What researchers published on Huntington's disease
735 papers, newest first.
Showing 200 of 735
Superpixel-ComBat multi-site harmonization of unpaired T1W MRI data in Huntington's disease.Neuroimage. Reports
ReviewMiro1 and mitochondrial dysfunction in Huntington's disease: Emerging mechanistic links and therapeutic perspectives.Mitochondrion
Qualitative insights from partners of individuals with Huntington's disease: the quality of life of an under-researched population.Orphanet journal of rare diseases
Primer site variations resulting in false-negative Huntington's disease testing.Journal of medical genetics
Isozyme-Specific Inhibition of GSK-3 Reveals Distinct Cellular Responses in Huntington's Disease Fibroblasts.Journal of neurochemistry
The SorCS2-derived macrocycle TT-P34 drives neuroprotection in animal models of neurodegeneration.Acta neuropathologica communications
ReviewThe hepatic secretome-microglia axis in huntington's disease: Linking peripheral metabolic dysfunction to neuroinflammation and novel therapeutic opportunities.Metabolic brain disease
In vivo assessment of brain microstructure in patients with Huntington's disease using quantitative MRI.Journal of neurology
NeuroD1-induced fate conversion partially restores GABAergic neuronal identity in Huntington's disease.Molecular therapy : the journal of the American Society of Gene Therapy
Forecasting and Dynamics of Huntington's disease: A Machine Learning approach for Fractional-Order Mathematical Model.Journal of advanced research
The Treatment of Psychiatric Symptoms in Huntington's Disease: A Systematic Review.Current neuropharmacology
Rhes as a Potential Modulator of PINK1/Parkin-Dependent Mitophagy in Huntington's Disease.Journal of integrative neuroscience
The postsynaptic scaffolding protein SAPAP3 shapes mitochondrial activity: the case of Huntington's disease.Cell death & disease
Cell-specific transcription dysregulation in human Huntington's disease-positive developing striatum.Brain : a journal of neurology
Bioinformatics Analysis to Reveal Potential Targets of Huntington's Disease.IET systems biology
CSF Leukocytes Transiently Increase Before Onset of Huntington Disease in Association With a Stage-Specific CSF Cytokine/Chemokine Pattern.Neurology(R) neuroimmunology & neuroinflammation
Computational modeling and preclinical evaluation support targeting somatic instability for Huntington's disease treatment.Nature communications
Somatic DNA-repeat expansions initiate distinct yet analogous changes in Huntington's disease cortical and striatal neurons.Cell
Multimodal spatial transcriptomics redefines cortical pathology in Huntington's disease.Cell
ReviewNeuroprotective roles of Klotho signaling in Huntington's disease: From molecular insights to clinical translation.IBRO neuroscience reports
Early Administration of Methylene Blue Attenuates Mitochondrial Dysfunction and Cognitive Deficits in a Model of Huntington's Disease.Biology
Should Huntington's Disease Remains the First Genetic Consideration in Adults Presenting with Combined Chorea and Ataxia in Resource-Limited Settings?Movement disorders clinical practice
Quantifying multidisciplinary collaboration in Huntington's disease before and after service redesign: a social network analysis.BMC health services research
HD-DRUM Rhythmic Training in Huntington's Disease: Feasibility, Motor, and Brain Microstructural Pilot Signals.Movement disorders clinical practice
PreprintCerebrospinal Fluid Myeloperoxidase Is Associated With Putamen Volume Beyond Neurofilament Light in Huntington's Disease.medRxiv : the preprint server for health sciences
Randomised trialAntidopaminergic Medications and Clinical Outcomes in Huntington Disease: Evidence From the PROOF-HD Placebo-Controlled Trial.Neurology
In plain wordsRead moreRead the paper on PubMedHealthcare trajectories diverge years before Huntington disease is recorded in claims: a nationwide French matched cohort study.Journal of neurology, neurosurgery, and psychiatry
