نتایج جستجو برای: genetic diagnosis

تعداد نتایج: 1054612  

سعیدی تهرانی, سعیده, لاریجانی, باقر, پارساپور‌, علیرضا,

Genetic research was initially limited to the screening and diagnosis of known hereditary diseases. After the completion of the Human Genome Project (HGP), studies became concerned with the diagnosis and treatment of many non-communicable diseases threatening the public health. Aside from this, genetic engineering, in its new form, is also concerned with the development of recombinant medicatio...

Journal: :genetics in the 3rd millennium 0
raheleh vazehan zohreh fattahi mahsa fadaee elham parsimehr mehrshid faraji mona montajebiniat

charcot-marie-tooth disease (cmt) is the most common inherited neurological disorder, affecting both motor and sensory peripheral nerves. neurophysiological patterns divide cmt into three main groups: demyelinating cmt1 (upper limb motor nerve conduction velocity (mncv) <38 m/s), axonal cmt2 (mncv >38 m/s) and intermediate cmt (mncv 25-45 m/s). cmt has been also categorized based on the mode of...

Journal: :journal of cell and molecular research 0
sarreh isakhani ardeshir bahmanimehr

the first step in the prenatal diagnosis of x-linked genetic disorders is determining fetus gender. current invasive methods to obtain the dna source of the fetus instead of its miscarriage risk, has harmful stress for high risk pregnancies. cell free fetal dna (cffdna) circulating in the maternal blood, has now become a useful source of noninvasive prenatal diagnosis. considering limitation of...

Mohammad Shahrokhi, Ramin Bozorgmehry Boozarjomehry Shokoufe Tayyebi

In this paper, the fuzzy system has been used for fault detection and diagnosis of a yeast fermentation bioreactor based on measurements corrupted by noise. In one case, parameters of membership functions are selected in a conventional manner. In another case, using certainty factors between normal and faulty conditions the optimal values of these parameters have been obtained through the g...

Journal: :iranian journal of neurology 0
abbas tafakhori department of neurology, school of medicine, imam khomeini hospital and iranian center of neurological research, tehran university of medical sciences, tehran, iran. vajiheh aghamollaii department of neurology, school of medicine, roozbeh hospital and iranian center of neurological research, tehran university of medical sciences, tehran, iran. sara faghihi-kashani department of neurology, school of medicine, tehran university of medical sciences, tehran, iran. payam sarraf department of neurology, school of medicine, imam khomeini hospital and iranian center of neurological research, tehran university of medical sciences, tehran, iran. laleh habibi department of medical genetics, school of medicine, tehran university of medical sciences, tehran, iran.

epilepsy is one of the most common neurological disorders. studies have demonstrated that genetic factors have a strong role in etiology of epilepsy. mutations in genes encoding ion channels, neurotransmitters and other proteins involved in the neuronal biology have been recognized in different types of this disease. moreover, some chromosomal aberration including ring chromosomes will result i...

Journal: :iranian journal of blood and cancer 0
mehrdad zeinalian department of genetics and molecular biology, school of medicine, isfahan university of medical sciences, isfahan, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی اصفهان (isfahan university of medical sciences)سازمان های دیگر: ala cancer prevention and control center, isfahan, iran nafiseh heidarzadeh ala cancer prevention and control center, isfahan, iran homayoun naji ala cancer prevention and control center, isfahan, iran, and department of anesthesia, nursing school, isfahan university of medical sciences, isfahan, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی اصفهان (isfahan university of medical sciences) mohammad reza sharbafchi department of psychiatry, school of medicine, isfahan university of medical sciences; isfahan, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی اصفهان (isfahan university of medical sciences)

background: breast cancer is one of the most common malignancies among iranian women; however, its clinicopathological feature is uncertain. we pioneered a genetic counseling program among patients with breast cancer and their families in isfahan. this is the first report of this program. methods: this was a descriptive cross-sectional study on women with breast cancer registered in ala cancer ...

Atekeh Bahadori, Dariush Farhud, Zahra Aryan,

The purpose of prenatal diagnosis tests is insisting of diagnosis of neonatal disorders, preparing a range of informed choices and making couples at risk to be ready for having children with genetic disorders as well. The aim of this article is to investigate all of the tests in order to determine the best one which has the lowest risk and the highest sensitivity. Screening tests (maternal bloo...

Background: Breast cancer is one of the most common malignancies among Iranian women; however, its clinicopathological feature is uncertain. We pioneered a genetic counseling program among patients with breast cancer and their families in Isfahan. This is the first report of this program. Methods: This was a descriptive cross-sectional study on women with breast cancer registered in Ala Cancer...

Introduction: Hamartomatous Polyposis Syndromes (HPS) are a rare group of dominant autosomal inheritance, which is characterized by the development of hamartomatous polyps in the gastrointestinal tract.  This syndrome included Juvenile Polyposis syndrome (JPS), Peutz-Jeghers syndrome (PJS), and PTEN Hamartoma Tumour Syndrome (PHTS). PTEN Hamartoma Tumour Syndrome (PHTS) itself includes Cowden ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید