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Mixed Dementia: Epidemiology, Diagnosis, and Treatment

Journal of the American Geriatrics Society (JAGS), 2002-08, Vol.50 (8), p.1431-1438

2002

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A stable proportion of Lewy body bearing neurons in the substantia nigra suggests a model in which the Lewy body causes neuronal death

Neurobiology of aging, 2010-01, Vol.31 (1), p.99-103

2010

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Effects of Antemortem and Postmortem Variables on Human Brain mRNA Quality: A BrainNet Europe Study

Journal of neuropathology and experimental neurology, 2010-01, Vol.69 (1), p.70-81

2010

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Cycline Efficacy on the Propagation of Human Prions in Primary Cultured Neurons is Strain-Specific

The Journal of infectious diseases, 2014-04, Vol.209 (7), p.1144-1148

2014

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Neuromelanin associated redox‐active iron is increased in the substantia nigra of patients with Parkinson's disease

Journal of neurochemistry, 2003-09, Vol.86 (5), p.1142-1148

2003

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How and why I fell into neuropathology

Free Neuropathology, 2023-11, Vol.4

Hauw, Jean Jacques

2023

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Nodes of ranvier and paranodes in chronic acquired neuropathies

PloS one, 2011-01, Vol.6 (1), p.e14533-e14533

2011

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Charcot identifies and illustrates amyotrophic lateral sclerosis

Free Neuropathology, 2021-01, Vol.2

2021

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Muscle Nogo-a expression is a prognostic marker in lower motor neuron syndromes

Annals of neurology, 2007-07, Vol.62 (1), p.15-20

2007

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Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders

Human molecular genetics, 2012-12, Vol.21 (26), p.5417-5428

2012

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Variant Creutzfeldt-Jakob disease in France and the United Kingdom: Evidence for the same agent strain

Annals of neurology, 2009-03, Vol.65 (3), p.249-256

2009

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Autopsy Prevalence of Intracranial Atherosclerosis in Patients With Fatal Stroke

Stroke (1970), 2008-04, Vol.39 (4), p.1142-1147

2008

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Nogo expression in muscle correlates with amyotrophic lateral sclerosis severity

Annals of neurology, 2005-04, Vol.57 (4), p.553-556

2005

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Is the urea cycle involved in Alzheimer's disease?

Journal of Alzheimer's disease, 2010-01, Vol.21 (3), p.1013-1021

2010

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Interlaboratory Comparison of Assessments of Alzheimer Disease-Related Lesions: A Study of the BrainNet Europe Consortium

Journal of neuropathology and experimental neurology, 2006-08, Vol.65 (8), p.740-757

2006

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Enhanced expression of aquaporin 4 in human brain with inflammatory diseases

Acta neuropathologica, 2005-09, Vol.110 (3), p.281-288

2005

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Degenerative and vascular lesions of the brain have synergistic effects in dementia of the elderly

Acta neuropathologica, 2002-05, Vol.103 (5), p.481-487

2002

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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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Transmission of the BSE agent to mice in the absence of detectable abnormal prion protein

Science (American Association for the Advancement of Science), 1997-01, Vol.275 (5298), p.402-405

1997

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Coronary and Basilar Artery Ectasia Are Associated: Results From an Autopsy Case–Control Study

Stroke (1970), 2016-01, Vol.47 (1), p.224-227

2016

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Inter-Laboratory Assessment of PrPSc Typing in Creutzfeldt-Jakob Disease: A Western Blot Study within the NeuroPrion Consortium

Brain pathology (Zurich, Switzerland), 2009-07, Vol.19 (3), p.384-391

2009

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Lack of up‐regulation of ferritin is associated with sustained iron regulatory protein‐1 binding activity in the substantia nigra of patients with Parkinson's disease

Journal of neurochemistry, 2002-10, Vol.83 (2), p.320-330

2002

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Amyloid Angiopathy in Brain Hemorrhage: A Postmortem Neuropathological-Magnetic Resonance Imaging Study

Cerebrovascular diseases (Basel, Switzerland), 2018-01, Vol.45 (3-4), p.124-131

2018

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Regulating factors of PrP glycosylation in Creutzfeldt-Jakob disease--implications for the dissemination and the diagnosis of human prion strains

PloS one, 2008-07, Vol.3 (7), p.e2786-e2786

2008

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Mixed Dementia: Epidemiology, Diagnosis, and Treatment

A stable proportion of Lewy body bearing neurons in the substantia nigra suggests a model in which the Lewy body causes neuronal death

Effects of Antemortem and Postmortem Variables on Human Brain mRNA Quality: A BrainNet Europe Study

Cycline Efficacy on the Propagation of Human Prions in Primary Cultured Neurons is Strain-Specific

Neuromelanin associated redox‐active iron is increased in the substantia nigra of patients with Parkinson's disease

How and why I fell into neuropathology

Nodes of ranvier and paranodes in chronic acquired neuropathies

Charcot identifies and illustrates amyotrophic lateral sclerosis

Muscle Nogo-a expression is a prognostic marker in lower motor neuron syndromes

Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders

Variant Creutzfeldt-Jakob disease in France and the United Kingdom: Evidence for the same agent strain

ADAM30 Downregulates APP-Linked Defects Through Cathepsin D Activation in Alzheimer's Disease

Autopsy Prevalence of Intracranial Atherosclerosis in Patients With Fatal Stroke

Nogo expression in muscle correlates with amyotrophic lateral sclerosis severity

Is the urea cycle involved in Alzheimer's disease?

Interlaboratory Comparison of Assessments of Alzheimer Disease-Related Lesions: A Study of the BrainNet Europe Consortium

Enhanced expression of aquaporin 4 in human brain with inflammatory diseases

Degenerative and vascular lesions of the brain have synergistic effects in dementia of the elderly

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

Transmission of the BSE agent to mice in the absence of detectable abnormal prion protein

Coronary and Basilar Artery Ectasia Are Associated: Results From an Autopsy Case–Control Study

Inter-Laboratory Assessment of PrPSc Typing in Creutzfeldt-Jakob Disease: A Western Blot Study within the NeuroPrion Consortium

Lack of up‐regulation of ferritin is associated with sustained iron regulatory protein‐1 binding activity in the substantia nigra of patients with Parkinson's disease

Amyloid Angiopathy in Brain Hemorrhage: A Postmortem Neuropathological-Magnetic Resonance Imaging Study

Regulating factors of PrP glycosylation in Creutzfeldt-Jakob disease--implications for the dissemination and the diagnosis of human prion strains

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