Emotion regulation difficulties are selectively associated with executive and behavioural apathy in Huntington's disease.Journal of neurology
Beyond Clinical Outcomes: What Antidopaminergic Medications Teach Us About Causal Inference in Huntington Disease.Neurology
Progenitor transcriptional alterations link fetal and adult pathology in Huntington's disease.Brain : a journal of neurology
ReviewBeyond inherited repeat length: somatic expansions in Huntington disease.Current opinion in genetics & development
Cas9 nickase-mediated contraction of CAG/CTG repeats is associated with phenotypic improvements in a Huntington's disease mouse model.Science translational medicine
ReviewThe potential of AI inspired approaches for patient monitoring in drug development for Huntington's disease: capturing the digital exhaust for activities of daily living.Frontiers in molecular medicine
Autonomic dysfunction in patients with Huntington's disease: Evidence from standardized cardiovascular reflex testing.Journal of Huntington's disease
Huntington's disease clinical trials update: August 2026.Journal of Huntington's disease
ReviewNeuroprotective Role of Withaferin A in Huntington's Disease: Current Evidence and Future Perspectives.Molecular neurobiology
The Power of Two: Combined MSH3/HTT Silencing in Huntington's Disease.Movement disorders : official journal of the Movement Disorder Society
iPSC neurodegenerative disease initiative isogenic CAG repeat iPSC line for Huntington's disease.Journal of Huntington's disease
Attentional emotional bias in Huntington's disease: The "Hyper-Positive" effect.Cognitive, affective & behavioral neuroscience
Neurofilament Light Chain and Mutant Huntingtin Across Huntington's Disease Integrated Staging System Stages in Huntington Disease: A Cross-Sectional Multimodal Analysis.Movement disorders : official journal of the Movement Disorder Society
Recent Advances in Pharmacological Interventions for Huntington's Disease: Evidence from Clinical Translation.Reviews on recent clinical trials
Huntington's disease vasculopathy is barrier-type-selective and arteriolar-dominant with spatially-coupled astrogliosis and reversible by S1pr1 stimulation.Nature communications
Unmasking Huntington Disease: How a Neuropsychiatric Crisis Overcame Cultural Barriers to a Delayed Diagnosis.Clinical case reports
Role of Miro1 in Mitochondrial Dysfunction and Neurodegeneration in Huntington's Disease.Current neurovascular research
Case reportJuvenile Huntington Disease With Cerebellar-Predominant Atrophy Identified by Genome Sequencing.Annals of clinical and translational neurology
Striatal astrocyte μ-crystallin (Crym) loss contributes to early-stage Huntington's disease pathophysiology.Neuron
Plasma Lipid Remodeling across Preclinical Burden, Disease Onset, and Early Motor Severity in Huntington's Disease.Movement disorders : official journal of the Movement Disorder Society
PreprintEffect of Vesicular Monoamine Transporter Type-2 Inhibitors on Motor Features in HD.medRxiv : the preprint server for health sciences
Safety and efficacy of SOM3355 in patients with Huntington's disease (SOMCT03): a phase 2b, randomised, placebo-controlled, multicentre, dose-ranging study.EClinicalMedicine
PreprintDepletion of border-associated macrophages impairs CSF flow and exacerbates extranuclear mutant Huntingtin aggregation in the zQ175DN mouse model of Huntington's disease.bioRxiv : the preprint server for biology
Pellagra encephalopathy in Huntington disease: An autopsy case.Journal of neuropathology and experimental neurology
Joint Analysis for Multivariate Longitudinal and Event Time Data With a Change Point Anchored at Interval-Censored Event Time.Statistics in medicine
Staging disease without illness: ethical issues of the Huntington's Disease Integrated Staging System (HD-ISS).Journal of medical ethics
ReviewMonitoring huntingtin aggregation in Huntington's disease: methods, challenges and future opportunities.Expert review of proteomics
