Search - Institut Pasteur de Tunis Access content directly

Filter your results

77 Results
Domains : sdv.gen
Image document

Modelling of seasonal influenza and estimation of the burden in Tunisia.

L Chlif , A Aissi , L Bettaieb , L Kharroubi , L Nouira , et al.
Eastern Mediterranean Health Journal, 2016, 22 (7), pp.460-467
Journal articles pasteur-01451663v1

Genetic heterogeneity of megaloblastic anaemia type 1 in Tunisian patients

Chiraz Bouchlaka , Chokri Maktouf , Bahri Mahjoub , Abdelkarim Ayadi , M. Tahar Sfar , et al.
Journal of Human Genetics, 2007, 52 (3), pp.262 - 270. ⟨10.1007/s10038-007-0110-0⟩
Journal articles pasteur-01375225v1
Image document

MTHFR gene polymorphisms and bladder cancer susceptibility: a meta-analysis including race, smoking status and tumour stage.

Soumaya Kouidhi , Kamel Rouissi , Sami Khedhiri , Slah Ouerhani , Mohamed Cherif , et al.
Asian Pacific Journal of Cancer Prevention, 2011, 12 (9), pp.2227-32
Journal articles pasteur-01375277v1
Image document

Using KASP technique to screen LRRK2 G2019S mutation in a large Tunisian cohort

Zied Landoulsi , Sawssan Benromdhan , Mouna Ben Djebara , Mariem Damak , Hamza Dallali , et al.
BMC Medical Genetics, 2017, 18 (1), pp.70. ⟨10.1186/s12881-017-0432-5⟩
Journal articles pasteur-01639043v1

Bathing suit ichthyosis caused by a TGM1 mutation in a Tunisian child

Rym Benmously-Mlika , Anissa Zaouak , Ridha Mrad , Nadia Laaroussi , Sonia Abdelhak , et al.
International Journal of Dermatology, 2014, 53 (12), pp.1478 - 1480. ⟨10.1111/ijd.12569⟩
Journal articles istex pasteur-01375053v1
Image document

La place des gènes non globine dans la modulation du syndrome drépanocytaire

Leila Chaouch
Hématologie. Université de Tunis El Manar (Tunisie), 2012. Français. ⟨NNT : ⟩
Theses tel-03540224v1

Specific aspects of consanguinity: some examples from the tunisian population.

Lilia Romdhane , Nizar Ben Halim , Insaf Rejeb , Rym Kefi , Yosra Bouyacoub , et al.
Human Heredity, 2014, 77 (1-4), pp.167-74. ⟨10.1159/000362167⟩
Journal articles pasteur-01061190v1
Image document

Adult gaucher disease in southern Tunisia: report of three cases.

Faten Ben Rhouma , Faten Kallel , Rym Kefi , Wafa Cherif , Majdi Nagara , et al.
Diagnostic Pathology, 2012, 7, pp.4. ⟨10.1186/1746-1596-7-4⟩
Journal articles pasteur-00682183v1

Clinical and genetic investigation of pediatric cases of Wolff-Parkinson-White syndrome in Tunisian families.

Sonia Nouira , Fatma Ouarda , Cherine Charfeddine , Imen Arfa , Houyem Ouragini , et al.
Heart & Lung, 2010, 39 (5), pp.432-6. ⟨10.1016/j.hrtlng.2009.10.012⟩
Journal articles istex pasteur-00612166v1

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

Nizar Ben Halim , Majdi Nagara , Béatrice Regnault , Sana Hsouna , Khaled Lasram , et al.
Annals of Human Genetics, 2015, 79 (6), pp.402 - 417. ⟨10.1111/ahg.12131⟩
Journal articles pasteur-01375019v1

A Tunisian patient with two rare syndromes: triple a syndrome and congenital hypogonadotropic hypogonadism.

Lamia Ben Abdallah , Youssef Lakhoua , Majdi Nagara , Karima Khiari , Sahar Elouej , et al.
Hormone Research in Paediatrics, 2014, 82 (5), pp.338-43. ⟨10.1159/000365888⟩
Journal articles pasteur-01375104v1

Rapid and inexpensive detection of common HBB gene mutations in Tunisian population by high-resolution melting analysis: Implication for molecular diagnosis

Houyem Ouragini , Fayrouz. Haddad , Imen Darragi , Salem Abbes
Hematology, 2014, 19 (2), pp.80 - 84. ⟨10.1179/1607845413Y.0000000096⟩
Journal articles pasteur-01375110v1
Image document

Lactase persistence in Tunisia as a result of admixture with other Mediterranean populations

Yosra Ben Halima , Rym Kefi , Marco Sazzini , Cristina Giuliani , Sara de Fanti , et al.
Genes and Nutrition, 2017, 12, pp.20. ⟨10.1186/s12263-017-0573-3⟩
Journal articles pasteur-01636913v1
Image document

A founder large deletion mutation in Xeroderma pigmentosum-Variant form in Tunisia: implication for molecular diagnosis and therapy.

Mariem Ben Rekaya , Nadia Laroussi , Olfa Messaoud , Mariem Jones , Manel Jerbi , et al.
BioMed Research International , 2014, 2014, pp.256245. ⟨10.1155/2014/256245⟩
Journal articles pasteur-01060291v1
Image document

Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the young

Hager Jaouadi , Yosra Bouyacoub , Sonia Chabrak , Lilia Kraoua , Amira Zaroui , et al.
Herz, 2020, 46 (S1), pp.94-102. ⟨10.1007/s00059-019-04883-1⟩
Journal articles hal-02965635v1

Molecular autopsy and clinical family screening in a case of sudden cardiac death reveals ACTN2 mutation related to hypertrophic/dilated cardiomyopathy and a novel LZTR1 variant associated with Noonan syndrome

Lilia Kraoua , Hager Jaouadi , Mohamed Allouche , Ahlem Achour , Hakim Kaouther , et al.
MOLECULAR GENETICS & GENOMIC MEDICINE, 2022, 10 (7), ⟨10.1002/mgg3.1954⟩
Journal articles hal-03780229v1

IL-17 T cells' defective differentiation in vitro despite normal range ex vivo in chronic mucocutaneous candidiasis due to STAT1 mutation.

