Effective housing and support models for people with Huntington's disease: A scoping review [0.03%]
亨廷顿病患者的高效住房与支持模式：一项概要性综述
Lee Cubis,Elise Davis,Sharyn McDonald et al.
Lee Cubis et al.
BackgroundPeople with Huntington's disease (HD) experience physical, cognitive, and psychiatric manifestations that can result in housing in settings that are inappropriate for care requirements.ObjectiveThe aim of this scoping review was t...
Isometric force matching in the TRACK-HD study - a novel quantitative assessment for clinical applications? [0.03%]
TRACK-HD研究中的等轴力匹配-一种新型的定量评估方法用于临床应用吗？
Robin Schubert,Pascal Barallon,Benjamin Habbel et al.
Robin Schubert et al.
BackgroundHuntington's disease is a rare, progressive, neurodegenerative disease. Capturing symptomatic progression and treatment effects reliably in clinical therapeutic trials has shown to be a challenging task, facing the problem of smal...
Reply to: In Response to Fuller et al., Functional Rating Scale 2.0 (FuRST 2.0): A patient-reported outcome measure of function for Huntington's disease [0.03%]
FuRST 2.0量表（ FuRST 2.0：亨廷顿病的功能预后评估量表）回复富勒等人的文章
Neha Sinha,Rebecca Lm Fuller,Glenn T Stebbins
Neha Sinha
Mapping the landscape of caregiver burden in Huntington's Disease: Current evidence and future directions [0.03%]
亨廷顿病照料负担研究现状及未来方向展望
Katerina Poprelka,Theodoros Fasilis,Panayiotis Patrikelis et al.
Katerina Poprelka et al.
IntroductionHuntington's Disease (HD) is a rare neurodegenerative disease that profoundly affects both individuals diagnosed with the condition and their caregivers. This review aims to examine the burden experienced by informal caregivers ...
Letter in response to Fuller et al., Functional Rating Scale 2.0 (FuRST 2.0): A patient-reported outcome measure of function for Huntington's disease [0.03%]
富尔尔等人关于功能性评分量表2.0（ FuRST 2.0）的来信：亨廷顿病的功能患者报告结局测量工具
Brett L Kinsler,Chad Heatwole
Brett L Kinsler
Tipping the PARylation scale: Dysregulation of PAR signaling in Huntington and neurodegenerative diseases [0.03%]
调控PAR修饰平衡的天平：亨廷顿病及其他神经退行性疾病中PAR信号转导异常
Christina Peng,Tamara Maiuri,Ray Truant
Christina Peng
Poly(ADP-ribosyl)ation (PARylation), a crucial post-translational modification, is catalyzed by ADP-ribosyltransferases (ARTs) and has significant implications in various cellular processes, including DNA damage response, cell signaling, an...
Understanding the relationship between patient-reported outcome measures, clinician-rated assessments, and performance-based measures (cognitive tests and device-based estimates) of symptoms and functioning in people with Huntington's disease [0.03%]
了解患者报告结果测量、临床医生评估和基于表现的测量（认知测试和设备估算）在亨廷顿病患者中症状和功能之间的关系
Noelle E Carlozzi,Jonathan P Troost,Wendy L Lombard et al.
Noelle E Carlozzi et al.
BackgroundGiven the progressive cognitive decline in Huntington's disease (HD), most research in this population relies solely on objective assessments of symptoms and function, rather than on patient-reported outcome (PRO) measures.Objecti...
Abnormal neurodevelopment predisposes to cortical hyperexcitability in Huntington's disease [0.03%]
神经发育异常易患亨廷顿舞蹈病皮质高兴奋性
Carlos Cepeda,Joshua Barry,Sandra M Holley
Carlos Cepeda
Accumulating morphological and electrophysiological evidence demonstrates that abnormal brain development is a key element in the progression of Huntington's disease (HD). Mutant huntingtin affects corticogenesis, cell migration, and differ...
Preface by the Editors-in-Chief [0.03%]
主编前言
Blair R Leavitt,Leslie M Thompson
Blair R Leavitt