Incidental Resolution of Dopamine Agonist Induced Impulse Control Disorder with GLP-1 Receptor Agonist [0.03%]
GLP-1受体激动剂意外缓解多巴胺激动剂诱导的冲动控制障碍
Hannah Kelly,Thomas Davis
Hannah Kelly
Case Reports
Movement disorders clinical practice. 2026 Jun 8. DOI:10.1002/mdc3.70704 2026
Bradley Lonergan,Peter Miller,Elisabete Marques et al.
Bradley Lonergan et al.
Quality and Readability of ChatGPT Performance on Parkinson's Disease [0.03%]
ChatGPT在帕金森病方面的表现质量与可读性
Gabriele Riccio,Rosa Coppola,Maria Rosaria Chiariello et al.
Gabriele Riccio et al.
Background: Chat Generative Pre-trained Transformer (ChatGPT) is increasingly used for medical education and healthcare counseling. Objective: ...
Pablo Rábano-Suárez,Álvaro Sánchez-Ferro,Ana Arteche-López et al.
Pablo Rábano-Suárez et al.
Case Reports
Movement disorders clinical practice. 2026 Jun 6. DOI:10.1002/mdc3.70701 2026
Tracking Genetic Parkinson's Disease with Molecular Imaging: A Systematic Review [0.03%]
基于分子影像的遗传性帕金森病系统评价研究
Chiara Meneghini,Luca Gallo,Arianna Sala et al.
Chiara Meneghini et al.
Background: Parkinson's disease (PD) is a worldwide, complex neurodegenerative disorder influenced by both genetic and environmental factors. Around 15-20% of PD cases are linked to genetic mutations, providing insights i...
Movement Disorders and Cerebellar Syndromes Associated with Mycoplasma pneumoniae Infection: A Systematic Review [0.03%]
与支原体感染相关的锥体系外症和小脑综合征：一项系统评价研究
Ravindra Kumar Garg,Shweta Pandey,Amita Jain et al.
Ravindra Kumar Garg et al.
Background: Mycoplasma pneumoniae is a well-recognized respiratory pathogen increasingly associated with diverse neurological manifestations beyond pulmonary disease involvement. ...
The m.14484T>C MT-ND6 Mutation Presenting with a Hereditary Spastic-Paraparesis Phenotype [0.03%]
线粒体DNA m14484T>C突变导致的遗传性痉挛性截瘫综合征一例报告
Gabriel Amorelli,Christelle Nilles,Gerald Pfeffer et al.
Gabriel Amorelli et al.
Atypical Atypical MECP2-Related Rett Syndrome Presenting with Movement Disorders- Predominating Phenotype [0.03%]
以运动障碍为主的非典型MECP2相关雷特综合征临床表型
Ján Necpál,Paula Stretavská,Elisabetta Indelicato et al.
Ján Necpál et al.
Background: Rett syndrome (RTT) is an X-linked neurodevelopmental disorder characterized by a typical natural history, including early stagnation, rapid regression, a pseudostationary phase, and late motor deterioration. ...
Case Reports
Movement disorders clinical practice. 2026 Jun 2. DOI:10.1002/mdc3.70697 2026
Apathy in Parkinson's Disease: Distinguishing Overlapping Symptoms Via Network Analysis [0.03%]
基于网络分析区分帕金森病中重叠症状中的淡漠症候群
Joseph Seemiller,Abhimanyu Mahajan,Christopher B Morrow et al.
Joseph Seemiller et al.
Background: Anxiety, fatigue, and excessive daytime sleepiness (EDS) frequently co-occur in Parkinson's disease (PD) and can influence the clinical determination of apathy. ...
Psychometric Evidence for an Augmented PDAQ for Improved Measurement of Cognition-Related IADLs in Parkinson's Disease [0.03%]
帕金森病中与认知相关的一般日常活动的心理测量学证据增强的PDAQ量表
Antoine Regnault,Laure Delbecque,Manal M&#x;Hari et al.
Antoine Regnault et al.
Background: The Penn Parkinson's Daily Activities Questionnaire-27 (PDAQ-27) is a 27-item measure of cognitive instrumental activities of daily living (IADLs) for Parkinson's disease (PD) patients developed by integrating...