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Morvan's syndrome: peripheral and central nervous system and cardiac involvement with antibodies to voltage-gated potassium channels

Brain (London, England : 1878), 2001-12, Vol.124 (12), p.2417-2426

2001

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Prion: the chameleon protein

Cellular and molecular life sciences : CMLS, 2007-12, Vol.64 (24), p.3266-3270

2007

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Consensus Recommendations for the Postmortem Diagnosis of Alzheimer’s Disease

Neurobiology of aging, 1997-07, Vol.18 (4), p.S1-S2

1997

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Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt-Jakob disease

Neurology, 2004-08, Vol.63 (3), p.436-442

2004

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Accessibility of a critical prion protein region involved in strain recognition and its implications for the early detection of prions

Cellular and molecular life sciences : CMLS, 2008-02, Vol.65 (4), p.631-643, Article 631

2008

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A subtype of sporadic prion disease mimicking fatal familial insomnia

Neurology, 1999-06, Vol.52 (9), p.1757-1757

1999

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Recovery rates: Uncertainty certainly matters

Journal of banking & finance, 2019-09, Vol.106, p.371-383

2019

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Sporadic fatal insomnia in a fatal familial insomnia pedigree

Neurology, 2008-03, Vol.70 (11), p.884-885

2008

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Presenilin-1 mutations in Alzheimer's disease

Nature (London), 2000-06, Vol.405 (6786), p.531-532

2000

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Fatal insomnia and agrypnia excitata: Sleep and the limbic system

Revue neurologique, 2008-08, Vol.164 (8-9), p.692-700

2008

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TREM2 VARIANTS INCREASE RISK OF TYPICAL EARLY-ONSET ALZHEIMER'S DISEASE BUT NOT OF PRION OR FRONTOTEMPORAL DEMENTIA

Journal of neurology, neurosurgery and psychiatry, 2014-08, Vol.85 (8), p.e3-e3

2014

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Typing prion isoforms

Nature (London), 1997-03, Vol.386 (6622), p.232-233

1997

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Familial and sporadic fatal insomnia

Lancet neurology, 2003-03, Vol.2 (3), p.167-176

2003

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Tau gene mutation in familial progressive subcortical gliosis

Nature medicine, 1999-04, Vol.5 (4), p.454-457

1999

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Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt–Jakob disease: its effect on the phenotype and prion-type characteristics

Brain (London, England : 1878), 2009-10, Vol.132 (10), p.2643-2658

2009

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Variably protease-sensitive prionopathy: A new sporadic disease of the prion protein

Annals of neurology, 2010-08, Vol.68 (2), p.162-172

2010

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Effect of the E200K Mutation on Prion Protein Metabolism : Comparative Study of a Cell Model and Human Brain

The American journal of pathology, 2000-08, Vol.157 (2), p.613-622

2000

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Sporadic and familial CJD: classification and characterisation

British medical bulletin, 2003-06, Vol.66 (1), p.213-239

2003

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Insomnia in Prion Diseases: Sporadic and Familial

The New England journal of medicine, 1999-05, Vol.340 (21), p.1675-1677

1999

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Transthyretin amyloidosis: A new mutation associated with dementia

Annals of neurology, 1997-03, Vol.41 (3), p.307-313

1997

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Creutzfeldt-Jakob disease associated with a deletion of two repeats in the prion protein gene

Neurology, 2002-11, Vol.59 (10), p.1628-1630

2002

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Human prion diseases

Current opinion in neurology, 1995-08, Vol.8 (4), p.286-293

1995

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Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

Annals of neurology, 1999-08, Vol.46 (2), p.224-233

1999

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Ubiquitin is Associated with Abnormal Cytoplasmic Filaments Characteristic of Neurodegenerative Diseases

Proceedings of the National Academy of Sciences - PNAS, 1988-06, Vol.85 (12), p.4501-4505

1988

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Soluble Amyloid β-Protein Is a Marker of Alzheimer Amyloid in Brain But Not in Cerebrospinal Fluid

Biochemical and biophysical research communications, 1994-05, Vol.200 (3), p.1598-1603

1994

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Morvan's syndrome: peripheral and central nervous system and cardiac involvement with antibodies to voltage-gated potassium channels

Prion: the chameleon protein

Consensus Recommendations for the Postmortem Diagnosis of Alzheimer’s Disease

Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt-Jakob disease

Accessibility of a critical prion protein region involved in strain recognition and its implications for the early detection of prions

A subtype of sporadic prion disease mimicking fatal familial insomnia

Recovery rates: Uncertainty certainly matters

Sporadic fatal insomnia in a fatal familial insomnia pedigree

Presenilin-1 mutations in Alzheimer's disease

Fatal insomnia and agrypnia excitata: Sleep and the limbic system

TREM2 VARIANTS INCREASE RISK OF TYPICAL EARLY-ONSET ALZHEIMER'S DISEASE BUT NOT OF PRION OR FRONTOTEMPORAL DEMENTIA

Typing prion isoforms

Familial and sporadic fatal insomnia

Tau gene mutation in familial progressive subcortical gliosis

Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt–Jakob disease: its effect on the phenotype and prion-type characteristics

Variably protease-sensitive prionopathy: A new sporadic disease of the prion protein

Effect of the E200K Mutation on Prion Protein Metabolism : Comparative Study of a Cell Model and Human Brain

Sporadic and familial CJD: classification and characterisation

Insomnia in Prion Diseases: Sporadic and Familial

Transthyretin amyloidosis: A new mutation associated with dementia

Creutzfeldt-Jakob disease associated with a deletion of two repeats in the prion protein gene

Human prion diseases

Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

Ubiquitin is Associated with Abnormal Cytoplasmic Filaments Characteristic of Neurodegenerative Diseases

Soluble Amyloid β-Protein Is a Marker of Alzheimer Amyloid in Brain But Not in Cerebrospinal Fluid

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