Observing Huntington's Disease: the European Huntington's Disease Network's REGISTRY - Wikidata - awgldk - TriplyDB

Observing Huntington's Disease: the European Huntington's Disease Network's REGISTRY

Observing Huntington's Disease: the European Huntington's Disease Network's REGISTRY

http://www.wikidata.org/entity/Q24598264

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Utilisation of Healthcare and Associated Services in Huntington's disease: a data mining study NMDA receptor gene variations as modifiers in Huntington disease: a replication study Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onset.Copy-number variation of the neuronal glucose transporter gene SLC2A3 and age of onset in Huntington's disease.Neuropsychiatric Burden in Huntington's Disease.RD-Connect: an integrated platform connecting databases, registries, biobanks and clinical bioinformatics for rare disease research.Use of Tetrabenazine in Huntington Disease Patients on Antidepressants or with Advanced Disease: Results from the TETRA-HD Study.Fetal striatal grafting slows motor and cognitive decline of Huntington's disease.Current Pharmacological Management in Juvenile Huntington's Disease.TOSCA - first international registry to address knowledge gaps in the natural history and management of tuberous sclerosis complex.The Q175 mouse model of Huntington's disease shows gene dosage- and age-related decline in circadian rhythms of activity and sleep.An exploratory double-blind, randomized clinical trial with selisistat, a SirT1 inhibitor, in patients with Huntington's disease.Identification of Genetic Factors that Modify Clinical Onset of Huntington's Disease.The personal experience of parenting a child with juvenile Huntington's disease: perceptions across Europe.Unified Huntington's disease rating scale for advanced patients: validation and follow-up study.The societal cost of Huntington's disease: are we underestimating the burden?Managing juvenile Huntington's disease.Health-related quality of life and unmet healthcare needs in Huntington's disease.Indirect tolerability comparison of Deutetrabenazine and Tetrabenazine for Huntington disease More alive than dead: non-apoptotic roles for caspases in neuronal development, plasticity and disease.Juvenile Huntington's Disease: Diagnostic and Treatment Considerations for the Psychiatrist.Psychiatric comorbidities in movement disorders.2016 William Allan Award: Human Disease Research: Genetic Cycling and Re-cycling.Quantification of huntingtin protein species in Huntington's disease patient leukocytes using optimised electrochemiluminescence immunoassays.Population-specific genetic modification of Huntington's disease in Venezuela.A Data-Driven Method for Generating Robust Symptom Onset Indicators in Huntington's Disease Registry Data.

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Observing Huntington's Disease: the European Huntington's Disease Network's REGISTRY

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Observing Huntington's Disease: the European Huntington's Disease Network's REGISTRY

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Aileen K Ho

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Carsten Schwenke

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P2860

European population substructure: clustering of northern and southern populations

A rating scale for depression

The Measurement of Observer Agreement for Categorical Data

An Inventory for Measuring Depression

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

A simple salting out procedure for extracting DNA from human nucleated cells

Huntington's disease

Trinucleotide Repeat Disorders

The nosological position of apathy in clinical practice.

The likelihood of being affected with Huntington disease by a particular age, for a specific CAG size

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10.1371/CURRENTS.RRN1184

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Sarah J. Tabrizi

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Huntington disease

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