ReviewExtracellular Vesicles and Exosomes as Biomarkers in Huntington's Disease: Uncovering Pathogenic Insights and Pioneering Therapies.Molecular neurobiology
ReviewHope or hype: novel disease-modifying treatments for Huntington disease.Parkinsonism & related disorders
Nationwide survey and epidemiology of Huntington's disease in Hungary.Neuroepidemiology
Lycium barbarum glycopeptide alleviates the neuropathology in Huntington's disease mouse models.Neural regeneration research
ReviewChaperone-mediated remodelling of mutant huntingtin.Philosophical transactions of the Royal Society of London. Series B, Biological sciences
ReviewMechanistic Differences in Adult-Onset and Juvenile-Onset Huntington's Disease and the Potential Role of Neurodevelopment.Cureus
PreprintRestoring Aquaporin-4 alleviates molecular and motor phenotypes in zQ175 mouse model of Huntington's disease.bioRxiv : the preprint server for biology
PreprintComputer vision-aided locomotor behavioral analysis identifies therapeutic motor signatures in a mouse model of Huntington's disease.bioRxiv : the preprint server for biology
Agentic AI for Clinical Outcomes Research, Population Health Management Analyses With Large Administrative Databases, and Generating Epidemiological Estimates of Diseases: Feasibility and Validation Study.Journal of medical Internet research
ReviewZebrafish as an Alternative Animal Model of Huntington's Disease: Challenges and Future Directions.Journal of integrative neuroscience
Development of Antisense Gapmers for the Treatment of Huntington's Disease.Methods in molecular biology (Clifton, N.J.)
Sex-dependent mild cardiac dysfunction and neurometabolic abnormalities in a model of Huntington's disease.Disease models & mechanisms
ReviewEstrogen and progesterone receptor signaling as candidate neuroendocrine modulators in Huntington's disease.Neurodegenerative disease management
Masking phosphatidylserine prevents neuronal loss in two distinct Drosophila models of neurodegeneration.Proceedings of the National Academy of Sciences of the United States of America
Expression of mutant Huntingtin induces proteasomal defects, mitochondrial abnormalities, and cell death in Drosophila muscles.Biochemical and biophysical research communications
ReviewPlanning advanced therapy trials for Huntington's disease: Ethical considerations.Molecular therapy : the journal of the American Society of Gene Therapy
Correction: Remote smartphone-based spoken language screening predicts clinical markers in Huntington's disease.Journal of neural transmission (Vienna, Austria : 1996)
ReviewUncovering hidden protein networks in Huntington's disease: implications for pathogenesis and therapy.Molecular biology reports
Exploring factors that influence meal management and eating behaviours in people living with Huntington's disease.Disability and rehabilitation
ReviewDefective membrane dynamics in Huntington's disease: A role of Rab11 dysfunction.Journal of Huntington's disease
Case reportChorea-predominant SCA5 mimicking Huntington's disease: A case report with a novel SPTBN2 variant.Clinical parkinsonism & related disorders
miR-196a reduces mutant Huntingtin aggregates by Rad23b-mediated degradation in Huntington's disease.Journal of biomedical science
ReviewFluid and Imaging Biomarkers in Huntington's Disease.Current neurology and neuroscience reports
ReviewImaging the glymphatic system in Huntington's disease: The benefits of a multimodal approach and clinical implications.International review of neurobiology
ReviewIndoleamine 2,3-dioxygenase 1 inhibitors: Molecular pharmacology, structural biology and medicinal chemistry with therapeutic perspectives for Huntington's disease.Biochimica et biophysica acta. Proteins and proteomics
uniQure Submits U.S., U.K. Applications for Huntington's Disease Candidate.Human gene therapy
Esketamine for treatment of depression in Huntington's disease: A case report.Journal of Huntington's disease
