نتایج جستجو برای: kurdish citizen

تعداد نتایج: 13867  

2012
Majid A Runnak Mohammed A Hazha Hassan A Hemin Abdulmahdi A Wasan Rashid M Rekawt Hughson D Michael

BACKGROUND Hormone receptor (HR) and HER2 expression predict the therapeutic response and prognosis of breast cancer. In the Middle-East, breast cancer is diagnosed at a young age, and Arabic women are reported to have a low frequency of HR positive tumors. This study investigates HR and HER2 expression among Kurdish and Arabic women. METHODS During 2008-2010, the Sulaimaniyah Directorate of ...

2016
Chiya Jalali Bayazid Ghaderi Sabrieh Amini Mohammad Abdi Daem Roshani

OBJECTIVES To evaluate the role of this polymorphism as a risk factor for breast cancer in Kurdish patients and to investigate the possible association between Arg194Trp x-ray repair cross-complementing group 1 (XRCC1) gene polymorphisms with clinical and histopathological outcomes of patients with breast cancer. METHODS A total of 100 breast cancer patients and 200 cancer-free controls in Ku...

رسته, داوود, عبداله پور, محمدرضا, محسنی, علی,

Diaspora, as a development agent, plays an important role in the political life of Iraqi Kurdish in recent years. In addition, it is a wave that has led to conflict and expansion of nationalist tendencies in the Middle East in recent decades. In this line, the Kurdish, who established the forth ethnical group in the Middle East, following mandatory deportations to the West, have created a rise ...

Trust, along with transparency, is an important indicator of a satisfactory relationship between a government and the public. Considering transparency as the key to trust in government, the purpose of this paper is to postulate a link between transparency and trust taking into account satisfaction as a psychological factor. This paper tries to find the answer of these questions: “Is there...

2010
Nasir Al-Allawi Adil A Eissa Jaladet MS Jubrael Shakir AR Jamal Hanan Hamamy

BACKGROUND Glucose-6-Phosphate dehydrogenase (G6PD) is a key enzyme of the pentose monophosphate pathway, and its deficiency is the most common inherited enzymopathy worldwide. G6PD deficiency is common among Iraqis, including those of the Kurdish ethnic group, however no study of significance has ever addressed the molecular basis of this disorder in this population. The aim of this study is t...

Journal: :Worldview 1975

2016
S. Rask P. Sainio A. E. Castaneda T. Härkänen S. Stenholm P. Koponen S. Koskinen

BACKGROUND Many ethnic minority populations have poorer health than the general population. However, there is limited knowledge on the possible ethnic gap in physical mobility. We aim to examine the prevalence of mobility limitations in working-age Russian, Somali and Kurdish origin migrants in comparison to the general population in Finland. We also determine whether the association between et...

Journal: :international journal of architectural engineering and urban planning 0
z. davoudpour department of urban planning and design, faculty of architecture, qazvin branch, islamic azad university, qazvin, iran. m. rezapour department of urban planning and design, faculty of architecture, qazvin branch, islamic azad university, qazvin, iran.

trust, along with transparency, is an important indicator of a satisfactory relationship between a government and the public. considering transparency as the key to trust in government, the purpose of this paper is to postulate a link between transparency and trust taking into account satisfaction as a psychological factor. this paper tries to find the answer of these questions: “is there any s...

Journal: :Torture : quarterly journal on rehabilitation of torture victims and prevention of torture 2006
Lloyd Bradley Nouran Tawfiq

There were over 2000 applications for asylum from Turkish nationals to the UK in 2003. A large proportion of these were person of Kurdish origin, many of whom claimed to have suffered torture. We sought to evaluate the physical and psychological effects of torture in those with physical injuries. A total of 97 Kurdish asylum seekers requiring medical evaluation for evidence of torture were exam...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1991
D Rund T Cohen D Filon C E Dowling T C Warren I Barak E Rachmilewitz H H Kazazian A Oppenheim

beta-Thalassemia is a hereditary disease caused by any of 90 different point mutations in the beta-globin gene. Specific populations generally carry a small number of mutations, the most common of which are those that are widely distributed regionally. The present study constitutes an extensive molecular characterization of this disease in a small, highly inbred ethnic group with a high inciden...

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