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Non‐recurrent laryngeal nerve and arteria lusoria: Rare and little known association

Clinical case reports, 2021-08, Vol.9 (8), p.e04723-n/a

2021

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Head and neck tuberculosis associated to sarcoidosis: A case report

Journal of clinical tuberculosis and other mycobacterial diseases, 2023-05, Vol.31, p.100364, Article 100364

2023

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Paradoxical reaction associated with cervical lymph node tuberculosis: Predictive factors and therapeutic management

International journal of infectious diseases, 2017-01, Vol.54 (C), p.4-7

2017

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Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients

PloS one, 2015-03, Vol.10 (3), p.e0120584-e0120584

2015

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Diagnostic performance of the EU TI‐RADS and ACR TI‐RADS scoring systems in predicting thyroid malignancy

Endocrinology, diabetes & metabolism, 2023-07, Vol.6 (4), p.e434-n/a

2023

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Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness

PloS one, 2014-06, Vol.9 (6), p.e99797-e99797

2014

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Ectopic thyroid tissue: unusual differential diagnosis of cervical paraganglioma

The Pan African medical journal, 2017, Vol.27 (43), p.43-43

2017

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Skeletal facial deformity in patients with β thalassemia major: Report of one Tunisian case and a review of the literature

International journal of pediatric otorhinolaryngology, 2015-11, Vol.79 (11), p.1955-1958

2015

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Nasopharyngeal Actinomycosis

Case reports in otolaryngology, 2011-01, Vol.2011, p.367364-4

2011

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Une tumeur thyroïdienne déroutante

Annales de pathologie, 2020-07, Vol.40 (4), p.309-312

2020

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A confusing tumor of the thyroid

Annales de pathologie, 2020-07, Vol.40 (4), p.309-312

2020

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Sudden Death Due to Neck Paraganglioma: A Pediatric Case Report and Review of the Literature

The American journal of forensic medicine and pathology, 2020-09, Vol.41 (3), p.199

2020

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Clinical and genetic analysis of two Tunisian otosclerosis families

American journal of medical genetics. Part A, 2007-07, Vol.143A (14), p.1653-1660

2007

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Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss

Gene, 2013-08, Vol.525 (1), p.1-4

2013

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A Tunisian family with a novel mutation in the gene CYP 4F22 for lamellar ichthyosis and co‐occurrence of hearing loss in a child due to mutation in the SLC 26A4 gene

International journal of dermatology, 2019-12, Vol.58 (12), p.1439-1443

2019

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Novel PAX3 mutations causing Waardenburg syndrome type 1 in Tunisian patients

International journal of pediatric otorhinolaryngology, 2017-12, Vol.103, p.14-19

2017

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Papillary thyroid tumors: Diagnostic value of CD56 and Cytokeratin 19

Tunisie Medicale, 2018-02, Vol.96 (2), p.113-121

2018

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Estimation of Recent and Ancient Inbreeding in a Small Endogamous Tunisian Community Through Genomic Runs of Homozygosity

Annals of human genetics, 2015-11, Vol.79 (6), p.402-417

2015

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GJB2 and GJB6 screening in Tunisian patients with autosomal recessive deafness

International journal of pediatric otorhinolaryngology, 2013-05, Vol.77 (5), p.714-716

2013

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Malignant transformation of nasal inverted papilloma into sarcomatoid carcinoma

Tunisie Medicale, 2017-06, Vol.95 (6), p.453-454

2017

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Agressive infection following a dental extraction in a diabetic patient :Rhinocerebral mucormycosis

Tunisie Medicale, 2017-05, Vol.95 (5), p.378-380

2017

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A confusing lesion of thyroid papillary carcinoma

Tunisie Medicale, 2017-03, Vol.95 (3), p.225-226

2017

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A confusing swelling of the buccal mucosa

Annales de pathologie, 2016-04, Vol.36 (2), p.139-142

2016

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Non‐recurrent laryngeal nerve and arteria lusoria: Rare and little known association

Head and neck tuberculosis associated to sarcoidosis: A case report

Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment

Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health

Paradoxical reaction associated with cervical lymph node tuberculosis: Predictive factors and therapeutic management

Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients

Diagnostic performance of the EU TI‐RADS and ACR TI‐RADS scoring systems in predicting thyroid malignancy

Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness

Ectopic thyroid tissue: unusual differential diagnosis of cervical paraganglioma

Skeletal facial deformity in patients with β thalassemia major: Report of one Tunisian case and a review of the literature

Nasopharyngeal Actinomycosis

Une tumeur thyroïdienne déroutante

A confusing tumor of the thyroid

Sudden Death Due to Neck Paraganglioma: A Pediatric Case Report and Review of the Literature

Clinical and genetic analysis of two Tunisian otosclerosis families

Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss

A Tunisian family with a novel mutation in the gene CYP 4F22 for lamellar ichthyosis and co‐occurrence of hearing loss in a child due to mutation in the SLC 26A4 gene

Novel PAX3 mutations causing Waardenburg syndrome type 1 in Tunisian patients

Papillary thyroid tumors: Diagnostic value of CD56 and Cytokeratin 19

Estimation of Recent and Ancient Inbreeding in a Small Endogamous Tunisian Community Through Genomic Runs of Homozygosity

GJB2 and GJB6 screening in Tunisian patients with autosomal recessive deafness

Malignant transformation of nasal inverted papilloma into sarcomatoid carcinoma

Agressive infection following a dental extraction in a diabetic patient :Rhinocerebral mucormycosis

A confusing lesion of thyroid papillary carcinoma

A confusing swelling of the buccal mucosa

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