Meal timing as medicine: clinical evidence for intermittent fasting in Huntington's disease.Nature metabolism
Trial resultEffects of time-restricted eating in early-stage Huntington's disease: a pilot study.Nature metabolism
In plain wordsRead moreRead the paper on PubMedVisualizing Synaptic Disruptions in the Release and Regulation of Dopamine Hotspots in Huntington's Disease.The Journal of neuroscience : the official journal of the Society for Neuroscience
An Atlas of Modifiers of Age at Onset in Huntington's Disease.Current neuropharmacology
Loss of interruption in the HTT CAG repeat is associated with somatic expansion and loss of medium spiny neurons in Huntington's disease.Neuron
Decreased cerebrospinal fluid TNFRSF8 (sCD30) confirmed as a biomarker of Huntington's disease progression.Journal of neurology
The Trail Making Test in healthy controls and Huntington's disease: Demographic effects and normative tables based on a large data set.Psychological assessment
Evaluation of curcumin as an exploratory pharmacological tool for modulating dysregulated molecular pathways in cellular models of Huntington's disease.Molecular biology reports
Neuroimaging Findings in Three Patients with Juvenile Huntington's Disease.AJNR. American journal of neuroradiology
ReviewMicroRNAs in polyglutamine diseases: Mechanistic insights, circulating biomarkers, and emerging microRNA-based therapeutic strategies.Neurobiology of disease
Sesamum indicum-derived valdiate as a novel neuroprotective agent targeting PDE10A2 and SIRT1 in Huntington's disease.Frontiers in bioinformatics
Combining Lycopene, Quercetin, and Poloxamer 188 Therapy Reduces Learning and Memory Deficits in the 3-nitropropionic Acid-induced Rat Model of Huntington's Disease.CNS & neurological disorders drug targets
Identification of Age-Associated Upstream Regulators to Promote Neuronal Resilience in HD Patient-Derived Neurons.Neuroscience bulletin
Targeting Klotho Signaling for Neuroprotection in Huntington's Disease: A Comprehensive Review.Current molecular medicine
Nanotechnological and in vivo characterization of a new generation of brain-permeable nanoparticles for brain-targeted cholesterol delivery in Huntington's disease.International journal of pharmaceutics
Mapping brain volume changes in the zQ175DN mouse model of Huntington's disease: a longitudinal MRI study.Biomarker research
Psychological interventions for individuals affected by Huntington's disease: effects on depression, anxiety, and emotional well-being.Journal of community genetics
Cross-species single-cell atlas of the striatum defines cell-type and subregion disease vulnerabilities.Cell
Multimodal Characterization of Glymphatic-Related Magnetic Resonance Imaging Markers in Huntington's Disease: A Multi-Cohort Retrospective Study.Annals of neurology
Unawareness of motor deficit in Huntington's disease.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Human-specific sequence features in HTT exon 1 promote toxic misprocessing via splicing factor SRSF7.Nature communications
L-theanine from Camellia sinensis (L.) attenuates 3-NP-induced Huntington's disease-like alterations by remedying behavioral patterns and modulating neurotransmitters across three distinct brain regions: evidence from in-vivo and in-silico approaches.Metabolic brain disease
A Cost-Effectiveness Analysis for Treatments of Patients with Early Stage Huntington's Disease in the USA.PharmacoEconomics - open
Case reportEarly Manifestations, Diagnostic Pathways, and Epilepsy in Juvenile-Onset Huntington Disease: A Three-Patient Case Series and Systematic Review.Brain sciences
Early reduction of myelin-associated glycoprotein at myelin membranes in Huntington's disease.Experimental neurology
ReviewRevealing the Mechanisms of Alzheimer's, Parkinson's and Huntington's Diseases Through Invertebrate Models.Biology
Geometric properties of caudate and putamen mark the progression of Huntington's disease.Imaging neuroscience (Cambridge, Mass.)
