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1 ythropoiesis, though K-Ras(-/-) embryos were anemic.
2 Cdc42GAP-/- mice were anemic.
3 s to decide whether the patient is, in fact, anemic.
4 6471 men (21.7%) and 4659 women (30.4%) were anemic.
5 n and 10.2% of women 65 years and older were anemic.
6 h chronic heart failure (CHF) are frequently anemic.
7 Sixty-one percent of the CHF patients were anemic.
8 dred men (4.8%) and 1,058 women (13.0%) were anemic.
9 , pancreas, and the digestive tract and were anemic.
10 ted that 60% of pregnant women worldwide are anemic.
11 were normal, and the mutant animals were not anemic.
12 all patients, and five of seven were mildly anemic.
13 of subjects were HIV positive and 15.1% were anemic.
14 s frequently delayed, and some donors become anemic.
15 ty-seven percent of the study population was anemic.
16 balamin concentrations; only one subject was anemic.
17 his infection persists and he remains mildly anemic.
18 s likely to smoke (41 versus 52%), were more anemic (23 versus 7%), and were more likely to live in p
20 ey rats weighing 200-300 g, 38 of which were anemic (80-90 g/L) and 11 with normal hemoglobin levels.
31 wever, IFNgamma-knockout mice did not become anemic and had greater numbers of splenic erythroid prec
32 e, which, like hypotransferrinemic mice, are anemic and incur iron loading, but have functional Tf.
34 57BL/6 mice given adult worms rapidly became anemic and lost weight in a manner similar to AWT hamste
35 attributable to ehrlichiosis, both dogs were anemic and neutropenic and the Thai dog was thrombocytop
37 ravenous iron improves exercise tolerance in anemic and nonanemic patients with symptomatic chronic h
38 fied as stunted and obese and 1.4% were both anemic and overweight compared with expected prevalences
40 phases at two hematocrit (Hct) values: 30% (anemic) and 42% (physiologic; normalized by treatment wi
42 a quarter of the world's population remains anemic, and about half of this burden is a result of iro
46 ntly older when HU was instituted, were more anemic, and more likely to have BAN or CAM haplotypes.
47 mice, SJL-Kit(W/W-v) mice are MC-deficient, anemic, and neutropenic and have normal T cell compartme
49 s died during gestation, frequently appeared anemic, and suffered from a lack of Ter-119-positive ery
51 sion of fresh blood to 100 g/L hemoglobin in anemic animals offers cardioprotection after acute myoca
52 survival were significantly improved in the anemic animals undergoing fresh blood transfusion compar
55 survival was dramatically decreased in these anemic animals, partially compensated by considerable en
57 ; 95% CI: -3.99, -0.96) in children who were anemic at baseline and decreased Atlantis delayed scores
59 all, 44.6% of women studied (n = 37/83) were anemic at delivery, and 18% of women (n = 11/61) had IDA
61 KLF1(-/-) KLF2(-/-) double knockout mice are anemic at embryonic day 10.5 (E10.5) and die by E11.5, i
62 anemia at one year in patients who were not anemic at entry and who were randomized to enalapril or
63 tudy with blinded end point assessment among anemic (average hemoglobin of 10.4+/-1 g/dL) older adult
71 at women complaining of fatigue who were not anemic but who had reduced or absent iron stores were sy
73 Surprisingly, the patient's father is not anemic, but he is a smoker with high levels of HbCO ( ap
76 lfa overcame much of the QOL deficit seen in anemic cancer patients compared with the norm population
77 the functional status and quality of life in anemic cancer patients receiving chemotherapy, as well a
78 meters, quality of life (QOL), and safety in anemic cancer patients receiving nonplatinum chemotherap
81 posterior mesoderm of wild-type embryos and anemic cdx4(-/-) mutants, indicating a link between the
82 Mice deficient for HDAC5 show resistance to anemic challenge and altered marrow responsiveness to er
85 on cognition and impaired working memory in anemic children and long-term memory and retrieval in gi
86 and peripheral blood (n = 70) of Mozambican anemic children by quantitative polymerase chain reactio
88 he change in the hemoglobin concentration of anemic children was significantly different between fort
91 ts were made in randomly selected 7-12-y-old anemic children with documented Schistosoma haematobium
94 on effect: 0.90; 95% CI: 0.18, 1.62), and in anemic children, iron increased scores in the Atlantis D
95 deficits were observed in iron-deficient or anemic children, particularly with longer-duration, lowe
97 itory factor (MIF) in the development of the anemic complications and bone marrow suppression that ar
100 1988-1994) revealed that only a minority of anemic CRI subjects in the United States met these K/DOQ
105 stored leukodepleted red cells to euvolemic, anemic, critically ill patients has no clinically signif
106 ese data, routine IV iron supplementation of anemic, critically ill trauma patients cannot be recomme
108 reatments) is superior to no iron therapy in anemic dialysis patients receiving adequate epoetin dosa
114 served during acute chest syndromes or acute anemic events (AAE), and extracranial internal carotid a
115 udin et al have identified the rate of acute anemic events (AAEs) and extracranial internal carotid a
119 Our aim was to follow patients discharged anemic from the intensive care unit (ICU) for up to 6 mo
120 according to hemoglobin levels (<12.5 g/dl [anemic group] vs. 12.5 to 14.5 g/dl [nonanemic group]).
