|
|
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.
Journal articles
pasteur-03561607v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
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
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
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
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
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.
Journal articles
pasteur-01374984v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
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 articles
pasteur-01374995v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
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.
Journal articles
pasteur-01553307v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
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.
Journal articles
pasteur-03546852v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
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.
Journal articles
hal-03477990v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Evaluation of the influenza-like illness surveillance system in Tunisia, 2012–2015
Rihab Yazidi
,
Wafa Aissi
,
Hind Bouguerra
,
Mariem Nouira
,
Ghassen Kharroubi
,
et al.
Journal articles
pasteur-03561232v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
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 articles
pasteur-01375025v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
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.
Journal articles
pasteur-01947926v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Thiamine responsive megaloblastic anemia mimicking mitochondrial disorders
F. Tinsa
,
M. Hechmi
,
I.B. Hadj
,
F. Khalsi
,
M. Chargui
,
et al.
Journal articles
pasteur-01999932v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
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.
Journal articles
hal-04133426v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|