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Grasping premanifest Huntington's disease - shaping new endpoints for new trials

Movement disorders, 2010-12, Vol.25 (16), p.2858-2862

2010

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Tongue force analysis assesses motor phenotype in premanifest and symptomatic Huntington's disease

Movement disorders, 2010-10, Vol.25 (13), p.2195-2202

2010

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Assessment of involuntary choreatic movements in Huntington's disease-Toward objective and quantitative measures

Movement disorders, 2011-10, Vol.26 (12), p.2267-2273

2011

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Huntington's Disease (HD): Neurodegeneration of Brodmann's Primary Visual Area 17 (BA17)

Brain pathology (Zurich, Switzerland), 2015-11, Vol.25 (6), p.701-711

2015

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Huntington's disease: Objective assessment of posture-A link between motor and functional deficits

Movement disorders, 2012-04, Vol.27 (4), p.555-559

2012

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Impaired Isometric Force Matching in Upper and Lower Limbs Revealed by Quantitative Motor Assessments in Huntington’s Disease

Journal of Huntington's disease, 2019-01, Vol.8 (4), p.483-492

2019

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Velocity modulation and rhythmic synchronization of gait in Huntington's disease

Movement disorders, 1999-09, Vol.14 (5), p.808-819

1999

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Differential effect of Huntington's and Parkinson's diseases in programming motor sequences of varied lengths

Journal of neurology, 2006-02, Vol.253 (2), p.186-193

2006

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Motor learning by imagery is differentially affected in Parkinson’s and Huntington’s diseases

Behavioural brain research, 1999-07, Vol.102 (1), p.115-127

1999

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Neurophysiological abnormalities in the westphal variant of Huntington's disease

Movement disorders, 1998-11, Vol.13 (6), p.920-928

1998

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LANGUAGE FUNCTIONS IN HUNTINGTON'S DISEASE

Brain (London, England : 1878), 1988-12, Vol.111 (6), p.1475-1503

1988

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Frequency dependent effects of rTMS on motor and cognitive functions in Huntington’s disease

Basal ganglia, 2012-03, Vol.2 (1), p.41-48

2012

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CORTICAL AND SUBCORTICAL GLUCOSE CONSUMPTION MEASURED BY PET IN PATIENTS WITH HUNTINGTON'S DISEASE

Brain (London, England : 1878), 1990-10, Vol.113 (5), p.1405-1423

1990

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IMPAIRMENT OF RAPID MOVEMENT IN HUNTINGTON'S DISEASE

Brain (London, England : 1878), 1987-06, Vol.110 (3), p.585-612

1987

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Huntington's Disease:N-Methyl-d-Aspartate Receptor Coagonist Glycine Is Increased in Platelets

Experimental neurology, 1997-04, Vol.144 (2), p.416-419

1997

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Huntington's disease: The neuroexcitotoxin aspartate is increased in platelets and decreased in plasma

Journal of the neurological sciences, 1994-12, Vol.127 (1), p.48-53

1994

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SPECT with HMPAO compared to PET with FDG in Huntington disease

Journal of computer assisted tomography, 1994-07, Vol.18 (4), p.542-548

1994

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Motor responses evoked by magnetic brain stimulation in Huntington's disease

Electroencephalography and clinical neurophysiology, 1992-06, Vol.85 (3), p.197-208

1992

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Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease

Neurology, 2009-10, Vol.73 (16), p.1280-1285

2009

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Observing Huntington's Disease: the European Huntington's Disease Network's REGISTRY

PLoS currents, 2011-04, Vol.2, p.RRN1184-RRN1184

2011

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Loss of disgust : Perception of faces and emotions in Huntington's disease

Brain (London, England : 1878), 1996-10, Vol.119 (5), p.1647-1665

1996

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Wie häufig werden Patienten im Durchschnitt pro Behandlungsjahr geschult? Darstellung der Schulungshäufigkeit bezüglich Alter, Diabetesdauer und Migrationshintergrund bei 26994 Patienten unterschiedlicher Altersgruppen mit Typ 1-Diabetes mellitus aus der DPV-Datenbank

Diabetologie und Stoffwechsel, 2012, Vol.7 (S 01)

2012

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Discrepancies in reporting the CAG repeat lengths for Huntington's disease

European journal of human genetics : EJHG, 2012-01, Vol.20 (1), p.20-26

2012

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Grasping premanifest Huntington's disease - shaping new endpoints for new trials

Tongue force analysis assesses motor phenotype in premanifest and symptomatic Huntington's disease

Assessment of involuntary choreatic movements in Huntington's disease-Toward objective and quantitative measures

Huntington's Disease (HD): Neurodegeneration of Brodmann's Primary Visual Area 17 (BA17)

Huntington's disease: Objective assessment of posture-A link between motor and functional deficits

Impaired Isometric Force Matching in Upper and Lower Limbs Revealed by Quantitative Motor Assessments in Huntington’s Disease

Velocity modulation and rhythmic synchronization of gait in Huntington's disease

Genetic analysis of candidate genes modifying the age-at-onset in Huntington's disease

Differential effect of Huntington's and Parkinson's diseases in programming motor sequences of varied lengths

The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington's disease

Motor learning by imagery is differentially affected in Parkinson’s and Huntington’s diseases

Neurophysiological abnormalities in the westphal variant of Huntington's disease

LANGUAGE FUNCTIONS IN HUNTINGTON'S DISEASE

Frequency dependent effects of rTMS on motor and cognitive functions in Huntington’s disease

CORTICAL AND SUBCORTICAL GLUCOSE CONSUMPTION MEASURED BY PET IN PATIENTS WITH HUNTINGTON'S DISEASE

IMPAIRMENT OF RAPID MOVEMENT IN HUNTINGTON'S DISEASE

Huntington's Disease:N-Methyl-d-Aspartate Receptor Coagonist Glycine Is Increased in Platelets

Huntington's disease: The neuroexcitotoxin aspartate is increased in platelets and decreased in plasma

SPECT with HMPAO compared to PET with FDG in Huntington disease

Motor responses evoked by magnetic brain stimulation in Huntington's disease

Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease

Observing Huntington's Disease: the European Huntington's Disease Network's REGISTRY

Loss of disgust : Perception of faces and emotions in Huntington's disease

Wie häufig werden Patienten im Durchschnitt pro Behandlungsjahr geschult? Darstellung der Schulungshäufigkeit bezüglich Alter, Diabetesdauer und Migrationshintergrund bei 26994 Patienten unterschiedlicher Altersgruppen mit Typ 1-Diabetes mellitus aus der DPV-Datenbank

Discrepancies in reporting the CAG repeat lengths for Huntington's disease

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