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Stages of the Pathologic Process in Alzheimer Disease: Age Categories From 1 to 100 Years

Journal of neuropathology and experimental neurology, 2011-11, Vol.70 (11), p.960-969

2011

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TDP-43 is intercellularly transmitted across axon terminals

The Journal of cell biology, 2015-11, Vol.211 (4), p.897-911

2015

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Microglial repopulation model reveals a robust homeostatic process for replacing CNS myeloid cells

Proceedings of the National Academy of Sciences - PNAS, 2012-10, Vol.109 (44), p.18150-18155

2012

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The relationship between subcortical tau pathology and Alzheimer's disease

Biochemical Society transactions, 2012-08, Vol.40 (4), p.711-715

2012

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Astrocyte-derived Jagged-1 mitigates deleterious Notch signaling in amyotrophic lateral sclerosis

Neurobiology of disease, 2018-11, Vol.119, p.26-40

2018

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Blood-brain barrier resealing in neuromyelitis optica occurs independently of astrocyte regeneration

The Journal of clinical investigation, 2021-03, Vol.131 (5), p.1-16

2021

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Peripheral monocytes are functionally altered and invade the CNS in ALS patients

Acta neuropathologica, 2016-09, Vol.132 (3), p.391-411

2016

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PART, a distinct tauopathy, different from classical sporadic Alzheimer disease

Acta neuropathologica, 2015-05, Vol.129 (5), p.757-762

2015

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Limited role of free TDP-43 as a diagnostic tool in neurodegenerative diseases

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2014-09, Vol.15 (5-6), p.351-356

2014

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Clearance of amyloid β-protein and its role in the spreading of Alzheimer's disease pathology

Frontiers in aging neuroscience, 2015-03, Vol.7, p.25-25

Thal, Dietmar R

2015

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Sporadic late-onset nemaline myopathy: clinico-pathological characteristics and review of 76 cases

Orphanet journal of rare diseases, 2017-05, Vol.12 (1), p.86-86, Article 86

2017

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Nonsteroidal Anti-Inflammatory Drugs Repress β-Secretase Gene Promoter Activity by the Activation of PPARγ

Proceedings of the National Academy of Sciences - PNAS, 2006-01, Vol.103 (2), p.443-448

2006

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Unravelling cell type-specific responses to Parkinson's Disease at single cell resolution

Molecular neurodegeneration, 2024-01, Vol.19 (1), p.7-7, Article 7

2024

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Histopathological correlations and fat replacement imaging patterns in recessive limb‐girdle muscular dystrophy type 12

Journal of cachexia, sarcopenia and muscle, 2023-06, Vol.14 (3), p.1468-1481

2023

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Correction: Unravelling cell type-specific responses to Parkinson's Disease at single cell resolution

Molecular neurodegeneration, 2024-03, Vol.19 (1), p.28-28, Article 28

2024

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The TGF-β System As a Potential Pathogenic Player in Disease Modulation of Amyotrophic Lateral Sclerosis

Frontiers in neurology, 2017-12, Vol.8, p.669-669

2017

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Abnormal Paraplegin Expression in Swollen Neurites, τ- and α-Synuclein Pathology in a Case of Hereditary Spastic Paraplegia SPG7 with an Ala510Val Mutation

International journal of molecular sciences, 2015-10, Vol.16 (10), p.25050-25066

2015

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Amyotrophic lateral sclerosis: dash-like accumulation of phosphorylated TDP-43 in somatodendritic and axonal compartments of somatomotor neurons of the lower brainstem and spinal cord

Acta neuropathologica, 2010-07, Vol.120 (1), p.67-74

2010

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Early loss of oligodendrocytes in human and experimental neuromyelitis optica lesions

Acta neuropathologica, 2014-04, Vol.127 (4), p.523-538

2014

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The Golgi-Localized γ-Ear-Containing ARF-Binding (GGA) Proteins Alter Amyloid-β Precursor Protein (APP) Processing through Interaction of Their GAE Domain with the Beta-Site APP Cleaving Enzyme 1 (BACE1)

PloS one, 2015-06, Vol.10 (6), p.e0129047-e0129047

2015

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Proteomics in cerebrospinal fluid and spinal cord suggests UCHL1, MAP2 and GPNMB as biomarkers and underpins importance of transcriptional pathways in amyotrophic lateral sclerosis

Acta neuropathologica, 2020, Vol.139 (1), p.119-134

2020

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Unraveling the Molecular Basis of the Dystrophic Process in Limb-Girdle Muscular Dystrophy LGMD-R12 by Differential Gene Expression Profiles in Diseased and Healthy Muscles

Cells (Basel, Switzerland), 2022-04, Vol.11 (9), p.1508

2022

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Mutant valosin-containing protein causes a novel type of frontotemporal dementia

Annals of neurology, 2005-03, Vol.57 (3), p.457-461

2005

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The Biphasic Relationship between Regional Brain Senile Plaque and Neurofibrillary Tangle Distributions: Modification by Age, Sex, and APOE Polymorphism

Annals of the New York Academy of Sciences, 2004-06, Vol.1019 (1), p.24-28

2004

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The Precapillary Segment of the Blood-Brain Barrier and Its Relation to Perivascular Drainage in Alzheimer's Disease and Small Vessel Disease

TheScientificWorld, 2009-01, Vol.9, p.557-563

Thal, Dietmar R

2009

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Stages of the Pathologic Process in Alzheimer Disease: Age Categories From 1 to 100 Years

TDP-43 is intercellularly transmitted across axon terminals

Microglial repopulation model reveals a robust homeostatic process for replacing CNS myeloid cells

The relationship between subcortical tau pathology and Alzheimer's disease

Astrocyte-derived Jagged-1 mitigates deleterious Notch signaling in amyotrophic lateral sclerosis

Blood-brain barrier resealing in neuromyelitis optica occurs independently of astrocyte regeneration

Peripheral monocytes are functionally altered and invade the CNS in ALS patients

PART, a distinct tauopathy, different from classical sporadic Alzheimer disease

Limited role of free TDP-43 as a diagnostic tool in neurodegenerative diseases

Clearance of amyloid β-protein and its role in the spreading of Alzheimer's disease pathology

Sporadic late-onset nemaline myopathy: clinico-pathological characteristics and review of 76 cases

Nonsteroidal Anti-Inflammatory Drugs Repress β-Secretase Gene Promoter Activity by the Activation of PPARγ

Unravelling cell type-specific responses to Parkinson's Disease at single cell resolution

Histopathological correlations and fat replacement imaging patterns in recessive limb‐girdle muscular dystrophy type 12

Correction: Unravelling cell type-specific responses to Parkinson's Disease at single cell resolution

The TGF-β System As a Potential Pathogenic Player in Disease Modulation of Amyotrophic Lateral Sclerosis

Abnormal Paraplegin Expression in Swollen Neurites, τ- and α-Synuclein Pathology in a Case of Hereditary Spastic Paraplegia SPG7 with an Ala510Val Mutation

Amyotrophic lateral sclerosis: dash-like accumulation of phosphorylated TDP-43 in somatodendritic and axonal compartments of somatomotor neurons of the lower brainstem and spinal cord

Early loss of oligodendrocytes in human and experimental neuromyelitis optica lesions

The Golgi-Localized γ-Ear-Containing ARF-Binding (GGA) Proteins Alter Amyloid-β Precursor Protein (APP) Processing through Interaction of Their GAE Domain with the Beta-Site APP Cleaving Enzyme 1 (BACE1)

Proteomics in cerebrospinal fluid and spinal cord suggests UCHL1, MAP2 and GPNMB as biomarkers and underpins importance of transcriptional pathways in amyotrophic lateral sclerosis

Unraveling the Molecular Basis of the Dystrophic Process in Limb-Girdle Muscular Dystrophy LGMD-R12 by Differential Gene Expression Profiles in Diseased and Healthy Muscles

Mutant valosin-containing protein causes a novel type of frontotemporal dementia

The Biphasic Relationship between Regional Brain Senile Plaque and Neurofibrillary Tangle Distributions: Modification by Age, Sex, and APOE Polymorphism

The Precapillary Segment of the Blood-Brain Barrier and Its Relation to Perivascular Drainage in Alzheimer's Disease and Small Vessel Disease

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