Bouzidi A - Search Results

1

Clinical and genetic spectrums of 413 North African families with inherited retinal dystrophies and optic neuropathies.

Bouzidi A, Charoute H, Charif M, Amalou G, Kandil M, Barakat A, Lenaers G. Bouzidi A, et al. Orphanet J Rare Dis. 2022 May 12;17(1):197. doi: 10.1186/s13023-022-02340-7. Orphanet J Rare Dis. 2022. PMID: 35551639 Free PMC article. Review.

2

Clinical and genetic investigations of three Moroccan families with retinitis pigmentosa phenotypes.

Bouzidi A, Charif M, Bouzidi A, Amalou G, Kandil M, Barakat A, Lenaers G. Bouzidi A, et al. Mol Vis. 2021 Jan 15;27:17-25. eCollection 2021. Mol Vis. 2021. PMID: 33633436 Free PMC article.

3

First characterization of LHON pedigrees in North Africa.

Bouzidi A, Aboussair N, Charif M, Amalou G, Goudenège D, Desquiret-Dumas V, Bris C, Sifeddine N, Nahili H, Elqabli M, Dafir K, Kandil M, Amati-Bonneau P, Procaccio V, Barakat A, Lenaers G. Bouzidi A, et al. Eye (Lond). 2020 Nov;34(11):2138-2139. doi: 10.1038/s41433-019-0755-x. Epub 2020 Jan 2. Eye (Lond). 2020. PMID: 31896800 Free PMC article. No abstract available.

4

A homozygous MPZL2 deletion is associated with non syndromic hearing loss in a moroccan family.

Amalou G, Bonnet C, Riahi Z, Bouzidi A, Elrharchi S, Bousfiha A, Charif M, Kandil M, Lenaers G, Petit C, Barakat A. Amalou G, et al. Among authors: bouzidi a. Int J Pediatr Otorhinolaryngol. 2021 Jan;140:110481. doi: 10.1016/j.ijporl.2020.110481. Epub 2020 Nov 2. Int J Pediatr Otorhinolaryngol. 2021. PMID: 33234333

5

A homozygous nonsense HECW2 variant is associated with neurodevelopmental delay and intellectual disability.

Krami AM, Bouzidi A, Charif M, Amalou G, Charoute H, Rouba H, Roky R, Lenaers G, Barakat A, Nahili H. Krami AM, et al. Among authors: bouzidi a. Eur J Med Genet. 2022 Jun;65(6):104515. doi: 10.1016/j.ejmg.2022.104515. Epub 2022 Apr 27. Eur J Med Genet. 2022. PMID: 35487419

6

First characterization of LTBP3 variants in two Moroccan families with hypoplastic amelogenesis imperfecta.

Nouara F, Amalou G, Bouzidi A, Charif M, Charoute H, Lenaers G, El Arabi S, Bousfiha B, Barakat A. Nouara F, et al. Among authors: bouzidi a. Arch Oral Biol. 2022 Oct;142:105518. doi: 10.1016/j.archoralbio.2022.105518. Epub 2022 Aug 6. Arch Oral Biol. 2022. PMID: 35998423

7

Identification of novel mutations by targeted NGS in Moroccan families clinically diagnosed with a neuromuscular disorder.

Rochdi K, Cerino M, Da Silva N, Delague V, Bouzidi A, Nahili H, Zouiri G, Kriouile Y, Gorokhova S, Bartoli M, Saïle R, Barakat A, Krahn M. Rochdi K, et al. Among authors: bouzidi a. Clin Chim Acta. 2022 Jan 1;524:51-58. doi: 10.1016/j.cca.2021.11.020. Epub 2021 Nov 28. Clin Chim Acta. 2022. PMID: 34852264

8

Hepatic peliosis in a newborn - A case report and review of the literature.

Lahlou W, Bourial A, Rami A, Al Bouzidi A, Nejjari M, Alammari I. Lahlou W, et al. Among authors: al bouzidi a. Int J Surg Case Rep. 2024 Dec;125:110476. doi: 10.1016/j.ijscr.2024.110476. Epub 2024 Oct 18. Int J Surg Case Rep. 2024. PMID: 39602925 Free PMC article.

9

Real-world effectiveness and safety of CT-P13, an infliximab biosimilar, for inflammatory bowel diseases: A prospective national observational cohort study (ReFLECT study).

Laharie D, Bouhnik Y, Vuitton L, Biron A, Pierron G, Brault Y, Assing M, Bouzidi A, Amiot A, Nancey S. Laharie D, et al. Among authors: bouzidi a. Clin Res Hepatol Gastroenterol. 2024 Dec;48(10):102483. doi: 10.1016/j.clinre.2024.102483. Epub 2024 Oct 22. Clin Res Hepatol Gastroenterol. 2024. PMID: 39448029 Free article.

10

Comprehensive behavioural assessment of TERT in bladder cancer.

El Azzouzi M, El Ahanidi H, Hassan I, Tetou M, Ameur A, Bensaid M, Al Bouzidi A, Oukabli M, Alaoui CH, Addoum B, Chaoui I, Benbacer L, Mzibri ME, Attaleb M. El Azzouzi M, et al. Among authors: al bouzidi a. Urol Oncol. 2024 Dec;42(12):451.e19-451.e29. doi: 10.1016/j.urolonc.2024.06.024. Epub 2024 Aug 14. Urol Oncol. 2024. PMID: 39147693

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