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Structure: Internal structure identifier : 477195
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Clinical and Genetic Heterogeneity in Six Tunisian Families With Horizontal Gaze Palsy With Progressive Scoliosis: A Retrospective Study of 13 Cases

Sami Bouchoucha , Asma Chikhaoui , Dorra Najjar , Hamza Dallali , Maleke Khammessi , et al.
Frontiers in Pediatrics, 2020, 8, pp.172. ⟨10.3389/fped.2020.00172⟩
Journal articles pasteur-03561607v1
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Heterogeneous clinical features in Cockayne syndrome-A patients with the same mutation and in siblings

Asma Chikhaoui , Ichraf Kraoua , Nadège Calmels , Sami Bouchoucha , Cathy Obringer , et al.
2022
Preprints, Working Papers, ... pasteur-03548783v1

Screening of three Mediterranean phenylketonuria mutations in Tunisian families

Sameh Khemir , Hajer Siala , Sameh Hadj Taieb , Wafa Cherif , Hatem Azzouz , et al.
Journal of Genetics, 2012, 91 (1), pp.91-94
Journal articles hal-01358543v1

Association of genetic variation in IKZF1, ARID5B, CDKN2A, and CEBPE with the risk of acute lymphoblastic leukemia in Tunisian children and their contribution to racial differences in leukemia incidence

Hanene Gharbi , Islem Ben Hassine , Ismail Soltani , Ines Safra , Slah Ouerhani , et al.
Pediatric Hematology-Oncology, 2016, 33 (3), pp.157-167. ⟨10.3109/08880018.2016.1161685⟩
Journal articles pasteur-01374984v1

A Founder Effect of c.257+2T > C Mutation in NCF2 Gene Underlies Severe Chronic Granulomatous Disease in Eleven Patients

Khaoula Ben-Farhat , Imen Ben-Mustapha , Meriem Ben-Ali , Karen Rouault , Saber Hamami , et al.
Journal of Clinical Immunology, 2016, 36 (6), pp.547-554. ⟨10.1007/s10875-016-0299-9⟩
Journal articles pasteur-01374995v1

Rare splicing defects of FAS underly severe recessive autoimmune lymphoproliferative syndrome.

N. Agrebi , I. Ben-Mustapha , N. Matoussi , N. Dhouib , M Ben-Ali , et al.
Clinical Immunology, 2017, 183, pp.17-23. ⟨10.1016/j.clim.2017.06.009⟩
Journal articles pasteur-01553307v1
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Phylogeography and phylogeny of Rhinoviruses collected from Severe Acute Respiratory Infection (SARI) cases over successive epidemic periods in Tunisia

Sondes Haddad-Boubaker , Cherif Ben Hamda , Kais Ghedira , Khaoula Mefteh , Aida Bouafsoun , et al.
PLoS ONE, 2021, 16 (11), pp.e0259859. ⟨10.1371/journal.pone.0259859⟩
Journal articles pasteur-03546852v1
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Identification and Characterization of a Novel Recurrent ERCC6 Variant in Patients with a Severe Form of Cockayne Syndrome B

Khouloud Zayoud , Ichraf Kraoua , Asma Chikhaoui , Nadège Calmels , Sami Bouchoucha , et al.
Genes, 2021, 12 (12), pp.1922. ⟨10.3390/genes12121922⟩
Journal articles hal-03477990v1
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Evaluation of the influenza-like illness surveillance system in Tunisia, 2012–2015

Rihab Yazidi , Wafa Aissi , Hind Bouguerra , Mariem Nouira , Ghassen Kharroubi , et al.
BMC Public Health, 2019, 19 (1), pp.694. ⟨10.1186/s12889-019-7035-3⟩
Journal articles pasteur-03561232v1

Report of the Tunisian Registry of Primary Immunodeficiencies: 25-Years of Experience (1988-2012)

Fethi Mellouli , Imen Ben Mustapha , Monia Ben Khaled , Habib Besbes , Monia Ouederni , et al.
Journal of Clinical Immunology, 2015, 35 (8), pp.745-753. ⟨10.1007/s10875-015-0206-9⟩
Journal articles pasteur-01375025v1

A novel large deletion in CCM1 gene in a Tunisian family

F. Tinsa , I. Bel Hadj , F. Riant , M. Ben Romdhane , I. Brini , et al.
Revue Neurologique, 2019, 175 (3), pp.194-197. ⟨10.1016/j.neurol.2018.04.013⟩
Journal articles pasteur-01947926v1

Thiamine responsive megaloblastic anemia mimicking mitochondrial disorders

F. Tinsa , M. Hechmi , I.B. Hadj , F. Khalsi , M. Chargui , et al.
Revue Neurologique, 2019, 175 (5), pp.324-327. ⟨10.1016/j.neurol.2018.07.008⟩
Journal articles pasteur-01999932v1
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Implementation of a prospective study for enhancing surveillance of invasive bacterial infections in North Africa

Hanen Smaoui , Hassiba Tali-Maamar , Saïd Zouhair , Selma Bouheraoua , Khaoula Mefteh , et al.
International Journal of Infectious Diseases, 2022, 115, pp.101-105. ⟨10.1016/j.ijid.2021.11.036⟩
Journal articles hal-04133426v1