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期刊名:Journal of huntingtons disease

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ISSN:1879-6397

e-ISSN:1879-6400

IF/分区:2.7/Q3

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共收录本刊相关文章索引495条
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Malin Sixt Börjesson,Mathias Hall,Elisabeth Winnberg Malin Sixt Börjesson
BackgroundIn the International guidelines for nutrition in Huntington's disease (HD) PEG-tubes may be considered in persons with HD (pwHD) with severe swallowing difficulties, but there are no general recommendations for when to initiate PE...
Tamine Tc Capato,Jorik Nonnekes,Jordache Ramjith et al. Tamine Tc Capato et al.
BackgroundBalance impairments in Huntington's Disease (HD) are common but difficult to treat.ObjectivesWe aimed to investigate the potential effects and feasibility of multimodal physiotherapy balance intervention in HD.MethodIn this prospe...
Beatriz Paiva,Ana Cristina Rego Beatriz Paiva
Emerging evidence suggests a central and early role of mitochondrial dysfunction, including altered mitochondrial dynamics, in Huntington's disease (HD) pathogenesis. Processes such as mitochondrial fission, fusion, transport and mitophagy ...
Michael G Friedrich,Gabrielle R Phillips,Reuben Se Young et al. Michael G Friedrich et al.
Huntington's disease (HD) is a fatal neurodegenerative disease caused by a CAG repeat expansion in the Huntingtin gene (HTT). While classically considered a disease of grey matter, recent imaging data have revealed presymptomatic abnormalit...
Vy Le,Edith Sigler,Jonathan Liu et al. Vy Le et al.
Following an abrupt medication switch from olanzapine to aripiprazole, a 61-year-old female with Huntington's disease developed psychosis that persisted despite olanzapine reinstitution. Subsequent hospitalization led to significant complic...
Lidia Gaffke,Estera Rintz,Magdalena Podlacha et al. Lidia Gaffke et al.
BackgroundRecent reports indicated that 4',5,7-trihydroxyisoflavone (genistein) can improve biochemical disorders and correct behavioral disturbances in cellular and animal models of Huntington's disease (HD), acting thorough stimulation of...
Lubna M Abu Zohair,Ruben Andriessen,Noor Mahmoud et al. Lubna M Abu Zohair et al.
Understanding the trajectory of Huntington's disease (HD) is critical for patient stratification and the development of targeted interventions. Traditionally, studies relied on age-CAG models to estimate disease onset and progression, based...
Erin Furr Stimming,Jee Bang,Amy Brown et al. Erin Furr Stimming et al.
Huntington's disease (HD) is a rare, autosomal dominant neurodegenerative disorder caused by a pathogenic CAG expansion in the huntingtin gene, classically characterized by a triad of cognitive, psychiatric, and motor symptoms. Involuntary ...
Andreas A Braun,Jonas Buff,Nora-Hjördis Moser et al. Andreas A Braun et al.
BackgroundSleep disturbances, including fragmentation and reduced slow-wave sleep (SWS), are common in Huntington's disease (HD). SWS contributes to synaptic homeostasis, metabolic clearance, and memory consolidation. Phase-targeted auditor...