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Clinical and genetic characteristics of Tunisian children with infantile nephropathic cystinosis

Pediatric nephrology (Berlin, West), 2023, Vol.38 (1), p.119-129

2023

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Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease

Journal of the American Society of Nephrology, 2016-03, Vol.27 (3), p.722-729

2016

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Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström Syndromes

Journal of medical genetics, 2012-08, Vol.49 (8), p.502-512

2012

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Partial Trisomy 4p Syndrome Diagnosed Prenatally

Fetal and pediatric pathology, 2024-03, Vol.43 (2), p.188-195

2024

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Perinatal-lethal Gaucher disease presenting as hydrops fetalis

The Pan African medical journal, 2015-06, Vol.21 (110), p.110-110

2015

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3M syndrome: A Tunisian seven-cases series

European journal of medical genetics, 2022-03, Vol.65 (3), p.104448-104448, Article 104448

2022

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Le syndrome de Kabuki : étude clinique d’une série de 23 patients tunisiens

Morphologie, 2021-09, Vol.105 (350), p.S33-S33

2021

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WDR73-related galloway mowat syndrome with collapsing glomerulopathy

European journal of medical genetics, 2019-09, Vol.62 (9), p.103550-103550, Article 103550

2019

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Genome Tunisia Project: paving the way for precision medicine in North Africa

Genome medicine, 2024-08, Vol.16 (1), p.104-19

2024

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Le syndrome Wolf–Hirschhorn : à propos de 9 cas

Morphologie, 2021-09, Vol.105 (350), p.S28-S28

2021

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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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Complete Trisomy 9 with unusual phenotypic associations

Tunisie Medicale, 2016-12, Vol.94 (12), p.895

2016

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Prevalence of Bardet–Biedl syndrome in Tunisia

Journal of community genetics, 2011-06, Vol.2 (2), p.97-99

2011

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Epidemiologic and clinical characteristics of 458 Tunisian patients with intellectual deficiency and a reconsidered diagnostic strategy

European journal of medical genetics, 2013-01, Vol.56 (1), p.13-19

2013

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Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström Syndromes

Journal of medical genetics, 2012, Vol.49 (8), p.502-512

2012

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Hexasomy of the Prader–Willi/Angelman critical region, including the OCA2 gene, in a patient with pigmentary dysplasia: Case report

European journal of medical genetics, 2011-07, Vol.54 (4), p.e446-e450

2011

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Clinical and Molecular Cytogenetic Study of 38 Williams-Beuren Syndrome Tunisian Patients

Open journal of genetics, 2014, Vol.4 (5), p.385-391

2014

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A 24-Mb deletion in 14q in a girl with corpus callosum hypoplasia

European journal of medical genetics, 2009-07, Vol.52 (4), p.256-259

2009

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Complete Trisomy 9 with unusual phenotypic associations

La Tunisie medicale, 2016, Vol.94 (12), p.895-895

2016

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Dental waste management among dentists in Tunisia

International dental journal, 2024-10, Vol.74, p.S215-S215

2024

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Evaluation de l’intéret des technologies de l’information et de la communication éducatives dans l’apprentissage par les étudiants en Médecine Dentaire

Journal de la faculté de médecine d'Oran (En ligne), 2023-12, Vol.7 (2), p.915-922

2023

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Two New Secreted Proteases Generate a Casein-Derived Antimicrobial Peptide in Bacillus cereus Food Born Isolate Leading to Bacterial Competition in Milk

Frontiers in microbiology, 2018-06, Vol.9, p.1148-1148

2018

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Unicystic ameloblastoma: Diagnostic challenges and uncommon treatment strategy: Case report

International journal of surgery case reports, 2024-11, Vol.124, p.110437, Article 110437

2024

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441 Endometrial stromal sarcomas: a retrospective analysis of 20 patients

International journal of gynecological cancer, 2024-03, Vol.34 (Suppl 1), p.A179-A179

2024

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The Miller-McKusick-Malvaux syndrome: a rare cause of short stature

Endocrine Abstracts, 2019-05

2019

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Clinical and genetic characteristics of Tunisian children with infantile nephropathic cystinosis

Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease

Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström Syndromes

Partial Trisomy 4p Syndrome Diagnosed Prenatally

Perinatal-lethal Gaucher disease presenting as hydrops fetalis

3M syndrome: A Tunisian seven-cases series

Le syndrome de Kabuki : étude clinique d’une série de 23 patients tunisiens

WDR73-related galloway mowat syndrome with collapsing glomerulopathy

Genome Tunisia Project: paving the way for precision medicine in North Africa

Le syndrome Wolf–Hirschhorn : à propos de 9 cas

Novel PAX3 mutations causing Waardenburg syndrome type 1 in Tunisian patients

Complete Trisomy 9 with unusual phenotypic associations

Prevalence of Bardet–Biedl syndrome in Tunisia

Epidemiologic and clinical characteristics of 458 Tunisian patients with intellectual deficiency and a reconsidered diagnostic strategy

Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström Syndromes

Hexasomy of the Prader–Willi/Angelman critical region, including the OCA2 gene, in a patient with pigmentary dysplasia: Case report

Clinical and Molecular Cytogenetic Study of 38 Williams-Beuren Syndrome Tunisian Patients

A 24-Mb deletion in 14q in a girl with corpus callosum hypoplasia

Complete Trisomy 9 with unusual phenotypic associations

Dental waste management among dentists in Tunisia

Evaluation de l’intéret des technologies de l’information et de la communication éducatives dans l’apprentissage par les étudiants en Médecine Dentaire

Two New Secreted Proteases Generate a Casein-Derived Antimicrobial Peptide in Bacillus cereus Food Born Isolate Leading to Bacterial Competition in Milk

Unicystic ameloblastoma: Diagnostic challenges and uncommon treatment strategy: Case report

441 Endometrial stromal sarcomas: a retrospective analysis of 20 patients

The Miller-McKusick-Malvaux syndrome: a rare cause of short stature

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