Multiple clinical features of Huntington’s disease correlate with mutant HTT gene CAG repeat lengths and neurodegeneration

Mapping the order and pattern of brain structural MRI changes using change-point analysis in premanifest Huntington's disease

(2017) Dan Wu et al.   HUMAN BRAIN MAPPING

HDNetDB: A Molecular Interaction Database for Network-Oriented Investigations into Huntington’s Disease

(2017) Ravi Kiran Reddy Kalathur et al.   Scientific Reports

The HTT CAG-Expansion Mutation Determines Age at Death but Not Disease Duration in Huntington Disease

(2016) Jae Whan Keum et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Current status of PET imaging in Huntington’s disease

(2016) Gennaro Pagano et al.   EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING

Natural variation in sensory-motor white matter organization influences manifestations of Huntington's disease

(2016) Michael Orth et al.   HUMAN BRAIN MAPPING

Visuospatial Processing Deficits Linked to Posterior Brain Regions in Premanifest and Early Stage Huntington’s Disease

(2016) Izelle Labuschagne et al.   JOURNAL OF THE INTERNATIONAL NEUROPSYCHOLOGICAL SOCIETY

The Biology of Huntingtin

(2016) Frédéric Saudou et al.   NEURON

Huntington’s Disease: Mechanisms of Pathogenesis and Therapeutic Strategies

(2016) Maria Jimenez-Sanchez et al.   Cold Spring Harbor Perspectives in Medicine

Network topology and functional connectivity disturbances precede the onset of Huntington’s disease

(2015) Deborah L. Harrington et al.   BRAIN

Huntington disease

(2015) Gillian P. Bates et al.   Nature Reviews Disease Primers

Predictors of Survival in a Huntington's Disease Population from Southern Italy

(2014) Carlo Rinaldi et al.   CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES

Cross sectional PET study of cerebral adenosine A1 receptors in premanifest and manifest Huntington’s disease

(2014) Andreas Matusch et al.   EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING

Reduced automatic frontal response to auditory deviance in Huntington’s disease as indexed by magnetic mismatch negativity

(2014) Chia-Hsiung Cheng et al.   JOURNAL OF CLINICAL NEUROSCIENCE

HD-CAB: A cognitive assessment battery for clinical trials in Huntington's disease1,2,3

(2014) Julie C. Stout et al.   MOVEMENT DISORDERS

The Phosphodiesterase 10 Positron Emission Tomography Tracer, [18F]MNI-659, as a Novel Biomarker for Early Huntington Disease

(2014) David S. Russell et al.   JAMA Neurology

Huntington's Disease (HD): Degeneration of Select Nuclei, Widespread Occurrence of Neuronal Nuclear and Axonal Inclusions in the Brainstem

(2013) Udo Rüb et al.   BRAIN PATHOLOGY

White matter integrity in premanifest and early Huntington's disease is related to caudate loss and disease progression

(2013) Marianne J.U. Novak et al.   CORTEX

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

(2013) Sarah J Tabrizi et al.   LANCET NEUROLOGY

Tractography of the Corpus Callosum in Huntington’s Disease

(2013) Owen Phillips et al.   PLoS One

Huntington's disease: underlying molecular mechanisms and emerging concepts

(2013) John Labbadia et al.   TRENDS IN BIOCHEMICAL SCIENCES

Huntingtin protein interactions altered by polyglutamine expansion as determined by quantitative proteomic analysis

(2012) Tamara Ratovitski et al.   CELL CYCLE

Huntingtonʼs disease

(2012) Ainhi D. Ha et al.   CURRENT OPINION IN NEUROLOGY

18F-FDG PET uptake in the pre-Huntington disease caudate affects the time-to-onset independently of CAG expansion size

(2012) Andrea Ciarmiello et al.   EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING

Proteomic Analysis of Wild-type and Mutant Huntingtin-associated Proteins in Mouse Brains Identifies Unique Interactions and Involvement in Protein Synthesis

(2012) Brady P. Culver et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Increased brain tissue sodium concentration in Huntington's Disease — A sodium imaging study at 4T

(2012) Kathrin Reetz et al.   NEUROIMAGE

Assessment of cortical and striatal involvement in 523 Huntington disease brains

(2012) T. C. Hadzi et al.   NEUROLOGY

CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion

(2012) J.- M. Lee et al.   NEUROLOGY

Network Organization of the Huntingtin Proteomic Interactome in Mammalian Brain

(2012) Dyna I. Shirasaki et al.   NEURON

Striatal Volume Contributes to the Prediction of Onset of Huntington Disease in Incident Cases

(2011) Elizabeth H. Aylward et al.   BIOLOGICAL PSYCHIATRY

Shape analysis of subcortical nuclei in Huntington's disease, global versus local atrophy — Results from the TRACK-HD study

(2011) S.J.A. van den Bogaard et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Basal ganglia atrophy in prodromal Huntington's disease is detectable over one year using automated segmentation

(2011) D.S. Adnan Majid et al.   MOVEMENT DISORDERS

Age, CAG repeat length, and clinical progression in Huntington's disease

(2011) Adam Rosenblatt et al.   MOVEMENT DISORDERS

A tale of two factors: What determines the rate of progression in Huntington's disease? A longitudinal MRI study

(2011) H. Diana Rosas et al.   MOVEMENT DISORDERS

Cell loss in the motor and cingulate cortex correlates with symptomatology in Huntington’s disease

(2010) Doris C. V. Thu et al.   BRAIN

Microglial activation in regions related to cognitive function predicts disease onset in Huntington's disease: A multimodal imaging study

(2010) Marios Politis et al.   HUMAN BRAIN MAPPING

Widespread Decrease of Type 1 Cannabinoid Receptor Availability in Huntington Disease In Vivo

(2010) K. Van Laere et al.   JOURNAL OF NUCLEAR MEDICINE

Huntington's disease: from molecular pathogenesis to clinical treatment

(2010) Christopher A Ross et al.   LANCET NEUROLOGY

A retrospective study of the impact of lifestyle on age at onset of Huntington disease

(2010) M. Kaye Trembath et al.   MOVEMENT DISORDERS

Molecular Mechanisms and Potential Therapeutical Targets in Huntington's Disease

(2010) Chiara Zuccato et al.   PHYSIOLOGICAL REVIEWS

Late onset Huntington Disease: Clinical and genetic characteristics of 34 cases

(2008) Hillary Lipe et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

The relationship between CAG repeat length and clinical progression in Huntington's disease

(2008) Bernard Ravina et al.   MOVEMENT DISORDERS

Weight loss in Huntington disease increases with higher CAG repeat number

(2008) N. A. Aziz et al.   NEUROLOGY

Longitudinal analysis of regional grey matter loss in Huntington disease: effects of the length of the expanded CAG repeat

(2007) H H Ruocco et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Detection of Huntington's disease decades before diagnosis: the Predict-HD study

(2007) J S Paulsen et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY