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Prognosis and Neuropathologic Correlation of Clinical Subtypes of Parkinson Disease

JAMA neurology, 2019-04, Vol.76 (4), p.470

2019

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Improving diagnostic accuracy of multiple system atrophy: a clinicopathological study

Brain (London, England : 1878), 2019-09, Vol.142 (9), p.2813-2827

2019

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A Histologic Study of the Circadian System in Parkinson Disease, Multiple System Atrophy, and Progressive Supranuclear Palsy

JAMA neurology, 2018-08, Vol.75 (8), p.1008

2018

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Neuropathological criteria of anti-IgLON5-related tauopathy

Acta neuropathologica, 2016-10, Vol.132 (4), p.531-543

2016

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Astrogliopathy predominates the earliest stage of corticobasal degeneration pathology

Brain (London, England : 1878), 2016-12, Vol.139 (Pt 12), p.3237-3252

2016

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Histological evidence of chronic traumatic encephalopathy in a large series of neurodegenerative diseases

Acta neuropathologica, 2015-12, Vol.130 (6), p.891-893

2015

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Dysregulation of glucose metabolism is an early event in sporadic Parkinson's disease

Neurobiology of aging, 2014-05, Vol.35 (5), p.1111-1115

2014

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Alpha-synuclein mRNA expression in oligodendrocytes in MSA

Glia, 2014-06, Vol.62 (6), p.964-970

2014

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Cerebral mitochondrial electron transport chain dysfunction in multiple system atrophy and Parkinson's disease

Scientific reports, 2019-04, Vol.9 (1), p.6559, Article 6559

2019

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Cognitive impairment in multiple system atrophy: A position statement by the neuropsychology task force of the MDS multiple system atrophy (MODIMSA) study group

Movement disorders, 2014-06, Vol.29 (7), p.857-867

2014

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Development of phospho-specific Rab protein antibodies to monitor in vivo activity of the LRRK2 Parkinson's disease kinase

Biochemical journal, 2018-01, Vol.475 (1), p.1-22

2018

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Genetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathies

Acta neuropathologica, 2009-07, Vol.118 (1), p.115-130

2009

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Research in motion: the enigma of Parkinson's disease pathology spread

Nature reviews. Neuroscience, 2008-10, Vol.9 (10), p.741-745

2008

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White matter DNA methylation profiling reveals deregulation of HIP1, LMAN2, MOBP, and other loci in multiple system atrophy

Acta neuropathologica, 2020-01, Vol.139 (1), p.135-156

2020

Volltextzugriff (PDF)

Prominent astrocytic alpha-synuclein pathology with unique post-translational modification signatures unveiled across Lewy body disorders

Acta neuropathologica communications, 2022-11, Vol.10 (1), p.163-163, Article 163

2022

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Association of clusterin with the BRI2-derived amyloid molecules ABri and ADan

Neurobiology of disease, 2021-10, Vol.158, p.105452-105452, Article 105452

2021

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The aftermath of boxing revisited: identifying chronic traumatic encephalopathy pathology in the original Corsellis boxer series

Acta neuropathologica, 2018-12, Vol.136 (6), p.973-974

2018

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Conventional magnetic resonance imaging in confirmed progressive supranuclear palsy and multiple system atrophy

Movement disorders, 2012-12, Vol.27 (14), p.1754-1762

2012

Volltextzugriff (PDF)

Cryptic Amyloidogenic Elements in the 3′ UTRs of Neurofilament Genes Trigger Axonal Neuropathy

American journal of human genetics, 2016-04, Vol.98 (4), p.597-614

2016

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Coenzyme Q10 Levels Are Decreased in the Cerebellum of Multiple-System Atrophy Patients

PloS one, 2016-02, Vol.11 (2), p.e0149557-e0149557

2016

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Identification of multiple system atrophy mimicking Parkinson's disease or progressive supranuclear palsy

Brain (London, England : 1878), 2021-05, Vol.144 (4), p.1138-1151

2021

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Proteomics of rimmed vacuoles define new risk allele in inclusion body myositis

Annals of neurology, 2017-02, Vol.81 (2), p.227-239

2017

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Pathological tau burden and distribution distinguishes progressive supranuclear palsy-parkinsonism from Richardson's syndrome

Brain (London, England : 1878), 2007-06, Vol.130 (6), p.1566-1576

2007

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Targeting protein homeostasis in sporadic inclusion body myositis

Science translational medicine, 2016-03, Vol.8 (331), p.331ra41

2016

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Early presentation of urinary retention in multiple system atrophy: can the disease begin in the sacral spinal cord?

Journal of neurology, 2020-03, Vol.267 (3), p.659-664

2020

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Prognosis and Neuropathologic Correlation of Clinical Subtypes of Parkinson Disease

Improving diagnostic accuracy of multiple system atrophy: a clinicopathological study

A Histologic Study of the Circadian System in Parkinson Disease, Multiple System Atrophy, and Progressive Supranuclear Palsy

Neuropathological criteria of anti-IgLON5-related tauopathy

Astrogliopathy predominates the earliest stage of corticobasal degeneration pathology

Histological evidence of chronic traumatic encephalopathy in a large series of neurodegenerative diseases

Dysregulation of glucose metabolism is an early event in sporadic Parkinson's disease

Alpha-synuclein mRNA expression in oligodendrocytes in MSA

Cerebral mitochondrial electron transport chain dysfunction in multiple system atrophy and Parkinson's disease

Cognitive impairment in multiple system atrophy: A position statement by the neuropsychology task force of the MDS multiple system atrophy (MODIMSA) study group

Development of phospho-specific Rab protein antibodies to monitor in vivo activity of the LRRK2 Parkinson's disease kinase

Genetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathies

Research in motion: the enigma of Parkinson's disease pathology spread

White matter DNA methylation profiling reveals deregulation of HIP1, LMAN2, MOBP, and other loci in multiple system atrophy

Prominent astrocytic alpha-synuclein pathology with unique post-translational modification signatures unveiled across Lewy body disorders

Association of clusterin with the BRI2-derived amyloid molecules ABri and ADan

The aftermath of boxing revisited: identifying chronic traumatic encephalopathy pathology in the original Corsellis boxer series

Conventional magnetic resonance imaging in confirmed progressive supranuclear palsy and multiple system atrophy

Cryptic Amyloidogenic Elements in the 3′ UTRs of Neurofilament Genes Trigger Axonal Neuropathy

Coenzyme Q10 Levels Are Decreased in the Cerebellum of Multiple-System Atrophy Patients

Identification of multiple system atrophy mimicking Parkinson's disease or progressive supranuclear palsy

Proteomics of rimmed vacuoles define new risk allele in inclusion body myositis

Pathological tau burden and distribution distinguishes progressive supranuclear palsy-parkinsonism from Richardson's syndrome

Targeting protein homeostasis in sporadic inclusion body myositis

Early presentation of urinary retention in multiple system atrophy: can the disease begin in the sacral spinal cord?

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