Lyahyai J - Search Results

1

AGXT Gene Mutations and Prevalence of Primary Hyperoxaluria Type 1 in Moroccan Population.

Boualla L, Tajir M, Oulahiane N, Lyahyai J, Laarabi FZ, Chafai Elalaoui S, Soulami K, Ait Ouamar H, Sefiani A. Boualla L, et al. Among authors: lyahyai j. Genet Test Mol Biomarkers. 2015 Nov;19(11):623-8. doi: 10.1089/gtmb.2015.0136. Epub 2015 Sep 18. Genet Test Mol Biomarkers. 2015. PMID: 26383609

2

Spinal muscular atrophy carrier frequency and estimated prevalence of the disease in Moroccan newborns.

Lyahyai J, Sbiti A, Barkat A, Ratbi I, Sefiani A. Lyahyai J, et al. Genet Test Mol Biomarkers. 2012 Mar;16(3):215-8. doi: 10.1089/gtmb.2011.0149. Epub 2011 Sep 27. Genet Test Mol Biomarkers. 2012. PMID: 21950724

3

CALR gene mutational profile in myeloproliferative neoplasms with non-mutated JAK2 in Moroccan patients: A case series and germline in-frame deletion.

Smaili W, Doubaj Y, Laarabi FZ, Lyahyai J, Kerbout M, Mikdame M, Sefiani A. Smaili W, et al. Among authors: lyahyai j. Curr Res Transl Med. 2017 Jan-Mar;65(1):15-19. doi: 10.1016/j.retram.2016.08.002. Epub 2016 Nov 3. Curr Res Transl Med. 2017. PMID: 28340692

4

Novel nonsense mutation of BRCA2 gene in a Moroccan man with familial breast cancer.

Guaoua S, Ratbi I, Lyahyai J, El Alaoui SC, Laarabi FZ, Sefiani A. Guaoua S, et al. Among authors: lyahyai j. Afr Health Sci. 2014 Jun;14(2):468-71. doi: 10.4314/ahs.v14i2.25. Afr Health Sci. 2014. PMID: 25320599 Free PMC article.

5

Further evidence for causal FAM20A mutations and first case of amelogenesis imperfecta and gingival hyperplasia syndrome in Morocco: a case report.

Cherkaoui Jaouad I, El Alloussi M, Chafai El Alaoui S, Laarabi FZ, Lyahyai J, Sefiani A. Cherkaoui Jaouad I, et al. Among authors: lyahyai j. BMC Oral Health. 2015 Jan 30;15:14. doi: 10.1186/1472-6831-15-14. BMC Oral Health. 2015. PMID: 25636655 Free PMC article.

6

Identification of a novel LAMA2 c.2217G > A, p.(Trp739*) mutation in a Moroccan patient with congenital muscular dystrophy: a case report.

El Kadiri Y, Ratbi I, Laarabi FZ, Kriouile Y, Sefiani A, Lyahyai J. El Kadiri Y, et al. Among authors: lyahyai j. BMC Med Genomics. 2021 Apr 21;14(1):113. doi: 10.1186/s12920-021-00959-2. BMC Med Genomics. 2021. PMID: 33882917 Free PMC article.

7

Clinical and molecular report of novel GALC mutations in Moroccan patient with Krabbe disease: case report.

Zerkaoui M, Ratbi I, Castellotti B, Gellera C, Lyahyai J, Kriouile Y, Sefiani A. Zerkaoui M, et al. Among authors: lyahyai j. BMC Pediatr. 2015 Nov 13;15:182. doi: 10.1186/s12887-015-0490-9. BMC Pediatr. 2015. PMID: 26567009 Free PMC article.

8

Clinical exome sequencing identifies two novel mutations of the SCN1A and SCN2A genes in Moroccan patients with epilepsy: a case series.

Sahli M, Zrhidri A, Elaloui SC, Smaili W, Lyahyai J, Oudghiri FZ, Sefiani A. Sahli M, et al. Among authors: lyahyai j. J Med Case Rep. 2019 Aug 23;13(1):266. doi: 10.1186/s13256-019-2203-8. J Med Case Rep. 2019. PMID: 31439038 Free PMC article.

9

Clinical, cytogenetic and molecular findings in nine Moroccan patients with Fanconi anemia.

Doubaj Y, Zrhidri A, Elalaoui SC, Lyahyai J, El Kadiri Y, Elkassimi N, Sbiti A, El Kababri M, Hessissen L, Sefiani A. Doubaj Y, et al. Among authors: lyahyai j. Pan Afr Med J. 2021 May 26;39:72. doi: 10.11604/pamj.2021.39.72.27220. eCollection 2021. Pan Afr Med J. 2021. PMID: 34422195 Free PMC article.

10

Mutational spectrum of BRCA1/2 genes in Moroccan patients with hereditary breast and/or ovarian cancer, and review of BRCA mutations in the MENA region.

Elalaoui SC, Laarabi FZ, Afif L, Lyahyai J, Ratbi I, Jaouad IC, Doubaj Y, Sahli M, Ouhenach M, Sefiani A. Elalaoui SC, et al. Among authors: lyahyai j. Breast Cancer Res Treat. 2022 Jul;194(1):187-198. doi: 10.1007/s10549-022-06622-3. Epub 2022 May 17. Breast Cancer Res Treat. 2022. PMID: 35578052

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