نتایج جستجو برای: israiliyyat traditions of jewish origin

تعداد نتایج: 21170008  

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه مراغه - دانشکده علوم پایه 1389

assume ? ? l2(rd) has fourier transform continuous at the origin, with ˆ ?(0) = 1, and thatcan be represented by an affine series f = j>0 k?zd c j,k?j,k for some coefficients satisfying c 1(2) = j>0 k?zd |c j,k|2 1/2 <?. here ?j,k(x) = |deta j |1/2?(a jx ?k) and the dilation matrices a j expand, for example a j = 2j i. the result improves an observation by daubechies that t...

Journal: :PLoS Genetics 2006
Michael F Seldin Russell Shigeta Pablo Villoslada Carlo Selmi Jaakko Tuomilehto Gabriel Silva John W Belmont Lars Klareskog Peter K Gregersen

Using a genome-wide single nucleotide polymorphism (SNP) panel, we observed population structure in a diverse group of Europeans and European Americans. Under a variety of conditions and tests, there is a consistent and reproducible distinction between "northern" and "southern" European population groups: most individual participants with southern European ancestry (Italian, Spanish, Portuguese...

Journal: :European review for medical and pharmacological sciences 2014
R Ghermandi A Mesfin S Terzi S Colangeli E Zamparini A Gasbarrini

Familial dysautomonia (FD, or Riley-Day syndrome) is a rare but fatal autosomal recessive peripheral neuropathy caused by a point mutation in I-κ-B kinase complex associated protein (IKBCAP) gene. The disease, that affects primarily people of Ashkenazi Jewish origin, prejudices the development of primary sensory neurons determining depletion of autonomic and sensory neurons. Musculoskeletal pro...

Journal: :Sao Paulo medical journal = Revista paulista de medicina 2001
R Rozenberg L da V Pereira

CONTEXT Tay-Sachs disease is an autosomal recessive disease characterized by progressive neurologic degeneration, fatal in early childhood. In the Ashkenazi Jewish population the disease incidence is about 1 in every 3,500 newborns and the carrier frequency is 1 in every 29 individuals. Carrier screening programs for Tay-Sachs disease have reduced disease incidence by 90% in high-risk populatio...

2014
Sergio Tofanelli Luca Taglioli Stefania Bertoncini Paolo Francalacci Anatole Klyosov Luca Pagani

Several authors have proposed haplotype motifs based on site variants at the mitochondrial genome (mtDNA) and the non-recombining portion of the Y chromosome (NRY) to trace the genealogies of Jewish people. Here, we analyzed their main approaches and test the feasibility of adopting motifs as ancestry markers through construction of a large database of mtDNA and NRY haplotypes from public genet...

Journal: :Suicide & life-threatening behavior 2013
Ora Nakash Irena Liphshitz Lital Keinan-Boker Itzhak Levav

Jewish-Israelis of European origin with cancer have higher suicide rates relative to their counterparts in the general population. We investigated whether this effect results from the high proportion of Holocaust survivors among them, due to vulnerabilities arising from the earlier traumas they sustained. The study was based on all Jewish-European persons with cancer, 60 years and over, diagnos...

Journal: :Jurnal Al-Mubarak: Jurnal Kajian Al-Qur'an dan Tafsir 2020

Journal: :Tattva journal of philosophy 2022

Vāda, the classical name for act of discussion/debate in Indian tradition, forms basis every conversation undertaken to reach correct knowledge. The paper explores tradition Vāda and its subcategories with intention highlighting all-encompassing holistic nature this tool cultural studies both theory praxis. It checks into evolution through contemporary times, wherein it has lost essence accommo...

2004
Petah Tiqva

Objectives-To assess the expression of systemic lupus erythematosus (SLE) in Jewish Israeli patients according to ethnic origin. Methods-Eighty four patients with SLE were divided into groups according to origin and compared for history, physical examination, and laboratory variables. Results-Patients of Sephardic origin had more serious disease manifestations than Ashkenazi patients in 60 ofth...

2013
T Kasifoglu S Bilge E Gonullu F Bekdemir C Korkmaz

Objectives The potential risk factors of amyloidosis are known as ethnic origin (Jewish, Armenian, Turkish, and North African origin), non-usage of colchicines, and family history. Various investigators suggest that M694V mutation, especially homozygote pattern, is a risk factor for amyloidosis. In literatures reported from Turkey, it is stated that there is only a limited association. In this ...

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