Results 261 to 270 of about 346,186 (307)

Supernumerary teeth in a Turkish population

American Journal of Orthodontics and Dentofacial Orthopedics, 2009
Our aim in this study was to investigate the frequency, distribution, sex differences, and characteristics of supernumerary teeth in a referred Turkish population.A total of 2599 patients' panoramic radiographs (1360 girls, 1239 boys) were evaluated, including children in both the mixed and the permanent dentitions.
Esenlik, Elcin, Atilla, A. Onur, Ozen, Tuncer, Altun, Ceyhan, Sayin, M. Ozgur, Basak, Feridun   +5 more
openaire   +3 more sources

Consanguineous marriages in the Turkish population

Clinical Genetics, 1988
This study of 55 175 marriages in Turkey, conducted from 1970 to 1987, showed an overall rate of consanguineous marriage of 21.21% (mostly first‐cousin liaisons) and an inbreeding coefficient of 0.0064532. However, considerable differences between areas are apparent.
N, Başaran, B S, Sayli, A, Başaran, M, Solak, S, Artan, J D, Stevenson   +5 more
openaire   +2 more sources

Nasalance Scores for Normal-Speaking Turkish Population

Journal of Craniofacial Surgery, 2011
ObjectiveObtain normative nasalance scores for adult and children subjects speaking Turkish language, and obtain a reference for normality when nasality is evaluated.MethodMean nasalance scores were obtained from 35 normal‐speaking children and 125 adults during the repetition of 3 passages that were categorized according to the amount of nasal ...
Omer, Karakoc, Timur, Akcam, Hakan, Birkent, Hasan Huseyin, Arslan, Mustafa, Gerek   +4 more
openaire   +2 more sources

Dtermination of coumarin metabolism in Turkish population

Human & Experimental Toxicology, 2001
Cytochrome P450 2A6 is an important human hepatic P450 which activates precarcinogens and oxidizes some drug constituents such as coumarin, halothane, and the major nicotine C-oxidase. Genetic polymorphism exists in the CYP2A6 gene. CYP2A6*1 (wild type)is responsible for the 7-hydroxylation of coumarin.
Karakaya, AE, Cholerton, S, Kocabas, NA, Cok, İSMET, Sardas, S   +4 more
openaire   +3 more sources

Raynaud’s phenomenon in a healthy Turkish population

Clinical Rheumatology, 2005
Raynaud's phenomenon (RP) is a vasospastic disease and is characterized by ischemia of the digits, nose, and ears. The vasospasm can be triggered by cold weather, cold water, or emotional stress and is followed by triphasic color changes. First white color (ischemia), then blue color (congestion and cyanosis), and finally red color change (reactive ...
Ustun, Y, Onbasi, K, Sahin, I, Onbasi, O, Koca, D   +4 more
openaire   +3 more sources

Turkish Population in the Great Depression

New Perspectives on Turkey, 2000
The “Professor” is not a machine for giving lectures, but is a resource to the students-one who inspires them to investigate and question, one who guides them and one who is able to sustain their enthusiasm for study and research. The real professor is himself a lifelong student. (Reşit Galip, Minister of Education, Istanbul University, 1933)During the
openaire   +2 more sources

Varicella seroprevalence in Turkish population in Cyprus

Acta Paediatrica, 2007
AbstractAim: This study was conducted to determine the age‐specific seroprevalence of varicella zoster virus (VZV) infection in Turkish population in Cyprus.Methods: A total of 600 unvaccinated individuals aged 1–30 years were selected for the study with cluster sampling.
Kurugol, Zafer, Koturoglu, Guldane, Aksit, Sadik, Ozacar, Tijen   +3 more
openaire   +3 more sources

Paraoxonase 1 Mutations in a Turkish Population

Toxicology and Applied Pharmacology, 1999
Human serum paraoxonase 1 (PON1) catalyzes the hydrolysis of certain organophosphate pesticides and nerve gases and so may alter significantly an individual's susceptibility to the toxicity of these chemicals. Moreover, PON1 hydrolyzes lipid peroxides complexed to low density lipoproteins (LDL) and therefore it was suggested that PON1 may be one of the
A S, Aynacioglu, I, Cascorbi, P M, Mrozikiewicz, M, Nacak, E E, Tapanyigit, I, Roots   +5 more
openaire   +2 more sources

RECURRENT RAB3GAP1 MUTATIONS IN THE TURKISH POPULATION.

Genetic counseling (Geneva, Switzerland), 2015
Warburg Micro Syndrome (WARBM, MIM 600118) is a rare, severe autosomal recessive neurodevelopmental disorder characterized by microcephaly, microphthalmia, microcornea, congenital cataract, cortical dysplasia, corpus callosum hypoplasia, intellectual disability, hypotonia and hypogonadism.
TATAR, Abdulgani, TAŞDEMİR, Şener, Sahini, I., Morris-Rosendahl, D. J., MARZİOĞLU, EBRU, ÇAYIR, ATİLLA, YÜCE, İhsan   +6 more
openaire   +3 more sources

Polymorphic debrisoquin metabolism in a turkish population

Clinical Pharmacology and Therapeutics, 1994
Debrisoquin hydroxylation polymorphism was studied in 326 unrelated healthy Turkish volunteers. Debrisoquin sulfate (10 mg) was administered to subjects, and debrisoquin and 4-hydroxydebrisoquin were determined in the 0- to 8-hour urine samples. Debrisoquin oxidation was polymorphic, with 11 subjects (3.37%; 95% confidence interval, 1.69% to 6.07 ...
A, Bozkurt, N E, Basci, A, Isimer, A, Sayal, S O, Kayaalp   +4 more
openaire   +2 more sources