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

Alpha-synuclein co-pathology in a real-world early Alzheimer's disease cohort

真实世界中早期阿尔茨海默病队列的α-突触核蛋白共病理学

Shiner, Tamara; Nathan, Talya; Levy, Mori Hai; David, Aya Bar; Omer, Nurit; Awad, Anan Abu; Ash, Elissa; Weisz, Mali Gana; Goldstein, Orly; Alcalay, Yifat; Regev, Keren; Lamoureux, Jennifer; Van Keuren-Jensen, Kendall; Blauwendraat, Cornelis; Alcalay, Roy N; Bregman, Noa

The GBA1 p.E427K (p.E388K) Variant is a Risk Factor for Synucleinopathies: A Meta-Analysis

GBA1 p.E427K (p.E388K) 变异是突触核蛋白病的一个风险因素:一项荟萃分析

Chifamba, Leah V; Parlar, Sitki Cem; Somerville, Emma N; Liu, Lang; Yu, Eric; Asayesh, Farnaz; Ahmad, Jamil; Teferra, Meron; Ruskey, Jennifer A; Waters, Cheryl; Monchi, Oury; Dauvilliers, Yves; Dupré, Nicolas; Timofeeva, Alla; Emelyanov, Anton; Pchelina, Sofya; Miliukhina, Irina; Greenbaum, Lior; Hassin-Baer, Sharon; Goldstein, Orly; Radefeldt, Mandy; Bauer, Peter; Beetz, Christian; Dilliott, Allison A; Beck, James C; Senkevich, Konstantin; Klein, Christine; Alcalay, Roy N; Gan-Or, Ziv

Radiological markers of CSF α-synuclein aggregation in Parkinson's disease patients

帕金森病患者脑脊液α-突触核蛋白聚集的放射学标志物

Droby, Amgad; Yoffe-Vasiliev, Avital; Atias, Daniel; Fraser, Kyle B; Mabrouk, Omar S; Omer, Nurit; Bar-Shira, Anat; Gana-Weisz, Mali; Goldstein, Orly; Artzi, Moran; Ben Bashat, Dafna; Alcalay, Roy N; Orr-Urtreger, Avi; Shirvan, Julia C; Cedarbaum, Jesse M; Giladi, Nir; Mirelman, Anat; Thaler, Avner

Effect of GBA1 Mutations and APOE Polymorphisms on Survival and Progression Among Ashkenazi Jews with Dementia with Lewy Bodies

GBA1基因突变和APOE基因多态性对患有路易体痴呆症的德系犹太人的生存和疾病进展的影响

Shiner, Tamara; Kavé, Gitit; Mirelman, Anat; Regev, Keren; Piura, Yoav; Goldstein, Orly; Gana Weisz, Mali; Bar-Shira, Anat; Gurevich, Tanya; Orr-Urtreger, Avi; Alcalay, Roy N; Giladi, Nir; Bregman, Noa

Validity of the Short Weekly Calendar Planning Activity in patients with Parkinson disease and nonmanifesting LRRK2 and GBA carriers

简短的每周日历计划活动在帕金森病患者和非显性LRRK2和GBA基因携带者中的有效性

Schejter-Margalit, Tamara; Binyamin, Noam Ben; Thaler, Avner; Maidan, Inbal; Cedarbaum, Jesse M; Orr-Urtreger, Avi; Gana Weisz, Mali; Goldstein, Orly; Giladi, Nir; Mirelman, Anat; Kizony, Rachel

MAPT Locus in Parkinson's Disease Patients of Ashkenazi Origin: A Stratified Analysis

阿什肯纳兹犹太人帕金森病患者的MAPT基因位点:一项分层分析

Shani, Shachar; Gana-Weisz, Mali; Bar-Shira, Anat; Thaler, Avner; Gurevich, Tanya; Mirelman, Anat; Giladi, Nir; Alcalay, Roy N; Goldstein, Orly; Orr-Urtreger, Avi

The Influence of GBA and LRRK2 on Mood Disorders in Parkinson's Disease

GBA和LRRK2对帕金森病情绪障碍的影响

DeBroff, Jake; Omer, Nurit; Cohen, Batsheva; Giladi, Nir; Kestenbaum, Meir; Shirvan, Julia C; Cedarbaum, Jesse M; Gana-Weisz, Mali; Goldstein, Orly; Orr-Urtreger, Avi; Mirelman, Anat; Thaler, Avner

The natural history study of preclinical genetic Creutzfeldt-Jakob Disease (CJD): a prospective longitudinal study protocol

克雅氏病(CJD)临床前遗传学自然史研究:一项前瞻性纵向研究方案

Bregman, Noa; Shiner, Tamara; Kavé, Gitit; Alcalay, Roy; Gana-Weisz, Mali; Goldstein, Orly; Glinka, Tal; Aizenstein, Orna; Bashat, Dafna Ben; Alcalay, Yifat; Mirelman, Anat; Thaler, Avner; Giladi, Nir; Omer, Nurit

Correction: The natural history study of preclinical genetic Creutzfeldt-Jakob Disease (CJD): a prospective longitudinal study protocol

更正:临床前遗传性克雅氏病(CJD)自然史研究:一项前瞻性纵向研究方案

Bregman, Noa; Shiner, Tamara; Kavé, Gitit; Alcalay, Roy; Gana-Weisz, Mali; Goldstein, Orly; Glinka, Tal; Aizenstein, Orna; Ben Bashat, Dafna; Alcalay, Yifat; Mirelman, Anat; Thaler, Avner; Giladi, Nir; Omer, Nurit

FUS-P525L Juvenile Amyotrophic Lateral Sclerosis and Intellectual Disability: Evidence for Association and Oligogenic Inheritance

FUS-P525L 青少年肌萎缩侧索硬化症和智力障碍:关联性和寡基因遗传的证据

Goldstein, Orly; Inbar, Talya; Kedmi, Merav; Gana-Weisz, Mali; Abramovich, Beatrice; Orr-Urtreger, Avi; Drory, Vivian E