نتایج جستجو برای: familial background

تعداد نتایج: 885024  

Journal: :Psychological medicine 2005
J Ormel A J Oldehinkel R F Ferdinand C A Hartman A F De Winter R Veenstra W Vollebergh R B Minderaa J K Buitelaar F C Verhulst

BACKGROUND We investigated the links between familial loading, preadolescent temperament, and internalizing and externalizing problems in adolescence, hereby distinguishing effects on maladjustment in general versus dimension-specific effects on either internalizing or externalizing problems. METHOD In a population-based sample of 2230 preadolescents (10-11 years) familial loading (parental l...

2011
Bengt Zöller Kristina Sundquist

Background—This nationwide study sought to determine ageand gender-specific familial risks in siblings hospitalized for venous thromboembolism (VTE). Methods and Results—The Swedish Multigeneration Register on 0to 75-year-old subjects was linked to the Hospital Discharge Register for the years 1987–2007. Standardized incidence ratios were calculated for individuals whose siblings were hospitali...

Journal: :گوارش 0
narimantas evaldassamalavicius

introduction: due to the whole network of polyposis registers worldwide and early prophylactic treatment, survival of familial adenomatosis (fap) patients is improved. extracolonic manifestations are remarkable feature of fap. two extracolonic manifestations (duodenal adenomatosis, leading duodenal cancer and desmoid tumours) play a very important role in the reasons of death in polyposis popul...

Journal: :international journal of molecular and cellular medicine 0
debarshi sanyal lilac insight pvt ltd, ambience court, 19th floor, unit 1901 & 1902, sec-19 vashi, navi mumbai 400705 maharashtra, india. vidya bhairi lilac insight pvt ltd, ambience court, 19th floor, unit 1901 & 1902, sec-19 vashi, navi mumbai 400705 maharashtra, india. jayarama s kadandale centre for human genetics, biotech park, electronic city, phase- i, bangalore-560100, karnataka, india.

we present 2 cases of likely rare event. in case 1, 3rd degree consanguineous marriage revealed inv(6) with same break points in parents who were found to be phenotypically normal. the same inv(6) being inherited in progeny but presented with low amh (anti mullerian hormone) and high level of fsh (follicular stimulating hormone) leading to polycystic ovarian syndrome/premature ovarian failure. ...

Journal: :فقه و اصول 0

financial and economic relationships are undeniable realities and impressive factors in familial relations, and there are reciprocal interactions between these two. the existence of this relationship has caused the familial relations to be realized as effective in the penal destiny of aggressions against properties in the penal jurisprudence and statutes. in islamic jurisprudence, familial immu...

2008
Mahnaz Ashrafi Masoumeh Fallahian Reza Salman Yazdi

Background: Premature ovarian failure (POF) is a disorder of multi causal etiology. Autoimmunity has been proposed as a mechanism for some cases of ovarian follicle dysfunction which is evident in POF. The aim of this study was to identify the level of auto-antibodies in POF and familial POF patients. Materials and Methods: In this study, auto-antibodies including anti-ovarian antibody (AOA), a...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2010
Iina Niittymäki Eevi Kaasinen Sari Tuupanen Auli Karhu Heikki Järvinen Jukka-Pekka Mecklin Ian P M Tomlinson Maria Chiara Di Bernardo Richard S Houlston Lauri A Aaltonen

BACKGROUND Genomewide association studies have identified 10 low-penetrance loci that confer modestly increased risk for colorectal cancer (CRC). Although they underlie a significant proportion of CRC in the general population, their impact on the familial risk for CRC has yet to be formally enumerated. The aim of this study was to examine the combined contribution of the 10 variants, rs6983267...

Journal: :American journal of epidemiology 2007
Monica Leu Kamila Czene Marie Reilly

Family history information is often incomplete in population-based disease registers because of truncation and/or missing family links. In this study, the authors simulated complete populations of related individuals with realistic age, family structure, and incidence rates. After mimicking the realities of register-based data, such as left truncation of family history and missing family links ...

Journal: :Haematologica 2004
Gerald E Marti

BACKGROUND AND OBJECTIVES Familial aggregation has been recognized in patients with several lymphoid neoplasms, but the genetic basis for this familial clustering is not known. Germ-line mutations in the ataxia-telangiectasia mutated (ATM) and CHK2 genes have been detected in patients with mantle cell lymphoma (MCL), suggesting a potential role of these genes in genetic predisposition to these ...

2011
Shomron Ben-Horin Shira Tamir Uri Kopylov Lion Katz Moshe Nadler Alon Lang Benjamin Avidan Yehuda Chowers

BACKGROUND A family history of inflammatory bowel disease (IBD) is present in some ulcerative colitis (UC) patients. We aimed to investigate the familial occurrence of UC and its impact on disease severity. METHODS A structured questionnaire was distributed to patients with UC. Parameters pertaining to disease severity were compared for patients with or without positive family history of IBD....

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