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Publications of S. Haik
Articles in journal or book chapters
  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. M. Soubrier, S. Haik, J. J. Hauw, J. C. Corvol, O. Lyon-Caen, and M. Dougados. Creutzfeldt-Jakob disease in a patient treated by etanercept for rheumatoid arthritis (RA): Just a coincidence?. Joint Bone Spine, 2010. Note: Journal articlerevue du rhumatisme. [WWW]


  4. 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]


  5. J. P. Brandel and S. Haik. [Doxycycline versus placebo trial in human prion diseases: A therapeutic challenge.]. Rev Neurol (Paris), 2009. Note: Editorial. [WWW]


  6. 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.


  7. 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]


  8. N. Limousin, P. Corcia, A. M. Guennoc, B. Lucas, V. Sazdovitch, S. Haik, B. De Toffol, and J. Praline. Sleep disturbances in variant of Creutzfeldt-Jakob disease. Sleep Med, 10(6):690, 2009. Note: Case ReportsLetterNetherlands. [WWW] Keyword(s): Adult, Codon, Creutzfeldt-Jakob Syndrome/*genetics, Female, Homozygote, Humans, Methionine, Polymorphism, Genetic, Polysomnography, Prions/genetics, Sleep Initiation and Maintenance Disorders/diagnosis/*genetics.


  9. P. Parchi, S. Notari, P. Weber, H. Schimmel, H. Budka, I. Ferrer, S. Haik, J. J. Hauw, M. W. Head, J. W. Ironside, L. Limido, A. Rodriguez, T. Strobel, F. Tagliavini, and H. A. Kretzschmar. Inter-laboratory assessment of PrPSc typing in creutzfeldt-jakob disease: a Western blot study within the NeuroPrion Consortium. Brain Pathol, 19(3):384-91, 2009. Note: Journal ArticleMulticenter StudyResearch Support, Non-U.S. Gov'tSwitzerland. [WWW] Keyword(s): *Blotting, Western/methods/standards, Brain Chemistry, Creutzfeldt-Jakob Syndrome/*classification, Humans, Laboratories, Hospital/*standards, PrPSc Proteins/*analysis.


  10. C. T. Pham, R. de Silva, S. Haik, M. Verny, A. Sachet, B. Forette, A. Lees, J. J. Hauw, and C. Duyckaerts. Tau-positive grains are constant in centenarians' hippocampus. Neurobiol Aging, 2009. Note: Journal article. [WWW]


  11. H. Zephir, T. Stojkovic, J. de Seze, C. A. Maurage, K. Peoc'h, S. Haik, and P. Vermersch. Severe and rapidly evolving peripheral neuropathy revealing sporadic Creutzfeldt-Jakob disease. J Neurol, 256(1):134-6, 2009. Note: LetterGermany. [WWW]


  12. I. Zerr, K. Kallenberg, D. M. Summers, C. Romero, A. Taratuto, U. Heinemann, M. Breithaupt, D. Varges, B. Meissner, A. Ladogana, M. Schuur, S. Haik, S. J. Collins, G. H. Jansen, G. B. Stokin, J. Pimentel, E. Hewer, D. Collie, P. Smith, H. Roberts, J. P. Brandel, C. van Duijn, M. Pocchiari, C. Begue, P. Cras, R. G. Will, and P. Sanchez-Juan. Updated clinical diagnostic criteria for sporadic Creutzfeldt Jakob disease. Brain, 132(Pt 10):2659-68, 2009. Note: Journal articlea journal of neurology. [WWW]


  13. V. Beringue, A. Le Dur, P. Tixador, F. Reine, L. Lepourry, A. Perret-Liaudet, S. Haik, J. L. Vilotte, M. Fontes, and H. Laude. Prominent and Persistent Extraneural Infection in Human PrP Transgenic Mice Infected with Variant CJD. PLoS ONE, 3(1):e1419, 2008. Note: Journal ArticleUnited States. [WWW]


  14. J. P. Brandel, D. Salomon, J. J. Hauw, S. Haik, and A. Alperovitch. [Creutzfeldt-Jakob disease in patients before and after 80 years of age.]. Psychol Neuropsychiatr Vieil, 6(3):219-24, 2008. Note: English AbstractJournal ArticleFrance. [WWW]


  15. D. Galanaud, D. Dormont, S. Haik, J. Chiras, J. P. Brandel, and J. P. Ranjeva. Differences of apparent diffusion coefficient values in patients with Creutzfeldt-Jakob disease according to the codon 129 genotype. AJNR Am J Neuroradiol, 29(7):E57;-author, 2008. Note: CommentLetterUnited States. [WWW] Keyword(s): Basal Ganglia/pathology, Caudate Nucleus/pathology, Cerebral Cortex/pathology, Codon/*genetics, Corpus Striatum/pathology, Creutzfeldt-Jakob Syndrome/*diagnosis/*genetics, *Diffusion Magnetic Resonance Imaging, *Genotype, Humans, Methionine/genetics, Polymorphism, Genetic, Prions/*genetics, Pulvinar/pathology, Retrospective Studies, Valine/genetics.


