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Differential overexpression of SERPINA3 in human prion diseases

Scientific reports, 2017-11, Vol.7 (1), p.15637-13, Article 15637

2017

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Sporadic Creutzfeldt-Jakob disease mimicking nonconvulsive status epilepticus

Neurology, 2010-06, Vol.74 (24), p.1995-1999

2010

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The French surveillance network of Creutzfeldt–Jakob disease. Epidemiological data in France and worldwide

Transfusion clinique et biologique (Paris), 2013-09, Vol.20 (4), p.395-397

2013

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Spreading of protein misfolding: A new paradigm in neurology

Revue neurologique, 2015-12, Vol.171 (12), p.825-831

2015

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Compassionate use of quinacrine in Creutzfeldt-Jakob disease fails to show significant effects

Neurology, 2004-12, Vol.63 (12), p.2413-2415

2004

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The 37-kDa/67-kDa laminin receptor acts as the cell-surface receptor for the cellular prion protein

The EMBO journal, 2001-11, Vol.20 (21), p.5863-5875

2001

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Tauopathy in human and experimental variant Creutzfeldt-Jakob disease

Neurobiology of aging, 2008-12, Vol.29 (12), p.1864-1873

2008

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Synergistic electrical and thermal transport properties of hybrid polymeric nanocomposites based on carbon nanotubes and graphite nanoplatelets

Carbon (New York), 2013-11, Vol.64, p.111-121

2013

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Identification of interaction domains of the prion protein with its 37-kDa/67-kDa laminin receptor

The EMBO journal, 2001-11, Vol.20 (21), p.5876-5886

2001

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La maladie de Parkinson est-elle une maladie à prion ?

Revue neurologique, 2015-12, Vol.171 (12), p.812-824

2015

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Is Parkinson's disease a prion disease?

Revue neurologique, 2015-12, Vol.171 (12), p.812-824

2015

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A novel mutation (G114V) in the prion protein gene in a family with inherited prion disease

Neurology, 2005-04, Vol.64 (8), p.1455-1457

2005

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Wernicke encephalopathy and Creutzfeldt-Jakob disease

Journal of neurology, 2009-06, Vol.256 (6), p.904-909

2009

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Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes

Neuropathology and applied neurobiology, 2011-08, Vol.37 (5), p.500-512

2011

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Interlaminar fracture toughness of hybrid carbon fiber‐carbon nanotubes‐reinforced polymer composites

Polymer composites, 2019-03, Vol.40 (S2), p.E1470-E1478

2019

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Mechanical properties of amorphous silicon carbonitride thin films at elevated temperatures

Journal of materials science, 2015-02, Vol.50 (4), p.1553-1564

2015

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Hybrid carbon fiber/carbon nanotube composites for structural damping applications

Nanotechnology, 2013-04, Vol.24 (15), p.155704-155704

2013

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Differences of apparent diffusion coefficient values in patients with Creutzfeldt-Jakob disease according to the codon 129 genotype

American journal of neuroradiology : AJNR, 2008-08, Vol.29 (7), p.E57; author reply E58-E57; author reply E58

2008

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Brain targeting through the autonomous nervous system: lessons from prion diseases

Trends in molecular medicine, 2004-03, Vol.10 (3), p.107-112

2004

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Sporadic CJD clinically mimicking variant CJD with bilateral increased signal in the pulvinar

Neurology, 2002-01, Vol.58 (1), p.148-149

2002

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Dementia with Lewy bodies in a neuropathologic series of suspected Creutzfeldt-Jakob disease

Neurology, 2000-11, Vol.55 (9), p.1401-1404

2000

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Na+-Dependent High-Affinity Glutamate Transport in Macrophages

The Journal of immunology (1950), 2000-05, Vol.164 (10), p.5430-5438

2000

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Doxycycline versus placebo trial in human prion diseases: a therapeutic challenge

Revue neurologique, 2010-03, Vol.166 (3), p.266-268

2010

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Alpha-synuclein-immunoreactive deposits in human and animal prion diseases

Acta neuropathologica, 2002-05, Vol.103 (5), p.516-520

2002

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Differential overexpression of SERPINA3 in human prion diseases

Sporadic Creutzfeldt-Jakob disease mimicking nonconvulsive status epilepticus

The French surveillance network of Creutzfeldt–Jakob disease. Epidemiological data in France and worldwide

Spreading of protein misfolding: A new paradigm in neurology

Compassionate use of quinacrine in Creutzfeldt-Jakob disease fails to show significant effects

The 37-kDa/67-kDa laminin receptor acts as the cell-surface receptor for the cellular prion protein

Tauopathy in human and experimental variant Creutzfeldt-Jakob disease

Synergistic electrical and thermal transport properties of hybrid polymeric nanocomposites based on carbon nanotubes and graphite nanoplatelets

Identification of interaction domains of the prion protein with its 37-kDa/67-kDa laminin receptor

La maladie de Parkinson est-elle une maladie à prion ?

Is Parkinson's disease a prion disease?

A novel mutation (G114V) in the prion protein gene in a family with inherited prion disease

Wernicke encephalopathy and Creutzfeldt-Jakob disease

Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes

Interlaminar fracture toughness of hybrid carbon fiber‐carbon nanotubes‐reinforced polymer composites

Mechanical properties of amorphous silicon carbonitride thin films at elevated temperatures

Potential human transmission of amyloid β pathology: surveillance and risks

Hybrid carbon fiber/carbon nanotube composites for structural damping applications

Differences of apparent diffusion coefficient values in patients with Creutzfeldt-Jakob disease according to the codon 129 genotype

Brain targeting through the autonomous nervous system: lessons from prion diseases

Sporadic CJD clinically mimicking variant CJD with bilateral increased signal in the pulvinar

Dementia with Lewy bodies in a neuropathologic series of suspected Creutzfeldt-Jakob disease

Na+-Dependent High-Affinity Glutamate Transport in Macrophages

Doxycycline versus placebo trial in human prion diseases: a therapeutic challenge

Alpha-synuclein-immunoreactive deposits in human and animal prion diseases

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