نتایج جستجو برای: tunisian climate

تعداد نتایج: 173401  

2011
Lilia Laadhar Fatma Harzallah Mondher Zitouni Maryam Kallel-Sellami Moncef Fekih Naziha Kaabachi Hádia Slimane Sondès Makni

We aimed to characterize the different subgroups of ketosis-prone diabetes (KPD) in a sample of Tunisian patients using the Aβ scheme based on the presence or absence of β-cell autoantibodies (A+ or A-) and β-cell functional reserve (β+ or β-) and we investigated whether HLA class II alleles could contribute to distinct KPD phenotypes. We enrolled 43 adult patients with a first episode of ketos...

2014
Rim Sassi Hela Sahli Chiraz Souissi Hejer El Mahmoudi Bechir Zouari Amel Ben Ammar ElGaaied Slaheddine Sellami Serge Livio Ferrari

BACKGROUND Osteoporosis is a highly heritable trait. Among the genes associated with bone mineral density (BMD), the low-density lipoprotein receptor-related protein 5 gene (LRP5) has been consistently identified in Caucasians. However LRP5 contribution to osteoporosis in populations of other ethnicities remains poorly known. METHODS To determine whether LRP5 polymorphisms Ala1330Val and Val6...

Journal: :Hereditas 2010
H Gouta E Ksia T Buhner M A Moreno M Zarrouk A Mliki Y Gogorcena

Genetic diversity of 50 Tunisian almond (Prunus dulcis Mill.) genotypes and their relationships to European and American cultivars were studied. In total 82 genotypes were analyzed using ten genomic SSRs. A total of 159 alleles were scored and their sizes ranged from 116 to 227 bp. The number of alleles per locus varied from 12 to 23 with an average of 15.9 alleles per locus. Mean expected and ...

Journal: :Investigative ophthalmology & visual science 2004
Nizar Smaoui Omar Beltaief Sonia BenHamed Ridha M'Rad Faouzi Maazoul Amel Ouertani Habiba Chaabouni J Fielding Hejtmancik

PURPOSE To map the locus and identify the gene causing autosomal recessive congenital cataracts in a large consanguineous Tunisian family. METHODS DNA was extracted from blood samples from a large Tunisian family with an autosomal recessive, congenital, total white cataract. A genome-wide scan was performed with microsatellite markers. All exons and the splice sites of the HSF4 gene were sequ...

2014
Sonia Rouatbi Mohamed Ali Chouchene Ines Sfaxi Mohamed Ben Rejeb Zouhair Tabka Helmi Ben Saad

AIMS To establish FeNO norms for healthy Tunisian adults aged 18-60 years and to prospectively assess their reliability. METHODS This was a cross-sectional analytical study. A convenience sample of healthy Tunisian adults was recruited. Subjects responded to a medical questionnaire, and then FeNO levels were measured by an online method (Medisoft, Sorinnes (Dinant), Belgium). Clinical, anthro...

2017
Lamia Lahouar Fatma Ghrairi Amira El Arem Sana Medimagh Mouledi El Felah Hichem Ben Salem Lotfi Achour

BACKGROUND Many experimental studies have suggested an important role for barley Rihane(BR)in the prevention of colon cancer and cardiovascular diseases. The objective of this study was to evaluate the physico-chemical properties and nutritional characterizations of BR compared to other varieties grown in Tunisia (Manel, Roho and Tej). MATERIAL AND METHODS Total, insoluble and soluble dietary...

Journal: :Journal of Arabic and Islamic Studies 2021

An array of Egyptian and Tunisian lifeworlds in 2016

Journal: :Journal of Arabic and Islamic Studies 2021

An array of Egyptian and Tunisian lifeworlds in 2016.

2011
Hakima Gharbi-Khelifi Nabil Ben Salem Abid Khira Sdiri Rafik Harrath Abir Beji Leila Bhiri Sylviane Billaudel Virginie Ferre Mahjoub Aouni

In the present study, epidemiological survey and molecular characterization of hepatitis A virus during an outbreak in five Tunisian childcare centers in El-Mahres during October and November 2006 were carried out. Five well-water and five drinking water samples were included in the present study. Serological investigation and molecular characterization were carried out. All patients were IgM s...

2014
Zied Riahi Crystel Bonnet Rim Zainine Malek Louha Yosra Bouyacoub Nadia Laroussi Mariem Chargui Rym Kefi Laurence Jonard Imen Dorboz Jean-Pierre Hardelin Sihem Belhaj Salah Jacqueline Levilliers Dominique Weil Kenneth McElreavey Odile Tanguy Boespflug Ghazi Besbes Sonia Abdelhak Christine Petit

Identification of the causative mutations in patients affected by autosomal recessive non syndromic deafness (DFNB forms), is demanding due to genetic heterogeneity. After the exclusion of GJB2 mutations and other mutations previously reported in Tunisian deaf patients, we performed whole exome sequencing in patients affected with severe to profound deafness, from four unrelated consanguineous ...

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