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A41 Olfactory bulb atrophy and caspase activation observed early in the bachd transgenic lines

Journal of neurology, neurosurgery and psychiatry, 2018-09, Vol.89 (Suppl 1), p.A15

2018

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Widespread thalamic and cerebellar degeneration in a patient with a complicated hereditary spastic paraplegia (HSP)

Annals of anatomy, 2009-04, Vol.191 (2), p.203-211

2009

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LRRK2 guides the actin cytoskeleton at growth cones together with ARHGEF7 and Tropomyosin 4

Biochimica et biophysica acta, 2013-12, Vol.1832 (12), p.2352-2367

2013

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The role of alpha-synuclein gene multiplications in early-onset Parkinson's disease and dementia with Lewy bodies

Journal of Neural Transmission, 2005-09, Vol.112 (9), p.1249-1254

2005

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Nuclear Localization of Ataxin-3 Is Required for the Manifestation of Symptoms in SCA3: In Vivo Evidence

The Journal of neuroscience, 2007-07, Vol.27 (28), p.7418-7428

2007

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Hereditäre Ataxien

Medizinische Genetik, 2013-06, Vol.102 (2), p.235-248

2013

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B15 Dysregulation of Gene Expression in the Striatum of Bachd Rats and Abnormalities Involved on Molecular and Protein Levels

Journal of neurology, neurosurgery and psychiatry, 2014-09, Vol.85 (Suppl 1), p.A14-A14

2014

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C07 The Influence Of Obesity And Reduced Food Intake On The Behavioural Characterisation Of The Bachd Rat Model Of Huntington Disease

Journal of neurology, neurosurgery and psychiatry, 2014-09, Vol.85 (Suppl 1), p.A27-A27

2014

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B15Dysregulation of Gene Expression in the Striatum of Bachd Rats and Abnormalities Involved on Molecular and Protein Levels

Journal of neurology, neurosurgery and psychiatry, 2014-09, Vol.85 (Suppl 1), p.A14-A14

2014

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APPLICATION OF NEXT GENERATION TECHNOLOGIES: EP.319 The Treatabolome flags treatable genes and variants: an emerging concept

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S146-S147

2021

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APPLICATION OF NEXT GENERATION TECHNOLOGIES

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S146-S147

2021

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In double-transgenic mouse models non-expanded ataxin-3 not suppresses polyglutamine neurodegeneration in the SCA3 disease – in vivo evidence

Aktuelle Neurologie, 2009-09, Vol.36 (S 02)

2009

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Normal sensitivity to excitotoxicity in a transgenic Huntington's disease rat

Brain research bulletin, 2006-04, Vol.69 (3), p.306-310

2006

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Unexpected high frequency of de novo unbalanced translocations in patients with Wolf-Hirschhorn syndrome (WHS)

Journal of medical genetics, 2000-10, Vol.37 (10), p.798-804

2000

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Klinisch-pathologische Charakterisierung von 1078 Ratsuchenden mit pathogener CHEK2 Mutation aus dem Deutschen Konsortium Familiärer Brust- und Eierstockkrebs (DK-FBREK)

Geburtshilfe und Frauenheilkunde, 2020, Vol.80 (6)

2020

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Multiple organ failure due to 5-fluorouracil chemotherapy in a patient with a rare dihydropyrimidine dehydrogenase gene variant

Oncology research and treatment, 2004-01, Vol.27 (6), p.559-562

2004

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Towards a European health research and innovation cloud (HRIC)

Genome medicine, 2020-02, Vol.12 (1), p.18-14, Article 18

2020

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Genome-wide association study identifies genetic factors that modify age at onset in Machado-Joseph disease

Aging (Albany, NY.), 2020-03, Vol.12 (6), p.4742-4756

2020

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Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease

Nature genetics, 1998-02, Vol.18 (2), p.106-108

1998

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Ubiquitylation of Synphilin-1 and α-Synuclein by SIAH and Its Presence in Cellular Inclusions and Lewy Bodies Imply a Role in Parkinson's Disease

Proceedings of the National Academy of Sciences - PNAS, 2004-04, Vol.101 (15), p.5500-5505