Najla Mekki , Imen Ben-Mustapha , Luyan Liu , Lobna Boussofara , Satoshi Okada , et al.
Journal of Investigative Dermatology, 2014, 134 (4), pp.1155-7. ⟨10.1038/jid.2013.480⟩
Journal articles pasteur-01061212v1

Mutational founder effect in recessive dystrophic epidermolysis bullosa families from Southern Tunisia.

Ahlem Sabrine Ben Brick , Nadia Laroussi , Hela Mesrati , Rym Kefi , Mbarka Bchetnia , et al.
Archives of Dermatological Research, 2014, 306 (4), pp.405-11. ⟨10.1007/s00403-013-1421-y⟩
Journal articles pasteur-01061249v1
Image document

Diagnosis of Theileria annulata infection of cattle in Tunisia: comparison of serology and blood smears

Mea Darghouth , A Bouattour , L Ben Miled , L Sassi
Veterinary Research, 1996, 27 (6), pp.613-621
Journal articles hal-00902453v1
Image document

A new AURKC mutation causing macrozoospermia: implications for human spermatogenesis and clinical diagnosis.

Mariem Ben Khelifa , Raoudha Zouari , Radu Harbuz , Lazhar Halouani , Christophe Arnoult , et al.
Molecular Human Reproduction, 2011, 17 (12), pp.762-8. ⟨10.1093/molehr/gar050⟩
Journal articles inserm-00639414v1

Assessment of the phenotype genotype variability and correlation in m.3243A > G mutation carriers requires prospective studies

Josef Finsterer , Sinda Zarrouk-Mahjoub
Molecular Genetics and Metabolism Reports, 2016, 8, pp.33. ⟨10.1016/j.ymgmr.2016.07.001⟩
Journal articles pasteur-01452827v1

Noncompaction in Duchenne Muscular Dystrophy

Josef Finsterer , Sinda Zarrouk-Mahjoub
Internal Medicine, 2016, 55 (9), pp.1241 - 1241. ⟨10.2169/internalmedicine.55.6547⟩
Journal articles pasteur-01357698v1
Image document

Nephrocalcinosis and retinal dystrophy, rare manifestations of MPV17-related mitochondrial depletion syndrome?

Josef Finsterer , Sinda Zarrouk-Mahjoub
Molecular Genetics and Metabolism Reports, 2016, 9 (18), ⟨10.1016/j.ymgmr.2016.09.002⟩
Journal articles pasteur-01457092v1

Omenn Syndrome: Two Case Reports

Nadia Siala , Ons Azzabi , Hakima Kebaier , Ridha Mrad , Olfa Rebah , et al.
Acta Dermatovenerologica Croatica, 2013, 21 (4), pp.259-262
Journal articles pasteur-01375120v1

[Genetic variability of type 3 echoviruses].

Wasfi Fares , Dorra Rezig , Ahlem Ben Yahia , Henda Touzi , Zina Meddeb , et al.
Annales de Biologie Clinique, 2012, 70 (2), pp.189-198. ⟨10.1684/abc.2012.0688⟩
Journal articles pasteur-01375130v1

NLRP7 and the genetics of post-molar choriocarcinomas in Senegal

R. Slim , P. Coullin , A. Diatta , W. Chebaro , D. Courtin , et al.
Molecular Human Reproduction, 2012, 18 (1), pp.52 - 56. ⟨10.1093/molehr/gar060⟩
Journal articles pasteur-01375139v1

[Clinical characterization of the Stargardt disease and molecular exploration of the c.2041C>T mutation (ABCA4 gene) in Tunisian patients].

Ibtissem Chouchene , Leila Largueche , Farah Ouechtati , Kawthar Derouiche , Ahmed Turki , et al.
Annales de Biologie Clinique, 2013, 71 (6), pp.645-51. ⟨10.1684/abc.2013.0912⟩
Journal articles pasteur-01061094v1

Prevalence of Y chromosome microdeletions in infertile Tunisian men.

Wajih Hammami , Olfa Kilani , Mariem Ben Khelifa , Wiem Ayed , Sonia Abdelhak , et al.
Annales de Biologie Clinique, 2014, 72 (3), pp.331-6. ⟨10.1684/abc.2014.0962⟩
Journal articles pasteur-01061201v1

Emergence of a BCR-ABL translocation in a patient with the JAK2V617F mutation: evidence for secondary acquisition of BCR-ABL in the JAK2V617F clone.

Osamu Yamada , Emna Mahfoudhi , Isabelle Plo , Kohji Ozaki , Mayuka Nakatake , et al.
Journal of Clinical Oncology, 2014, 32 (21), pp.e76-9. ⟨10.1200/JCO.2012.47.8669⟩
Journal articles pasteur-01060955v1
Image document

Mutations in DNAH1, which encodes an inner arm heavy chain dynein, lead to male infertility from multiple morphological abnormalities of the sperm flagella.

Mariem Ben Khelifa , Charles Coutton , Raoudha Zouari , Thomas Karaouzène , John Rendu , et al.
American Journal of Human Genetics, 2014, 94 (1), pp.95-104. ⟨10.1016/j.ajhg.2013.11.017⟩
Journal articles pasteur-01061012v1