V. Sazdovitch

发表

Elevated levels of IFNγ and LIGHT in the spinal cord of patients with sporadic amyotrophic lateral sclerosis

V. Meininger, C. Raoul, A. Moumen, 2012, European journal of neurology.

Neuropathologic variants of sporadic Creutzfeldt–Jakob disease and codon 129 of PrP gene

J. Hauw, D. Dormont, J. Laplanche, 2000, Neurology.

Prion‐like protein Doppel expression is not modified in scrapie‐infected cells and in the brains of patients with Creutzfeldt–Jakob disease

J. Laplanche, P. Beaudry, S. Lehmann, 2003, FEBS letters.

The neuropathologic diagnostic criteria of frontal lobe dementia revisited. A study of ten consecutive cases.

C. Duyckaerts, J. Hauw, D. Seilhean, 1996, Journal of neural transmission. Supplementum.

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

C. Duyckaerts, J. Hauw, D. Dormont, 2002, Acta Neuropathologica.

A brain bank in a neuropathology laboratory (with some emphasis on diagnostic criteria).

C. Duyckaerts, J. Hauw, P. Delaère, 1993, Journal of neural transmission. Supplementum.

Creutzfeldt-Jakob disease with slow progression. A mimickry of progressive supranuclear palsy.

D. Droste, U. Heinemann, N. Diederich, 2007, Bulletin de la Societe des sciences medicales du Grand-Duche de Luxembourg.

Effects of vigabatrin and of GABA on myelinated rat cerebellar cultures: preliminary data.

C. Duyckaerts, J. Hauw, J. Boutry, 1989, British journal of clinical pharmacology.

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

J. Hauw, J. Laplanche, A. Alpérovitch, 2004, Neurology.

Prion Protein is Not Detectable in Dental Pulp from Patients with Creutzfeldt-Jakob Disease

J. Hauw, J. Cesbron, D. Dormont, 2000, Journal of dental research.

Foscarnet and crystals in glomerular capillary lumens

C. Katlama, D. Henin, C. Jouanneau, 1990, The Lancet.

Human immunodeficiency virus type 1 DNA and RNA load in brains of demented and nondemented patients with acquired immunodeficiency syndrome.

C. Duyckaerts, J. Hauw, C. Katlama, 1997, Journal of neurovirology.

Human immunode ® ciency virus type 1 DNA and RNA load in brains of demented and nondemented patients with acquired immunode ® ciency syndrome

C. Duyckaerts, J. Hauw, C. Katlama, 1997 .

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

J. Hauw, J. Laplanche, S. Haïk, 2011, Neuropathology and applied neurobiology.

Sporadic Creutzfeldt-Jakob disease mimicking nonconvulsive status epilepticus

M. Baulac, V. Navarro, D. Galanaud, 2010, Neurology.

Wernicke encephalopathy and Creutzfeldt-Jakob disease

J. Hauw, F. Chapon, C. Maurage, 2009, Journal of Neurology.

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

C. Duyckaerts, J. Laplanche, A. Laquérriere, 2000, Neurology.

The nosology and neuropathology of human conditions related to unconventional infectious agents or prions

C. Duyckaerts, N. Delasnerie‐Lauprêtre, S. Camilleri, 1996 .

The neuropathology of vigabatrin.

S. Trottier, C. Duyckaerts, J. Hauw, 1988, British journal of clinical practice. Supplement.

[Fronto-temporal degenerative dementia. A modern neuropathologic approach].

C. Duyckaerts, J. Hauw, D. Seilhean, 1999, Bulletin de l'Academie nationale de medecine.

Creutzfeldt-Jak ob disease in French West Indies

D. Caparros-Lefebvre, J. Laplanche, V. Sazdovitch, 1999, The Lancet.

[Usefulness of molecular genetic analysis of the PRNP gene in patients with cerebellar ataxia: a new case of fatal familial insomnia].

J. Hauw, J. Laplanche, P. Beaudry, 2003, Revue neurologique.

Astrocytic adhesion molecules are increased in HIV‐1‐associated cognitive/motor complex

C. Duyckaerts, J. Hauw, C. Katlama, 1997, Neuropathology and applied neurobiology.

[The anatomo-pathologic examination of the brain].

C. Duyckaerts, J. Hauw, D. Henin, 2000, Annales de Pathologie.

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

C Marsault, C. Oppenheim, C. Marsault, 2002, Neurology.