Search Results - "Reilmann, Ralf"
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Predictors of phenotypic progression and disease onset in premanifest and early-stage Huntington's disease in the TRACK-HD study: analysis of 36-month observational data
Published in Lancet neurology (01-07-2013)“…Summary Background TRACK-HD is a multinational prospective observational study of Huntington's disease (HD) that examines clinical and biological findings of…”
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Huntington's disease: Current and future therapeutic prospects
Published in Movement disorders (01-07-2018)“…ABSTRACT Huntington's disease is a progressive neurodegenerative disorder for which therapies are woefully inadequate and do not prevent inevitable…”
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Biological and clinical changes in premanifest and early stage Huntington's disease in the TRACK-HD study: the 12-month longitudinal analysis
Published in Lancet neurology (2011)“…Summary Background TRACK-HD is a prospective observational study of Huntington's disease (HD) that examines disease progression in premanifest individuals…”
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Huntington disease: natural history, biomarkers and prospects for therapeutics
Published in Nature reviews. Neurology (01-04-2014)“…Key Points No disease-modifying treatments are currently available for Huntington disease (HD), but clinical trials of potential compounds are imminent;…”
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Potential endpoints for clinical trials in premanifest and early Huntington's disease in the TRACK-HD study: analysis of 24 month observational data
Published in Lancet neurology (2012)“…Summary Background TRACK-HD is a prospective observational biomarker study in premanifest and early Huntington's disease (HD). In this report we define a…”
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Effects of age and sex on outcomes of the Q-Motor speeded finger tapping and grasping and lifting tests-findings from the population-based BiDirect Study
Published in Frontiers in neurology (30-09-2022)“…Background Q-Motor is a suite of motor tests originally designed to assess motor symptoms in Huntington's disease. Among others, Q-Motor encompasses a finger…”
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Biological and clinical manifestations of Huntington's disease in the longitudinal TRACK-HD study: cross-sectional analysis of baseline data
Published in Lancet neurology (01-09-2009)“…Summary Background Huntington's disease (HD) is an autosomal dominant, fully penetrant, neurodegenerative disease that most commonly affects adults in…”
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Gait variability as digital biomarker of disease severity in Huntington’s disease
Published in Journal of neurology (01-06-2020)“…Background Impaired gait plays an important role for quality of life in patients with Huntington’s disease (HD). Measuring objective gait parameters in HD…”
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International Guidelines for the Treatment of Huntington's Disease
Published in Frontiers in neurology (2019)“…The European Huntington's Disease Network (EHDN) commissioned an international task force to provide global evidence-based recommendations for everyday…”
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Cognitive decline in Huntington's disease in the Digitalized Arithmetic Task (DAT)
Published in PloS one (23-08-2021)“…Efficient cognitive tasks sensitive to longitudinal deterioration in small cohorts of Huntington's disease (HD) patients are lacking in HD research. We thus…”
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Pridopidine for the treatment of motor function in patients with Huntington's disease (MermaiHD): a phase 3, randomised, double-blind, placebo-controlled trial
Published in Lancet neurology (01-12-2011)“…Summary Background Huntington's disease is a progressive neurodegenerative disorder, characterised by motor, cognitive, and behavioural deficits. Pridopidine…”
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Digitomotography in Parkinson's disease: a cross-sectional and longitudinal study
Published in PloS one (22-04-2015)“…Motor symptoms in Parkinson's disease (PD) are usually assessed with semi-quantitative tests such as the Unified PD Rating Scale (UPDRS) which are limited by…”
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Behavioral testing of minipigs transgenic for the Huntington gene-A three-year observational study
Published in PloS one (09-10-2017)“…Large animal models of Huntington's disease (HD) may increase the reliability of translating preclinical findings to humans. Long live expectancy offers…”
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Objectively characterizing Huntington’s disease using a novel upper limb dexterity test
Published in Journal of neurology (01-07-2021)“…Background The Clinch Token Transfer Test (C3t) is a bi-manual coin transfer task that incorporates cognitive tasks to add complexity. This study explored the…”
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Evaluation of walking activity and gait to identify physical and mental fatigue in neurodegenerative and immune disorders: preliminary insights from the IDEA-FAST feasibility study
Published in Journal of neuroengineering and rehabilitation (05-06-2024)“…Many individuals with neurodegenerative (NDD) and immune-mediated inflammatory disorders (IMID) experience debilitating fatigue. Currently, assessments of…”
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Multifeature quantitative motor assessment of upper limb ataxia including drawing and reaching
Published in Annals of clinical and translational neurology (01-05-2024)“…Objective Voluntary upper limb movements are an ecologically important yet insufficiently explored digital‐motor outcome domain for trials in degenerative…”
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Correction to: Gait variability as digital biomarker of disease severity in Huntington’s disease
Published in Journal of neurology (01-06-2020)“…The original version of this article unfortunately contained a mistake. The name of one author is not presented correctly in the author group…”
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Assessing fatigue and sleep in chronic diseases using physiological signals from wearables: A pilot study
Published in Frontiers in physiology (14-11-2022)“…Problems with fatigue and sleep are highly prevalent in patients with chronic diseases and often rated among the most disabling symptoms, impairing their…”
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Compensation in Preclinical Huntington's Disease: Evidence From the Track-On HD Study
Published in EBioMedicine (01-10-2015)“…Cognitive and motor task performance in premanifest Huntington's disease (HD) gene-carriers is often within normal ranges prior to clinical diagnosis, despite…”
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Symptomatic treatment options for Huntington’s disease (guidelines of the German Neurological Society)
Published in Neurological research and practice (16-11-2023)“…Abstract Introduction Ameliorating symptoms and signs of Huntington’s disease (HD) is essential to care but can be challenging and hard to achieve. The…”
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