ReviewThe pathophysiology of depression in Huntington's disease.Neuroscience and biobehavioral reviews
Decoding neuronal vulnerability: Multidimensional analysis of D1R- and D2R- medium-sized spiny neurons in Huntington's disease.Brain pathology (Zurich, Switzerland)
ReviewUnraveling Neurodegeneration: Common Molecular Mechanisms and Novel Therapeutic Concepts in Major Neurodegenerative Disorders.Brain and behavior
A porcine spectral assay library to quantify brain proteome by DIA-MS.Scientific data
Network-based stratification of allele-specific expression reveals patient subgroups in Huntington's disease.Bioinformatics (Oxford, England)
ReviewHuntingtin, signaling endosomes and neuronal survival in health and Huntington disease.Journal of Huntington's disease
ReviewDysfunction of Primary Cilium in Huntington's Disease: How Mutant Huntingtin Disrupts This Cellular Signaling Hub.Biochemistry. Biokhimiia
Systematic reviewThe Role of MicroRNA in Diagnosis of Huntington's Disease: A Systematic Review.Molecular neurobiology
In plain wordsRead moreRead the paper on PubMedIndicators of need and timing of percutaneous endoscopic gastrostomy (PEG) in people with Huntington's disease: A medical chart review study.Journal of Huntington's disease
PreprintTargeted quantification assays for DNA repair and handling proteins and interactions in Huntington's disease models.bioRxiv : the preprint server for biology
Intracerebroventricular Administration of Gangliosides for In Vivo Functional Studies in Mice.Methods in molecular biology (Clifton, N.J.)
ReviewThe potential of vitamins in Huntington's disease: bridging mechanistic evidence with translational limitations and future strategies.Metabolic brain disease
The Role of PolyQ in Global Conformational Dynamics and Stability of Huntingtin.ACS chemical neuroscience
ReviewCurrent landscape and future perspectives of small-molecule therapeutics for Huntington's disease: From rational design to clinical translation.European journal of medicinal chemistry
Multimodal balance training with rhythmical auditory cueing in Huntington's disease: A pilot randomized controlled trial.Journal of Huntington's disease
Dissociable Effects of Dysarthria Etiology and Severity on the Minimally Detectable Change of Speech Intelligibility.Journal of speech, language, and hearing research : JSLHR
Observational studyCSF Leukocytes Transiently Increase Before Onset of Huntington Disease in Association With a Stage-Specific CSF Cytokine/Chemokine Pattern.Neurology(R) neuroimmunology & neuroinflammation
ReviewMitochondrial dynamics in Huntington's disease.Journal of Huntington's disease
Real-world treatment patterns and outcomes of deutetrabenazine in patients with chorea associated with Huntington disease: A retrospective chart review study.Journal of Huntington's disease
ReviewAlternative splicing dysregulation in CAG repeat expansion diseases.Trends in neurosciences
Cholesterol restores corticostriatal synaptic connectivity in Huntington's disease through BDNF/TrkB signalling, supporting a role for cholesterol pathways implicated by human genetic modifier studies.Pharmacological research
Blocking somatic repeat expansion and lowering huntingtin by RNAi synergize to attenuate Huntington's disease pathogenesis in mice.Science translational medicine
Missed Opportunities for Goals-of-Care Conversations in a Patient With End-Stage Juvenile Huntington's Disease: A Case Report.The American journal of hospice & palliative care
In vivo mapping of striatal neurodegeneration in Huntington's disease with Soma and Neurite Density Imaging.eLife
Emerging Pharmacological Therapies for Huntington's Disease: Translational Insights from Recent Clinical Trials.Current pharmaceutical biotechnology
An automated speech measure for Huntington's disease: how can it take the field forward?The Lancet. Digital health
Early Longitudinal Brain Network Changes in Huntington's Disease Before Clinical Motor Onset.Movement disorders : official journal of the Movement Disorder Society
Gelatin methacryloyl hydrogel as a potential scaffold for cell transplantation for Huntington's disease.Brain communications
Wild-type C9orf72 drives proteasomal dysfunction and mutant aggregates via a Stat1-Isg15 axis in Huntington's disease.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics
Juvenile-onset Huntington's disease: a challenging diagnosis.Practical neurology
