Search Results - "Privat, N"

Evaluating the behaviour of instrumented prototype rockfill dams by SIDDIQUA, S, BLATZ, J. A, PRIVAT, N. C

“…This paper studies the behaviour of prototype rockfill dams under turbulent flow conditions to identify the flow-through characteristics of rockfill materials…”
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Amplification techniques and diagnosis of prion diseases by Brandel, J.-P., Culeux, A., Grznarova, K., Levavasseur, E., Lamy, P., Privat, N., Welaratne, A., Denouel, A., Laplanche, J.-L., Haik, S.

“…Protein misfolding cyclic amplification assay (PMCA) and real-time quaking-induced conversion (RT-QuIC) are two amplification techniques based on the ability…”
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Evaluating Turbulent Flow in Large Rockfill by Siddiqua, S, Blatz, J. A, Privat, N. C

“…This paper describes a laboratory testing program developed to assess the hydraulic properties of coarse rockfill by using a custom-built large-scale…”
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Wernicke encephalopathy and Creutzfeldt-Jakob disease by Bertrand, A., Brandel, J. P., Grignon, Y., Sazdovitch, V., Seilhean, D., Faucheux, B., Privat, N., Brault, J. L., Vital, A., Uro-Coste, E., Pluot, M., Chapon, F., Maurage, C. A., Letournel, F., Vespignani, H., Place, G., Degos, C. F., Peoc’h, K., Haïk, S., Hauw, J. J.

“…We assessed the prevalence of Wernicke encephalopathy (WE) in all 657 cases suspected of Creutzfeldt-Jakob (CJD) referred from 2001 to 2006 to the French…”
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Olig2 expression, GFAP, p53 and 1p loss analysis contribute to glioma subclassification by Mokhtari, K., Paris, S., Aguirre-Cruz, L., Privat, N., Crinière, E., Marie, Y., Hauw, J.-J., Kujas, M., Rowitch, D., Hoang-Xuan, K., Delattre, J.-Y., Sanson, M.

“…The expression of Olig2, a basic helix–loop–helix (bHLH) transcription factor involved in oligodendroglial specification, was investigated by…”
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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 by Faucheux, B. A., Morain, E., Diouron, V., Brandel, J.-P., Salomon, D., Sazdovitch, V., Privat, N., Laplanche, J.-L., Hauw, J.-J., Haïk, S.

“…B. A. Faucheux, E. Morain, V. Diouron, J.‐P. Brandel, D. Salomon, V. Sazdovitch, N. Privat, J.‐L. Laplanche, J.‐J. Hauw and S. Haïk (2011) Neuropathology and…”
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Siah-1 Binds and Regulates the Function of Numb by Susini, Laurent, Passer, Brent J., Amzallag-Elbaz, Nathalie, Juven-Gershon, Tamar, Prieur, Sylvie, Privat, Nicolas, Tuynder, Marcel, Gendron, Marie-Claude, Israël, Alain, Amson, Robert, Oren, Moshe, Telerman, Adam

“…The Drosophila Seven in absentia (Sina) gene product originally was described as a protein that controls cell fate decisions during eye development. Its…”
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Alpha-synuclein-immunoreactive deposits in human and animal prion diseases by HAÏK, S, PRIVAT, N, ADJOU, K. T, SAZDOVITCH, V, DORMONT, D, DUYCKAERTS, C, HAUW, J. J

“…Prion related disorders are associated with the accumulation of a misfolded isoform (PrPsc) of the host-encoded prion protein, PrP. There is strong evidence…”
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Neuropathologic variants of sporadic Creutzfeldt-Jakob disease and codon 129 of PrP gene by HAUW, J.-J, SAZDOVITCH, V, DORMONT, D, ALPEROVITCH, A, LAPLANCHE, J.-L, PEOC'H, K, KOPP, N, KEMENY, J, PRIVAT, N, DELASNERIE-LAUPRETRE, N, BRANDEL, J. P, DESLYS, J. P

“…To determine the contribution of methionine/valine (Met/Val) polymorphism at codon 129 of the prion protein (PrP) gene in the neuropathologic pattern and…”
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Dementia with Lewy bodies in a neuropathologic series of suspected Creutzfeldt-Jakob disease by HAIK, S, BRANDEL, J. P, LAQUERRIERE, A, MOHR, M, DESLYS, J. P, DORMONT, D, HAUW, J. J, SAZDOVITCH, V, DELASNERIE-LAUPRETRE, N, PEOC'H, K, LAPLANCHE, J.-L, PRIVAT, N, DUYCKAERTS, C, KEMENY, J. L, KOPP, N

