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Page 1
Phenotype and molecular characterization of Wilson's disease in Morocco.
Abbassi N, Bourrahouat A, Bedoya EC, Pagan C, Qabli ME, Maidoumi S, Belmalih A, Guillaud O, Kissani N, Abkari A, Chahid I, Rafai MA, Mouane N, Kriouile Y, Aidi S, Hida M, Idrissi ML, Belahsen MF, Abkari ME, Rkain M, Ismaili Z, Sedki A, Bost M, Aboussair N, Lachaux A. Abbassi N, et al. Among authors: rkain m. Clin Res Hepatol Gastroenterol. 2024 May;48(5):102335. doi: 10.1016/j.clinre.2024.102335. Epub 2024 Apr 6. Clin Res Hepatol Gastroenterol. 2024. PMID: 38588792
[Hemophilia: situation in a pediatric ward in eastern Morocco].
Benajiba N, Boussaadni YE, Aljabri M, Bentata Y, Amrani R, Rkain M. Benajiba N, et al. Among authors: rkain m. Pan Afr Med J. 2014 Jun 10;18:126. doi: 10.11604/pamj.2014.18.126.4007. eCollection 2014. Pan Afr Med J. 2014. PMID: 25404986 Free PMC article. French.
Salmonella Meningitis in a Young Infant: A Case Report.
Elouali A, Ouerradi N, Ayad G, Babakhouya A, Rkain M. Elouali A, et al. Among authors: rkain m. Cureus. 2023 Aug 26;15(8):e44147. doi: 10.7759/cureus.44147. eCollection 2023 Aug. Cureus. 2023. PMID: 37753016 Free PMC article.
Severe Kawasaki Disease and Thrombocytopenia: A Case Report.
Souni G, Ayad G, Elouali A, Rkain M, Babakhouya A. Souni G, et al. Among authors: rkain m. Cureus. 2023 Aug 3;15(8):e42916. doi: 10.7759/cureus.42916. eCollection 2023 Aug. Cureus. 2023. PMID: 37664379 Free PMC article.
First report on chromosomal abnormalities in Eastern Morocco: Identification of a new case of a de novo partial trisomy 13q using single-nucleotide polymorphism array.
Elidrissi Errahhali M, Elidrissi Errahhali M, Ramdani S, Lhousni S, Benajiba N, Rkain M, Babakhouya A, Elouali A, Ghanam A, Amrani R, Messaoudi S, Ayyad A, Oneib B, Mimouni A, Saadi H, Allaoui S, Ouarzane M, Guichet A, Charif M, Boulouiz R, Bellaoui M. Elidrissi Errahhali M, et al. Among authors: rkain m. Arch Pediatr. 2024 Feb;31(2):112-116. doi: 10.1016/j.arcped.2023.10.002. Epub 2024 Jan 22. Arch Pediatr. 2024. PMID: 38262863
[Varicella is not always benign].
Ayyad A, Rkain M, Babakhouya A, Benajiba N. Ayyad A, et al. Among authors: rkain m. Pan Afr Med J. 2018 Sep 13;31:30. doi: 10.11604/pamj.2018.31.30.16730. eCollection 2018. Pan Afr Med J. 2018. PMID: 30918557 Free PMC article. French.
[Congenital factor VII deficiency: about two family cases].
Benajiba N, Ayyad A, Aabdi C, Amrani R, Rkain M, Benajiba M. Benajiba N, et al. Among authors: rkain m. Pan Afr Med J. 2018 Oct 31;31:156. doi: 10.11604/pamj.2018.31.156.6123. eCollection 2018. Pan Afr Med J. 2018. PMID: 31065316 Free PMC article. French.
Triple-A Syndrome in Morocco: Founder Effect, Age Estimation of the AAAS c.1331+1G>A Variant, and Implications for Genetic Diagnosis.
Belmokhtar KY, Cherkaoui I, Lhousni S, Elidrissi Errahhali M, Elidrissi Errahhali M, Charif M, Boulouiz R, Ouarzane M, Elouali A, Ghanam A, Babakhouya A, Rkain M, Benajiba N, Bellaoui M. Belmokhtar KY, et al. Among authors: rkain m. Mol Syndromol. 2024 Mar;15(2):96-103. doi: 10.1159/000533894. Epub 2023 Sep 29. Mol Syndromol. 2024. PMID: 38585542 Free PMC article.
62 results