نتایج جستجو برای: iranian families

تعداد نتایج: 162129  

2014
Mehdi Hosseini-Mazinani Roberto Mariotti Bahareh Torkzaban Massoma Sheikh-Hassani Saeedeh Ataei Nicolò G. M. Cultrera Saverio Pandolfi Luciana Baldoni

BACKGROUND Olive trees (Olea europaea subsp. europaea var. europaea) naturally grow in areas spanning the Mediterranean basin and towards the East, including the Middle East. In the Iranian plateau, the presence of olives has been documented since very ancient times, though the early history of the crop in this area is shrouded in uncertainty. METHODS The varieties presently cultivated in Ira...

2009
Seyed Morteza Taghavi Seyedeh Seddigheh Fatemi Houshang Rafatpanah Rashin Ganjali Jalil Tavakolafshari Narges Valizadeh

Hepatocyte nuclear factor 4alpha (HNF4alpha) is a nuclear receptor involved in glucose homeostasis and is required for normal beta cell function. Mutations in the HNF4alpha gene are associated with maturity onset diabetes of the young type 1 (MODY1). The aim of the present study was to determine the prevalence and nature of mutations in HNF4alpha gene in Iranian patients with a clinical diagnos...

2014
Zeinab Ahadi Ramin Heshmat Maryam Sanaei Gita Shafiee Maryam Ghaderpanahi Mohsen Rezaei Homami Forouzan Salehi Zahra Abdollahi Bahar Azemati Bagher Larijani

BACKGROUND The aim of this study was to assess knowledge, attitude and practice of urban and rural households toward principles of nutrition in Iran. METHODS The study population was Iranian households who live in rural and urban areas in all provinces of the country. The sampling method at households' level in each province was single stage cluster sampling with equal size clusters. The incu...

2015
Nahid Dehghan Nayeri Mahlagha Dehghan Sedigheh Iranmanesh

BACKGROUND Treatment adherence is often an important issue in the management of hypertension. Deep understanding of adherence behavior as well as its influential factors can expand knowledge about treatment adherence among hypertensives. OBJECTIVE The aim of this study was to explore patients, their families, and healthcare providers' experiences about hypertension treatment adherence in sout...

2016
Maryam Sedghi Elham Esfandiari Esmat Fazel-Najafabadi Mansoor Salehi Abbas Salavaty Shirin Fattahpour Leila Dehghani Nayerossadat Nouri Fariborz Mokarian

BACKGROUND The second leading cause of cancer deaths in women is breast cancer. Germline mutations in susceptibility breast cancer gene BRCA1 increase the lifetime risk of breast cancer. Eighty-one large genomic rearrangements (LGRs) have been reported up to date in BRCA1 gene, and evaluation of these rearrangements helps with precise risk assessment in high-risk individuals. In this study, we ...

Journal: :The Malaysian journal of medical sciences : MJMS 2014
Maryam Javadi Amir Javadi Naser Kalantari Shabnam Jaliloghadr Hamed Mohamad

BACKGROUND Sleep problems are one of the main health issues raised by families. Therefore, we aimed to evaluate the sleep problems of pre-school children in Iran. METHODS Five hundred and seventy-nine children aged 3-6 years were randomly recruited from 15 kindergartens in the city of Qazvin in Iran. The Iranian version of BEARS (Bedtime problems, Excessive daytime sleepiness, Awakenings duri...

Journal: :genetics in the 3rd millennium 0
کیمیا کهریزی kimia kahrizi assoc prof of pediatrics, university of social welfare and rehabilitation sciences, tehran, iran لیا عباسی موهب lia abbasi moheb مرضیه محسنی marzieh mohseni ساناز ارژنگی sanaz arzhangi سوسن بنی هاشمی susan banihashemi حسین نجم آبادی hossein najmabadi

the hereditary ataxias are a group of genetically defined neurological diseases which are characterized by heterogeneous clinical presentations. ataxia is defined as imbalance and lack of coordination. mental retardation associated with ataxia has been reported in some of the known and recently identified syndromes. in this review, we describe some known and novel genes that cause familial ment...

Journal: :Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology 2008
Mehdi Yeganeh Marzieh Heidarzade Zahra Pourpak Nima Parvaneh Nima Rezaei Mohammad Gharagozlou Masoud Movahedi Mahnaz Sadeghi Shabestari Setareh Mamishi Asghar Aghamohammadi Mostafa Moin

Severe Combined Immunodeficiency (SCID) consists of a heterogeneous group of genetic disorders characterized by an arrest in T lymphocyte development which is variably associated with an abnormal differentiation of B and NK cells. In order to depict the clinical state of Iranian patients with SCID, records of forty patients were reviewed. Patients were classified based on the flow cytometry dat...

Journal: :Molecular Vision 2009
Shiva Akbari Birgani Zivar Salehi Masoud Houshmand Mohamad Javad Mohamadi Leila Azizade Promehr Zahra Mozafarzadeh

PURPOSE To characterize mutations within the carbohydrate sulfotransferase 6 (CHST6) gene in Iranian subjects from 12 families with macular corneal dystrophy (MCD). METHODS Genomic DNA was extracted from peripheral blood of 20 affected patients and 60 healthy volunteers followed by polymerase chain reaction (PCR) and direct sequencing of the CHST6 coding region. The observed nucleotide sequen...

2011
Hamid Galehdari Roya Monajemzadeh Habibolah Nazem Gholamreza Mohamadian Mohammad Pedram

BACKGROUND Cornelia de Lange syndrome is characterized by dysmorphic facial features, hirsutism, severe growth and developmental delay. Germline mutations in the NIPBL gene with an autosomal dominant pattern and in the SMC1A gene with an X-linked pattern have been identified in Cornelia de Lange syndrome. CASE PRESENTATION A two-month-old Iranian boy who showed multiple congenital anomalies w...

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