M. Drira

发表

In nasopharyngeal carcinoma‐bearing patients, tumors and lymphocytes are infected by different epstein‐barr virus strains

C. Sacaze, S. Henry, J. Icart, 2001, International journal of cancer.

A. Khabir, J. Daoud, M. Frikha, 2003, Cancer detection and prevention.

Contrasted frequencies of p53 accumulation in the two age groups of North African nasopharyngeal carcinomas.

J. Daoud, M. Frikha, P. Busson, 2000, Clinical cancer research : an official journal of the American Association for Cancer Research.

Comparison of three different serological techniques for primary diagnosis and monitoring of nasopharyngeal carcinoma in two age groups from Tunisia

J. Daoud, M. Frikha, Jaap M Middeldorp, 2005, Journal of medical virology.

Contrasted Frequencies of p 53 Accumulation in the Two Age Groups of North African Nasopharyngeal Carcinomas 1

J. Daoud, M. Frikha, P. Busson, 2000 .

A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene.

J. Weissenbach, D. Le Paslier, H. Chaib, 1994, Human molecular genetics.

From DFNB2 to Usher syndrome: variable expressivity of the same disease.

C. Petit, S. Masmoudi, H. Ayadi, 2001, American journal of medical genetics.

Nasopharyngeal carcinoma in childhood and adolescence: analysis of a series of 32 patients treated with combined chemotherapy and radiotherapy.

N. Toumi, J. Daoud, M. Frikha, 2003, European journal of cancer.

Results of a prospective randomised trial comparing conventional radiotherapy to split course bifractionated radiation therapy in patients with nasopharyngeal carcinoma.

N. Toumi, J. Daoud, M. Frikha, 2007, Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.

[Facial mucormycosis: observations from three cases].

I. Charfeddine, M. Abdelmoula, T. Sellami-Boudawara, 2002, Revue de Stomatologie et de Chirurgie Maxillo-Faciale.

Pendred syndrome: phenotypic variability in two families carrying the same PDS missense mutation.

J. Hardelin, M. Grati, S. Masmoudi, 2000, American journal of medical genetics.

A Novel Autosomal Recessive Non-Syndromic Deafness Locus, DFNB66, Maps to Chromosome 6p21.2-22.3 in a Large Tunisian Consanguineous Family

L. Ala‐Kokko, M. Männikkö, M. Ben Amor, 2006, Human Heredity.

Conventional and array-based comparative genomic hybridization analysis of nasopharyngeal carcinomas from the Mediterranean area.

A. Bernheim, P. Busson, A. Valent, 2005, Cancer genetics and cytogenetics.

Various 30 and 69 bp deletion variants of the Epstein-Barr virus LMP1 may arise by homologous recombination in nasopharyngeal carcinoma of Tunisian patients.

B. Hadhri-Guiga, A. Khabir, J. Daoud, 2006, Virus research.

[Radiation-induced glioblastoma and myxoma after treatment for undifferentiated carcinoma of the naspharynx].

J. Daoud, M. Frikha, A. Ghorbel, 2000, Cancer radiotherapie : journal de la Societe francaise de radiotherapie oncologique.

The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene

C. Petit, D. Weil, S. Blanchard, 1997, Nature Genetics.

A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23–24.2

C. Petit, H. Ayadi, Z. B. Zina, 1999, European Journal of Human Genetics.

Contribution of DFNB1 and DFNB2 loci to neurosensory deafness in affected Tunisian families.

H. Chaib, C. Petit, S. Masmoudi, 1997, Archives de l'Institut Pasteur de Tunis.

Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non‐syndromic autosomal recessive deafness

S. Antonarakis, C. Rossier, M. Guipponi, 2001, Human mutation.

Prognostic factors in metastatic nasopharyngeal carcinoma.

J. Daoud, M. Frikha, A. Ghorbel, 2007, Cancer radiotherapie : journal de la Societe francaise de radiotherapie oncologique.

[Perrault's syndrome: two cases].

M. Abid, S. Kammoun, A. Ghorbel, 2001, Annales d'Endocrinologie.

Mutational analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in Tunisian patients with nonsyndromic hearing loss.

M. Ben Amor, A. Tlili, S. Masmoudi, 2006, Biochemical and biophysical research communications.

Determination of the frequency of connexin 26 mutations in inherited sensorineural deafness and carrier rates in the Tunisian population using DGGE

C. Petit, S. Blanchard, S. Masmoudi, 2000 .

Analysis of GJB2 mutation: evidence for a Mediterranean ancestor for the 35delG mutation

E. Chouery, A. Mégarbané, Ahmed Rebai, 2005, Clinical genetics.

[Metastatic nasopharyngeal carcinoma: clinical study and therapeutic results of 95 cases].

J. Daoud, M. Frikha, A. Ghorbel, 2006, Cancer radiotherapie : journal de la Societe francaise de radiotherapie oncologique.

Identification of a novel frameshift mutation in the DFNB31/WHRN gene in a Tunisian consanguineous family with hereditary non‐syndromic recessive hearing loss

D. Weil, A. Tlili, S. Masmoudi, 2005, Human mutation.

[North African and Southeast Asian nasopharyngeal carcinomas: between the resemblance and the dissemblance].

B. Hadhri-Guiga, N. Toumi, J. Daoud, 2010, Bulletin du cancer.

Localization of a Novel Autosomal Recessive Non‐syndromic Hearing Impairment Locus DFNB63 to Chromosome 11q13.3‐q13.4

A. Tlili, S. Masmoudi, H. Ayadi, 2007, Annals of human genetics.

Distinctive audiometric features between USH2A and USH2B subtypes of Usher syndrome

W. Kimberling, H. Ayadi, D. Orten, 2002, Journal of medical genetics.

Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1

M. Lathrop, C. Petit, D. Weil, 2003, European Journal of Human Genetics.

Refined mapping of the autosomal recessive non‐syndromic deafness locus DFNB13 using eight novel microsatellite markers

C. Petit, Ahmed Rebai, A. Tlili, 2004, Clinical genetics.

Determination of the frequency of connexin26 mutations in inherited sensorineural deafness and carrier rates in the Tunisian population using DGGE

C. Petit, S. Blanchard, S. Masmoudi, 2000, Journal of Medical Genetics.