نتایج جستجو برای: iranian family

تعداد نتایج: 457338  

2013
Rokhsareh Meamar Maryam Ostadsharif Mohammad Saadatnia Abbas Ghorbani Nayereh Nouri Leila Dehghani Mansoor Salehi

BACKGROUND There are contrary results about the role of CACNA1A gene in the causation of common migraine in different populations. However, migraine may be genetically heterogeneous and more studies in different families and populations are required for a definite conclusion. The aim of this study was to surveyed leukocyte genomic DNA mutation of CACNA1A in Iranian migraine patients with [MA] a...

2015
Reza Chaman Ahmad Khosravi Sima Sajedinejad Saeed Nazemi Khadije Fereidoon Mohasseli Behzad Valizade Hamid Vahedi Ehsan Hosseinzadeh Mohammad Amiri

BACKGROUND In different studies, the prevalence of tobacco consumption has been growing in high schools boys. OBJECTIVES This study was conducted to determine the prevalence of smoking and its related factors among Iranian high school students in 2011. MATERIALS AND METHODS In this cross-sectional study, 450 male students from 15 high schools of Shahroud (northeast of Iran) were selected fo...

2015
Azad Teimori Hamid Reza Esmaeili Golnaz Sayyadzadeh Neda Zarei Ali Gholamhosseini

The Iranian Persian chub is an endemic species of the family Cyprinidae known only from few localities in drainages of Southern Iran. It was originally described in the genus Pseudophoxinus as (Pseudophoxinus persidis) and then Petroleuciscus (as Petroleuciscus persidis). In this study, we examined phylogenetic relationships of the Iranian Persian chub with other relatives in the family Cyprini...

2013
Nader Mansouri Narges Chimeh Mohsen Dehghani Seyed Kazem Malakouti Hamid Taherkhani Zohreh Abarashi

OBJECTIVE Psychiatric hospitalization of patients imposes heavy burdens on caregivers, but little is known about this issue in Iran. The present cross-sectional study aimed to investigate the risk factors associated with psychiatric hospitalization of patients with schizophrenia who were the regular clients for the educational programs of The Iranian Society for Supporting Individuals with Schi...

2016
Sadegh Chinikar Saeid Bouzari Mohammad Ali Shokrgozar Ehsan Mostafavi Tahmineh Jalali Sahar Khakifirouz Norbert Nowotny Anthony R. Fooks Nariman Shah-Hosseini

BACKGROUND Crimean Congo hemorrhagic fever virus (CCHFV) is a member of the Bunyaviridae family and Nairovirus genus. It has a negative-sense, single stranded RNA genome approximately 19.2 kb, containing the Small, Medium, and Large segments. CCHFVs are relatively divergent in their genome sequence and grouped in seven distinct clades based on S-segment sequence analysis and six clades based on...

2013
Mojgan Gharipour Alireza Khosravi Masoumeh Sadeghi Hamidreza Roohafza Mohammad Hashemi Nizal Sarrafzadegan

BACKGROUND Hypertension is a major risk factor for cardiovascular diseases. It affects approximately 18.0% of Iranian adults. This study aimed to estimate age-adjusted prevalence of hypertension and its control among Iranian persons older 19 years of age. It also tried to find and socioeconomic factors associated with hypertension control in Iranian population. METHODS In Isfahan Healthy Hear...

2017
Susan Akbaroghli Maryam Balali Behnam Kamalidehghan Siamak Saber Omid Aryani Goh Yong Meng Massoud Houshmand

BACKGROUND Hereditary multiple osteochondromas (HMO), previously named hereditary multiple exostoses (HME), is an autosomal dominant skeletal disorder characterized by the growth of multiple osteochondromas and is associated with bony deformity, skeletal growth reduction, nerve compression, restriction of joint motion, and premature osteoarthrosis. HMO is genetically heterogeneous, localized on...

2016
Masoud Mehrpour Faeze Gohari Majid Zaki Dizaji Ali Ahani May Christine V. Malicdan Babak Behnam

OBJECTIVES Current study was the first to report a consanguineous Iranian pedigree with ABCD1 mutation. METHODS Targeted molecular analysis was initially performed in three affected individuals in one family suspected to have X-ALD due to chronic progressive spasticity. Upon confirmation of genetic diagnosis, further neurologic and genetic evaluation of all family members was done. RESULTS ...

Journal: :Acta medica Iranica 2011
Fardeen Ali Malayeri Mojtaba Panjehpour Ahmad Movahedian Majid Ghaffarpour Gholam Reza Zamani Mina Hajifaraj Tabrizi Mahdi Zamani

This study determines the value of linkage analysis using six RFLP markers for carrier detection and prenatal diagnosis in familial DMD/BMD cases and their family members for the first time in the Iranian population. We studied the dystrophin gene in 33 unrelated patients with clinical diagnosis of DMD or BMD. Subsequently, we determined the rate of heterozygosity for six intragenic RFLP marker...

2014
Nahid Dehghan-Nayeri Mansooreh Tajvidi

BACKGROUND Pregnancy rate among Iranian adolescents below 20 years of age is increasing. Pregnancy during adolescence is considered a social issue associated with medical, emotional, and social outcomes for the mother, child, and family. The current research examines the experience of pregnancy among Iranian adolescents. MATERIALS AND METHODS The qualitative content analysis method was used. ...

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