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Is All Inflammation within Temporal Artery Biopsies Temporal Arteritis?

Human pathology, 2016-11, Vol.57, p.17-21

2016

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Structural determinants of phenotypic diversity and replication rate of human prions

PLoS pathogens, 2015-04, Vol.11 (4), p.e1004832-e1004832

2015

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Molecular subtypes of glioblastoma are relevant to lower grade glioma

PloS one, 2014-03, Vol.9 (3), p.e91216-e91216

2014

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Feasibility of Remote Assessment of Human Prion Diseases for Research and Surveillance

Dementia and geriatric cognitive disorders, 2019-05, Vol.47 (1-2), p.79

2019

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Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study

Acta neuropathologica communications, 2018-01, Vol.6 (1), p.5-5, Article 5

2018

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Novel histotypes of sporadic Creutzfeldt-Jakob disease linked to 129MV genotype

Acta neuropathologica communications, 2023-08, Vol.11 (1), p.141-141, Article 141

2023

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Characterization of Prion Disease Associated with a Two-Octapeptide Repeat Insertion

Viruses, 2021-09, Vol.13 (9), p.1794

2021

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Abnormal brain iron homeostasis in human and animal prion disorders

PLoS pathogens, 2009-03, Vol.5 (3), p.e1000336-e1000336

2009

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Diagnostic and prognostic value of human prion detection in cerebrospinal fluid

Annals of neurology, 2017-01, Vol.81 (1), p.79-92

2017

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Pathological findings in autoimmune encephalitis autopsy specimens from cases of suspected prion disease

Journal of neurology, 2024, Vol.271 (1), p.446-456

2024

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The Emerging Role of Inhaled Heroin in the Opioid Epidemic: A Review

JAMA neurology, 2018-11, Vol.75 (11), p.1423

2018

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C19orf12 ablation causes ferroptosis in mitochondrial membrane protein-associated with neurodegeneration

Free radical biology & medicine, 2022-03, Vol.182, p.23-33

2022

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Whole-genome and multisector exome sequencing of primary and post-treatment glioblastoma reveals patterns of tumor evolution

Genome research, 2015-03, Vol.25 (3), p.316

2015

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The disturbance of gaze in progressive supranuclear palsy: implications for pathogenesis

Frontiers in neurology, 2010, Vol.1, p.147-147

2010

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DNA damage and cell cycle events implicate cerebellar dentate nucleus neurons as targets of Alzheimer's disease

Molecular neurodegeneration, 2010-12, Vol.5 (1), p.60-60, Article 60

2010

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Rapidly progressive Alzheimer's disease features distinct structures of amyloid-β

Brain (London, England : 1878), 2015-04, Vol.138 (Pt 4), p.1009-1022

2015

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Adult Diffuse Astrocytic and Oligodendroglial Tumors

Neurosurgery, 2021-11, Vol.89 (5), p.737-749

2021

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Evaluation of a New Criterion for Detecting Prion Disease With Diffusion Magnetic Resonance Imaging

JAMA neurology, 2020-09, Vol.77 (9), p.1141

2020

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Treatable neurological disorders misdiagnosed as Creutzfeldt-Jakob disease

Annals of neurology, 2011-09, Vol.70 (3), p.437-444

2011

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Efficient transmission of human prion diseases to a glycan-free prion protein-expressing host

Brain (London, England : 1878), 2023-11, Vol.147 (4), p.1539-1552

2023

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EphA2 Mediates Ligand-Dependent Inhibition and Ligand-Independent Promotion of Cell Migration and Invasion via a Reciprocal Regulatory Loop with Akt

Cancer cell, 2009-07, Vol.16 (1), p.9-20

2009

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Subtype Diagnosis of Sporadic Creutzfeldt–Jakob Disease with Diffusion Magnetic Resonance Imaging

Annals of neurology, 2021-03, Vol.89 (3), p.560-572

2021

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Prion seeding activity and infectivity in skin samples from patients with sporadic Creutzfeldt-Jakob disease

Science translational medicine, 2017-11, Vol.9 (417)

2017

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Distinct conformers of amyloid beta accumulate in the neocortex of patients with rapidly progressive Alzheimer's disease

The Journal of biological chemistry, 2021-11, Vol.297 (5), p.101267-101267, Article 101267

2021

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Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA

Acta neuropathologica, 2012-10, Vol.124 (4), p.517-529

2012

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Is All Inflammation within Temporal Artery Biopsies Temporal Arteritis?

Structural determinants of phenotypic diversity and replication rate of human prions

Molecular subtypes of glioblastoma are relevant to lower grade glioma

Feasibility of Remote Assessment of Human Prion Diseases for Research and Surveillance

Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study

Novel histotypes of sporadic Creutzfeldt-Jakob disease linked to 129MV genotype

Characterization of Prion Disease Associated with a Two-Octapeptide Repeat Insertion

Abnormal brain iron homeostasis in human and animal prion disorders

Diagnostic and prognostic value of human prion detection in cerebrospinal fluid

Pathological findings in autoimmune encephalitis autopsy specimens from cases of suspected prion disease

The Emerging Role of Inhaled Heroin in the Opioid Epidemic: A Review

C19orf12 ablation causes ferroptosis in mitochondrial membrane protein-associated with neurodegeneration

Whole-genome and multisector exome sequencing of primary and post-treatment glioblastoma reveals patterns of tumor evolution

The disturbance of gaze in progressive supranuclear palsy: implications for pathogenesis

DNA damage and cell cycle events implicate cerebellar dentate nucleus neurons as targets of Alzheimer's disease

Rapidly progressive Alzheimer's disease features distinct structures of amyloid-β

Adult Diffuse Astrocytic and Oligodendroglial Tumors

Evaluation of a New Criterion for Detecting Prion Disease With Diffusion Magnetic Resonance Imaging

Treatable neurological disorders misdiagnosed as Creutzfeldt-Jakob disease

Efficient transmission of human prion diseases to a glycan-free prion protein-expressing host

EphA2 Mediates Ligand-Dependent Inhibition and Ligand-Independent Promotion of Cell Migration and Invasion via a Reciprocal Regulatory Loop with Akt

Subtype Diagnosis of Sporadic Creutzfeldt–Jakob Disease with Diffusion Magnetic Resonance Imaging

Prion seeding activity and infectivity in skin samples from patients with sporadic Creutzfeldt-Jakob disease

Distinct conformers of amyloid beta accumulate in the neocortex of patients with rapidly progressive Alzheimer's disease

Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA

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