Examples of using Study entry in English and their translations into Greek
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Medicine
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Colloquial
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Ecclesiastic
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Financial
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Official/political
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Computer
I at study entry.
Characteristic at study entry.
The mean age at study entry was 62 years(with 8.5% of the patients≥75 years).
A KRAS mutation was reported in 57% of patients at study entry.
Infusions will be given at study entry and Weeks 2, 6, and 14.
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KRAS status was wild(49%)or mutant(51%) at study entry.
For study entry, patients were required to have ALT levels of≥1.5 X upper limit of normal(ULN).
Visits will occur at screening, study entry, and Weeks 6 and 12.
Patients had a median platelet count of 19 x 109/ l at study entry.
At study entry patients were randomised to receive twice-daily doses of either 0.6 mg or 0.9 mg Signifor.
Bone marrow involvement at time of diagnosis or study entry, n(%).
At study entry, the mean HBV DNA was 8.1 log10 IU/ml and mean ALT was 103 U/l across the study population.
Skin biopsies of unaffected skin will be done at study entry and Weeks 10, 18, and 26;
All patients had leukapheresis starting material collected andcryopreserved prior to or during study entry.
Of the patients who had been clinically diagnosed with MCI at study entry, 9(19%) converted to clinical AD 36 months later.
Amongst these women were almost 5,500 cases of NMSC previously diagnoses at study entry.
No characteristics at study entry identified patients who would later receive one or more additional courses.
All patients had leukapheresis products collected and cryopreserved prior to or during study entry.
At study entry, the women answered questions about physical activity, and their height and weight were measured.
More than 80% of patients in both treatment groups had a history of transfusion within 12 months of study entry.
At study entry, 41% of randomised patients had PSA progression only, whereas 59% of patients had radiographic progression.
A majority of patients(73%)had not received disease-modifying therapy during the 2 years before study entry.
At study entry, approximately 30% of the patients were 10-13 years and approximately 17%, 18%, 40%, and 25% were Tanner stage II, III, IV, and V, respectively.
There was no evidence of protection from disease caused by the HPV types for which subjects were HPV DNA positive at study entry.
Mean HbA1c increases were less pronounced in patients with normal glycaemia at study entry in comparison to pre-diabetic patients or diabetic patients.
The study treated 155(65%) subjects with AML or MDS, and 82(35%) subjects with HSCT,as the primary diseases at study entry.
The majority of patients(58%) had LDLcholesterol>190 mg/dl at study entry, and 24% of patients with LDL-cholesterol> 190 mg/dl were on lipid lowering medicinal products.
Overall, 74% of women enrolled were naïve to both HPV-16 andHPV-18(i.e. DNA negative and seronegative at study entry).
Characteristics of the patients at study entry were the following: mean age 14.2 years(range 9-17 years), 50% female, 50% male, 93.8% White, 26.7% Hispanic and 6.3% were Black.
The first was an open label study of 214 patients(aged 1-30 years)who were receiving stable doses of anti epileptic drugs before study entry.