Cognitive impairment in Huntington disease: diagnosis and treatment. - Wikidata - awgldk - TriplyDB

Cognitive impairment in Huntington disease: diagnosis and treatment.

Cognitive impairment in Huntington disease: diagnosis and treatment.

http://www.wikidata.org/entity/Q36773397

about

Mood disorders in Huntington's disease: from behavior to cellular and molecular mechanisms Huntingtin is critical both pre- and postsynaptically for long-term learning-related synaptic plasticity in Aplysia Cholinesterase inhibitors for rarer dementias associated with neurological conditions Cholinesterase inhibitors for neurological conditions associated with rarer dementias Treatment of Huntington's disease.Maintenance of basal levels of autophagy in Huntington's disease mouse models displaying metabolic dysfunction Deep Brain Stimulation in Huntington's Disease-Preliminary Evidence on Pathophysiology, Efficacy and Safety Mass Spectrometry-Based Approaches to Understand the Molecular Basis of Memory A two years longitudinal study of a transgenic Huntington disease monkey.Longitudinal Psychiatric Symptoms in Prodromal Huntington's Disease: A Decade of Data.Psychiatric Aspects of Dementia.Neural correlates of impaired emotion processing in manifest Huntington's disease.Participants', caregivers', and professionals' experiences with a group-based rehabilitation program for Huntington's disease: a qualitative study.Onset of Huntington's disease: can it be purely cognitive?Current Pharmacological Approaches to Reduce Chorea in Huntington's Disease.Everyday cognition in prodromal Huntington disease Functional connectivity modeling of consistent cortico-striatal degeneration in Huntington's disease.NIH EXAMINER: conceptualization and development of an executive function battery.Medication Use in Early-HD Participants in Track-HD: an Investigation of its Effects on Clinical Performance Delayed identification and diagnosis of Huntington's disease due to psychiatric symptoms.Brain metabolite alterations and cognitive dysfunction in early Huntington's disease.Unmet needs for healthcare and social support services in patients with Huntington's disease: a cross-sectional population-based study Quality of Life of Cypriot Patients Suffering with Huntington's Disease.The BACHD Rat Model of Huntington Disease Shows Signs of Fronto-Striatal Dysfunction in Two Operant Conditioning Tests of Short-Term Memory.Multivariate prediction of motor diagnosis in Huntington's disease: 12 years of PREDICT-HD Translational research in Huntington's disease: opening up for disease modifying treatment Effect of mesenchymal stem cell transplantation on brain-derived neurotrophic factor expression in rats with Tourette syndrome.Cognitive decline in prodromal Huntington Disease: implications for clinical trials.Patterns of Co-Occurring Gray Matter Concentration Loss across the Huntington Disease Prodrome.Problem solving, impulse control and planning in patients with early- and late-stage Huntington's disease A review of quality of life after predictive testing for and earlier identification of neurodegenerative diseases.Unified Huntington's disease rating scale for advanced patients: validation and follow-up study.Assistive Technology for Cognition and Health-related Quality of Life in Huntington's Disease.Effects of a One Year Intensive Multidisciplinary Rehabilitation Program for Patients with Huntington's Disease: a Prospective Intervention Study.Beyond and below the cortex: the contribution of striatal dysfunction to cognition and behaviour in neurodegeneration.The cognitive burden in Huntington's disease: pathology, phenotype, and mechanisms of compensation.Reassessing models of basal ganglia function and dysfunction.Animal models of Huntington's disease for translation to the clinic: best practices.Practice Effects and Stability of Neuropsychological and UHDRS Tests Over Short Retest Intervals in Huntington Disease.The Complexity of Clinical Huntington's Disease: Developments in Molecular Genetics, Neuropathology and Neuroimaging Biomarkers.

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P2860

Cognitive impairment in Huntington disease: diagnosis and treatment.

http://www.wikidata.org/entity/Q36773397

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Cognitive impairment in Huntington disease: diagnosis and treatment.

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Current Neurology and Neuroscience Reports

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Cognitive impairment in Huntington disease: diagnosis and treatment.

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P2860

Huntington's disease: a clinical review.

Therapeutic interventions for disease progression in Huntington's disease

Brain imaging and cognitive dysfunctions in Huntington's disease

An item response analysis of the motor and behavioral subscales of the unified Huntington's disease rating scale in huntington disease gene expansion carriers

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

Self-paced timing detects and tracks change in prodromal Huntington disease.

Longitudinal change in regional brain volumes in prodromal Huntington disease

Start/stop signals emerge in nigrostriatal circuits during sequence learning

Development of the Huntington disease family concerns and strategies survey from focus group data

Huntington's disease: from molecular pathogenesis to clinical treatment.

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