N. Driss

发表

[What are the alternative criteria for fine needle aspiration biopsy of a thyroid nodule?].

H. Essabbah, R. Sfar, I. Lahmar, 2008, Annales d'oto-laryngologie et de chirurgie cervico faciale : bulletin de la Societe d'oto-laryngologie des hopitaux de Paris.

A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation.

X. Liu, S. Blanton, A. Farooq, 2015, Human molecular genetics.

Mutation in gap and tight junctions in patients with non-syndromic hearing loss.

S. Masmoudi, H. Ayadi, I. Lahmar, 2009, Biochemical and biophysical research communications.

Spontaneous cholesteatoma of the external auditory canal: the utility of CT.

M. Saidi, N. Driss, M. Dakkem, 2013, Diagnostic and interventional imaging.

Genetic variants in RELN are associated with otosclerosis in a non‐European population from Tunisia

E. Fransen, S. Masmoudi, Richard J. H. Smith, 2010, Annals of human 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.

TMC1 but Not TMC2 Is Responsible for Autosomal Recessive Nonsyndromic Hearing Impairment in Tunisian Families

A. Tlili, S. Masmoudi, H. Ayadi, 2008, Audiology and Neurotology.

Association of COL1A1 and TGFB1 Polymorphisms with Otosclerosis in a Tunisian Population

Mohamed Ali Mosrati, S. Masmoudi, H. Ayadi, 2011, Annals of human genetics.

Imaging of congenital cysts and fistulas of the neck: what radiologists need to know

N. Driss, S. Jerbi, Omar Bradai, 2013 .

[Congenital cholesteatoma in children].

I. Lahmar, N. Driss, C. Hafsa, 2011, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Screening of the DFNB3 locus: identification of three novel mutations of MYO15A associated with hearing loss and further suggestion for two distinctive genes on this locus.

S. Masmoudi, H. Ayadi, I. Lahmar, 2009, Genetic testing and molecular biomarkers.

Calcific tendinitis of the longus colli: diagnosis by CT.

I. Lahmar, N. Driss, C. Hafsa, 2008, Joint, bone, spine : revue du rhumatisme.

Ultrasound-Guided Intermediate Cervical Plexus Block effects on per and Post-Operative Opioids Consumption during Total Thyroidectomy under General Anesthesia Article Information

N. Driss, A. Majdoub, Mouna Ouaz, 2019 .

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.

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

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

[A rare cause of multiple lacunae of the cranial vault and temporal bone in adults: histiocytosis X].

M. Ladeb, N. Driss, N. Hattab, 1994, Journal de radiologie.

Calcific tendinitis of the longus colli: diagnosis by CT.

I. Lahmar, N. Driss, C. Hafsa, 2008 .

Predictive epidemiological and clinical factors of nasopharyngeal carcinoma diagnosis: Adult versus pediatric population.

N. Driss, M. Masmoudi, A. Ben Mabrouk, 2020, International journal of pediatric otorhinolaryngology.

Orbital complication of acute ethmoiditis: A Tunisian paediatric cross sectional study.

N. Driss, S. Jerbi, B. Mahjoub, 2019, American journal of otolaryngology.

Solitary Fibrous Tumor of the External Auditory Canal

N. Driss, N. Ben Abdeljalil, M. Masmoudi, 2021, Ear, nose, & throat journal.