  16. 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]


  17. 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]


  18. N. Limousin, P. Corcia, A. M. Guennoc, B. Lucas, V. Sazdovitch, S. Haik, B. D. Toffol, and J. Praline. Sleep disturbances in variant of Creutzfeldt-Jakob disease. Sleep Med, 2008. Note: Letter. [WWW]


  19. 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]


  20. P. Parchi, S. Notari, P. Weber, H. Schimmel, H. Budka, I. Ferrer, S. Haik, J. J. Hauw, M. W. Head, J. W. Ironside, L. Limido, A. Rodriguez, T. Strobel, F. Tagliavini, and H. A. Kretzschmar. Inter-Laboratory Assessment of PrP(Sc) Typing in Creutzfeldt-Jakob Disease: A Western Blot Study within the NeuroPrion Consortium. Brain Pathol, 2008. Note: Journal article. [WWW]


  21. 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]


  22. E. Uro-Coste, H. Cassard, S. Simon, S. Lugan, J. M. Bilheude, A. Perret-Liaudet, J. W. Ironside, S. Haik, C. Basset-Leobon, C. Lacroux, K. Peoch, N. Streichenberger, J. Langeveld, M. W. Head, J. Grassi, J. J. Hauw, F. Schelcher, M. B. Delisle, and O. Andreoletti. Beyond PrP res type 1/type 2 dichotomy in Creutzfeldt-Jakob disease. PLoS Pathog, 4(3):e1000029, 2008. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW]


  23. G. Giaccone, M. Mangieri, R. Capobianco, L. Limido, J. J. Hauw, S. Haik, P. Fociani, O. Bugiani, and F. Tagliavini. Tauopathy in human and experimental variant Creutzfeldt-Jakob disease. Neurobiol Aging, 2007. Note: Journal article. [WWW]


  24. F. M. Huber, V. Sazdovitch, U. Heinemann, S. Haik, J. J. Hauw, F. Zanini, D. W. Droste, and N. J. Diederich. Creutzfeldt-Jacob disease mimicking progressive supranuclear palsy. Mov Disord, 22:S264-S264, 2007. Note: Suppl. 16. [WWW]


  25. 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.


  26. F. Tagliavini, M. Mangieri, R. Capobianco, J. J. Hauw, S. Haik, L. Limido, P. Fociani, O. Bugiam, and G. Giaccone. Tauopathy in human and experimental variant Creutzfeldt-Jakob disease. Faseb J, 21(5):A29-A29, 2007. [WWW]


  27. F. Tagliavini, M. Mangieri, R. Capobianco, J. J. Hauw, S. Haik, L. Limido, P. Fociani, O. Bugiani, and G. Giaccone. Tauopathy in human and experimental variant Creutzfeldt-Jakob disease. Journal of Neuropathology and Experimental Neurology, 66(5):430-430, 2007. [WWW]


  28. C. Basset-Leobon, E. Uro-Coste, K. Peoc'h, S. Haik, V. Sazdovitch, M. Rigal, O. Andreoletti, J. J. Hauw, and M. B. Delisle. Familial Creutzfeldt-Jakob disease with an R208H-129V haplotype and Kuru plaques. Arch Neurol, 63(3):449-52, 2006. Note: Case ReportsComparative StudyJournal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Amyloid/*genetics/metabolism, Arginine/*genetics, Blotting, Western/methods, Brain/pathology, Creutzfeldt-Jakob Syndrome/*genetics/metabolism/*pathology/physiopathology, Haplotypes, Histidine/*genetics, Humans, Immunohistochemistry/methods, Male, Middle Aged, *Mutation, Prions, Protein Precursors/*genetics/metabolism, Senile Plaques/pathology, Valine/genetics.


  29. 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]


  30. I. Laffont-Proust, R. Hassig, S. Haik, S. Simon, J. Grassi, C. Fonta, B. A. Faucheux, and K. L. Moya. Truncated PrP(c) in mammalian brain: interspecies variation and location in membrane rafts. Biol Chem, 387(3):297-300, 2006. Note: Journal ArticleGermany. [WWW] Keyword(s): Animals, Brain/*metabolism, Cell Membrane/*metabolism, Cricetinae, Detergents/pharmacology, Electrophoresis, Polyacrylamide Gel, Membrane Microdomains/*metabolism, Papio, PrPC Proteins/chemistry/genetics/*metabolism, PrPSc Proteins/chemistry/genetics/*metabolism, Primates, Prion Diseases/etiology/*metabolism, Rodentia, Species Specificity.