“…Discriminating Creutzfeldt-Jakob disease (CJD) from dementia with Lewy bodies (DLB) may be clinically difficult to achieve. The authors describe 10 patients…”
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MS-8209, amphotericin B analogue, delays the appearance of spongiosis, astrogliosis and PrPres accumulation in the brain of scrapie-infected hamsters by Adjou, K.T, Privat, N, Demart, S, Deslys, J.P, Seman, M, Hauw, J.J, Dormont, D

“…The histopathological response of scrapie-infected hamsters treated at the late stage of the infection with an "anti-scrapie" drug, a polyene macrolide…”
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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 by Peoc'h, K., Levavasseur, E., Delmont, E., De Simone, A., Laffont-Proust, I., Privat, N., Chebaro, Y., Chapuis, C., Bedoucha, P., Brandel, J.-P., Laquerriere, A., Kemeny, J.-L., Hauw, J.-J., Borg, M., Rezaei, H., Derreumaux, P., Laplanche, J.-L., Haik, S.

“…Human prion diseases are a heterogeneous group of fatal neurodegenerative disorders, characterized by the deposition of the partially protease-resistant prion…”
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Senile plaques do not induce susceptibility effects in T 2-weighted MR microscopic images by Dhenain, Marc, Privat, Nicolas, Duyckaerts, Charles, Jacobs, Russell E.

“…Senile plaques are the hallmarks of Alzheimer's disease. They typically range from 16 to 150 µm in size with most less than 25 µm. Mechanisms by which they…”
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Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrP Sc ) deposition in sporadic Creutzfeldt–Jakob disease supports a pathogenic role for small PrP Sc deposits common to the various molecular subtypes by Faucheux, B. A., Morain, E., Diouron, V., Brandel, J.‐P., Salomon, D., Sazdovitch, V., Privat, N., Laplanche, J.‐L., Hauw, J.‐J., Haïk, S.

“…B. A. Faucheux, E. Morain, V. Diouron, J.‐P. Brandel, D. Salomon, V. Sazdovitch, N. Privat, J.‐L. Laplanche, J.‐J. Hauw and S. Haïk (2011) Neuropathology and…”
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The sympathetic nervous system is involved in variant Creutzfeldt-Jakob disease by Haïk, Stéphane, Faucheux, Baptiste A, Sazdovitch, Véronique, Privat, Nicolas, Kemeny, Jean-Louis, Perret-Liaudet, Armand, Hauw, Jean-Jacques

“…Prion epizoonoses spread from animals consumed by humans raise the question of which pathways lead to prion neuroinvasion after oral exposure of humans. Here…”
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Striking PrPsc heterogeneity in inherited prion diseases with the D178N mutation by Haïk, Stéphane, Peoc'h, Katell, Brandel, Jean-Philippe, Privat, Nicolas, Laplanche, Jean-Louis, Faucheux, Baptiste A., Hauw, Jean-Jacques

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MRI description of cerebral atrophy in mouse lemur primates by Dhenain, Marc, Michot, Jean–Luc, Privat, Nicolas, Picq, Jean–Luc, Boller, Francois, Duyckaerts, Charles, Volk, Andreas

“…We assessed cerebral atrophy in mouse lemur primates ( Microcebus murinus) by estimating CSF volume in their brains from 4.7 Tesla T2-weighted magnetic…”
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PrP immunohistochemistry: Different protocols, including a procedure for long formalin fixation, and a proposed schematic classification for deposits in sporadic Creutzfeldt-Jakob disease by Privat, Nicolas, Sazdovitch, Véronique, Seilhean, Danielle, LaPlanche, Jean-Louis, Hauw, Jean-Jacques

“…The use of immunohistochemistry on formalin‐fixed and paraffin‐embedded tissue has greatly improved the neuropathological diagnosis of Creutzfeldt‐Jakob…”
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Age-Related Changes in Serotonergic and Catecholaminergic Brain Systems in the Lemurian Primate Microcebus murinus by JALLAGEAS, VÉRONIQUE, PRIVAT, NICOLAS, MESTRE-FRANCÉS, NADINE, BONS, NOËLLE

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MS-8209, an Amphotericin B Analogue,Delays the Appearance of Spongiosis, Astrogliosis and PrPres Accumulation inthe Brain of Scrapie-infected Hamsters by Adjou, KT, Privat, N, Demart, S, Deslys, J -P, Seman, M, Hauw, J -J, Dormont, D

“…The histopathological response of scrapie-infected hamsters treated at the late stage of the infection with an “anti-scrapie” drug, a polyene macrolide…”
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