نتایج جستجو برای: familial history

تعداد نتایج: 402168  

Journal: :British heart journal 1979
A M Rissanen E A Nikkilä

The occurrence of main coronary risk factors was assessed in the families of 211 men under age 56 from East Finland. Fifty men were survivors of a recent myocardial infarction, 55 had died of myocardial infarction, 53 suffered from uncomplicated angina, and 53 were healthy reference men. Familial hyperlipidaemia was twice and familial hypertension three times as common in case as in reference f...

2014
Yedong Son Myong Cheol Lim Sang Soo Seo Sokbom Kang Sang-Yoon Park

OBJECTIVE To investigate the completeness of pedigree and of number of pedigree analysis to know the acceptable familial history in Korean women with ovarian cancer. METHODS Interview was conducted in 50 ovarian cancer patients for obtaining familial history three times over the 6 weeks. The completeness of pedigree is estimated in terms of familial history of disease (cancer), health status ...

Journal: :acta medica iranica 0
z. n. hatmi m. shaterian m. a. kazemi

heart failure (hf) is a common disease with high health care costs and high mortality rate knowledge of the health-related quality of life (qol) outcomes of hf may guide decision making and be useful in assessing new therapies for population. yet little is known about qol of hf patients in iran. objectives: to assess health related qol of patients with hf with two different instrument and to co...

Journal: :Blood 2011
Susan L Slager Kari G Rabe Sara J Achenbach Celine M Vachon Lynn R Goldin Sara S Strom Mark C Lanasa Logan G Spector Laura Z Rassenti Jose F Leis Nicola J Camp Martha Glenn Neil E Kay Julie M Cunningham Curtis A Hanson Gerald E Marti J Brice Weinberg Vicki A Morrison Brian K Link Timothy G Call Neil E Caporaso James R Cerhan

Prior genome-wide association (GWA) studies have identified 10 susceptibility loci for risk of chronic lymphocytic leukemia (CLL). To identify additional loci, we performed a GWA study in 407 CLL cases (of which 102 had a family history of CLL) and 296 controls. Moreover, given the strong familial risk of CLL, we further subset our GWA analysis to the CLL cases with a family history of CLL to i...

2017
Mahmood Moosazadeh Ravanbakhsh Esmaeili Mohammad Mehdi Nasehi Ghasem Abedi Mahdi Afshari Fereshteh Farshidi Motahareh Kheradmand

Background: Familial history of multiple sclerosis (MS) has been considered as one of the etiologic factors of MS by several studies. It is valuable to combine the results of these studies. The aim of this study is to estimate the pooled prevalence of familial MS in Iran using meta-analysis. Methods: Using relevant keywords, national and international databanks were searched. Considering the si...

Journal: :Journal of Crohn's & colitis 2014
Eduard Cabré Míriam Mañosa Valle García-Sánchez Ana Gutiérrez Elena Ricart Maria Esteve Jordi Guardiola Mariam Aguas Olga Merino Angel Ponferrada Javier P Gisbert Esther Garcia-Planella Gloria Ceña José L Cabriada Miguel Montoro Eugeni Domènech

BACKGROUND & AIMS Disease outcome has been found to be poorer in familial inflammatory bowel disease (IBD) than in sporadic forms, but assessment of phenotypic concordance in familial IBD provided controversial results. We assessed the concordance for disease type and phenotypic features in IBD families. METHODS Patients with familial IBD were identified from the IBD Spanish database ENEIDA. ...

Journal: :Brain and language 1996
H K van der Lely L Stollwerck

The aim of this study is to provide further characterization of a subgroup of so-called "Grammatical specific language-impaired (SLI)" children. The Grammatical SLI children have a persistent and disproportionate impairment in grammatical comprehension and expression of language. Previous research has indicated that their language impairment may be characterized by a domain-specific and modular...

Journal: :avicenna journal of neuro psycho physiology 0
mehrdokht mazdeh department of neurology, hamadan university of medical sciences, hamadan, ir iran mojtaba khazaei department of neurology, hamadan university of medical sciences, hamadan, ir iran; department of neurology, hamadan university of medical sciences, hamadan, ir iran. tel: +98-8118380315, fax: +98-08138276010 nasrin hashemi-firouzi neurophysiology research center, hamadan university of medical sciences, hamadan, ir iran masoud ghiasian department of neurology, hamadan university of medical sciences, hamadan, ir iran

patients and methods this cross-sectional study was performed on 1202 ms patients in farshchian hospital, hamadan, in 2013. all patients were diagnosed with definite ms. a questionnaire was used to gather information; demographic characteristics, medical history, signs and symptoms at onset, course of disease, relatives with ms, and degree and type of relationship were recorded. conclusions the...

2014
Delshad Saleh Akrawi Xinjun Li Jan Sundquist Kristina Sundquist Bengt Zöller

BACKGROUND The value of family history as a risk factor for kidney failure has not been determined in a nationwide setting. AIM This nationwide family study aimed to determine familial risks for kidney failure in Sweden. METHODS The Swedish multi-generation register on 0-78-year-old subjects were linked to the Swedish patient register and the Cause of death register for 1987-2010. Individua...

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