1. N. Bizat, J. M. Peyrin, S. Haik, V. Cochois, P. Beaudry, J. L. Laplanche, and C. Neri. Neuron dysfunction is induced by prion protein with an insertional mutation via a Fyn kinase and reversed by sirtuin activation in Caenorhabditis elegans. J Neurosci, 30(15):5394-403, 2010. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited Statesthe official journal of the Society for Neuroscience. [WWW]



2. J. P. Brandel, D. Galanaud, L. Freeman, J. L. Laplanche, and S. Haik. Variant or sporadic Creutzfeldt-Jakob disease?. Lancet, 375(9718):889;-author, 2010. Note: CommentLetterEngland. [WWW]



3. J. P. Brandel, C. A. Heath, M. W. Head, E. Levavasseur, R. Knight, J. L. Laplanche, J. P. Langeveld, J. W. Ironside, J. J. Hauw, J. Mackenzie, A. Alperovitch, R. G. Will, and S. Haik. Variant Creutzfeldt-Jakob disease in France and the United Kingdom: Evidence for the same agent strain. Ann Neurol, 65(3):249-56, 2009. Note: Comparative StudyJournal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Adolescent, Adult, Blood Transfusion/adverse effects, Brain/pathology, Child, Creutzfeldt-Jakob Syndrome/*epidemiology/*genetics/pathology, Female, France/epidemiology, Great Britain/epidemiology, Humans, Male, Medical Records/statistics & numerical data, Middle Aged, PrPSc Proteins/metabolism, Questionnaires, Retrospective Studies, Risk Factors, Young Adult.



4. 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]



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. A. Privat, I. Laffont-Proust, B. Faucheux, V. Sazdovitch, Y. Frobert, J. L. Laplanche, J. Grassi, J. J. Hauw, and S. Haik. PrP immunohistochemistry in human prion diseases: from antibody screening to a standardized fast immunodiagnosis using automation. Modern Pathol, pp sous-presse, 2007.



8. S. Chasseigneaux, S. Haik, I. Laffont-Proust, O. De Marco, M. Lenne, J. P. Brandel, J. J. Hauw, J. L. Laplanche, and K. Peoc'h. V180I mutation of the prion protein gene associated with atypical PrP(Sc) glycosylation. Neurosci Lett, 408(3):165-9, 2006. Note: Journal ArticleIreland. [WWW]



9. D. Dimitri, L. Jehel, A. Durr, M. Levy-Soussan, V. Andreux, J. L. Laplanche, P. Fossati, and D. Cohen. Fatal familial insomnia presenting as psychosis in an 18-year-old man. Neurology, 67(2):363-4, 2006. Note: Case ReportsJournal ArticleUnited States. [WWW] Keyword(s): Adolescent, Depressive Disorder, Major/*diagnosis, Diagnosis, Differential, Fatal Outcome, Humans, Insomnia, Fatal Familial/*diagnosis, Male.



10. M. M. Rodriguez, K. Peoc'h, S. Haik, C. Bouchet, L. Vernengo, G. Manana, R. Salamano, L. Carrasco, M. Lenne, P. Beaudry, J. M. Launay, and J. L. Laplanche. A novel mutation (G114V) in the prion protein gene in a family with inherited prion disease. Neurology, 64(8):1455-7, 2005. Note: Case ReportsJournal ArticleUnited States. [WWW] Keyword(s): Adolescent, Adult, Age of Onset, Amino Acid Substitution/genetics, Amyloid/*genetics, Biopsy, Brain/metabolism/pathology/*physiopathology, Chromosome Aberrations, DNA Mutational Analysis, Dementia/genetics/pathology/physiopathology, Disease Progression, Fatal Outcome, Female, Frontal Lobe/metabolism/pathology/physiopathology, Genetic Predisposition to Disease/*genetics, Genetic Screening, Humans, Male, Mutation/*genetics, Personality Disorders/genetics/pathology/physiopathology, Prion Diseases/*genetics/pathology/physiopathology, Prions, Protein Precursors/*genetics, Pyramidal Tracts/metabolism/pathology/physiopathology, Uruguay.



11. S. Haik, J. P. Brandel, D. Salomon, V. Sazdovitch, N. Delasnerie-Laupretre, J. L. Laplanche, B. A. Faucheux, C. Soubrie, E. Boher, C. Belorgey, J. J. Hauw, and A. Alperovitch. Compassionate use of quinacrine in Creutzfeldt-Jakob disease fails to show significant effects. Neurology, 63(12):2413-5, 2004. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Brain/pathology, Creutzfeldt-Jakob Syndrome/*drug therapy/mortality/pathology, Disease Progression, Drug Evaluation, Humans, Quinacrine/administration & dosage/adverse effects/*therapeutic use, Survival Analysis, Treatment Failure.



12. 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.



13. J. P. Brandel, M. Preece, P. Brown, E. Croes, J. L. Laplanche, Y. Agid, R. Will, and A. Alperovitch. Distribution of codon 129 genotype in human growth hormone-treated CJD patients in France and the UK. Lancet, 362(9378):128-30, 2003. Note: Journal ArticleResearch Support, Non-U.S. Gov'tEngland. [WWW] Keyword(s): Codon, Creutzfeldt-Jakob Syndrome/*genetics/*transmission, France, Great Britain, *Homozygote, Human Growth Hormone/*adverse effects, Humans, Iatrogenic Disease, Polymorphism, Genetic, PrPSc Proteins/*genetics, Risk Factors.

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