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authFullName_s : Rachid Saile

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

Zahra Aadam , Nadia Kechout , Abdelhamid Barakat , Koon-Wing Chan , Meriem Ben-Ali , et al.
Journal of Clinical Immunology, 2016, 36 (3), pp.187-194. ⟨10.1007/s10875-016-0251-z⟩
Journal articles pasteur-01374987v1
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Identification of novel mutations by targeted NGS in Moroccan families clinically diagnosed with a neuromuscular disorder

Khaoula Rochdi , Mathieu Cerino , Nathalie da Silva , Valérie Delague , Aymane Bouzidi , et al.
Clinica Chimica Acta, 2022, 524, pp.51-58. ⟨10.1016/j.cca.2021.11.020⟩
Journal articles hal-03678846v1

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

Imane Morjane , Rym Kefi , Hicham Charoute , Fouzia Lakbakbi El Yaagoubi , Meryem Hechmi , et al.
Diabetes & Metabolic Syndrome: Clinical Research & Reviews, 2017, 11 (supplement 2), pp.S853-S857. ⟨10.1016/j.dsx.2017.07.005⟩
Journal articles hal-01571303v1

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

Fatima Zahra Jadid , Hajar Chihab , Hanane Salih Alj , Raouia Elfihry , Imane Zaidane , et al.
Infection, Genetics and Evolution, 2018, 66, pp.1-8. ⟨10.1016/j.meegid.2018.08.027⟩
Journal articles pasteur-02611922v1