نتایج جستجو برای: muscular disease

تعداد نتایج: 1522672  

Journal: :international journal of endocrinology and metabolism 0
chiu chi tsang department of medicine, alice ho miu ling nethersole hospital, hong kong, china; department of medicine, alice ho miu ling nethersole hospital, hong kong, china. tel: +852-26892000, fax: +852-26892472 wai shan hui department of medicine, alice ho miu ling nethersole hospital, hong kong, china kwun man lo department of medicine, alice ho miu ling nethersole hospital, hong kong, china jonas hon ming yeung department of medicine, alice ho miu ling nethersole hospital, hong kong, china yuk lun cheng department of medicine, alice ho miu ling nethersole hospital, hong kong, china

case presentation a 28-year old chinese female was treated with carbimazole (cmz) for graves’ disease with hyperthyroidism. two weeks later, she developed myalgia and proximal muscle weakness. investigations showed evidence of myopathy. cmz was stopped and rapid improvement of clinical condition and biochemical parameters ensued. conclusions rapid decrement of thyroid hormone level is recognize...

Journal: :international clinical neurosciences journal 0
behdad behnam functional neurosurgery research center, shahid beheshti university of medical sciences, tehran, iran mehran arab ahmadi functional neurosurgery research center, shahid beheshti university of medical sciences, tehran, iran farzad ashrafi functional neurosurgery research center, shahid beheshti university of medical sciences, tehran, iran

kennedy disease is a rare x-linked neurodegenerative disorder that affects patients in 30-50 years of age. it is caused by cag-repeat in androgen receptor gen. there is no known effective treatment for kennedy disease. we report a 60-year-old man who had fasciculations and proximal and distal muscle weakness. physical examination showed involvement of the bulbar musculature accompanied by tongu...

Journal: :genetics in the 3rd millennium 0
غلامرضا زمانی gholamreza zamani child neurologist, children's medical center, tehran university of medical sciences (tums)

muscular dystrophies are inherited disorders that cause progressive muscle weakness (myopathy) and atrophy (loss of muscle mass) due to defects in one or more genes required for normal muscle function. some of the genes responsible for these conditions have been identified .there are a number of different types of muscular dystrophy. the primary symptom for most types is muscle weakness, althou...

Journal: :caspian journal of neurological sciences 0
fariborz rezaeitalab assistant professor, department of neurology, school of medicine, mashhad university of medical sciences, mashhad, iran reza boostani associate professor, department of neurology, school of medicine, mashhad university of medical sciences, mashhad, iran ali ghabeli-juibary neurologist, student research committee, school of medicine, mashhad university of medical sciences, mashhad, iran sara mali resident of neurology, department of neurology, school of medicine, mashhad university of medical sciences, mashhad, iran; [email protected]

pompe disease, also termed glycogen storage disease type ii or acid maltase deficiency, caused by deficient activity of acid alpha-glucosidase (gaa), the glycogen degrading lysosomal enzyme. as a result, massive lysosomal glycogen deposits in the numerous organs including the muscles. in pompe disease weakness of truncal muscles is a prominent presentation which results in respiratory failure a...

Journal: :American Journal of PharmTech Research 2018

Ali Ghabeli-Juibary, Fariborz Rezaeitalab, Reza Boostani, Sara Mali,

Pompe disease, also termed glycogen storage disease type II or acid maltase deficiency, caused by deficient activity of acid alpha-glucosidase (GAA), the glycogen degrading lysosomal enzyme. As a result, massive lysosomal glycogen deposits in the numerous organs including the muscles. In Pompe disease weakness of truncal muscles is a prominent presentation which results in respiratory failure a...

A Arzi M Rezaei

L-tyrosine, B6 and folic acid are involved in biosynthesis of DOPA and consequently dopamine. The aim of this study was to investigate the antiparkinsonian effect of these agents in perphenazine-induced catatonia in rats. Murprogo method or scored muscular rigidity, which is induced by a phenothiazine, was used to evaluate the antiparkinsonian effect of these agents. A significant decrease in m...

daniali, samira, Ghavidel, Somayeh, Riyahi Nia, Nosrat,

Introduction:  The purpose of this article is to evaluate the status of articles in the field of Spinal Muscular Atrophy According to the Scientometrics indices Word co-occurrence map of this field . Methods: The present study is an applied one with a quantitative approach and a descriptive approach. It has been done using scientometrics and the co-occurrence words analysis technique. Document...

Journal: :iranian journal of pharmaceutical research 0
a arzi m rezaei

l-tyrosine, b6 and folic acid are involved in biosynthesis of dopa and consequently dopamine. the aim of this study was to investigate the antiparkinsonian effect of these agents in perphenazine-induced catatonia in rats. murprogo method or scored muscular rigidity, which is induced by a phenothiazine, was used to evaluate the antiparkinsonian effect of these agents. a significant decrease in m...

A Arzi M Rezaei

L-tyrosine, B6 and folic acid are involved in biosynthesis of DOPA and consequently dopamine. The aim of this study was to investigate the antiparkinsonian effect of these agents in perphenazine-induced catatonia in rats. Murprogo method or scored muscular rigidity, which is induced by a phenothiazine, was used to evaluate the antiparkinsonian effect of these agents. A significant decrease in m...

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