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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486
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
Jessica Y Winder,Wilco P Achterberg,Raymund A C Roos Jessica Y Winder
Background: Huntington's disease is a progressive, incurable neurodegenerative disorder and it is not possible to delay onset or progression of the disease. Consequently, the disease leads to functional decline and loss o...
Lorena Rieke,Robin Schubert,Tamara Matheis et al. Lorena Rieke et al.
Background: Large animal models, such as the transgenic (tg) Huntington disease (HD) minipig, have been proposed to improve translational reliability and assessment of safety, efficacy and tolerability in preclinical stud...
Rebecca A G De Souza,Natalia Kosior,Sarah B Thomson et al. Rebecca A G De Souza et al.
Background: Huntington's disease is a late onset neurological disorder caused by a trinucleotide CAG repeat expansion mutation in the HTT gene encoding for the protein huntingtin. Despite considerable ongoing research, th...
Paul McNulty,Richard Pilcher,Raviram Ramesh et al. Paul McNulty et al.
Background: People with Huntington's disease (HD) have been observed to have lower rates of cancers. Objective: To investigate the rela...
Melissa Wesson,Nicholas R Boileau,Joel S Perlmutter et al. Melissa Wesson et al.
Background: Huntington disease (HD) is associated with increased risk of suicide. Objective: This study compares suicide ideation in HD...
Karen E Anderson,Erik van Duijn,David Craufurd et al. Karen E Anderson et al.
Background: In clinical practice, several strategies and pharmacological options are available to treat neuropsychiatric symptoms of Huntington disease (HD). However, there is currently insufficient data for evidence-base...
Morgane Sonia Thion,Sandrine Humbert Morgane Sonia Thion
Huntingtin (HTT) is a scaffold protein mostly known because it gives rise to the severe and incurable inherited neurological disorder Huntington's disease (HD) when mutated. The Huntingtin gene (HTT) carries a polymorphic trinucleotide expa...
Jan Kobal,Kolenc Matej,Matic Koželj et al. Jan Kobal et al.
Background: Huntington's disease (HD) patients often report anorectal dysfunction; however, in HD research no detailed analysis of these complaints has been published. ...
Lindsay Romo,Emily S Mohn,Neil Aronin Lindsay Romo
Huntington's disease (HD) is an inherited neurodegenerative disorder caused by a mutation that expands the polyglutamine (CAG) repeat in exon 1 of the huntingtin (HTT) gene. Wild-type HTT protein interacts with other proteins to protect cel...
Ruth Veenhuizen,Hanneke Nijsten,Paul van Roosmalen et al. Ruth Veenhuizen et al.
Huntington's disease (HD) patients and families deserve expert treatment and care throughout their lives, but uniformity in functional diagnosis and treatment was lacking. In the aim of reaching this uniformity on day-to-day treatment and c...