Gut microbiome composition in Huntington's disease: Stage-dependent differences between premanifest and manifest patients.Life sciences
Cholesterol nose-to-brain delivery as a possible therapeutic strategy in Huntington's disease.Translational neurodegeneration
ReviewMolecular insights of peroxisome proliferator-activated receptor-γ signalling in amyotrophic lateral sclerosis and Huntington's disease.International review of neurobiology
Altered myelin sphingolipid and glycerophospholipid profiles in Huntington disease.Journal of Huntington's disease
ReviewWhat can clinical disorders involving the basal ganglia tell us about the pathophysiology of obsessive and compulsive symptoms?Journal of neural transmission (Vienna, Austria : 1996)
Enhancing the detection of HTT1a with neoepitope antibodies in mouse models of Huntington's disease.Brain communications
Falls in Huntington's Disease: A Cross-Sectional Analysis of Clinical Features and Potential Contributors.Movement disorders clinical practice
Accelerated prefrontal intermittent theta-burst stimulation in Huntington's disease: a within-subject study of domain-specific behavioral and event-related potential changes.Frontiers in human neuroscience
Revisiting the Link Between Huntington's Disease and Cancer: Evidence from the Enroll-HD dataset.Neuroepidemiology
In vivo CRISPR base editing for treatment of Huntington's disease.Nature biomedical engineering
Psychosis in Huntington's disease: A case supporting multidisciplinary and early palliative care.Journal of Huntington's disease
HDDF2-A Novel Patient-Derived Fibroblast Line from Huntington's Disease with Prominent Cellular Senescence and polyQ Pathology.Biomedicines
ReviewGrape Seed Extract as an Adjuvant Therapy for Huntington Disease; A Narrative Review of Biological Plausibility and Potential Clinical Outcomes.Molecules (Basel, Switzerland)
Prevention of appearance of severe Huntington's disease symptoms in the R6/1 mouse model by early administration of 4',5,7-trihydroxyisoflavone.Journal of Huntington's disease
IL17A disrupts autophagy-lysosomal function and lysosome reformation through the GSK3B-TFE3 signaling pathway in Huntington disease.Autophagy
A novel machine learning approach for the classification of Huntington disease manifestation using motor features.Parkinsonism & related disorders
A deep learning model for speech-based prediction of clinical scores in people with Huntington's disease: a longitudinal study with cross-sectional replication.The Lancet. Digital health
Do young carriers of Huntington's disease mature earlier?Journal of Huntington's disease
ReviewMachine learning applications in Huntington's disease prognosis: A review.Journal of Huntington's disease
Relationship Between miRNA and Neurodegenerative Diseases Such as Alzheimer's disease, Parkinson's, Huntington's disease, Amyotrophic Lateral Sclerosis.Mini reviews in medicinal chemistry
USP28 Deficiency is Linked to Impaired Ubiquitin-dependent Proteostasis in Huntington's Disease.Molecular neurobiology
ReviewFrom glycemic control to neuroprotection: alogliptin as a repurposed candidate for Huntington's disease.Metabolic brain disease
The Recommendation Paradox: Perspectives on Genetic Testing in Huntington's Disease Families.Journal of genetic counseling
Emotion regulation across disease stages in Huntington's disease gene expansion carriers.Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists
Therapeutic potential of flavonoids and rutin against inflammation-induced on a huntington animal model.PloS one
Understanding Energy Expenditure: An Approach to Improving Activities of Daily Living in Huntington's Disease.Journal of clinical medicine
Understanding the cellular architecture of Huntington's disease.eLife
ReviewPractical recommendations for the treatment of chorea associated with Huntington's disease: An expert consensus.Journal of Huntington's disease
ReviewThe nano-intervention in Huntington's disease: A theragnostic approach.Neuroscience
Effects of Vitamin C Supplementation on Tetrabenazine Treatment in a Caenorhabditis elegans Huntington's Disease Model.microPublication biology
ReviewCRISPR-Cas9-based therapies for Huntington's disease and Friedreich's ataxia: mechanisms, advances, and future perspectives.Neurogenetics
ReviewTargeting DNA mismatch repair in Huntington's disease.Trends in neurosciences
