نتایج جستجو برای: metabolic disease

تعداد نتایج: 1658666  

Journal: :gene, cell and tissue 0
james p hardwick department of integrative medical sciences, northeast medical university (neomed), rootstown, usa; department of integrative medical sciences, northeast medical university (neomed), 4209 state route 44, rootstown, ohio 44272, usa. tel/fax: +1-3303256684

Ebrahim pour, P, Fakhrzadeh, H, Heshmat, R, Larijani, B, Nouri, M, Pourebrahim, R, Shoushtarizadeh, P,

Introduction: Metabolic syndrome includes obesity, hypertriglyceridemia, glucose intolerance, hypertension and lipid profile abnormalities. The risk of cardiovascular diseases with this syndrome is higher than every components alone. In view of its burden and high mortality rate, this syndrome should be noted. Methods: The 25-64 aged individuals in 17th zone of Tehran were studied. It was des...

Journal: :BJOG: An International Journal of Obstetrics & Gynaecology 2019

Journal: :iranian journal of basic medical sciences 0
majid khazaei department of physiology; isfahan university of medical sciences, isfahan, iran mehdi nematbakhsh water and electrolytes research center, isfahan university of medical sciences, isfahan, iran

objective(s)cardiovascular disease causes a major clinical problem in patients with end stage renal disease. since metabolic acidosis is very common in patients with end stage renal disease, we aimed to investigate the effect of experimentally-induced metabolic acidosis on serum lipid profile and aortic fatty streak (fs) formation in normal and high-cholesterol fed rabbits.materials and methods...

Non-alcoholic fatty liver disease (NAFLD) is emerging as a major health problem worldwide. NAFLD is a continuum of disease ranging from mild liver steatosis to severe steatohepatitis, which will ultimately lead to end-stage liver disease with high morbidity and mortality rates. This disorder is considered as a silent liver disease. The metabolic syndrome and its components are accounted as the ...

Journal: :iranian red crescent medical journal 0
ali sheikh md sayed department of cardiology, xiangya hospital, central south university, changsha, china zhenyu zhao institute of clinical pharmacology, central south university, changsha, china lanyan guo xijing hospital, fourth military medical university, xi an, china fei li department of cardiology, xiangya hospital, central south university, changsha, china xu deng department of cardiology, xiangya hospital, central south university, changsha, china hai deng department of cardiology, xiangya hospital, central south university, changsha, china

conclusions patient with cad and ms had higher risk than those with only cad because of lipid and glucose metabolism abnormalities. combination measurements of serum lox-1 and adiponectin levels may be helpful to evaluate the severity of cad together with ms. results serum lox-1 level was highest in cad + ms group; the difference between control and disease groups was statistically significant ...

مظهری, سیدضیاء الدین,

Phenylketonuria (PKU) is a hereditary metabolic disorder which is caused by complete or near complete deficiency of phenylalanin hydroxylase or other cofactors of the phenylalanin metabolic cycle. In this paper the data are collected from 312 patients who were referred to Shahid Akbarabadi Hospital . These patients were the result of 215 marriages which were familial in 192 instances. Most of t...

Journal: :مجله دیابت و متابولیسم ایران 0
h fakhrzadeh p ebrahim pour m nouri r pourebrahim r heshmat p shoushtarizadeh

introduction: metabolic syndrome includes obesity, hypertriglyceridemia, glucose intolerance, hypertension and lipid profile abnormalities. the risk of cardiovascular diseases with this syndrome is higher than every components alone. in view of its burden and high mortality rate, this syndrome should be noted. methods: the 25-64 aged individuals in 17th zone of tehran were studied. it was desig...

I-cell disease is a rare inherited metabolic disorder resulting from a defective phosphotransferase, characterized by coarse facial features, skeletal abnormalities and mental retardation. As clinical features of this condition mimic that of Hurler disease mutation studies help in the diagnosis. We present a case of I-cell disease in a neonate with GNPTAB gene mutation.

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