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

Headache and Status Epilepticus Reveal Paget's Disease of the Bone

头痛和癫痫持续状态提示佩吉特骨病

Ouhabi, Dahab; Tibar, Houyam; Benomar, Ali; Jiddane, Mohamed; Regragui, Wafa

Contribution of fibrin glue in the surgery of cyanogenic and non-cyanogenic congenital cardiopathies: retrospective cohort study

纤维蛋白胶在致绀型和非致绀型先天性心脏病手术中的作用:回顾性队列研究

Cheikh, Amine; Ajaja, Mohamed Rida; Rhazali, Hicham; Bouatia, Mustapha; Benomar, Ali; Slaoui, Anas; Cherrah, Yahia; Abouqal, Redouane; El Hassani, Amine; Cheikhaoui, Younes

A case of bilateral thalamic infarct complicating tuberculous meningoencephalitis

结核性脑膜脑炎并发双侧丘脑梗死的病例报告

Aasfara, Jehanne; Regragui, Wafa; Ouardi, Loubna El; Haddou, El Hachmia Ait Ben; Benomar, Ali; Yahyaoui, Mohammed

Non-Motor Symptoms of Parkinson's Disease and Their Impact on Quality of Life in a Cohort of Moroccan Patients

帕金森病非运动症状及其对摩洛哥患者生活质量的影响

Tibar, Houyam; El Bayad, Khalil; Bouhouche, Ahmed; Ait Ben Haddou, El Hachmia; Benomar, Ali; Yahyaoui, Mohamed; Benazzouz, Abdelhamid; Regragui, Wafa

Deep Brain Stimulation in Moroccan Patients With Parkinson's Disease: The Experience of Neurology Department of Rabat

摩洛哥帕金森病患者的深部脑刺激治疗:拉巴特神经病学系的经验

Rahmani, Mounia; Benabdeljlil, Maria; Bellakhdar, Fouad; Faris, Mustapha El Alaoui; Jiddane, Mohamed; Bayad, Khalil El; Boutbib, Fatima; Razine, Rachid; Gana, Rachid; Hassani, Moulay R El; Fatemi, Nizar El; Fikri, Meryem; Sanhaji, Siham; Tassine, Hennou; Balrhiti, Imane El Alaoui; Hadri, Souad El; Kettani, Najwa Ech-Cherif; Abbadi, Najia El; Amor, Mourad; Moussaoui, Abdelmjid; Semlali, Afifa; Aidi, Saadia; Benhaddou, El Hachmia Ait; Benomar, Ali; Bouhouche, Ahmed; Yahyaoui, Mohamed; Khamlichi, Abdeslam El; Ouahabi, Abdessamad El; Maaqili, Rachid El; Tibar, Houyam; Arkha, Yasser; Melhaoui, Adyl; Benazzouz, Abdelhamid; Regragui, Wafa

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