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

Association study of the JAK/STAT signaling pathway with susceptibility to COVID-19 in moroccan patient and in-silico analysis of rare variants

摩洛哥患者JAK/STAT信号通路与COVID-19易感性的关联研究及罕见变异的计算机分析

El Houdi, Meriem; Skhoun, Hanaa; El Fessikh, Meriem; Benmansour, Reda; El Yousfi, Fatima-Zahra; Nebhani, Chaimae; Tagajdid, Mohamed Rida; Lahlou Amine, Idriss; El Annaz, Hicham; Ameziane El Hassani, Rabii; Ouzzif, Zohra; Abouqal, Redouane; Ennibi, Khalid; Bouhouche, Ahmed; El Baghdadi, Jamila

The Genetic Architecture of Parkinson's Disease in Morocco: Highlighting a Predominance of Mendelian Genes

摩洛哥帕金森病遗传结构:凸显孟德尔基因的优势地位

Bouhouche, Ahmed; Tibar, Houyam; Regragui, Wafa

A Novel Loss-of-Function Variant in COL4A3 in a Consanguineous Moroccan Family Displaying the Alport Syndrome with Variable Clinical Expression

在摩洛哥一个近亲结婚的家庭中发现一种新的COL4A3功能缺失变异,该变异导致阿尔波特综合征的临床表现多样。

Taroua, Oumayma; Askander, Omar; Rhou, Hakima; Bouhouche, Ahmed

De novo p.Glu61Ter mutation in GCH1 in a Moroccan patient with dopa-responsive dystonia: a case report

摩洛哥一名多巴反应性肌张力障碍患者GCH1基因新发p.Glu61Ter突变:病例报告

Bouhouche, Ahmed; Tamaoui, Leila; Birouk, Nazha

Novel ITGB2 Mutation Is Responsible for a Severe Form of Leucocyte Adhesion Deficiency Type 1

一种新的ITGB2基因突变是导致严重型白细胞黏附缺陷1型的原因

Bouhouche, Ahmed; Tabache, Yasmin; Askander, Omar; Charoute, Hicham; Mesnaoui, Nada; Belayachi, Lamiae; El Hafidi, Naima; Hardizi, Houyam; El Fahime, Elmostafa; Erreimi, Naima; Barakat, Abdelhamid; Khattab, Mohammed; Seghrouchni, Fouad; El Hassani, Amine

Characterization of Recessive Parkinson Disease in a Large Multicenter Study

一项大型多中心研究中隐性帕金森病的特征分析

Lesage, Suzanne; Lunati, Ariane; Houot, Marion; Romdhan, Sawssan Ben; Clot, Fabienne; Tesson, Christelle; Mangone, Graziella; Toullec, Benjamin Le; Courtin, Thomas; Larcher, Kathy; Benmahdjoub, Mustapha; Arezki, Mohamed; Bouhouche, Ahmed; Anheim, Mathieu; Roze, Emmanuel; Viallet, François; Tison, François; Broussolle, Emmanuel; Emre, Murat; Hanagasi, Hasmet; Bilgic, Basar; Tazir, Meriem; Djebara, Mouna Ben; Gouider, Riadh; Tranchant, Christine; Vidailhet, Marie; Le Guern, Eric; Corti, Olga; Mhiri, Chokri; Lohmann, Ebba; Singleton, Andrew; Corvol, Jean-Christophe; Brice, Alexis

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

Identification of single nucleotide variants in the Moroccan population by whole-genome sequencing

利用全基因组测序鉴定摩洛哥人群中的单核苷酸变异

Crooks, Lucy; Cooper-Knock, Johnathan; Heath, Paul R; Bouhouche, Ahmed; Elfahime, Mostafa; Azzouz, Mimoun; Bakri, Youssef; Adnaoui, Mohammed; Ibrahimi, Azeddine; Amzazi, Saaïd; Tazi-Ahnini, Rachid

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