Naima Bouslam - Faculty of Medicine and Pharmacy, University Mohammed V

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论文共 37 篇作者统计合作学者相似作者

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Novel WFS1 Variants in Two Moroccan Families with Wolfram Syndrome

Ahmed Bouhouche, Sara Sefiani,Hicham Charoute,Tibar Houyam,Naima Bouslam, Fatima-Zahra El Yousfi, Wadi Bnouhana,Ali Benomar, Fatima-Zahra Ouadghiri,Wafaa Regragui

Genetic Testing and Molecular Biomarkersno. 6 (2024): 257-262

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Exercise Habits in People with Parkinson's: A Multinational Survey

MOVEMENT DISORDERS CLINICAL PRACTICE (2024)

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

Imane Smaili,Houyam Tibar,Mounia Rahmani, Najlaa Machkour,Rachid Razine,Hajar Naciri Darai,Naima Bouslam,Ali Benomar,Wafa Regragui,Ahmed Bouhouche

Journal of Molecular Neuroscience（2023）

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Novel Pathogenic VPS13A Mutation in Moroccan Family with Choreoacanthocytosis: a Case Report

Fatima Ouchkat,Wafaa Regragui,Imane Smaili,Hajar Naciri Darai,Naima Bouslam,Mounia Rahmani,Adyl Melhaoui,Yasser Arkha,Elmostafa El Fahime,Ahmed Bouhouche

BMC medical genetics（2020）

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A Specific Diplotype H1j/H2 of the MAPT Gene Could Be Responsible for Parkinson's Disease with Dementia

Imane Smaili, Imane Hajjaj,Rachid Razine,Houyam Tibar,Ayyoub Salmi,Naima Bouslam,Ahmed Moussa,Wafa Regragui,Ahmed Bouhouche

Case reports in genetics（2020）

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

Smaili Imane,Tesson Christelle, Specialties hospital,Bertrand Hélène,Bouslam Naima,Brice Alexis,Lesage Suzanne

Journal of Molecular Neuroscience（2020）

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

Ahmed Bouhouche,Houyam Tibar, Yamna Kriouale,Mohammed Jiddane,Imane Smaili,Naima Bouslam,Ali Benomar,Mohamed Yahyaoui,Elmostafa El Fahime

Case Reports in Genetics（2018）

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Evidence for Prehistoric Origins of the G2019S Mutation in the North African Berber Population

Rafiqua Ben El Haj,Ayyoub Salmi,Wafa Regragui,Ahmed Moussa,Naima Bouslam,Houyam Tiber,Ali Benomar,Mohamed Yahyaoui,Ahmed Bouhouche

PLoS ONE（2017）

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

Ahmed Bouhouche,Houyam Tibar,Rafiqua Ben El Haj,Khalil El Bayad,Rachid Razine, Sanaa Tazrout,Asmae Skalli,Naima Bouslam, Loubna Elouardi,Ali Benomar,Mohammed Yahyaoui,Wafa Regragui

Parkinson s Disease（2017）

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

Ahmed Bouhouche,Christelle Tesson,Wafaa Regragui,Mounia Rahmani,Valerie Drouet,Houyam Tibar,Zouhayr Souirti,Rafiqua Ben El Haj,Naima Bouslam,Mohamed Yahyaoui,Alexis Brice,Ali Benomar,Suzanne Lesage

Frontiers in neurology（2017）

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