نتایج جستجو برای: intra familial

تعداد نتایج: 153072  

Journal: :گوارش 0
homayoon vahedi peyman arab

cronkhite-canada syndrome (ccs) is a rare, non-familial disorder of unknown etiology associated with alopecia, cutaneous hyperpigmentation, gastrointestinal polyposis, onychodystrophy, diarrhea, weight loss and abdominal pain.the prevalence ofâ gastrointestinal malignancy in ccs patients is about 13%, and especially is high in colorectal and gastric areas; 5 year mortality rate is 55%. in this ...

Journal: :basic and clinical cancer research 0
kourosh ghanadi department of internal medicine, faculty of medicine, lorestan university of medical sciences, khorramabad, iran khatereh anbari department of social medicine, faculty of medicine, lorestan university of medical sciences, khorramabad, iran zia obeidavi faculty of medicine, lorestan university of medical sciences, khorramabad, iran behrouz beiranvand kermanshah university of medical sciences, kermanshah, iran mohammad almasian faculty of medicine, lorestan university of medical sciences, khorramabad, iran omid beiki kermanshah university of medical sciences, kermanshah, iran / department of clinical neuroscience, karolinska institutet, sweden

introduction: the objective of the present study is to investigate the relationship between the familial history of digestive system cancers and development of gastric cancer. methods: in this case-control study conducted in 2012, 84 patients with a definite diagnosis of gastric cancer, diagnosed using endoscopy and pathological study of biopsies, were compared with 84 people with the same age ...

Journal: :iranian red crescent medical journal 0
maryam zarkesh cellular and molecular endocrine research center, research institute for endocrine sciences, shahid beheshti university of medical sciences, tehran, ir iran golaleh asghari nutrition and endocrine research center, research institute for endocrine sciences, shahid beheshti university of medical sciences, tehran, ir iran parisa amiri research center for social determinants of endocrine health and obesity research center, research institute for endocrine sciences, shahid beheshti university of medical sciences, tehran, ir iran; research center for social determinants of endocrine health and obesity research center, research institute for endocrine sciences, shahid beheshti university of medical sciences, p. o. box: 19395-4763, tehran, ir iran. tel: +98-212409309, fax: +98-212402463 nima hosseinzadeh cellular and molecular endocrine research center, research institute for endocrine sciences, shahid beheshti university of medical sciences, tehran, ir iran mehdi hedayati cellular and molecular endocrine research center, research institute for endocrine sciences, shahid beheshti university of medical sciences, tehran, ir iran arash ghanbarian prevention of metabolic disorders research center, research institute for endocrine sciences, shahid beheshti university of medical sciences, tehran, ir iran

background since genetic and most environmental factors shape the context of families, some studies have been initiated to investigate the role of familial relationships in metabolic syndrome (mets). objectives to estimate the familial aggregation of mets and its components by identifying both case and control probands among tehranian adults with different socio-behavioral and reproductive char...

Journal: :archives of cardiovascular imaging 0
laxman dubey department of cardiology, college of medical sciences and teaching hospital, bharatpur-10, chitwan, nepal; department of cardiology, college of medical sciences and teaching hospital, bharatpur-10, chitwan, nepal. tel: +977-9851123288, fax: +977-56521527

introduction dilated cardiomyopathy (dcm) is the leading cause of heart failure and arrhythmia. case presentation a 47-year-old male, diagnosed with dilated cardiomyopathy, died due to heart failure. during the screening of his family members, his 17-year-old daughter and 9-year-old son also had dilated cardiomyopathy. another daughter had died suddenly at the age of 12 years. conclusions we he...

ژورنال: Medical Laboratory Journal 2012
Alizadeh Sharg Sh, , Dolatkhah H, , Movahedian A, , Rahmani S Z, ,

Abstract Background and objectives: Familial hypercholesterolemia (FH) is an autosomal disorder characterized by increased levels of total cholesterol and low density lipoprotein cholesterol. The FH clinical phenotype has been associated with increased risk of coronary heart disease and premature death. The mutation in LDLR gene in most cases is responsible for FH phenotype. Furthermore, other ...

2017
Masoumeh Simbar Shiva Alizadeh Mahboubeh Hajifoghaha Fatemeh Dabiri

BACKGROUND Women's empowerment was defined as their ability to achieve awareness and control their personal, social, economic and political forces aiming at taking measures in order to improve their lives. This study aimed to compare the empowerment of the married women in medical sciences university in social, economic and familial domains in three cities, IRAN. METHODS This was a descriptiv...

Journal: :European journal of endocrinology 2014
H E Ramos A Carré L Chevrier G Szinnai E Tron T L O Cerqueira J Léger S Cabrol O Puel C Queinnec N De Roux L Guillot M Castanet M Polak

CONTEXT Within the last two decades, heterozygous loss-of-function PAX8 mutations have been reported in patients with a wide degree of thyroid gland dysfunction and growth despite the presence of identical mutations. OBJECTIVES To search for PAX8 mutations in a cohort of patients with congenital hypothyroidism (CH) and various types of thyroid gland defects. DESIGN A cross-sectional study w...

I Esfandyar pour

sarcoidosis is a granulomatius disease of unknown etiology involving multiple body systems.approximately 10-35% of patients with systemic disease have cutaneous involvement.skin lesions commonly observed in sarcoidosis include:erythema nodosum,macular or parpular rashes,nodules,hypopigmented or hyperpigmented patches,scarsarcoid,lupus pernio,plaques,and rarely mocusal lesions.this report descri...

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