Tebib N - Search Results

1

Molecular characterization of CTNS mutations in Tunisian patients with ocular cystinosis.

Chkioua L, Amri Y, Saheli C, Mili W, Mabrouk S, Chabchoub I, Boudabous H, Azzouz WB, Turkia HB, Ferchichi S, Tebib N, Massoud T, Ghorbel M, Laradi S. Chkioua L, et al. Among authors: tebib n. Diagn Pathol. 2022 May 6;17(1):44. doi: 10.1186/s13000-022-01221-8. Diagn Pathol. 2022. PMID: 35524314 Free PMC article.

2

Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III.

Mili A, Ben Charfeddine I, Mamaï O, Abdelhak S, Adala L, Amara A, Pagliarani S, Lucchiarri S, Ayadi A, Tebib N, Harbi A, Bouguila J, H'Mida D, Saad A, Limem K, Comi GP, Gribaa M. Mili A, et al. Among authors: tebib n. J Hum Genet. 2012 Mar;57(3):170-5. doi: 10.1038/jhg.2011.122. Epub 2011 Nov 17. J Hum Genet. 2012. PMID: 22089644

3

Molecular confirmation of founder mutation c.-167A>G in Tunisian patients with PMLD disease.

Kammoun Jellouli N, Salem IH, Ellouz E, Louhichi N, tlili A, Kammoun F, Triki C, Fakhfakh F; Tunisian Network on Mental Retardation Study. Kammoun Jellouli N, et al. Gene. 2013 Jan 25;513(2):233-8. doi: 10.1016/j.gene.2012.10.070. Epub 2012 Nov 7. Gene. 2013. PMID: 23142375

4

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

Mellouli F, Mustapha IB, Khaled MB, Besbes H, Ouederni M, Mekki N, Ali MB, Larguèche B, Hachicha M, Sfar T, Gueddiche N, Barsaoui S, Sammoud A, Boussetta K, Becher SB, Meherzi A, Guandoura N, Boughammoura L, Harbi A, Amri F, Bayoudh F, Jaballah NB, Tebib N, Bouaziz A, Mahfoudh A, Aloulou H, Mansour LB, Chabchoub I, Boussoffara R, Chemli J, Bouguila J, Hassayoun S, Hammami S, Habboul Z, Hamzaoui A, Ammar J, Barbouche MR, Bejaoui M. Mellouli F, et al. Among authors: tebib n. J Clin Immunol. 2015 Nov;35(8):745-53. doi: 10.1007/s10875-015-0206-9. Epub 2015 Oct 13. J Clin Immunol. 2015. PMID: 26464197 Review.

5

Clinical and Genetic Characterization of 26 Tunisian Patients with Allgrove Syndrome.

Kallabi F, Belghuith N, Aloulou H, Kammoun T, Ghorbel S, Hajji M, Gallas S, Chemli J, Chabchoub I, Azzouz H, Ben Chehida A, Sfaihi L, Makni S, Amouri A, Keskes L, Tebib N, Ben Becher S, Hachicha M, Kamoun H. Kallabi F, et al. Among authors: tebib n. Arch Med Res. 2016 Feb;47(2):105-10. doi: 10.1016/j.arcmed.2016.04.004. Epub 2016 Apr 28. Arch Med Res. 2016. PMID: 27133709

6

A Novel Mutation c.153 C>A in a Tunisian Girl With Wolman Disease and Unusual Presentation: Hemophagocytic Lymphohistiocytosis.

Tinsa F, Ben Romdhane M, Boudabous H, Bel Hadj I, Brini I, Tebib N, Louati H, Bekri S, Boussetta K. Tinsa F, et al. Among authors: tebib n. J Pediatr Hematol Oncol. 2019 Apr;41(3):e193-e196. doi: 10.1097/MPH.0000000000001192. J Pediatr Hematol Oncol. 2019. PMID: 29702543

7

Novel splice site IDUA gene mutation in Tunisian pedigrees with hurler syndrome.

Chkioua L, Boudabous H, Jaballi I, Grissa O, Turkia HB, Tebib N, Laradi S. Chkioua L, et al. Among authors: tebib n. Diagn Pathol. 2018 May 29;13(1):35. doi: 10.1186/s13000-018-0710-3. Diagn Pathol. 2018. PMID: 29843745 Free PMC article.

8

High Frequency of Cardiovascular Complications in Tunisian Kawasaki Disease Patients: Need for a Further Awareness.

Ben Chehida A, Ben Messaoud S, Ben Abdelaziz R, Boudabous H, Oujra M, Ben Turkia H, Abdelmoula MS, Azzouz H, Hakim K, Tebib N. Ben Chehida A, et al. Among authors: tebib n. J Trop Pediatr. 2019 Jun 1;65(3):217-223. doi: 10.1093/tropej/fmy036. J Trop Pediatr. 2019. PMID: 29982732

9

Neuromuscular Involvement in Glycogen Storage Disease Type III in Fifty Tunisian Patients: Phenotype and Natural History in Young Patients.

Ben Chehida A, Ben Messaoud S, Ben Abdelaziz R, Ben Ali N, Boudabous H, Ben Abdelaziz I, Ben Ameur Z, Sassi Y, Kaabachi N, Abdelhak S, Abdelmoula MS, Fradj M, Azzouz H, Tebib N. Ben Chehida A, et al. Among authors: tebib n. Neuropediatrics. 2019 Feb;50(1):22-30. doi: 10.1055/s-0038-1669786. Epub 2018 Oct 11. Neuropediatrics. 2019. PMID: 30308687

10

Hemophagocytic Lymphohistiocytosis: A Rare Complication of an Ultrarare Lysosomal Storage Disease.

Chabchoub I, Boudabbous H, Maaloul I, Ben Abdelaziz R, Ben Chehida A, Ayadi L, Kamoun T, Tebib N, Boudaouara T, Bekri S, Hachicha M. Chabchoub I, et al. Among authors: tebib n. J Pediatr Hematol Oncol. 2020 May;42(4):310-312. doi: 10.1097/MPH.0000000000001552. J Pediatr Hematol Oncol. 2020. PMID: 31318819

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