with disease wa

55 Sickle cell trait was also associated with albuminuria (

56 The odds ratio for pulmonary embolism and sickle cell trait was higher, 3.9 (2.2-6.9).

57 Sickle cell trait was more common in this cohort than th

58 Sickle cell trait was not associated with a higher risk

59 Sickle cell trait was seen in all districts.

60 The odds that a patient had sickle cell trait were approximately twice that of a con

61 When children with sickle cell trait were compared with 31 control subjects

62 A patient with sickle cell trait who presented with gross hematuria and