نتایج جستجو برای: genetic disorder

تعداد نتایج: 1161670  

احمدخانیها , حمیدرضا , تابان , مژگان , قدیری, محمد , مصطفوی عبدالملکی, حمید , نوحه‌سرا , شبنم ,

Objectives: In most advanced countries, there are tissue, deoxyribonucleic acid (DNA) and ribonucleic acid (RNA) banks which have been made to provide samples for researchers in order to speed up genetic studies in different medical disorders. This may save time and materials in comparison to self-governing projects that usually spend months to collect samples independently. In these banks pati...

Journal: :Neuroscience & Biobehavioral Reviews 2018

Journal: :genetics in the 3rd millennium 0
محمد روحانی mohammad rohani assist prof of neurology, rasul akram hospital, iran university of medical sciences, tehran, iran غلام علی شهیدی gholam ali shahidi

after parkinsonism, dystonia is the movement disorder most commonly encountered in movement disorder clinics. it is defined as a syndrome of sustained muscle contractions, frequently causing twisting and repetitive movements or abnormal postures. dystonia is classified in three ways: age at onset, body distribution of abnormal movements, and etiology. the etiologic classification identifies fou...

Journal: :Folia medica 2015
Hristo Y Ivanov Vili K Stoyanova Nikolay T Popov Tihomir I Vachev

Autism spectrum disorder is an entity that reflects a scientific consensus that several previously separated disorders are actually a single spectrum disorder with different levels of symptom severity in two core domains - deficits in social communication and interaction, and restricted repetitive behaviors. Autism spectrum disorder is diagnosed in all racial, ethnic and socioeconomic groups an...

Journal: :iranian red crescent medical journal 0
mohammad reza eslami amirabadi behavioral sciences research center, shahid beheshti university of medical sciences, tehran, ir iran rozita davari-ashtiani department of psychiatry, imam hosein hospital, shahid beheshti university of medical sciences, tehran, ir iran mojgan khademi department of psychiatry, imam hosein hospital, shahid beheshti university of medical sciences, tehran, ir iran sepideh rajeziesfahani behavioral sciences research center, shahid beheshti university of medical sciences, tehran, ir iran babak emamalizadeh department of medical genetics, shahid beheshti university of medical sciences, tehran, ir iran abolfazl movafagh department of medical genetics, shahid beheshti university of medical sciences, tehran, ir iran

conclusions the results of the study show no significant association between norepinephrine transporter polymorphism scl6a2 and adhd. results the percentages of adhd subtypes for combined, inattentive, and hyperactive/impulsive were 72.2%, 17.2%, and 11.9%, respectively. there was no significant association between norepinephrine transporter polymorphism and adhd (p = 0.81). moreover, no signif...

2012
Gonzalo Alvarez Celsa Quinteiro Francisco C. Ceballos

Inbreeding is usually defined as the mating between relatives and the progeny that result of a consanguineous mating between two related individuals is said to be inbred (CavalliSforza & Bodmer, 1971; Hedrick, 2005; Vogel & Motulsky, 1997). As a result of inheriting the same chromosomal segment through both parents, who inherited it from a common ancestor, the individuals born of consanguineous...

Brahmbhatt Vinita Maan Pratibha Patel Pratik Popat Vijay Vora Deval

Ehlers-Danlos syndrome (EDS) is a clinically heterogeneous groupof inherited disorders with ten different types, all involving agenetic defect in collagen and connective-tissue synthesis andstructure that affecting the skin, joints, and blood vessels. EDStype VIA, a very rare kyphoscoliotic type, is autosomal recessiveand clinically characterized by soft extensible skin, laxity ofjoints and kyp...

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