1. A. Bertrand, J. P. Brandel, Y. Grignon, V. Sazdovitch, D. Seilhean, B. Faucheux, N. Privat, J. L. Brault, A. Vital, E. Uro-Coste, M. Pluot, F. Chapon, C. A. Maurage, F. Letournel, H. Vespignani, G. Place, C. F. Degos, K. Peoc'h, S. Haik, and J. J. Hauw. Wernicke encephalopathy and Creutzfeldt-Jakob disease. J Neurol, 256(6):904-9, 2009. Note: Journal ArticleResearch Support, Non-U.S. Gov'tGermany. [WWW]



2. B. A. Faucheux, N. Privat, J. P. Brandel, V. Sazdovitch, J. L. Laplanche, C. A. Maurage, J. J. Hauw, and S. Haik. Loss of cerebellar granule neurons is associated with punctate but not with large focal deposits of prion protein in Creutzfeldt-Jakob disease. J Neuropathol Exp Neurol, 68(8):892-901, 2009. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW]



3. S. Haik, D. Galanaud, M. G. Linguraru, K. Peoc'h, N. Privat, B. A. Faucheux, N. Ayache, J. J. Hauw, D. Dormont, and J. P. Brandel. In Vivo Detection of Thalamic Gliosis: A Pathoradiologic Demonstration in Familial Fatal Insomnia. Arch Neurol, 65(4):545-549, 2008. Note: Journal article. [WWW]



4. E. Levavasseur, I. Laffont-Proust, E. Morain, B. A. Faucheux, N. Privat, K. Peoc'h, V. Sazdovitch, J. P. Brandel, J. J. Hauw, and S. Haik. Regulating factors of PrP glycosylation in Creutzfeldt-Jakob disease--implications for the dissemination and the diagnosis of human prion strains. PLoS ONE, 3(7):e2786, 2008. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW]



5. C. Paquet, N. Privat, R. Kaci, M. Polivka, O. Dupont, S. Haik, J. L. Laplanche, J. J. Hauw, and F. Gray. Cerebral amyloid angiopathy with co-localization of prion protein and beta-amyloid in an 85-year-old patient with sporadic Creutzfeldt-Jakob disease. Acta Neuropathol, 2008. Note: Journal article. [WWW]



6. N. Privat, I. Laffont-Proust, B. A. Faucheux, V. Sazdovitch, Y. Frobert, J. L. Laplanche, J. Grassi, J. J. Hauw, and S. Haik. Human prion diseases: from antibody screening to a standardized fast immunodiagnosis using automation. Mod Pathol, 21(2):140-9, 2008. Note: Journal ArticleUnited Statesan official journal of the United States and Canadian Academy of Pathology, Inc. [WWW]



7. K. Mokhtari, S. Paris, L. Aguirre-Cruz, N. Privat, E. Criniere, Y. Marie, J. J. Hauw, M. Kujas, D. Rowitch, K. Hoang-Xuan, J. Y. Delattre, and M. Sanson. Olig2 expression, GFAP, p53 and 1p loss analysis contribute to glioma subclassification. Neuropathol Appl Neurobiol, 31(1):62-9, 2005. Note: Comparative StudyJournal ArticleResearch Support, Non-U.S. Gov'tEngland. [WWW] Keyword(s): Basic Helix-Loop-Helix Transcription Factors, Brain Neoplasms/*classification/metabolism/pathology, Chromosomes, Human, Pair 1, Glial Fibrillary Acidic Protein/*metabolism, Glioma/*classification/metabolism/pathology, Humans, Immunohistochemistry, Loss of Heterozygosity, Nerve Tissue Proteins/*metabolism, Tumor Suppressor Protein p53/*metabolism.



8. S. Haik, K. Peoc'h, J. P. Brandel, N. Privat, J. L. Laplanche, B. A. Faucheux, and J. J. Hauw. Striking PrPsc heterogeneity in inherited prion diseases with the D178N mutation. Ann Neurol, 56(6):909-10;, 2004. Note: CommentLetterResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Asparagine/genetics, Aspartic Acid/genetics, Brain/pathology, Humans, *Mutation, PrPSc Proteins/*genetics, Prion Diseases/*genetics/pathology.



9. S. Haik, B. A. Faucheux, V. Sazdovitch, N. Privat, J. L. Kemeny, A. Perret-Liaudet, and J. J. Hauw. The sympathetic nervous system is involved in variant Creutzfeldt-Jakob disease. Nat Med, 9(9):1121-3, 2003. Note: Case ReportsJournal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Adult, Catecholamines/metabolism, Creutzfeldt-Jakob Syndrome/*etiology/*physiopathology, Female, Ganglia, Sympathetic/metabolism, Humans, Magnetic Resonance Imaging, Neurons/*metabolism/pathology, PrPSc Proteins/*metabolism, Stellate Ganglion/metabolism, Sympathetic Nervous System/*metabolism/pathology.

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