日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

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

帕金森病患者运动习惯:一项多国调查

Jagota, Priya; Phutrakool, Phanupong; Kamble, Nitish; Dang, Thuong Huyen Thi; Aldaajani, Zakiyah; Hatano, Taku; Hoskere Sreenivasa, Deva Kumar; Tripura, Telugu; Kukkle, Prashanth Lingappa; Jeon, Beomseok; Nishikawa, Noriko; Oji, Yutaka; Tran, Tai Ngoc; Susatia, Frandy; Fabbri, Margherita; Leung, Clémence; Alonso Canovas, Araceli; Kamel, Walaa A; Pal, Pramod Kumar; Rakesh, Kempaiah; Abu Snineh, Muneer; Chairangsaris, Parnsiri; Lolekha, Praween; Jamora, Roland Dominic G; Mohamed Ibrahim, Norlinah; Desa, Siti Hajar Mat; Tan, Ai Huey; Toh, Tzi Shin; Obaid, Mona; Fung, Victor S C; Lang, Anthony; Lin, Chin-Hsien; Regragui, Wafa; Bouslam, Naima; Bhidayasiri, Roongroj

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

摩洛哥舞蹈棘红细胞增多症家族中新的致病性 VPS13A 突变:一例病例报告

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

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

MAPT基因的特定二倍型H1j/H2可能是导致帕金森病伴痴呆症的原因

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

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

利用微阵列和外显子组测序对未确诊的青少年GM1神经节苷脂病进行基因分析

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

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

结合微阵列和基因组检测技术对摩洛哥近亲结婚的帕金森病患者进行突变分析

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

Evidence for prehistoric origins of the G2019S mutation in the North African Berber population

北非柏柏尔人群中G2019S突变史前起源的证据

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

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

LRRK2 G2019S 突变:摩洛哥帕金森病患者的患病率和临床特征

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

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

在一名患有帕金森病的摩洛哥患者中,PINK1基因中发现了一种新的纯合p.L539F突变

Ben El Haj, Rafiqua; Regragui, Wafaa; Tazi-Ahnini, Rachid; Skalli, Asmae; Bouslam, Naima; Benomar, Ali; Yahyaoui, Mohamed; Bouhouche, Ahmed

Clinical and genetic data of Huntington disease in Moroccan patients

摩洛哥亨廷顿病患者的临床和遗传数据

Bouhouche, Ahmed; Regragui, Wafaa; Lamghari, Hind; Khaldi, Khadija; Birouk, Nazha; Lytim, Safaa; Bellamine, Soufiane; Kriouile, Yamna; Bouslam, Naima; Haddou, El Hachmia Ait Ben; Faris, Mustapha Alaoui; Benomar, Ali; Yahyaoui, Mohamed

KIF1C mutations in two families with hereditary spastic paraparesis and cerebellar dysfunction

两个患有遗传性痉挛性截瘫和小脑功能障碍的家族中的 KIF1C 突变

Talya Dor, Yuval Cinnamon, Laure Raymond, Avraham Shaag, Naima Bouslam, Ahmed Bouhouche, Marion Gaussen, Vincent Meyer, Alexandra Durr, Alexis Brice, Ali Benomar, Giovanni Stevanin, Markus Schuelke, Simon Edvardson