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1 y cancer in patients of African descent with sickle cell trait.
2 th sickle cell disease than in patients with sickle cell trait.
3 ia, despite a newborn-screening diagnosis of sickle cell trait.
4  Among 26 siblings screened, 21 children had sickle cell trait.
5  disease and resistance to severe malaria in sickle cell trait.
6  loss of SMARCB1 and tightly associated with sickle cell trait.
7                   The prevalence of both the sickle cell trait (10/218 [4.6%]) and homozygous alpha+t
8             We identified 1251 patients with sickle cell trait, 230 with sickle cell disease, and 872
9 medullar iron concentrations associated with sickle cell trait, an environment propitious to the muta
10                   Among 5002 patients (10.3% sickle cell trait and 2.4% hemoglobin C trait) receiving
11                                              Sickle cell trait and disease are associated with faster
12                                Prevalence of sickle cell trait and disease were high in Uganda, with
13  of the study was to calculate prevalence of sickle cell trait and disease.
14    Our findings suggest that the presence of sickle cell trait and hemoglobin C trait may explain, at
15 duced compared with the number released from sickle cell trait and nonsickle clots in both mice and h
16 lysis to manage anemia, but the influence of sickle cell trait and other hemoglobinopathy traits on a
17 rial disease, and a lower prevalence of both sickle cell trait and sickle cell anemia.
18                                              Sickle cell trait and sickle cell disease are thought to
19 degree of protection to that afforded by the sickle-cell trait and considerably greater than that off
20             Heterozygous hemoglobin (Hb) AS (sickle-cell trait) and HbAC are hypothesized to protect
21 -American patients, 542 (10.2%) patients had sickle cell trait, and 129 (2.4%) patients had hemoglobi
22  with hemoglobin SS disease, 13 (24.1%) with sickle cell trait, and 3 (5.6%) with sickle cell-beta th
23  cells in normal blood donors, patients with sickle cell trait, and patients with hemolytic anemias n
24       Sudden death in military recruits with sickle cell trait appears to be related to hyperthermia
25 mes, including sickle cell disease (SCD) and sickle cell trait, are associated with multiple kidney a
26                  Since the identification of sickle cell trait as a heritable form of resistance to m
27 (+) thalassemia (S beta(+)-thal), and 4 were sickle cell trait (AS).
28 nce in the risk of death among soldiers with sickle cell trait, as compared with those without the tr
29 th sickle cell trait except for the cases of sickle cell trait associated with systemic arterial hype
30   Driven by the malaria-protective effect of sickle-cell trait, balancing selection results in hemogl
31 S was associated with faster eGFR decline in sickle cell trait but may be confounded by concurrent he
32 in status (healthy control subjects, n = 10; sickle cell trait carriers, n = 10; and SCA patients, n
33 eased approximately 2-fold among blacks with sickle cell trait compared with those with the wild-type
34 he mechanisms by which alpha-thalassemia and sickle cell traits confer protection from severe Plasmod
35 ex, Lynch, Xp11.2 translocation/TFE3 fusion, Sickle cell trait, DICER1 mutation, Hereditary hyperpara
36                      These data suggest that sickle-cell trait does not reduce the risk of malaria by
37                  Studies have suggested that sickle cell trait elevates the risks of exertional rhabd
38 an uncommon complication in individuals with sickle cell trait except for the cases of sickle cell tr
39 n babies' identifies sickle cell disease and sickle cell trait, guidelines direct preconception genet
40 ian genetics wherein a patient who inherited sickle cell trait has mild SCD resulting from postzygoti
41 th many protective polymorphisms-such as the sickle-cell trait-having been selected to high frequenci
42 , and occurred at the following frequencies: sickle cell trait (HbAS) 220 (14%), HbC heterozygosity (
43                                              Sickle cell trait (HbAS) associates with impaired urinar
44                                              Sickle cell trait (HbAS) is known to be protective again
45 des of genetic epidemiological research, the sickle cell trait (HbAS) sickle cell polymorphism, ABO b
46 gic responses in pregnant Gambian women with sickle cell trait (HbAS) than in similar women with the
47              Among children aged 2-10 years, sickle cell trait (HbAS) was associated with a 34-day de
48                                              Sickle cell trait (HbAS) was present in 17.7% of the chi
49                                              Sickle cell trait (HbAS) was protective against symptoma
50 ygous for HbS and HbC (HbSC), 740 (21%) with sickle cell trait (HbAS), 34 (1%) heterozygous for HbA a
51 's health in a case-control study, using the sickle cell trait (HbAS), a condition associated with a
52 othesis that malaria might cause ID, we used sickle cell trait (HbAS, rs334 ), a genetic variant that
53               Infections in individuals with sickle-cell trait (HbAS) were more likely to have gameto
54 OL1 alleles that were directly genotyped and sickle cell trait (hemoglobin subunit beta gene [HBB] va
55                             In subjects with sickle cell trait, heterozygosity for PIEZO1 E756del did
56                      Although his father has sickle cell trait, his mother has no abnormal hemoglobin
57                      We conducted a study of sickle cell trait in relation to these outcomes, control
58 e with normal hemoglobin or with nondisease, sickle-cell trait in under 12 min.
