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Targeting Huntingtin Expression in Patients with Huntington’s Disease

The New England journal of medicine, 2019-06, Vol.380 (24), p.2307-2316

2019

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Speech biomarkers in Huntington's disease: A cross‐sectional study in pre‐symptomatic, prodromal and early manifest stages

European journal of neurology, 2023-05, Vol.30 (5), p.1262-1271

2023

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Suicidal ideation and suicidal behavior according to the C-SSRS in a European cohort of Huntington's disease gene expansion carriers

Journal of affective disorders, 2018-03, Vol.228, p.194-204

2018

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Ubiquitination and the proteasome rather than caspase‐3‐mediated C‐terminal cleavage are involved in the EAAT2 degradation by staurosporine‐induced cellular stress

Journal of neurochemistry, 2021-05, Vol.157 (4), p.1284-1299

2021

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Olfactory screening of Parkinson's Disease patients and healthy subjects in China and Germany: A study of cross-cultural adaptation of the Sniffin' Sticks 12-identification test

PloS one, 2019-11, Vol.14 (11), p.e0224331-e0224331

2019

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Tominersen in Adults with Manifest Huntington's Disease

The New England journal of medicine, 2023-12, Vol.389 (23), p.2203-2205

2023

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Huntingtin HTT1a is generated in a CAG repeat-length-dependent manner in human tissues

Molecular medicine (Cambridge, Mass.), 2024-03, Vol.30 (1), p.36-36

2024

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Correction: Huntingtin HTT1a is generated in a CAG repeat-length-dependent manner in human tissues

Molecular medicine (Cambridge, Mass.), 2024-04, Vol.30 (1), p.49-49

2024

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A greatly extended PPARGC1A genomic locus encodes several new brain-specific isoforms and influences Huntington disease age of onset

Human molecular genetics, 2012-08, Vol.21 (15), p.3461-3473

2012

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HAP40 protein levels are huntingtin-dependent and decrease in Huntington disease

Neurobiology of disease, 2021-10, Vol.158, p.105476-105476, Article 105476

2021

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Riluzole in Huntington's disease: a 3-year, randomized controlled study

Annals of neurology, 2007-09, Vol.62 (3), p.262-272

2007

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Dorsolateral prefrontal cortex dysfunction in presymptomatic Huntington's disease: evidence from event-related fMRI

Brain (London, England : 1878), 2007-11, Vol.130 (11), p.2845-2857

2007

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Disease severity and progression in progressive supranuclear palsy and multiple system atrophy: validation of the NNIPPS--Parkinson Plus Scale

PloS one, 2011-08, Vol.6 (8), p.e22293-e22293

2011

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Fast-to-Slow Transition of Skeletal Muscle Contractile Function and Corresponding Changes in Myosin Heavy and Light Chain Formation in the R6/2 Mouse Model of Huntington's Disease

PloS one, 2016-11, Vol.11 (11), p.e0166106-e0166106

2016

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How to Arrange Follow-Up Time-Intervals for Longitudinal Brain MRI Studies in Neurodegenerative Diseases

Frontiers in neuroscience, 2021-07, Vol.15, p.682812-682812

2021

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Research priorities for rare neurological diseases: a representative view of patient representatives and healthcare professionals from the European Reference Network for Rare Neurological Diseases

Orphanet journal of rare diseases, 2021-03, Vol.16 (1), p.135-135, Article 135

2021

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Enroll-HD: An Integrated Clinical Research Platform and Worldwide Observational Study for Huntington's Disease

Frontiers in neurology, 2021-08, Vol.12, p.667420-667420

2021

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Commentary: Acanthocytes identified in Huntington's disease

Frontiers in neuroscience, 2022-11, Vol.16, p.1049676-1049676

2022

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

Human brain mapping, 2016-12, Vol.37 (12), p.4615-4628

2016

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Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy

PloS one, 2009-09, Vol.4 (9), p.e7114-e7114

2009

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Monitoring the Motor Phenotype in Huntington's Disease by Analysis of Keyboard Typing During Real Life Computer Use

Journal of Huntington's disease, 2021-01, Vol.10 (2), p.259

2021

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High-resolution respirometry of fine-needle muscle biopsies in pre-manifest Huntington's disease expansion mutation carriers shows normal mitochondrial respiratory function

PloS one, 2017-04, Vol.12 (4), p.e0175248-e0175248

2017

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Catatonia: looking back and moving forward

Brain (London, England : 1878), 2022-09, Vol.145 (9), p.2939-2942

2022

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Brain activation and functional connectivity in premanifest Huntington's disease during states of intrinsic and phasic alertness

Human brain mapping, 2012-09, Vol.33 (9), p.2161-2173

2012

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Targeting Huntingtin Expression in Patients with Huntington’s Disease

Speech biomarkers in Huntington's disease: A cross‐sectional study in pre‐symptomatic, prodromal and early manifest stages

Suicidal ideation and suicidal behavior according to the C-SSRS in a European cohort of Huntington's disease gene expansion carriers

Exome sequencing of individuals with Huntington's disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onset

Ubiquitination and the proteasome rather than caspase‐3‐mediated C‐terminal cleavage are involved in the EAAT2 degradation by staurosporine‐induced cellular stress

Olfactory screening of Parkinson's Disease patients and healthy subjects in China and Germany: A study of cross-cultural adaptation of the Sniffin' Sticks 12-identification test

Tominersen in Adults with Manifest Huntington's Disease

Huntingtin HTT1a is generated in a CAG repeat-length-dependent manner in human tissues

Correction: Huntingtin HTT1a is generated in a CAG repeat-length-dependent manner in human tissues

A greatly extended PPARGC1A genomic locus encodes several new brain-specific isoforms and influences Huntington disease age of onset

HAP40 protein levels are huntingtin-dependent and decrease in Huntington disease

Riluzole in Huntington's disease: a 3-year, randomized controlled study

Dorsolateral prefrontal cortex dysfunction in presymptomatic Huntington's disease: evidence from event-related fMRI

Disease severity and progression in progressive supranuclear palsy and multiple system atrophy: validation of the NNIPPS--Parkinson Plus Scale

Fast-to-Slow Transition of Skeletal Muscle Contractile Function and Corresponding Changes in Myosin Heavy and Light Chain Formation in the R6/2 Mouse Model of Huntington's Disease

How to Arrange Follow-Up Time-Intervals for Longitudinal Brain MRI Studies in Neurodegenerative Diseases

Research priorities for rare neurological diseases: a representative view of patient representatives and healthcare professionals from the European Reference Network for Rare Neurological Diseases

Enroll-HD: An Integrated Clinical Research Platform and Worldwide Observational Study for Huntington's Disease

Commentary: Acanthocytes identified in Huntington's disease

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

Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy

Monitoring the Motor Phenotype in Huntington's Disease by Analysis of Keyboard Typing During Real Life Computer Use

High-resolution respirometry of fine-needle muscle biopsies in pre-manifest Huntington's disease expansion mutation carriers shows normal mitochondrial respiratory function

Catatonia: looking back and moving forward

Brain activation and functional connectivity in premanifest Huntington's disease during states of intrinsic and phasic alertness

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