Amplification techniques and diagnosis of prion diseases
Brandel, J.-P., Culeux, A., Grznarova, K., Levavasseur, E., Lamy, P., Privat, N., Welaratne, A., Denouel, A., Laplanche, J.-L., Haik, S.
Published in Revue neurologique (01.09.2019)
Published in Revue neurologique (01.09.2019)
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Evaluating Turbulent Flow in Large Rockfill
Siddiqua, S, Blatz, J. A, Privat, N. C
Published in Journal of hydraulic engineering (New York, N.Y.) (01.11.2011)
Published in Journal of hydraulic engineering (New York, N.Y.) (01.11.2011)
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Wernicke encephalopathy and Creutzfeldt-Jakob disease
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.
Published in Journal of neurology (01.06.2009)
Published in Journal of neurology (01.06.2009)
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Olig2 expression, GFAP, p53 and 1p loss analysis contribute to glioma subclassification
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.
Published in Neuropathology and applied neurobiology (01.02.2005)
Published in Neuropathology and applied neurobiology (01.02.2005)
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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
Faucheux, B. A., Morain, E., Diouron, V., Brandel, J.-P., Salomon, D., Sazdovitch, V., Privat, N., Laplanche, J.-L., Hauw, J.-J., Haïk, S.
Published in Neuropathology and applied neurobiology (01.08.2011)
Published in Neuropathology and applied neurobiology (01.08.2011)
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Siah-1 Binds and Regulates the Function of Numb
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
Published in Proceedings of the National Academy of Sciences - PNAS (18.12.2001)
Published in Proceedings of the National Academy of Sciences - PNAS (18.12.2001)
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Alpha-synuclein-immunoreactive deposits in human and animal prion diseases
HAÏK, S, PRIVAT, N, ADJOU, K. T, SAZDOVITCH, V, DORMONT, D, DUYCKAERTS, C, HAUW, J. J
Published in Acta neuropathologica (01.05.2002)
Published in Acta neuropathologica (01.05.2002)
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Neuropathologic variants of sporadic Creutzfeldt-Jakob disease and codon 129 of PrP gene
Hauw, J J, Sazdovitch, V, Laplanche, J L, Peoc'h, K, Kopp, N, Kemeny, J, Privat, N, Delasnerie-Lauprêtre, N, Brandel, J P, Deslys, J P, Dormont, D, Alpérovitch, A
Published in Neurology (25.04.2000)
Published in Neurology (25.04.2000)
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Dementia with Lewy bodies in a neuropathologic series of suspected Creutzfeldt-Jakob disease
Haïk, S, Brandel, J P, Sazdovitch, V, Delasnerie-Lauprêtre, N, Peoc'h, K, Laplanche, J L, Privat, N, Duyckaerts, C, Kemeny, J L, Kopp, N, Laquerrière, A, Mohr, M, Deslys, J P, Dormont, D, Hauw, J J
Published in Neurology (14.11.2000)
Published in Neurology (14.11.2000)
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Journal Article
MS-8209, amphotericin B analogue, delays the appearance of spongiosis, astrogliosis and PrPres accumulation in the brain of scrapie-infected hamsters
Adjou, K.T, Privat, N, Demart, S, Deslys, J.P, Seman, M, Hauw, J.J, Dormont, D
Published in Journal of comparative pathology (2000)
Published in Journal of comparative pathology (2000)
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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
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.
Published in Human molecular genetics (15.04.2014)
Published in Human molecular genetics (15.04.2014)
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Senile plaques do not induce susceptibility effects in T 2-weighted MR microscopic images
Dhenain, Marc, Privat, Nicolas, Duyckaerts, Charles, Jacobs, Russell E.
Published in NMR in biomedicine (01.05.2002)
Published in NMR in biomedicine (01.05.2002)
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Journal Article
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
Faucheux, B. A., Morain, E., Diouron, V., Brandel, J.‐P., Salomon, D., Sazdovitch, V., Privat, N., Laplanche, J.‐L., Hauw, J.‐J., Haïk, S.
Published in Neuropathology and applied neurobiology (01.08.2011)
Published in Neuropathology and applied neurobiology (01.08.2011)
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MRI description of cerebral atrophy in mouse lemur primates
Dhenain, Marc, Michot, Jean–Luc, Privat, Nicolas, Picq, Jean–Luc, Boller, Francois, Duyckaerts, Charles, Volk, Andreas
Published in Neurobiology of aging (01.01.2000)
Published in Neurobiology of aging (01.01.2000)
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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
Privat, Nicolas, Sazdovitch, Véronique, Seilhean, Danielle, LaPlanche, Jean-Louis, Hauw, Jean-Jacques
Published in Microscopy research and technique (01.07.2000)
Published in Microscopy research and technique (01.07.2000)
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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
Adjou, KT, Privat, N, Demart, S, Deslys, J -P, Seman, M, Hauw, J -J, Dormont, D
Published in Journal of comparative pathology (01.01.2000)
Published in Journal of comparative pathology (01.01.2000)
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