PreprintiPSC Neurodegenerative Disease Initiative isogenic CAG repeat iPSC line for Huntington's disease.bioRxiv : the preprint server for biology
PreprintShared and disease-specific human brain vascular signatures in Alzheimer's disease, frontotemporal dementia, and Huntington's disease.bioRxiv : the preprint server for biology
xHD-Vox, an Automated Speech Model for Estimating Motor and Cognitive Scores in Huntington Disease: Development and Longitudinal Validation.JMIR neurotechnology
The experiences of partners of individuals with pre-symptomatic Huntington's disease: a reflexive thematic analysis.Psychology & health
Cortistatin as a modulator of inflammatory and mitochondrial dysfunction in Huntington´s disease.Journal of neuroinflammation
ReviewHuntington's disease in the era of somatic instability, biomarkers, and targeted therapies: A narrative review.Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion
Genistein (5,7-dihydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one) Is Effective in Reducing Symptoms of Huntington's Disease in Females of the R6/1 Mouse Model.Frontiers in bioscience (Landmark edition)
Berbamine improves behavioral impairments in Huntington's disease mice models through inhibiting Src/AKT1/NFκB signaling pathway and attenuating Src-mediated mitophagy suppression.International immunopharmacology
Structural insights into the MLH1-FAN1 interaction reveal an uncharacterized binding interface on MLH1.Nature communications
Data mining revealed no other trinucleotide repeat expansion associated with the Huntington's disease biomarker (CAG).Clinical parkinsonism & related disorders
CDKN1A protects medium spiny neurons from Huntington's disease pathology.Neurobiology of disease
ReviewNeuroprotective potential of resveratrol in Parkinson, Huntington, amyotrophic lateral sclerosis, and multiple sclerosis: a comprehensive review.Molecular biology reports
Phase-targeted auditory stimulation enhances slow-wave activity during sleep in Huntington's disease: A pilot crossover study.Journal of Huntington's disease
PreprintMismatch repair dissection by in vivo RNAi reveals dose-dependent modulators of somatic instability and proteome remodeling in Huntington's disease.bioRxiv : the preprint server for biology
PreprintWWOX contributes to DNA damage, but not somatic instability in Huntington's disease.bioRxiv : the preprint server for biology
A Multi-Regional Single-nucleus Atlas of the Huntington's Disease Brain.Scientific data
Restoring cortical disinhibition improves Huntington's disease phenotypes.Nature
Factors influencing receipt of specialty neurologic care for patients with Huntington's disease in Colorado.Clinical parkinsonism & related disorders
Development and validation of a machine learning model to detect psychiatric symptoms in Huntington's disease using speech analysis.PloS one
Hyperhomocysteinemia and Vitamin B Deficiency as Potential Aggravating Factors in Huntington's Disease: A Prospective Monocentric Study.Movement disorders : official journal of the Movement Disorder Society
Visuospatial working memory in Huntington's disease: behavioural and structural brain correlates.Journal of neurology, neurosurgery, and psychiatry
Assessing the prognostic value of early oculomotor abnormalities in Huntington's disease.Frontiers in neurology
Topological modeling of gene expression in the brain with Huntington's disease reveals selective disruption of co-expression network.Scientific reports
Proteomic Impact of Peripheral Expression of Mutant Huntingtin in C. elegans.Journal of proteome research
Differential sensitivity of the MMSE and MoCA for staging and longitudinal cognitive change in Huntington's disease.Journal of Huntington's disease
Nuclear RNA clusters are dynamic structural entities in Huntington's disease.Communications biology
Stage-dependent tau-PET signatures in Huntington's disease revealed by [¹⁸F]PI-2620.European journal of nuclear medicine and molecular imaging
The impedance mismatch theory: A non-equilibrium thermodynamic framework for a shared energetic stress pathway in neurodegeneration.Bio Systems
Anle138b ameliorates pathological phenotypes in mouse and cellular models of Huntington's disease.EMBO molecular medicine
Mutant huntingtin in the extracellular matrix: A new perspective on Huntington's disease pathology.Neurobiology of disease