Saile R - Search Results

1

X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations.

Aadam Z, Kechout N, Barakat A, Chan KW, Ben-Ali M, Ben-Mustapha I, Zidi F, Ailal F, Attal N, Doudou F, Abbadi MC, Kaddache C, Smati L, Touri N, Chemli J, Gargah T, Brini I, Bakhchane A, Charoute H, Jeddane L, El Atiqi S, El Hafidi N, Hida M, Saile R, Alj HS, Boukari R, Bejaoui M, Najib J, Barbouche MR, Lau YL, Mellouli F, Bousfiha AA. Aadam Z, et al. Among authors: saile r. J Clin Immunol. 2016 Apr;36(3):187-94. doi: 10.1007/s10875-016-0251-z. Epub 2016 Mar 1. J Clin Immunol. 2016. PMID: 26931785

2

Chronic granulomatous disease in Morocco: genetic, immunological, and clinical features of 12 patients from 10 kindreds.

Baba LA, Ailal F, El Hafidi N, Hubeau M, Jabot-Hanin F, Benajiba N, Aadam Z, Conti F, Deswarte C, Jeddane L, Aglaguel A, El Maataoui O, Tissent A, Mahraoui C, Najib J, Martinez-Barricarte R, Abel L, Habti N, Saile R, Casanova JL, Bustamante J, Salih Alj H, Bousfiha AA. Baba LA, et al. Among authors: saile r. J Clin Immunol. 2014 May;34(4):452-8. doi: 10.1007/s10875-014-9997-3. Epub 2014 Mar 5. J Clin Immunol. 2014. PMID: 24596025

3

The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan population.

Naamane H, El Maataoui O, Ailal F, Barakat A, Bennani S, Najib J, Hassar M, Saile R, Bousfiha AA. Naamane H, et al. Among authors: saile r. Eur J Pediatr. 2010 Sep;169(9):1069-74. doi: 10.1007/s00431-010-1179-6. Epub 2010 Apr 23. Eur J Pediatr. 2010. PMID: 20414676

4

Research of anti-GAD and anti-IA2 autoantibodies by ELISA test in a series of Moroccan pediatric patients with diabetes type 1.

Belhiba O, Aadam Z, Jeddane L, Saile R, Salih Alj H, Bousfiha AA, Jennane F. Belhiba O, et al. Among authors: saile r. Afr Health Sci. 2020 Sep;20(3):1337-1343. doi: 10.4314/ahs.v20i3.40. Afr Health Sci. 2020. PMID: 33402983 Free PMC article.

5

Association study of HNF1A polymorphisms with metabolic syndrome in the Moroccan population.

Morjane I, Kefi R, Charoute H, Lakbakbi El Yaagoubi F, Hechmi M, Saile R, Abdelhak S, Barakat A. Morjane I, et al. Among authors: saile r. Diabetes Metab Syndr. 2017 Dec;11 Suppl 2:S853-S857. doi: 10.1016/j.dsx.2017.07.005. Epub 2017 Jul 3. Diabetes Metab Syndr. 2017. PMID: 28712822

6

Prediction and Structural Comparison of Deleterious Coding Nonsynonymous Single Nucleotide Polymorphisms (nsSNPs) in Human LEP Gene Associated with Obesity.

Bouafi H, Bencheikh S, Mehdi Krami AL, Morjane I, Charoute H, Rouba H, Saile R, Benhnini F, Barakat A. Bouafi H, et al. Among authors: saile r. Biomed Res Int. 2019 Dec 4;2019:1832084. doi: 10.1155/2019/1832084. eCollection 2019. Biomed Res Int. 2019. PMID: 31871931 Free PMC article.

7

Association of c.56C > G (rs3135506) Apolipoprotein A5 Gene Polymorphism with Coronary Artery Disease in Moroccan Subjects: A Case-Control Study and an Updated Meta-Analysis.

Morjane I, Charoute H, Ouatou S, Elkhattabi L, Benrahma H, Saile R, Rouba H, Barakat A. Morjane I, et al. Among authors: saile r. Cardiol Res Pract. 2020 Aug 4;2020:5981971. doi: 10.1155/2020/5981971. eCollection 2020. Cardiol Res Pract. 2020. PMID: 32832146 Free PMC article.

8

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: saile r. 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

9

Control of progression towards liver fibrosis and hepatocellular carcinoma by SOCS3 polymorphisms in chronic HCV-infected patients.

Jadid FZ, Chihab H, Alj HS, Elfihry R, Zaidane I, Tazi S, Badre W, Marchio A, El Filali KM, Tahiri M, Saile R, Pineau P, Ezzikouri S, Benjelloun S. Jadid FZ, et al. Among authors: saile r. Infect Genet Evol. 2018 Dec;66:1-8. doi: 10.1016/j.meegid.2018.08.027. Epub 2018 Aug 30. Infect Genet Evol. 2018. PMID: 30172885

10

In Silico Analysis of Coding/Noncoding SNPs of Human RETN Gene and Characterization of Their Impact on Resistin Stability and Structure.

Elkhattabi L, Morjane I, Charoute H, Amghar S, Bouafi H, Elkarhat Z, Saile R, Rouba H, Barakat A. Elkhattabi L, et al. Among authors: saile r. J Diabetes Res. 2019 May 20;2019:4951627. doi: 10.1155/2019/4951627. eCollection 2019. J Diabetes Res. 2019. PMID: 31236417 Free PMC article.

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