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Mohamed Drira

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Mohamed Drira; Ali Gargouri; Khaled Masmoudi; Walid Saibi; Faïçal Brini; Moez Hanin
The K-Segments of the Wheat Dehydrin DHN-5 are Essential for the Protection of Lactate Dehydrogenase and β-Glucosidase Activities In Vitro.
Afef Khanfir; Mounir Frikha; Ali Ghorbel; Mohamed Drira; Jamel Daoud
Prognostic factors in metastatic nasopharyngeal carcinoma.
Abdelaziz Tlili; Saber Masmoudi; H Dhouib; S Bouaziz; I Ben Rebeh; J Chouchen; K Turki; Zeineb Benzina; Ilhem Charfedine; Mohamed Drira; Hammadi Ayadi
Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB63 to chromosome 11q13.3-q13.4.

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All Publications

2013: Mohamed Drira; Ali Gargouri; Khaled Masmoudi; Walid Saibi; Faïçal Brini; Moez Hanin
The K-Segments of the Wheat Dehydrin DHN-5 are Essential for the Protection of Lactate Dehydrogenase and β-Glucosidase Activities In Vitro.
Molecular biotechnology 2013;54(2):643-50.
2007: Afef Khanfir; Mounir Frikha; Ali Ghorbel; Mohamed Drira; Jamel Daoud
Prognostic factors in metastatic nasopharyngeal carcinoma.
Cancer radiothérapie : journal de la Société française de radiothérapie oncologique 2007;11(8):461-4.
2007: Abdelaziz Tlili; Saber Masmoudi; H Dhouib; S Bouaziz; I Ben Rebeh; J Chouchen; K Turki; Zeineb Benzina; Ilhem Charfedine; Mohamed Drira; Hammadi Ayadi
Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB63 to chromosome 11q13.3-q13.4.
Annals of human genetics 2007;71(Pt 2):271-5.
2006: Afef Khanfir; Mounir Frikha; Ali Ghorbel; Hela Karray; Mohamed Drira; Jamel Daoud
[Metastatic nasopharyngeal carcinoma: clinical study and therapeutic results of 95 cases].
Cancer radiothérapie : journal de la Société française de radiothérapie oncologique 2006;10(8):545-9.
2006: Emna Mkaouar-Rebai; Abdelaziz Tlili; Saber Masmoudi; Nacim Louhichi; Ilhem Charfeddine; Mohamed Ben Amor; Imed Lahmar; Nabil Driss; Mohamed Drira; Hammadi Ayadi; Faiza Fakhfakh
Mutational analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in Tunisian patients with nonsyndromic hearing loss.
Biochemical and biophysical research communications 2006;340(4):1251-8.
2006: Boutheina Hadhri-Guiga; Abdelmajid Khabir; Raja Mokdad-Gargouri; Ali Ghorbel; Mohamed Drira; Jamel Daoud; Mounir Frikha; Rachid Jlidi; Ali Gargouri
Various 30 and 69 bp deletion variants of the Epstein-Barr virus LMP1 may arise by homologous recombination in nasopharyngeal carcinoma of Tunisian patients.
Virus research 2006;115(1):24-30.
2005: Jamel Daoud; F Elloumi; Imed Maaloul; Nabil Toumi; Ali Ghorbel; Mounir Ben Jemaa; Mounir Frikha; Mohamed Drira
[Erysipela after treatment of nasopharyngeal carcinoma].
Cancer radiothérapie : journal de la Société française de radiothérapie oncologique 2005;9(8):587-9.
2005: Hanen Belguith; S Hajji; N Salem; Ilhem Charfeddine; Imed Lahmar; M B Amor; Karim Ouldim; Eliane Chouery; Nabil Driss; Mohamed Drira; André Mégarbané; Ahmed Rebai; abdelaziz sefiani; Saber Masmoudi; Hammadi Ayadi
Analysis of GJB2 mutation: evidence for a Mediterranean ancestor for the 35delG mutation.
Clinical genetics 2005;68(2):188-9.
2005: Jamel Daoud; Wissem Siala; FADHEL GUERMAZI; Mounir Besbes; Mounir Frikha; M Ghorbel; Mohamed Drira; Mohamed Abid
[Hypothyroidism following cervical irradiation in the management of carcinoma of the nasopharynx and of the breast: a prospective study on eighty-four cases].
Cancer radiothérapie : journal de la Société française de radiothérapie oncologique 2005;9(3):140-7.
2005: Abdelaziz Tlili; Ilhem Charfedine; Imed Lahmar; Zeineb Benzina; Ben Amor Mohamed; Dominique Weil; Nabil Idriss; Mohamed Drira; Saber Masmoudi; Hammadi Ayadi
Identification of a novel frameshift mutation in the DFNB31/WHRN gene in a Tunisian consanguineous family with hereditary non-syndromic recessive hearing loss.
