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A MDS evidence‐based review on treatments for Huntington's Disease

Movement disorders, 2022-01, Vol.37 (1), p.25-35

2022

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Mechanisms underlying phenotypic variation in neurogenetic disorders

Nature reviews. Neurology, 2023-06, Vol.19 (6), p.363-370

Burgunder, Jean-Marc

2023

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International Guidelines for the Treatment of Huntington's Disease

Frontiers in neurology, 2019, Vol.10, p.710-710

2019

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Quality of Life in Huntington's Disease: Critique and Recommendations for Measures Assessing Patient Health‐Related Quality of Life and Caregiver Quality of Life

Movement disorders, 2018-05, Vol.33 (5), p.742-749

2018

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Recent progress in the genetics of motor neuron disease

European journal of medical genetics, 2014-02, Vol.57 (2), p.103-112

2014

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Defining pediatric huntington disease: Time to abandon the term Juvenile Huntington Disease?

Movement disorders, 2019-04, Vol.34 (4), p.584-585

2019

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Brain alterations with deep brain stimulation: New insight from a neuropathological case series

Movement disorders, 2015-07, Vol.30 (8), p.1125-1130

2015

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Development and Evaluation of Maze-Like Puzzle Games to Assess Cognitive and Motor Function in Aging and Neurodegenerative Diseases

Frontiers in aging neuroscience, 2020-04, Vol.12, p.87-87

2020

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The characteristic and prognostic role of blood inflammatory markers in patients with Huntington's disease from China

Frontiers in neurology, 2024-03, Vol.15, p.1374365-1374365

2024

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Evaluation of Blood Glial Fibrillary Acidic Protein as a Potential Marker in Huntington's Disease

Frontiers in neurology, 2021-11, Vol.12, p.779890-779890

2021

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Factors influencing cognitive function in patients with Huntington's disease from China: A cross‐sectional clinical study

Brain and behavior, 2023-11, Vol.13 (11), p.e3258-e3258

2023

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Symptomatic treatment options for Huntington’s disease (guidelines of the German Neurological Society)

Neurological research and practice, 2023-11, Vol.5 (1), p.61-61, Article 61

2023

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Differential diagnosis of chorea (guidelines of the German Neurological Society)

Neurological research and practice, 2023-11, Vol.5 (1), p.63-63, Article 63

2023

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Combining Literature Review With a Ground Truth Approach for Diagnosing Huntington's Disease Phenocopy

Frontiers in neurology, 2022-02, Vol.13, p.817753-817753

2022

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Multiple LRRK2 variants modulate risk of Parkinson disease: a chinese multicenter study

Human mutation, 2010-05, Vol.31 (5), p.561-568

2010

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Interrater Reliability of the Unified Huntington's Disease Rating Scale‐Total Motor Score Certification

Movement disorders clinical practice (Hoboken, N.J.), 2018-05, Vol.5 (3), p.290-295

2018

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Rating Scales and Performance‐based Measures for Assessment of Functional Ability in Huntington's Disease: Critique and Recommendations

Movement disorders clinical practice (Hoboken, N.J.), 2018-07, Vol.5 (4), p.361-372

2018

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Model-Based Magnetization Transfer Imaging Markers to Characterize Patients and Asymptomatic Gene Carriers in Huntington's Disease

Frontiers in neurology, 2017-09, Vol.8, p.465-465

2017

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Myotonia congenita-associated mutations in chloride channel-1 affect zebrafish body wave swimming kinematics

PloS one, 2014-08, Vol.9 (8), p.e103445-e103445

2014

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Better global and cognitive functioning in choreatic versus hypokinetic-rigid Huntington's disease

Movement disorders, 2013-07, Vol.28 (8), p.1142-1145

2013

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Recent advances in the management of choreas

Therapeutic Advances in Neurological Disorders, 2013-03, Vol.6 (2), p.117-127

Burgunder, Jean-Marc

2013

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Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

Nature genetics, 1999-11, Vol.23 (3), p.296-303

1999

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Association of GWAS loci with PD in China

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2011-04, Vol.156B (3), p.334-339

2011

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Genetics of Huntington's disease and related disorders

Drug discovery today, 2014-07, Vol.19 (7), p.985-989

Burgunder, Jean-Marc

2014

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A MDS evidence‐based review on treatments for Huntington's Disease

European Academy of Neurology guidance for developing and reporting clinical practice guidelines on rare neurological diseases

Mechanisms underlying phenotypic variation in neurogenetic disorders

International Guidelines for the Treatment of Huntington's Disease

Quality of Life in Huntington's Disease: Critique and Recommendations for Measures Assessing Patient Health‐Related Quality of Life and Caregiver Quality of Life

Recent progress in the genetics of motor neuron disease

Defining pediatric huntington disease: Time to abandon the term Juvenile Huntington Disease?

Brain alterations with deep brain stimulation: New insight from a neuropathological case series

Development and Evaluation of Maze-Like Puzzle Games to Assess Cognitive and Motor Function in Aging and Neurodegenerative Diseases

The characteristic and prognostic role of blood inflammatory markers in patients with Huntington's disease from China

Evaluation of Blood Glial Fibrillary Acidic Protein as a Potential Marker in Huntington's Disease

Factors influencing cognitive function in patients with Huntington's disease from China: A cross‐sectional clinical study

Symptomatic treatment options for Huntington’s disease (guidelines of the German Neurological Society)

Differential diagnosis of chorea (guidelines of the German Neurological Society)

Combining Literature Review With a Ground Truth Approach for Diagnosing Huntington's Disease Phenocopy

Multiple LRRK2 variants modulate risk of Parkinson disease: a chinese multicenter study

Interrater Reliability of the Unified Huntington's Disease Rating Scale‐Total Motor Score Certification

Rating Scales and Performance‐based Measures for Assessment of Functional Ability in Huntington's Disease: Critique and Recommendations

Model-Based Magnetization Transfer Imaging Markers to Characterize Patients and Asymptomatic Gene Carriers in Huntington's Disease

Myotonia congenita-associated mutations in chloride channel-1 affect zebrafish body wave swimming kinematics

Better global and cognitive functioning in choreatic versus hypokinetic-rigid Huntington's disease

Recent advances in the management of choreas

Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

Association of GWAS loci with PD in China

Genetics of Huntington's disease and related disorders

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