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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492
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
Katharine Huynh,Nellie Georgiou-Karistianis,Amit Lampit et al. Katharine Huynh et al.
BackgroundComputerized cognitive training (CCT) has been found to improve cognition by altering functional activity and functional connectivity of brain networks in people with and without cognitive impairment. The effects of CCT on functio...
Mena Farag,Sarah J Tabrizi,Edward J Wild Mena Farag
In this edition of the Huntington's Disease Clinical Trials Update, we expand on the launch of the phase II/III clinical trial of SKY-0515 from Skyhawk Therapeutics and the phase I/II clinical trial of SPK-10001 from Spark Therapeutics. We ...
Mallory R Shin,Marco M Hefti Mallory R Shin
Huntington's disease (HD) is classically characterized as a late-onset neurodegenerative disorder of adulthood caused by CAG expansion in the HTT gene. However, mounting evidence from both human and experimental studies suggests that both w...
Jordan L Schultz,Peg C Nopoulos Jordan L Schultz
Recent findings suggest that neurodevelopment plays a critical role in Huntington's Disease (HD) pathogenesis. This review integrates data from human studies of children and young adults at risk for HD (the Kids-HD study) with the theory of...
Nicolò Zarotti,Alice Storey,Sarah Lloyd et al. Nicolò Zarotti et al.
BackgroundDeficits of emotion recognition have received increasing attention in people with Huntington's disease (HD) in the three decades since the discovery of the HD gene. However, the characterisation of such deficits across different d...
Gianna M Fote,Nicolette R McClure,Robert M Bragg et al. Gianna M Fote et al.
BackgroundThe HTT protein, mutated in Huntington's disease, is expressed throughout the body, and loss of HTT function as an autophagic scaffold may affect tissues and cellular processes. These processes include lipid metabolism potentially...
Behnaz Nateghi,Mohamed Lala Bouali,Zineb Bouredji et al. Behnaz Nateghi et al.
Background: Huntington's disease (HD) is a progressive neurodegenerative disorder primarily affecting the central nervous system (CNS). However, emerging evidence suggests that peripheral tissues, including skeletal muscle and bone, also un...
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...
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...