Human mutation 2005;25(5):503.
2005: Hela Karray; W Ayadi; L Fki; Adnane Hammami; Jamel Daoud; Mohamed Drira; Mounir Frikha; Rachid Jlidi; Jaap Middeldorp
Comparison of three different serological techniques for primary diagnosis and monitoring of nasopharyngeal carcinoma in two age groups from Tunisia.
Journal of medical virology 2005;75(4):593-602.
2005: S Rodriguez; Abdelmajid Khabir; Cécile Keryer; C Perrot; Mohamed Drira; Ali Ghorbel; Rachid Jlidi; Alain BERNHEIM; Alexander Valent; Pierre Busson
Conventional and array-based comparative genomic hybridization analysis of nasopharyngeal carcinomas from the Mediterranean area.
Cancer genetics and cytogenetics 2005;157(2):140-7.
2005: Abdelaziz Tlili; Minna Männikkö; Ilhem Charfedine; Imed Lahmar; Zeineb Benzina; Mohamed Ben Amor; Nabil Driss; Leena Ala-Kokko; Mohamed Drira; Saber Masmoudi; Hammadi Ayadi
A novel autosomal recessive non-syndromic deafness locus, DFNB66, maps to chromosome 6p21.2-22.3 in a large Tunisian consanguineous family.
Human heredity 2005;60(3):123-8.
2004: Saber Masmoudi; Ilhem Charfedine; I B Rebeh; Ahmed Rebai; Abdelaziz Tlili; Ali Ghorbel; Hanen Belguith; Christine Petit; Mohamed Drira; Hammadi Ayadi
Refined mapping of the autosomal recessive non-syndromic deafness locus DFNB13 using eight novel microsatellite markers.
Clinical genetics 2004;66(4):358-64.
2003: Jamel Daoud; Nabil Toumi; Mounir Bouaziz; Ali Ghorbel; Rachid Jlidi; Mohamed Drira; Mounir Frikha
Nasopharyngeal carcinoma in childhood and adolescence: analysis of a series of 32 patients treated with combined chemotherapy and radiotherapy.
European journal of cancer (Oxford, England : 1990) 2003;39(16):2349-54.
2003: Saber Masmoudi; Abdelaziz Tlili; Marja Majava; Ali Ghorbel; Sébastien Chardenoux; Arnaud Lemainque; Zeineb Ben Zina; Jihene Moala; Minna Männikkö; Dominique Weil; Mark Lathrop; Leena Ala-Kokko; Mohamed Drira; Christine Petit; Hammadi Ayadi
Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1.
European journal of human genetics : EJHG 2003;11(2):185-8.
2003: Abdelmajid Khabir; Ali Ghorbel; Jamel Daoud; Mounir Frikha; Mohamed Drira; Agnès Laplanche; Pierre Busson; Rachid Jlidi
Similar BCL-X but different BCL-2 levels in the two age groups of north African nasopharyngeal carcinomas.
Cancer detection and prevention 2003;27(4):250-5.
2002: Tahya Sellami-Boudawara; Naourez Gouiaa; Ilhem Charfeddine; M Abdelmoula; Mohamed Drira; Rachid Jlidi
[Facial mucormycosis: observations from three cases].
Revue de stomatologie et de chirurgie maxillo-faciale 2002;103(6):369-72.
2002: Lobna Ayadi; Tahia Boudawara; Abdelmajid Khabir; Mohamed Drira; Habib Ben Mansour; Rachid Jlidi
[Mastoid tumor simulating meningitis].
Annales de pathologie 2002;22(4):335-6.
2002: M Hmani-Aifa; Saida Ben Arab; K Kharrat; Dana J Orten; A Boulila-Elgaied; Mohamed Drira; Slah Hachicha; William J Kimberling; Hammadi Ayadi
Distinctive audiometric features between USH2A and USH2B subtypes of Usher syndrome.
Journal of medical genetics 2002;39(4):281-3.
2002: Ibtissem Bahri; Tahia Boudawara; Abdelhafidh Sellami; Abdelmajid Khabir; M Ghorgel; Mohamed Drira; Jamel Daoud; Rachid Jlidi
[A rare tumor of the parapharyngeal space: myxoid chondrosarcoma].
Revue de laryngologie - otologie - rhinologie 2002;123(4):255-8.
2001: M Bellassoued; Mouna Mnif; H Marouene; Samir Kammoun; Ali Ghorbel; J Mnif; F Ayadi; Mohamed Drira; MS Kchaou; Mohamed Abid
[Perrault's syndrome: two cases].
Annales d'endocrinologie 2001;62(6):534-7.
