A randomized, placebo-controlled trial of latrepirdine in Huntington disease.
about
The importance of integrating basic and clinical research toward the development of new therapies for Huntington diseaseA review on mitochondrial restorative mechanism of antioxidants in Alzheimer's disease and other neurological conditionsTreatment of Huntington's disease.The rise and fall of Dimebon.Current Pharmacological Approaches to Reduce Chorea in Huntington's Disease.Preclinical study of dimebon on β-amyloid-mediated neuropathology in Alzheimer's diseaseRuthenium-catalyzed γ-carbolinium ion formation from aryl azides; synthesis of dimebolin.Mitochondria and antioxidant targeted therapeutic strategies for Alzheimer's disease.The acute effects of dimebolin, a potential Alzheimer's disease treatment, on working memory in rhesus monkeysMutant huntingtin, abnormal mitochondrial dynamics, defective axonal transport of mitochondria, and selective synaptic degeneration in Huntington's diseaseDimebon slows progression of proteinopathy in γ-synuclein transgenic mice.Video Rating in Neurodegenerative Disease Clinical Trials: The Experience of PRION-1.Dimebon alters hippocampal amyloid pathology in 3xTg-AD mice.Latrepirdine stimulates autophagy and reduces accumulation of α-synuclein in cells and in mouse brain.Intermediate CAG Repeats in Huntington's Disease: Analysis of COHORT.Latrepirdine improves cognition and arrests progression of neuropathology in an Alzheimer's mouse model.Neuronal calcium signaling, mitochondrial dysfunction, and Alzheimer's disease.5-hydroxytryptamine subtype 6 receptor modulators: a patent survey.The clinical and genetic features of Huntington disease.Pharmacologic approaches to the treatment of Huntington's disease.Mitochondrial dysfunction--a pharmacological target in Alzheimer's disease.Latrepirdine: molecular mechanisms underlying potential therapeutic roles in Alzheimer's and other neurodegenerative diseasesThe most appropriate primary outcomes to design clinical trials on Huntington's disease: meta-analyses of cohort studies and randomized placebo-controlled trials.Corticostriatal circuit dysfunction in Huntington's disease: intersection of glutamate, dopamine and calcium.Dimebon does not ameliorate pathological changes caused by expression of truncated (1-120) human alpha-synuclein in dopaminergic neurons of transgenic mice.Discovery of Therapeutic Approaches for Polyglutamine Diseases: A Summary of Recent Efforts.Huntington's Disease: Mechanisms of Pathogenesis and Therapeutic Strategies.The gramine route to pyrido[4,3-b]indol-3-ones - identification of a new cytotoxic lead.Latrepirdine (dimebon) enhances autophagy and reduces intracellular GFP-Aβ42 levels in yeast.The impact of oculomotor functioning on neuropsychological performance in Huntington disease.Rating scales for cognition in Huntington's disease: Critique and recommendations.Rating Scales and Performance-based Measures for Assessment of Functional Ability in Huntington's Disease: Critique and Recommendations
P2860
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P2860
A randomized, placebo-controlled trial of latrepirdine in Huntington disease.
description
2010 nî lūn-bûn
@nan
2010 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
A randomized, placebo-controlled trial of latrepirdine in Huntington disease.
@ast
A randomized, placebo-controlled trial of latrepirdine in Huntington disease.
@en
type
label
A randomized, placebo-controlled trial of latrepirdine in Huntington disease.
@ast
A randomized, placebo-controlled trial of latrepirdine in Huntington disease.
@en
prefLabel
A randomized, placebo-controlled trial of latrepirdine in Huntington disease.
@ast
A randomized, placebo-controlled trial of latrepirdine in Huntington disease.
@en
P2093
P2860
P50
P1433
P1476
A randomized, placebo-controlled trial of latrepirdine in Huntington disease.
@en
P2093
Andrew Feigin
Bernard Ravina
Dimebon in Subjects with Hunti ...... of the Huntington Study Group
E Ray Dorsey
Elise Kayson
Francis Walker
Huntington Disease Study Group DIMOND Investigators
Jody Corey-Bloom
Karen Hodgeman
Karen Rabinowitz
P2860
P304
P356
10.1001/ARCHNEUROL.2009.334
P577
2010-02-01T00:00:00Z