121 erence in one-year survival was noted in the anemic groups compared with no anemia group (adjusted ha
122 e, alleviating anemia, and improving HRQL in anemic (Hb < or = 12 g/dL) HCV-infected patients receivi
123 l infarction was two to five times higher in anemic (Hb <12 g/dl) patients than in people with Hb fro
124 ndomized hemoglobin (Hb) correction study in anemic (Hb</=10.0 g/dl) patients incident to hemodialysi
125 ness of growth factor therapy in maintaining anemic HCV-infected patients on target drug levels durin
127 intained RBV dose and improved QOL and Hb in anemic HCV-infected patients receiving combination thera
129 iesis-stimulating agents in the treatment of anemic heart failure patients, clinical trial data, to d
130 ic gluconate to improve hemoglobin levels in anemic hemodialysis patients who were receiving adequate
132 hemoglobin and allows lower epoetin doses in anemic hemodialysis patients with low TSAT and ferritin
134 7, target hemoglobin of 14 +/- 1 g/dl) or an anemic hemoglobin group (n = 18, target hemoglobin 10 +/
139 SP) on erythropoietin production in severely anemic (hemoglobin < or = 70 g/L) preschool children in
141 concentrations and hematocrit percentages in anemic (hemoglobin concentration <12 g/dL) Indian women
142 lled treatment trial was conducted among 546 anemic (hemoglobin concentration, 7-11 g/dL) children ag
143 es and malaria after iron supplementation in anemic (hemoglobin: 70-109 g/L) children aged 2-35 mo.
146 omen) who enrolled in a prospective study of anemic HIV-1-infected patients requiring transfusion.
150 al and urban families were less likely to be anemic if they received fortified milk [odds ratio (OR):
151 nts were significantly less likely to become anemic if uninterrupted postpartum participation lasted
153 n in nonpregnant Cambodian women screened as anemic.In this 2 x 2 factorial, double-blind, randomized
155 e major cause of tissue-iron accumulation in anemic iron-overload disorders caused by hemolytic anemi
157 kely contributing to an otherwise relatively anemic level of horizontal gene transfer, which neverthe
159 matopoietic growth factors for patients with anemic low/intermediate-1 IPSS (n = 94), and hypomethyla
163 OBHRE-Epo corrected the hematocrit level in anemic mice to a normal physiologic level that stabilize
164 rythropoiesis was induced in both normal and anemic mice, a process that was completely reversible.
165 EPO-generating organs of hypoxic or acutely anemic mice, acetate levels rise and ACSS2 is required f
167 e marrow cells from phenylhydrazine-treated, anemic mice, we find that both gp55-A and gp55-P induce
171 GM-CSF) and erythropoietin (epoetin alfa) in anemic, neutropenic patients with myelodysplastic syndro
173 n (odds ratio: 3.47; 95% CI: 1.51, 7.96) and anemic (odds ratio: 2.92; 95% CI: 1.24, 6.90) children h
174 icians, and the target patient population is anemic or iron-deficient adult patients with heart disea
176 st this stage have normal morphology but are anemic owing to failed definitive erythropoiesis, caused
178 ous and binary outcomes, respectively.Of 179 anemic participants, 136 (76.0%) completed all follow-up
187 reduce the risk of transfusion in moderately anemic patients controlling for patient and ICU factors.
192 ed to trigger red blood cell transfusions in anemic patients in critical care and acute care settings
195 Strikingly, it also identifies many pre-anemic patients several weeks before anemia becomes clin
197 alence of hypoglycemia in critically ill and anemic patients treated with insulin and tight glucose c
202 escribe PS exposure in RBCs of 56 comparably anemic patients with different genetic backgrounds of th
205 on was assessed in a subset of 37 ambulatory anemic patients with I131-tagged albumin to measure red
206 ersus SC alone (n = 57) for the treatment of anemic patients with lower-risk myelodysplastic syndrome
209 -elevation acute coronary syndrome, although anemic patients with ST-elevation myocardial infarction
211 uation of anemia was found in only 3% of all anemic patients, and better in internal medicine than in
212 s one of the main therapeutics used to treat anemic patients, greatly improving their quality of life
220 gle-dose (500 mg) mebendazole among severely anemic pregnant women in periurban Karachi, Pakistan.
221 Alzheimer disease etiology in iron-deficient anemic rat pups at the time of hippocampal differentiati
223 sed infarct size and myocardial apoptosis in anemic rats when compared to anemic animals not undergoi
226 oduct improved iron status in iron-deficient anemic soldiers but not in iron-normal or iron-deficient
227 concentrations were lower in iron-deficient anemic soldiers than in those with normal iron status (P
228 ed declines in iron status in iron-deficient anemic soldiers; a group-by-time interaction was observe
230 induced erythropoiesis, such as during acute anemic states (see the related article beginning on page
231 impact upon erythropoiesis, particularly in anemic states that may require output from the spleen.
232 ematocrit (Hct) or hemoglobin to correct for anemic status (e.g., 20.7 +/- 5.7 mumol/L per % Hct [day
235 lycythemic strain (gp55-P), but not from the anemic strain (gp55-A), activates the erythropoietin rec
236 terestingly, we find that the env gene of an anemic strain of Friend virus, Rauscher virus envelope g
237 -/- mice displayed exaggerated recovery from anemic stress and persistent cell cycling consistent wit
244 blast differentiation in vivo and alleviated anemic symptoms in a chronic anemia mouse model by regul
246 ugh rbc-specific Sphk1 Sphk2-KO embryos were anemic, the erythropoietic capacity of hematopoietic ste
251 erozygous Lyn(+/up) mice became increasingly anemic with age, indicating that the mutation was domina
254 receiving Sod2(-/-) cells were persistently anemic, with findings suggestive of a hemolytic process.
255 hemoglobin concentrations in rural Cambodian anemic women (aged 18-49 y) who cooked with the iron ing
256 ough the benefits of iron supplementation in anemic women are well recognized, insufficient data are
260 n multivariate models, but the proportion of anemic women who were iron deficient was considerably lo
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