59 high-transmission season, and absence of the sickle cell trait increased severe-malaria risk and para
60                             We conclude that sickle cell trait is a risk factor for venous thromboemb
61 ology of renal abnormalities associated with sickle cell trait is described.
62                                           In sickle cell trait, low hemoglobin S and elevated hemoglo
63 2018) and included adult black patients with sickle cell trait or disease (exposures) or normal hemog
64                          No correlation with sickle cell trait or glucose-6-phosphate-dehydrogenase d
65 y in individuals with SCD than in those with sickle cell trait or in healthy individuals.
66 clined significantly faster in patients with sickle cell trait or sickle cell disease compared with r
67 s states of hemoglobin (Hb) A and HbS (HbAS, sickle-cell trait) or HbC (HbAC) protect against Plasmod
68 s significantly more common in children with sickle cell trait (P =.014).
69                            Within subgroups, sickle cell trait patients received 13.2% (P=0.003) high
70                          Among children with sickle cell trait, percentage of hemoglobin S was signif
71                                     Although sickle cell trait protects against severe disease due to
72   These disorders may not be associated with sickle cell trait-related sudden death in this populatio
73                                              Sickle cell trait (relative risk [RR], 0.68 [95% confide
74 ompared with matched controls without SCD or sickle cell trait (SCT) also evaluated by an ophthalmolo
75                      The association between sickle cell trait (SCT) and chronic kidney disease (CKD)
76 sk genotypes, hemoglobin variants, including sickle cell trait (SCT) and hemoglobin C trait, have a r
77 ost exclusively develops in individuals with sickle cell trait (SCT) and is always characterized by l
78 s relationship may differ between those with sickle cell trait (SCT) and those without it.
79 f stem cell mobilization in individuals with sickle cell trait (SCT) has not been documented.
80                                              Sickle cell trait (SCT) is a risk factor of collapse and
81                          The contribution of sickle cell trait (SCT) to racial disparities in cardiop
82 rature regarding management of patients with sickle cell trait (SCT) undergoing cardiac surgery, sinc
83                                              Sickle cell trait (SCT), defined as the presence of 1 he
84 y, an estimated 300 million individuals have sickle cell trait (SCT), the carrier state for sickle ce
85 ozygous state for the sickle cell variant or sickle cell trait (SCT).
86 um malaria in its heterozygous state, called sickle cell trait (SCT).
87 aining are the most serious complications of sickle cell trait (SCT).
88  of pregnancy complications among those with sickle cell trait (SCT).
89 rhabdomyolysis and death varied according to sickle cell trait status among 47,944 black soldiers who
90                                              Sickle cell trait status was evaluated by either direct
91 ficantly higher levels on infected RBCs from sickle cell trait subjects compared to those lacking hem
92 -matched control (n = 11) volunteers without sickle cell trait to assess whole-brain oxygen extractio
93 rst reported case of conversion of inherited sickle cell trait to SCD by uniparental disomy (UPD) res
94 ntrolled vocabulary and keywords related to "sickle cell trait," "vaso-occlusive pain," and "death,"
95          The overall number of children with sickle cell trait was 12,979 (13.3%) and with disease wa
96                                              Sickle cell trait was also associated with albuminuria (
97    The odds ratio for pulmonary embolism and sickle cell trait was higher, 3.9 (2.2-6.9).
98                                              Sickle cell trait was more common in this cohort than th
99                                              Sickle cell trait was not associated with a higher risk
100                                              Sickle cell trait was present in 7.8% of individuals of
101                                              Sickle cell trait was seen in all districts.
102                  The odds that a patient had sickle cell trait were approximately twice that of a con
103                           When children with sickle cell trait were compared with 31 control subjects
104                               A patient with sickle cell trait who presented with gross hematuria and

 
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