Boudabous H - 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: boudabous h. Diagn Pathol. 2022 May 6;17(1):44. doi: 10.1186/s13000-022-01221-8. Diagn Pathol. 2022. PMID: 35524314 Free PMC article.

2

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: boudabous h. Diagn Pathol. 2018 May 29;13(1):35. doi: 10.1186/s13000-018-0710-3. Diagn Pathol. 2018. PMID: 29843745 Free PMC article.

3

The mutational spectrum of hunter syndrome reveals correlation between biochemical and clinical profiles in Tunisian patients.

Chkioua L, Grissa O, Leban N, Gribaa M, Boudabous H, Turkia HB, Ferchichi S, Tebib N, Laradi S. Chkioua L, et al. Among authors: boudabous h. BMC Med Genet. 2020 May 24;21(1):111. doi: 10.1186/s12881-020-01051-9. BMC Med Genet. 2020. PMID: 32448126 Free PMC article.

4

Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme.

Chkioua L, Amri Y, Chaima S, Fenni F, Boudabous H, Ben Turkia H, Messaoud T, Tebib N, Laradi S. Chkioua L, et al. Among authors: boudabous h. BMC Med Genomics. 2021 Aug 23;14(1):208. doi: 10.1186/s12920-021-01061-3. BMC Med Genomics. 2021. PMID: 34425818 Free PMC article.

5

Correction to: Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme.

Chkioua L, Amri Y, Chaima S, Fenni F, Boudabous H, Ben Turkia H, Messaoud T, Tebib N, Laradi S. Chkioua L, et al. Among authors: boudabous h. BMC Med Genomics. 2021 Dec 15;14(1):293. doi: 10.1186/s12920-021-01149-w. BMC Med Genomics. 2021. PMID: 34911538 Free PMC article. No abstract available.

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: boudabous h. J Pediatr Hematol Oncol. 2019 Apr;41(3):e193-e196. doi: 10.1097/MPH.0000000000001192. J Pediatr Hematol Oncol. 2019. PMID: 29702543

7

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: boudabous h. J Trop Pediatr. 2019 Jun 1;65(3):217-223. doi: 10.1093/tropej/fmy036. J Trop Pediatr. 2019. PMID: 29982732

8

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: boudabous h. Neuropediatrics. 2019 Feb;50(1):22-30. doi: 10.1055/s-0038-1669786. Epub 2018 Oct 11. Neuropediatrics. 2019. PMID: 30308687

9

A lower energetic, protein and uncooked cornstarch intake is associated with a more severe outcome in glycogen storage disease type III: an observational study of 50 patients.

Ben Chehida A, Ben Messaoud S, Ben Abdelaziz R, Mansouri H, Boudabous H, Hakim K, Ben Ali N, Ben Ameur Z, Sassi Y, Kaabachi N, Abdelhak S, Abdelmoula MS, Azzouz H, Tebib N. Ben Chehida A, et al. Among authors: boudabous h. J Pediatr Endocrinol Metab. 2018 Sep 25;31(9):979-986. doi: 10.1515/jpem-2018-0151. J Pediatr Endocrinol Metab. 2018. PMID: 30110253

10

Peripheral venous catheter complications in children: predisposing factors in a multicenter prospective cohort study.

Ben Abdelaziz R, Hafsi H, Hajji H, Boudabous H, Ben Chehida A, Mrabet A, Boussetta K, Barsaoui S, Sammoud A, Hamzaoui M, Azzouz H, Tebib N. Ben Abdelaziz R, et al. Among authors: boudabous h. BMC Pediatr. 2017 Dec 19;17(1):208. doi: 10.1186/s12887-017-0965-y. BMC Pediatr. 2017. PMID: 29258474 Free PMC article.

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