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CSF biomarkers in frontotemporal lobar degeneration with known pathology

Neurology, 2008-05, Vol.70 (19 Pt 2), p.1827

2008

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Progression of alpha‐synuclein pathology in multiple system atrophy of the cerebellar type

Neuropathology and applied neurobiology, 2017-06, Vol.43 (4), p.315-329

2017

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Novel conformation‐selective alpha‐synuclein antibodies raised against different in vitro fibril forms show distinct patterns of Lewy pathology in Parkinson's disease

Neuropathology and applied neurobiology, 2017-12, Vol.43 (7), p.604-620

2017

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Distinct cerebral perfusion patterns in FTLD and AD

Neurology, 2010-09, Vol.75 (10), p.881

2010

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Glucocerebrosidase mutations are an important risk factor for Lewy body disorders

Neurology, 2006-09, Vol.67 (5), p.908

2006

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Multimodal predictors for Alzheimer disease in nonfluent primary progressive aphasia

Neurology, 2010-08, Vol.75 (7), p.595

2010

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Comparison of family histories in FTLD subtypes and related tauopathies

Neurology, 2005-12, Vol.65 (11), p.1817

2005

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Modulation of protein-protein interactions as a therapeutic strategy for the treatment of neurodegenerative tauopathies

Current topics in medicinal chemistry, 2011-02, Vol.11 (3), p.317

2011

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Longitudinal decline in autopsy-defined frontotemporal lobar degeneration

Neurology, 2008-05, Vol.70 (22), p.2036

2008

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TDP-43 pathology occurs infrequently in multiple system atrophy

Neuropathology and applied neurobiology, 2011-06, Vol.37 (4), p.358-365

2011

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A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology

Brain (London, England : 1878), 2007-05, Vol.130 (5), p.1360-1374

2007

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Cortical biochemistry in MCI and Alzheimer disease: lack of correlation with clinical diagnosis

Neurology, 2007-03, Vol.68 (10), p.757

2007

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Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations

Neurology, 2008-02, Vol.70 (7), p.521

2008

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Axonopathy and amyotrophy in mice transgenic for human four-repeat tau protein

Acta neuropathologica, 2000-05, Vol.99 (5), p.469-481

2000

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NTera 2 Cells: A human cell line which displays characteristics expected of a human committed neuronal progenitor cell

Journal of neuroscience research, 1993-08, Vol.35 (6), p.585-602

1993

Volltextzugriff (PDF)

Monoclonal antibody PHF-1 recognizes tau protein phosphorylated at serine residues 396 and 404

Journal of neuroscience research, 1994-12, Vol.39 (6), p.669-673

1994

Volltextzugriff (PDF)

The North American Multiple System Atrophy Study Group

Journal of Neural Transmission, 2005-12, Vol.112 (12), p.1687-1694

2005

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Novel CSF biomarkers for frontotemporal lobar degenerations

Neurology, 2010-12, Vol.75 (23), p.2079

2010

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The Neuropathology of a Chromosome 17-Linked Autosomal Dominant Parkinsonism and Dementia (“Pallido-Ponto-Nigral Degeneration”)

Journal of neuropathology and experimental neurology, 1998-06, Vol.57 (6), p.588-601

1998

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Cognitive and motor assessment in autopsy-proven corticobasal degeneration

Neurology, 2007-04, Vol.68 (16), p.1274

2007

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Mutations in TDP-43 link glycine-rich domain functions to amyotrophic lateral sclerosis

Human molecular genetics, 2009-10, Vol.18 (R2), p.R156-R162

2009

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Functions of neurofilaments in synapses

Molecular psychiatry, 2015-08, Vol.20 (8), p.915-915

2015

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Neurofilament subunits are integral components of synapses and modulate neurotransmission and behavior in vivo

Molecular psychiatry, 2015-08, Vol.20 (8), p.986-994

2015

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Clinical and neuropathologic variation in neuronal intermediate filament inclusion disease

Neurology, 2004-10, Vol.63 (8), p.1376

2004

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Radioiodinated Styrylbenzenes and Thioflavins as Probes for Amyloid Aggregates

Journal of medicinal chemistry, 2001-06, Vol.44 (12), p.1905-1914

2001

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CSF biomarkers in frontotemporal lobar degeneration with known pathology

Progression of alpha‐synuclein pathology in multiple system atrophy of the cerebellar type

Novel conformation‐selective alpha‐synuclein antibodies raised against different in vitro fibril forms show distinct patterns of Lewy pathology in Parkinson's disease

Distinct cerebral perfusion patterns in FTLD and AD

Glucocerebrosidase mutations are an important risk factor for Lewy body disorders

Multimodal predictors for Alzheimer disease in nonfluent primary progressive aphasia

Comparison of family histories in FTLD subtypes and related tauopathies

Modulation of protein-protein interactions as a therapeutic strategy for the treatment of neurodegenerative tauopathies

Longitudinal decline in autopsy-defined frontotemporal lobar degeneration

TDP-43 pathology occurs infrequently in multiple system atrophy

A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology

Cortical biochemistry in MCI and Alzheimer disease: lack of correlation with clinical diagnosis

Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations

Axonopathy and amyotrophy in mice transgenic for human four-repeat tau protein

NTera 2 Cells: A human cell line which displays characteristics expected of a human committed neuronal progenitor cell

Monoclonal antibody PHF-1 recognizes tau protein phosphorylated at serine residues 396 and 404

The North American Multiple System Atrophy Study Group

Novel CSF biomarkers for frontotemporal lobar degenerations

The Neuropathology of a Chromosome 17-Linked Autosomal Dominant Parkinsonism and Dementia (“Pallido-Ponto-Nigral Degeneration”)

Cognitive and motor assessment in autopsy-proven corticobasal degeneration

Mutations in TDP-43 link glycine-rich domain functions to amyotrophic lateral sclerosis

Functions of neurofilaments in synapses

Neurofilament subunits are integral components of synapses and modulate neurotransmission and behavior in vivo

Clinical and neuropathologic variation in neuronal intermediate filament inclusion disease

Radioiodinated Styrylbenzenes and Thioflavins as Probes for Amyloid Aggregates

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