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Topography of cerebral atrophy in early Huntington’s disease: a voxel based morphometric MRI study

Journal of neurology, neurosurgery and psychiatry, 2004-02, Vol.75 (2), p.213-220

2004

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Apolipoprotein E genotypes do not influence the age of onset in Huntington’s disease

Journal of neurology, neurosurgery and psychiatry, 2004-12, Vol.75 (12), p.1692-1696

2004

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Autonomic nervous system function in Huntington's disease

Journal of neurology, neurosurgery and psychiatry, 2002-06, Vol.72 (6), p.726-731

2002

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Cardiovagal modulation upon postural change is altered in Huntington's disease

European journal of neurology, 2008-08, Vol.15 (8), p.869-871

2008

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Sonographic detection of bilateral striopallidodentate calcinosis

Journal of neurology, 2009-02, Vol.256 (2), p.266-267

2009

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Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington’s disease-like phenotype

Journal of medical genetics, 2004-03, Vol.41 (3), p.230-232

2004

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NR2A and NR2B receptor gene variations modify age at onset in Huntington disease

Neurogenetics, 2005-02, Vol.6 (1), p.25-28

2005

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Mitochondrial impairment in patients and asymptomatic mutation carriers of Huntington's disease

Movement disorders, 2005-06, Vol.20 (6), p.674-679

2005

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Relation between electroconvulsive therapy, cognitive side effects, neuron specific enolase, and protein S-100

Journal of neurology, neurosurgery and psychiatry, 2001-09, Vol.71 (3), p.394-396

2001

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69. Voluntary movement execution in Huntington’s disease – a combined neurophysiological and morphometric magnetic resonance imaging study

Clinical neurophysiology, 2009, Vol.120 (1), p.e31-e31

2009

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Relationship between major depression and heart rate variability.: Clinical consequences and implications for antidepressive treatment

Psychiatry research, 2002-12, Vol.113 (1), p.139-149

2002

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Weight loss in Huntington disease increases with higher CAG repeat number

Neurology, 2008-11, Vol.71 (19), p.1506

2008

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Basal ganglia alterations and brain atrophy in Huntington’s disease depicted by transcranial real time sonography

Journal of neurology, neurosurgery and psychiatry, 1999-10, Vol.67 (4), p.457-462

1999

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Chronic subdural haematoma in patients with Huntington's disease

British journal of neurosurgery, 2006-10, Vol.20 (5), p.327-329

2006

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Asymmetric anhidrosis in MSA

Neurology, 2003-07, Vol.61 (2), p.231

2003

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Assessment of simple movements and progression of Huntington’s disease

Journal of neurology, neurosurgery and psychiatry, 2007-04, Vol.78 (4), p.405-407

2007

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Coenzyme Q10 serum levels in Huntington's disease

Journal of neural transmission. Supplementum, 2004 (68), p.111

2004

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High Cholesterol Feeding in C57/Blc6 Mice Alters Expression within The VEGF Receptor-Ligand Family in Corporal Tissue

Journal of sexual medicine, 2008-05, Vol.5 (5), p.1137-1148

2008

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Short-term effects of intravenous benzodiazepines on autonomic neurocardiac regulation in humans: A comparison between midazolam, diazepam, and lorazepam

Critical care medicine, 2002-05, Vol.30 (5), p.997-1006

2002

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Placebo effect characteristics observed in a single, international, longitudinal study in Huntington's disease

Movement disorders, 2012-03, Vol.27 (3), p.439-442

2012

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Kontinuierliche dopaminerge Stimulation mittels DuoDopa®-Therapie – Praktikabilität, klinischer Benefit und Risiken der duodenalen Applikation

Aktuelle Neurologie, 2007, Vol.34 (S 2)

2007

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Segmentale Schweisssekretionsstorung bei Multisystematrophie

Hautarzt, 2005-08, Vol.56 (8), p.773-777

2005

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Congruent deterioration of complex and simple movements in patients with Huntington's disease

Journal of neural transmission. Supplementum, 2004 (68), p.97

2004

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Is the retina affected in Huntington disease?

Acta neuropathologica, 2005-11, Vol.110 (5), p.523-525

2005

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Morbus Huntington - a human genetic model disease

Cytogenetics and cell genetics, 2000, Vol.91 (1-4), p.90

2000

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Topography of cerebral atrophy in early Huntington’s disease: a voxel based morphometric MRI study

Apolipoprotein E genotypes do not influence the age of onset in Huntington’s disease

Autonomic nervous system function in Huntington's disease

Cardiovagal modulation upon postural change is altered in Huntington's disease

Sonographic detection of bilateral striopallidodentate calcinosis

Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington’s disease-like phenotype

NR2A and NR2B receptor gene variations modify age at onset in Huntington disease

Mitochondrial impairment in patients and asymptomatic mutation carriers of Huntington's disease

Relation between electroconvulsive therapy, cognitive side effects, neuron specific enolase, and protein S-100

69. Voluntary movement execution in Huntington’s disease – a combined neurophysiological and morphometric magnetic resonance imaging study

Relationship between major depression and heart rate variability.: Clinical consequences and implications for antidepressive treatment

Weight loss in Huntington disease increases with higher CAG repeat number

Basal ganglia alterations and brain atrophy in Huntington’s disease depicted by transcranial real time sonography

Chronic subdural haematoma in patients with Huntington's disease

Asymmetric anhidrosis in MSA

Assessment of simple movements and progression of Huntington’s disease

Coenzyme Q10 serum levels in Huntington's disease

High Cholesterol Feeding in C57/Blc6 Mice Alters Expression within The VEGF Receptor-Ligand Family in Corporal Tissue

Short-term effects of intravenous benzodiazepines on autonomic neurocardiac regulation in humans: A comparison between midazolam, diazepam, and lorazepam

Placebo effect characteristics observed in a single, international, longitudinal study in Huntington's disease

Kontinuierliche dopaminerge Stimulation mittels DuoDopa®-Therapie – Praktikabilität, klinischer Benefit und Risiken der duodenalen Applikation

Segmentale Schweisssekretionsstorung bei Multisystematrophie

Congruent deterioration of complex and simple movements in patients with Huntington's disease

Is the retina affected in Huntington disease?

Morbus Huntington - a human genetic model disease

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