نتایج جستجو برای: iranian families

تعداد نتایج: 162129  

Journal: :International journal of pediatric otorhinolaryngology 2012
Behzad Davarnia Mojgan Babanejad Zohreh Fattahi Nooshin Nikzat Niloofar Bazazzadegan Akbar Pirzade Reza Farajollahi Carla Nishimura Khadijeh Jalalvand Sanaz Arzhangi Kimia Kahrizi Richard J H Smith Hossein Najmabadi

OBJECTIVE Hereditary hearing impairment is a genetically heterogeneous disorder. In spite of this, mutations in the GJB2 gene, encoding connexin 26 (Cx26), are a major cause of nonsyndromic recessive hearing loss in many countries and are largely dependent on ethnic groups. The purpose of our study was to characterize the type and prevalence of GJB2 mutations among Azeri population of Iran. M...

2018
Jing Guan Hongyang Wang Lan Lan Li Wang Ju Yang Linyi Xie Zifang Yin Wenping Xiong Lidong Zhao Dayong Wang Qiuju Wang

Autosomal recessive non-syndromic hearing loss (ARNSHL) is a highly heterogeneous genetic condition. PDZD7 has emerged as a new genetic etiology of ARNSHL. Biallelic mutations in the PDZD7 gene have been reported in two German families, four Iranian families, and a Pakistani family with ARNSHL. The effect of PDZD7 on ARNSHL in other population has yet to be elucidated. Two Chinese ARNSHL famili...

A. A Motallebi, B Coad , F Owfi, S.M. R. Fatemi,

This study focuses on Anguilliformes specimens revising which collected during 2006-08 in some Iranian museums. For this study, all museum samples from Iranian coastal waters of the Persian Gulf and Oman Sea were investigated. The results indicated that species diversity in the Iranian waters can be classified into six families of Anguiliformes (Eels and Morays fishes). A total of 11 species...

Journal: :shiraz e medical journal 2022

Background: The neonate's birth and subsequent hospitalization cause families to experience various needs. Identifying the family's needs can lead provision of qualitative services implementation family-centered development care (FCDC) by nurses. Objectives: This study aimed assess Iranian with neonates in Neonatal Intensive Care Units (NICUs). Methods: cross-sectional was conducted northern Ir...

Journal: :Investigative ophthalmology & visual science 2007
Afagh Alavi Elahe Elahi Mehdi Hosseini Tehrani Fahimeh Asadi Amoli Mohammad-Ali Javadi Nasrin Rafati Mohsen Chiani Setareh Sadat Banihosseini Behnaz Bayat Reza Kalhor Seyed S H Amini

PURPOSE To perform a mutation screening of TACSTD2 in 13 Iranian Gelatinous Drop-like Corneal Dystrophy (GDLD) pedigrees. To assess genotype-phenotype correlations. To determine intragenic SNP haplotypes associated with the mutations, so as to gain information on their origin. METHODS The coding region of TACSTD2 was sequenced in the probands of 13 unrelated Iranian GDLD pedigrees. Variations...

2015
Mahmoud Babaeian Mohsen Naseri Mohammad Kamalinejad Farzaneh Ghaffari Fatemeh Emadi Awat Feizi Nafiseh Hosseini Yekta Peyman Adibi

CONTEXT Functional dyspepsia (FD) is a functional gastro-intestinal disorder with high prevalence. Among various treatment options, treatment by complementary and alternative medicines especially herbal remedies also practiced. Traditional Iranian medicine (TIM), a valuable resource of valid applied studies of ancient Iranian scholars, recommends numerous medicinal plants to treat dyspepsia sym...

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