Bouslam N - Search Results

1

Novel WFS1 Variants in Two Moroccan Families with Wolfram Syndrome.

Bouhouche A, Sefiani S, Charoute H, Houyam T, Bouslam N, El Yousfi FZ, Bnouhana W, Benomar A, Ouadghiri FZ, Regragui W. Bouhouche A, et al. Among authors: bouslam n. Genet Test Mol Biomarkers. 2024 Jun;28(6):257-262. doi: 10.1089/gtmb.2023.0550. Epub 2024 May 9. Genet Test Mol Biomarkers. 2024. PMID: 38721948

2

A Novel Homozygous p.L539F Mutation Identified in PINK1 Gene in a Moroccan Patient with Parkinsonism.

Ben El Haj R, Regragui W, Tazi-Ahnini R, Skalli A, Bouslam N, Benomar A, Yahyaoui M, Bouhouche A. Ben El Haj R, et al. Among authors: bouslam n. Biomed Res Int. 2016;2016:3460234. doi: 10.1155/2016/3460234. Epub 2016 Jun 20. Biomed Res Int. 2016. PMID: 27413743 Free PMC article.

3

Mutation Analysis of Consanguineous Moroccan Patients with Parkinson's Disease Combining Microarray and Gene Panel.

Bouhouche A, Tesson C, Regragui W, Rahmani M, Drouet V, Tibar H, Souirti Z, Ben El Haj R, Bouslam N, Yahyaoui M, Brice A, Benomar A, Lesage S. Bouhouche A, et al. Among authors: bouslam n. Front Neurol. 2017 Oct 31;8:567. doi: 10.3389/fneur.2017.00567. eCollection 2017. Front Neurol. 2017. PMID: 29163333 Free PMC article.

4

Novel pathogenic VPS13A mutation in Moroccan family with Choreoacanthocytosis: a case report.

Ouchkat F, Regragui W, Smaili I, Naciri Darai H, Bouslam N, Rahmani M, Melhaoui A, Arkha Y, El Fahime E, Bouhouche A. Ouchkat F, et al. Among authors: bouslam n. BMC Med Genet. 2020 Mar 4;21(1):47. doi: 10.1186/s12881-020-0983-8. BMC Med Genet. 2020. PMID: 32131761 Free PMC article.

5

Gene Panel Sequencing Identifies Novel Pathogenic Mutations in Moroccan Patients with Familial Parkinson Disease.

Smaili I, Tesson C, Regragui W, Bertrand H, Rahmani M, Bouslam N, Benomar A, Brice A, Lesage S, Bouhouche A. Smaili I, et al. Among authors: bouslam n. J Mol Neurosci. 2021 Jan;71(1):142-152. doi: 10.1007/s12031-020-01635-3. Epub 2020 Jun 16. J Mol Neurosci. 2021. PMID: 32557143

6

Gene Panel Sequencing Analysis Revealed a Strong Contribution of Rare Coding Variants to the Risk of Parkinson's Disease in Sporadic Moroccan Patients.

Smaili I, Tibar H, Rahmani M, Machkour N, Razine R, Darai HN, Bouslam N, Benomar A, Regragui W, Bouhouche A. Smaili I, et al. Among authors: bouslam n. J Mol Neurosci. 2023 Jun;73(6):391-402. doi: 10.1007/s12031-023-02128-9. Epub 2023 May 31. J Mol Neurosci. 2023. PMID: 37256495

7

Clinical and genetic data of Huntington disease in Moroccan patients.

Bouhouche A, Regragui W, Lamghari H, Khaldi K, Birouk N, Lytim S, Bellamine S, Kriouile Y, Bouslam N, Haddou el HA, Faris MA, Benomar A, Yahyaoui M. Bouhouche A, et al. Among authors: bouslam n. Afr Health Sci. 2015 Dec;15(4):1232-8. doi: 10.4314/ahs.v15i4.23. Afr Health Sci. 2015. PMID: 26958025 Free PMC article.

8

Genetic Analysis of Undiagnosed Juvenile GM1-Gangliosidosis by Microarray and Exome Sequencing.

Bouhouche A, Tibar H, Kriouale Y, Jiddane M, Smaili I, Bouslam N, Benomar A, Yahyaoui M, El Fahime E. Bouhouche A, et al. Among authors: bouslam n. Case Rep Genet. 2018 Nov 15;2018:8635698. doi: 10.1155/2018/8635698. eCollection 2018. Case Rep Genet. 2018. PMID: 30581635 Free PMC article.

9

LRRK2 G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson's Disease.

Bouhouche A, Tibar H, Ben El Haj R, El Bayad K, Razine R, Tazrout S, Skalli A, Bouslam N, Elouardi L, Benomar A, Yahyaoui M, Regragui W. Bouhouche A, et al. Among authors: bouslam n. Parkinsons Dis. 2017;2017:2412486. doi: 10.1155/2017/2412486. Epub 2017 Mar 30. Parkinsons Dis. 2017. PMID: 28465860 Free PMC article.

10

Clinical comparison between AVED patients with 744 del A mutation and Friedreich ataxia with GAA expansion in 15 Moroccan families.

Benomar A, Yahyaoui M, Meggouh F, Bouhouche A, Boutchich M, Bouslam N, Zaim A, Schmitt M, Belaidi H, Ouazzani R, Chkili T, Koenig M. Benomar A, et al. Among authors: bouslam n. J Neurol Sci. 2002 Jun 15;198(1-2):25-9. doi: 10.1016/s0022-510x(02)00057-6. J Neurol Sci. 2002. PMID: 12039660

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