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

A plasma proteomics-based candidate biomarker panel predictive of amyotrophic lateral sclerosis

基于血浆蛋白质组学的肌萎缩侧索硬化症预测候选生物标志物组合

Chia, Ruth; Moaddel, Ruin; Kwan, Justin Y; Rasheed, Memoona; Ruffo, Paola; Landeck, Natalie; Reho, Paolo; Vasta, Rosario; Calvo, Andrea; Moglia, Cristina; Canosa, Antonio; Manera, Umberto; Snyder, Allison; Saez-Atienzar, Sara; Grassano, Maurizio; Brunetti, Maura; Casale, Federico; Ray, Anindita; Arvind, Kumar; Comertpay, Betul; Zhu, Min; Gibbs, J Raphael; Alba, Camille; Dawson, Ted M; Rosenthal, Liana S; Hall, Anna J; Pantelyat, Alexander Y; Narendra, Derek P; Ehrlich, Debra J; Walker, Keenan A; Kosa, Peter; Bielekova, Bibiana; Egan, Josephine M; Candia, Julián; Tanaka, Toshiko; Ferrucci, Luigi; Dalgard, Clifton L; Scholz, Sonja W; Chiò, Adriano; Traynor, Bryan J

Clinical Neurophysiological Study for the Diagnosis of Functional Cranial-Cervical Dystonia

功能性颅颈肌张力障碍的临床神经生理学诊断研究

Ni, Zhen; Halhouli, Oday; Cho, Hyun Joo; Hallett, Mark; Ehrlich, Debra

Olfactory network reorganization in Parkinson's disease

帕金森病中的嗅觉网络重组

Saqib, Mohammed; Pacheco, Laura Pesantez; Ehrlich, Debra J; Horovitz, Silvina G

Persistent GDNF Expression 45 Months after Putaminal Infusion of AAV2-GDNF in a Patient with Parkinson's Disease

帕金森病患者壳核内注射AAV2-GDNF 45个月后,GDNF表达持续存在

Heiss, John D; Ray-Chaudhury, Abhik; Kleiner, David E; Ehrlich, Debra J; Scott, Gretchen; Edwards, Nancy A; Goldstein, David S; Hammoud, Dima A; Hadaczek, Piotr; Van Laar, Victor S; Graff, Shantelle A; Herscovitch, Peter; Lungu, Codrin; Hallett, Mark; Lonser, Russell R; Zaghloul, Kareem A; Bankiewicz, Krystof S

A randomized feasibility trial of medium chain triglyceride-supplemented ketogenic diet in people with Parkinson's disease

一项针对帕金森病患者的补充中链甘油三酯的生酮饮食随机可行性试验

Choi, Alexander H; Delgado, Melanie; Chen, Kong Y; Chung, Stephanie T; Courville, Amber; Turner, Sara A; Yang, Shanna; Airaghi, Kayla; Dustin, Irene; McGurrin, Patrick; Wu, Tianxia; Hallett, Mark; Ehrlich, Debra J

Large-scale rare variant burden testing in Parkinson's disease

帕金森病大规模罕见变异负荷检测

Makarious, Mary B; Lake, Julie; Pitz, Vanessa; Ye Fu, Allen; Guidubaldi, Joseph L; Solsberg, Caroline Warly; Bandres-Ciga, Sara; Leonard, Hampton L; Kim, Jonggeol Jeffrey; Billingsley, Kimberley J; Grenn, Francis P; Jerez, Pilar Alvarez; Alvarado, Chelsea X; Iwaki, Hirotaka; Ta, Michael; Vitale, Dan; Hernandez, Dena; Torkamani, Ali; Ryten, Mina; Hardy, John; Scholz, Sonja W; Traynor, Bryan J; Dalgard, Clifton L; Ehrlich, Debra J; Tanaka, Toshiko; Ferrucci, Luigi; Beach, Thomas G; Serrano, Geidy E; Real, Raquel; Morris, Huw R; Ding, Jinhui; Gibbs, J Raphael; Singleton, Andrew B; Nalls, Mike A; Bhangale, Tushar; Blauwendraat, Cornelis

Genome-Wide Analysis of Structural Variants in Parkinson Disease

帕金森病结构变异的全基因组分析

Billingsley, Kimberley J; Ding, Jinhui; Jerez, Pilar Alvarez; Illarionova, Anastasia; Levine, Kristin; Grenn, Francis P; Makarious, Mary B; Moore, Anni; Vitale, Daniel; Reed, Xylena; Hernandez, Dena; Torkamani, Ali; Ryten, Mina; Hardy, John; Chia, Ruth; Scholz, Sonja W; Traynor, Bryan J; Dalgard, Clifton L; Ehrlich, Debra J; Tanaka, Toshiko; Ferrucci, Luigi; Beach, Thomas G; Serrano, Geidy E; Quinn, John P; Bubb, Vivien J; Collins, Ryan L; Zhao, Xuefang; Walker, Mark; Pierce-Hoffman, Emma; Brand, Harrison; Talkowski, Michael E; Casey, Bradford; Cookson, Mark R; Markham, Androo; Nalls, Mike A; Mahmoud, Medhat; Sedlazeck, Fritz J; Blauwendraat, Cornelis; Gibbs, J Raphael; Singleton, Andrew B

Electrophysiological Characterization of a MYH7 Variant with Tremor Phenotype

MYH7 变异体震颤表型的电生理特征

Vial, Felipe; McGurrin, Patrick; Osterholt, Thomas; Ehrlich, Debra J; Iannacone, Susan T; Donkervoort, Sandra; Neuhaus, Sarah B; Chao, Katherine C; Bönnemann, Carsten G; Haubenberger, Dietrich; Hallett, Mark

Association of polygenic risk score with response to deep brain stimulation in Parkinson's disease

多基因风险评分与帕金森病深部脑刺激反应的相关性

Yoon, Esther; Ahmed, Sarah; Li, Ryan; Bandres-Ciga, Sara; Blauwendraat, Cornelis; Dustin, Irene; Scholz, Sonja; Hallett, Mark; Ehrlich, Debra

Heterozygous PRKN mutations are common but do not increase the risk of Parkinson's disease.

PRKN 杂合突变很常见,但不会增加患帕金森病的风险

Zhu William, Huang Xiaoping, Yoon Esther, Bandres-Ciga Sara, Blauwendraat Cornelis, Billingsley Kimberly J, Cade Joshua H, Wu Beverly P, Williams Victoria H, Schindler Alice B, Brooks Janet, Gibbs J Raphael, Hernandez Dena G, Ehrlich Debra, Singleton Andrew B, Narendra Derek P