Messaoud T - Search Results

1

Seminal vesicle agenesis: An uncommon cause of azoospermia.

Bouzouita A, Kerkeni W, Abouda H, Khrouf M, Elloumi H, Mnif N, Messaoud T, Zhioua A, Zhioua F, Chebil M. Bouzouita A, et al. Among authors: messaoud t. Can Urol Assoc J. 2014 Mar;8(3-4):E266-9. doi: 10.5489/cuaj.1663. Can Urol Assoc J. 2014. PMID: 24839497 Free PMC article.

2

Identification of mutations that causes glucose-6-phosphate transporter defect in tunisian patients with glycogenosis type 1b.

Chkioua L, Amri Y, Sahli C, Rhouma FB, Chehida AB, Tebib N, Messaoud T, Abdennebi HB, Laradi S. Chkioua L, et al. Among authors: messaoud t. Diabetol Metab Syndr. 2023 Apr 28;15(1):86. doi: 10.1186/s13098-023-01065-2. Diabetol Metab Syndr. 2023. PMID: 37118808 Free PMC article.

3

Epidemiological and clinical characteristics of 66 Tunisian Sickle cell syndrome patients.

Sahli A, Ouali F, Dabboubi R, Fredj SH, Meddeb N, Mzoughi N, Messaoud T. Sahli A, et al. Among authors: messaoud t. Afr Health Sci. 2023 Sep;23(3):213-222. doi: 10.4314/ahs.v23i3.26. Afr Health Sci. 2023. PMID: 38357153 Free PMC article.

4

Cystic fibrosis transmembrane conductance regulator mutations and polymorphisms associated with congenital bilateral absence of vas deferens in a restricted group of patients from North Africa.

Boudaya M, Fredj SH, Haj RB, Khrouf M, Bouker A, Halouani L, Messaoud T. Boudaya M, et al. Among authors: messaoud t. Ann Hum Biol. 2012 Jan;39(1):76-9. doi: 10.3109/03014460.2011.642892. Epub 2011 Dec 8. Ann Hum Biol. 2012. PMID: 22148899 Free article.

5

Identification of a cystic fibrosis mutation W19X in Tunisia.

Boudaya M, Fredj SH, Siala H, Bibi A, Messaoud T. Boudaya M, et al. Among authors: messaoud t. Ann Biol Clin (Paris). 2013 Mar-Apr;71(2):223-6. doi: 10.1684/abc.2013.0790. Ann Biol Clin (Paris). 2013. PMID: 23587593 Free article.

6

Preliminary study of haplotypes linked to the rare cystic fibrosis E1104X mutation.

Oueslati S, Hadj Fredj S, Belhaj R, Siala H, Bibi A, Messaoud T. Oueslati S, et al. Among authors: messaoud t. Acta Physiol Hung. 2015 Mar;102(1):86-93. doi: 10.1556/APhysiol.101.2014.013. Acta Physiol Hung. 2015. PMID: 25481366 Free article.

7

Prenatal diagnosis of cystic fibrosis: 10-years experience.

Hadj Fredj S, Ouali F, Siala H, Bibi A, Othmani R, Dakhlaoui B, Zouari F, Messaoud T. Hadj Fredj S, et al. Among authors: messaoud t. Pathol Biol (Paris). 2015 Jun;63(3):126-9. doi: 10.1016/j.patbio.2015.04.002. Epub 2015 May 20. Pathol Biol (Paris). 2015. PMID: 26002249

8

Association of M470V polymorphism of CFTR gene with variability of clinical expression of asthma: Case-report study.

Wahabi I, Hadj Fredj S, Nefzi M, Dabboubi R, Siala H, Khalsi F, Bousetta K, Messaoud T. Wahabi I, et al. Among authors: messaoud t. Allergol Immunopathol (Madr). 2019 Mar-Apr;47(2):159-165. doi: 10.1016/j.aller.2018.06.007. Epub 2018 Sep 27. Allergol Immunopathol (Madr). 2019. PMID: 30268379

9

Distribution of CFTR mutations in cystic fibrosis patients of Tunisian origin: identification of two novel mutations.

Messaoud T, Verlingue C, Denamur E, Pascaud O, Quéré I, Fattoum S, Elion J, Férec C. Messaoud T, et al. Eur J Hum Genet. 1996;4(1):20-4. doi: 10.1159/000472165. Eur J Hum Genet. 1996. PMID: 8800923

10

[Molecular epidemiology of cystic fibrosis in Tunisia].

Messaoud T, Bel Haj Fredj S, Bibi A, Elion J, Férec C, Fattoum S. Messaoud T, et al. Ann Biol Clin (Paris). 2005 Nov-Dec;63(6):627-30. Ann Biol Clin (Paris). 2005. PMID: 16330381 Free article. French.

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