نتایج جستجو برای: familial chylomicronemia

تعداد نتایج: 56099  

Journal: :gastroenterology and hepatology from bed to bench 0
seyed mohammad hossein kashfi basic and molecular epidemiology of gastroenterology disorders research center, shahid beheshti university of medical sciences, tehran, iran mina golmohammadi basic and molecular epidemiology of gastroenterology disorders research center, shahid beheshti university of medical sciences, tehran, iran faeghe behboudi basic and molecular epidemiology of gastroenterology disorders research center, shahid beheshti university of medical sciences, tehran, iran ehsan nazemalhosseini- mojarad gastroenterology and liver diseases research center, shahid beheshti university of medical science, tehran, iran mohammad reza zali gastroenterology and liver diseases research center, shahid beheshti university of medical science, tehran, iran

normal 0 false false false en-us x-none ar-sa microsoftinternetexplorer4 colorectal cancer is classified in to three forms: sporadic (70-75%), familial (20-25%) and hereditary (5-10%). hereditary colorectal cancer syndromes classified into two different subtypes: polyposis and non polyposis. familial adenomatous polyposis (fap; omim #175100) is the most common polyposis syndrome, account for <1...

Journal: :iranian journal of diabetes and obesity 0
elaheh asadi department of genetics, faculty of medicine, shahid sadoughi university of medical sciences, yazd, iran. ehsan farashahi yazd department of genetics, faculty of medicine, shahid sadoughi university of medical sciences, yazd, iran.research and clinical centre for infertility, shahid sadoughi university of medical sciences, yazd, iran. mohammad hassan sheikhha department of genetics, faculty of medicine, shahid sadoughi university of medical sciences, yazd, iran.research and clinical centre for infertility, shahid sadoughi university of medical sciences, yazd, iran. nasrin ghasemi department of genetics, faculty of medicine, shahid sadoughi university of medical sciences, yazd, iran. razieh zarifian yeganeh department of medical genetics, tehran university of medical sciences, tehran, iran.

familial hypercholesterolemia (fh) is an inherited common autosomal mendelian disorder of lipoprotein metabolism with a population prevalence of 1 in 500. fh is characterized by severely elevated levels of low-density lipoprotein cholesterol (ldl-c), which result in surplus deposition of cholesterol in tissues. this condition leads to premature at hero sclerosis and early-onset of coronary hear...

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: :archives of clinical infectious diseases 0
ali fani department of infectious diseases and tropical medicine, arak university of medical sciences, arak, ir iran masoomeh sofian department of infectious diseases and tropical medicine, arak university of medical sciences, arak, ir iran; department of infectious diseases and tropical medicine, arak university of medical sciences, arak, ir iran. email: majid fathollahi department of infectious diseases and tropical medicine, arak university of medical sciences, arak, ir iran poorya adeli department of infectious diseases and tropical medicine, arak university of medical sciences, arak, ir iran parisa fani department of infectious diseases and tropical medicine, arak university of medical sciences, arak, ir iran

background hepatitis c virus (hcv) is a major cause of chronic liver disease worldwide. the role of intra familial hcv transmission is still controversial. the aim of the present study is to determine intra familial transmission (sexual and non sexual contacts) of hcv in a group of iranian population. patients and methods in this historical cohort study, 270 first degree relatives of hepatitis ...

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 ...

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