2001: Saber Masmoudi; Stylianos E Antonarakis; Torsten Schwede; Ali Ghorbel; M Gratri; M P Pappasavas; Mohamed Drira; A Elgaied-Boulila; Marie Wattenhofer; Colette Rossier; Hamish Scott; Hammadi Ayadi; Michel Guipponi
Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness.
Human mutation 2001;18(2):101-8.
2001: Zeineb Ben Zina; Saber Masmoudi; Hammadi Ayadi; F Chaker; Ali Ghorbel; Mohamed Drira; Christine Petit
From DFNB2 to Usher syndrome: variable expressivity of the same disease.
American journal of medical genetics 2001;101(2):181-3.
2001: S Henry; C Sacaze; L Berrajah; Hela Karray; Mohamed Drira; Adnane Hammami; J Icart; B Mariame
In nasopharyngeal carcinoma-bearing patients, tumors and lymphocytes are infected by different Epstein-Barr virus strains.
International journal of cancer. Journal international du cancer 2001;91(5):698-704.
2000: Jamel Daoud; H Ben Salah; W Kammoun; Ali Ghorbel; Mounir Frikha; Rachid Jlidi; Mounir Besbes; Mohamed Drira; Mongi Maalej
[Radiation-induced glioblastoma and myxoma after treatment for undifferentiated carcinoma of the naspharynx].
Cancer radiothérapie : journal de la Société française de radiothérapie oncologique 2000;4(6):469-72.
2000: Saber Masmoudi; A Elgaied-Boulila; I Kassab; Saida Ben Arab; S Blanchard; J E Bouzouita; Mohamed Drira; A Kassab; Slah Hachicha; Christine Petit; Hammadi Ayadi
Determination of the frequency of connexin26 mutations in inherited sensorineural deafness and carrier rates in the Tunisian population using DGGE.
Journal of medical genetics 2000;37(11):E39.
2000: Abdelmajid Khabir; Abdelhafidh Sellami; M Sakka; Ali Ghorbel; Jamel Daoud; Mounir Frikha; Mohamed Drira; Pierre Busson; Rachid Jlidi
Contrasted frequencies of p53 accumulation in the two age groups of North African nasopharyngeal carcinomas.
Clinical cancer research : an official journal of the American Association for Cancer Research 2000;6(10):3932-6.
2000: Saber Masmoudi; Ilhem Charfedine; M Hmani; M'hamed Grati; Ali Ghorbel; A Elgaied-Boulila; Mohamed Drira; J P Hardelin; Hammadi Ayadi
Pendred syndrome: phenotypic variability in two families carrying the same PDS missense mutation.
American journal of medical genetics 2000;90(1):38-44.
1999: M Hmani; Ali Ghorbel; A Boulila-Elgaied; Zeineb Ben Zina; W Kammoun; Mohamed Drira; Mohamed Chaabouni; Christine Petit; Hammadi Ayadi
A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23-24.2.
European journal of human genetics : EJHG 1999;7(3):363-7.
1997: Dominique Weil; P Küssel; Stéphane Blanchard; G Lévy; F Levi-Acobas; Mohamed Drira; Hammadi Ayadi; Christine Petit
The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene.
Nature genetics 1997;16(2):191-3.
1997: Jamel Daoud; M Ghorbel; Mounir Frikha; Y Ben Hamed; Rachid Jlidi; J Walha; M Sellami; Mohamed Drira
[Verrucous carcinoma of the larynx. Diagnostic and therapeutic problems].
Bulletin du cancer 1997;84(3):329-30.
1997: Mounir Frikha; Mounir Bouaziz; Jamel Daoud; Ali Ghorbel; Moez Elloumi; M Boudaya; Rachid Jlidi; Taoufik Souissi; Mohamed Salah Kechaou; Mohamed Drira
[Evaluation of tumoral and lymph node response to neoadjuvant chemotherapy in undifferentiated nasopharyngeal carcinoma].
Bulletin du cancer 1997;84(3):273-6.
1997: A Boulila-Elgaïed; Saber Masmoudi; Mohamed Drira; M Gouia; Hassan Chaib; Christine Petit; Hammadi Ayadi
Contribution of DFNB1 and DFNB2 loci to neurosensory deafness in affected Tunisian families.
Archives de l'Institut Pasteur de Tunis 1997;74(1-2):5-8.
1994: P Guilford; Hammadi Ayadi; Stéphane Blanchard; Hassan Chaib; D Le Paslier; Jean Weissenbach; Mohamed Drira; Christine Petit
A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene.
Human molecular genetics 1994;3(6):989-93.
1989: F Kharrat; S Mnif; MS Kechaou; H Turki; M Jaouadi; Mohamed Drira; R Fourati; B Haddouk
[Sideropenic dysphagia].
Journal de radiologie 1989;70(10):563-7.