  31. M. G. Linguraru, N. Ayache, E. Bardinet, M. A. Ballester, D. Galanaud, S. Haik, B. Faucheux, J. J. Hauw, P. Cozzone, D. Dormont, and J. P. Brandel. Differentiation of sCJD and vCJD forms by automated analysis of basal ganglia intensity distribution in multisequence MRI of the brain--definition and evaluation of new MRI-based ratios. IEEE Trans Med Imaging, 25(8):1052-67, 2006. Note: Evaluation StudiesJournal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Algorithms, *Artificial Intelligence, Basal Ganglia/*pathology, Computer Simulation, Creutzfeldt-Jakob Syndrome/classification/*diagnosis, Diagnosis, Differential, Image Enhancement/*methods, Image Interpretation, Computer-Assisted/*methods, Imaging, Three-Dimensional/methods, Information Storage and Retrieval/methods, Magnetic Resonance Imaging/*methods, Models, Biological, Pattern Recognition, Automated/*methods, Reproducibility of Results, Sensitivity and Specificity, Subtraction Technique.


  32. I. Laffont-Proust, B. A. Faucheux, R. Hassig, V. Sazdovitch, S. Simon, J. Grassi, J. J. Hauw, K. L. Moya, and S. Haik. The N-terminal cleavage of cellular prion protein in the human brain. FEBS Lett, 579(28):6333-7, 2005. Note: Journal ArticleResearch Support, Non-U.S. Gov'tNetherlands. [WWW] Keyword(s): ADAM Proteins/*metabolism, Age Factors, Amyloid Precursor Protein Secretases, Cerebral Cortex/*enzymology/metabolism, Humans, Membrane Proteins/*metabolism, Oxidation-Reduction, PrPC Proteins/*metabolism, Protein Structure, Tertiary.


  33. P. Millet, C. S. Lages, S. Haik, E. Nowak, I. Allemand, C. Granotier, and F. D. Boussin. Amyloid-beta peptide triggers Fas-independent apoptosis and differentiation of neural progenitor cells. Neurobiol Dis, 19(1-2):57-65, 2005. Note: Comparative StudyJournal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Amyloid beta-Protein/*pharmacology, Animals, Antigens, CD95, Apoptosis/drug effects/*physiology, Cell Differentiation/drug effects/*physiology, Cells, Cultured, Cerebral Cortex/cytology/drug effects/physiology, Mice, Mice, Congenic, Mice, Inbred C57BL, Neurons/cytology/drug effects/*physiology, Receptors, Tumor Necrosis Factor/*deficiency/genetics, Stem Cells/cytology/drug effects/*physiology.


  34. 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.


  35. 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.


  36. S. Haik, B. A. Faucheux, and J. J. Hauw. Brain targeting through the autonomous nervous system: lessons from prion diseases. Trends Mol Med, 10(3):107-12, 2004. Note: Journal ArticleReviewEngland. [WWW] Keyword(s): Adrenergic Fibers/metabolism, Autonomic Nervous System/*metabolism, Brain/*metabolism/pathology, Lymph Nodes/pathology, Prion Diseases/metabolism/pathology/*transmission, Prions/*metabolism.


  37. 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.


  38. 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.


  39. C. M. Rangon, S. Haik, B. A. Faucheux, M. H. Metz-Boutigue, F. Fierville, J. P. Fuchs, J. J. Hauw, and D. Aunis. Different chromogranin immunoreactivity between prion and a-beta amyloid plaque. Neuroreport, 14(5):755-8, 2003. Note: Comparative StudyJournal ArticleResearch Support, Non-U.S. Gov'tEngland. [WWW] Keyword(s): Adult, Aged, Aged, 80 and over, Alzheimer Disease/metabolism/pathology, Amyloid beta-Protein/*metabolism, Cerebellum/metabolism/pathology, Chromogranin A, Chromogranins/*metabolism, Creutzfeldt-Jakob Syndrome/*metabolism/pathology, Humans, Immunohistochemistry, Middle Aged, Neurites/pathology, Prions/*metabolism, Senile Plaques/*metabolism/pathology, Temporal Lobe/metabolism/pathology.


  40. S. Simoneau, S. Haik, C. Leucht, D. Dormont, J. P. Deslys, S. Weiss, and C. Lasmezas. Different isoforms of the non-integrin laminin receptor are present in mouse brain and bind PrP. Biol Chem, 384(2):243-6, 2003. Note: Journal ArticleResearch Support, Non-U.S. Gov'tGermany. [WWW] Keyword(s): Animals, Antibodies/chemistry/immunology, Blotting, Western, Brain/*metabolism, Humans, Integrins/*metabolism, Mice, Prions/immunology/*metabolism, Protein Binding, Protein Isoforms/isolation & purification/metabolism, Radioligand Assay/methods, Receptors, Laminin/genetics/immunology/isolation &, purification/*metabolism.



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