2004

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Screening for mutations of the IRP2 gene in Parkinson's disease patients with hyperechogenicity of the substantia nigra

Journal of Neural Transmission, 2004-04, Vol.111 (4), p.515-521

2004

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M12 A769662 Leads to AMPK Activation, Induces Autophagy and has Beneficial Effects IN HD Cells

Journal of neurology, neurosurgery and psychiatry, 2014-09, Vol.85 (Suppl 1), p.A98-A98

2014

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C07The Influence Of Obesity And Reduced Food Intake On The Behavioural Characterisation Of The Bachd Rat Model Of Huntington Disease

Journal of neurology, neurosurgery and psychiatry, 2014-09, Vol.85 (Suppl 1), p.A27-A27

2014

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M12A769662 Leads to AMPK Activation, Induces Autophagy and has Beneficial Effects IN HD Cells

Journal of neurology, neurosurgery and psychiatry, 2014-09, Vol.85 (Suppl 1), p.A98-A98

2014

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E01Analysis of mitochondrial genes as potential genetic modifiers of the age-at-onset in Huntington disease

Journal of neurology, neurosurgery and psychiatry, 2012-09, Vol.83 (Suppl 1), p.A19-bh-A20

2012

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A41 Olfactory bulb atrophy and caspase activation observed early in the bachd transgenic lines

Widespread thalamic and cerebellar degeneration in a patient with a complicated hereditary spastic paraplegia (HSP)

LRRK2 guides the actin cytoskeleton at growth cones together with ARHGEF7 and Tropomyosin 4

The role of alpha-synuclein gene multiplications in early-onset Parkinson's disease and dementia with Lewy bodies

Nuclear Localization of Ataxin-3 Is Required for the Manifestation of Symptoms in SCA3: In Vivo Evidence

Hereditäre Ataxien

B15 Dysregulation of Gene Expression in the Striatum of Bachd Rats and Abnormalities Involved on Molecular and Protein Levels

C07 The Influence Of Obesity And Reduced Food Intake On The Behavioural Characterisation Of The Bachd Rat Model Of Huntington Disease

B15Dysregulation of Gene Expression in the Striatum of Bachd Rats and Abnormalities Involved on Molecular and Protein Levels

APPLICATION OF NEXT GENERATION TECHNOLOGIES: EP.319 The Treatabolome flags treatable genes and variants: an emerging concept

APPLICATION OF NEXT GENERATION TECHNOLOGIES

In double-transgenic mouse models non-expanded ataxin-3 not suppresses polyglutamine neurodegeneration in the SCA3 disease – in vivo evidence

Normal sensitivity to excitotoxicity in a transgenic Huntington's disease rat

Unexpected high frequency of de novo unbalanced translocations in patients with Wolf-Hirschhorn syndrome (WHS)

Klinisch-pathologische Charakterisierung von 1078 Ratsuchenden mit pathogener CHEK2 Mutation aus dem Deutschen Konsortium Familiärer Brust- und Eierstockkrebs (DK-FBREK)

Multiple organ failure due to 5-fluorouracil chemotherapy in a patient with a rare dihydropyrimidine dehydrogenase gene variant

Towards a European health research and innovation cloud (HRIC)

Genome-wide association study identifies genetic factors that modify age at onset in Machado-Joseph disease

Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease

Ubiquitylation of Synphilin-1 and α-Synuclein by SIAH and Its Presence in Cellular Inclusions and Lewy Bodies Imply a Role in Parkinson's Disease

Screening for mutations of the IRP2 gene in Parkinson's disease patients with hyperechogenicity of the substantia nigra

M12 A769662 Leads to AMPK Activation, Induces Autophagy and has Beneficial Effects IN HD Cells

C07The Influence Of Obesity And Reduced Food Intake On The Behavioural Characterisation Of The Bachd Rat Model Of Huntington Disease

M12A769662 Leads to AMPK Activation, Induces Autophagy and has Beneficial Effects IN HD Cells

E01Analysis of mitochondrial genes as potential genetic modifiers of the age-at-onset in Huntington disease

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