A Genetic Variation of Cathepsin D Is a Major Risk Factor for Alzheimer's Disease (English)
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In:
ANNALS OF NEUROLOGY
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47
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399-403
;
2000
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ISSN:
- Article (Journal) / Print
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Title:A Genetic Variation of Cathepsin D Is a Major Risk Factor for Alzheimer's Disease
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Contributors:Papassotiropoulos, A. ( author ) / Bagli, M. ( author ) / Kurz, A. ( author ) / Kornhuber, J. ( author ) / Forstl, H. ( author ) / Maier, W. ( author ) / Pauls, J. ( author ) / Lautenschlager, N. ( author ) / Heun, R. ( author )
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Published in:ANNALS OF NEUROLOGY ; 47 ; 399-403
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Publisher:
- New search for: LITTLE BROWN AND COMPANY
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Publication date:2000-01-01
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Size:5 pages
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ISSN:
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Type of media:Article (Journal)
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Type of material:Print
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Language:English
- New search for: 616.8005 / 161
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© Metadata Copyright the British Library Board and other contributors. All rights reserved.
Table of contents – Volume 47
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 4
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Cytotoxic T Cells in Paraneoplastic Cerebellar DegenerationGreenlee, J. E. et al. | 2000
- 6
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Recessive Charcot-Marie-Tooth DiseaseLupski, J. R. et al. | 2000
- 9
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Detection and Treatment of Activated T Cells in the Cerebrospinal Fluid of Patients with Paraneoplastic Cerebellar DegenerationAlbert, M. L. / Austin, L. M. / Darnell, R. B. et al. | 2000
- 18
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Meningeal Cells Can Communicate with Astrocytes by Calcium SignalingGrafstein, B. / Liu, S. / Cotrina, M. L. / Goldman, S. A. / Nedergaard, M. et al. | 2000
- 26
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Up-Regulation of the Metabotropic Glutamate Receptor mGluR4 in Hippocampal Neurons with Reduced Seizure VulnerabilityLie, A. A. / Becker, A. / Behle, K. / Beck, H. / Malitschek, B. / Conn, P. J. / Kuhn, R. / Nitsch, R. / Plaschke, M. / Schramm, J. et al. | 2000
- 36
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A Voxel-Based Morphometry Study of Semantic Dementia: Relationship between Temporal Lobe Atrophy and Semantic MemoryMummery, C. J. / Patterson, K. / Price, C. J. / Ashburner, J. / Frackowiak, R. S. / Hodges, J. R. et al. | 2000
- 46
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Randomized Trials of Dichlorphenamide in the Periodic ParalysesTawil, R. / McDermott, M. P. / Brown, R. / Shapiro, B. C. / Ptacek, L. J. / McManis, P. G. / Dalakas, M. C. / Spector, S. A. / Mendell, J. R. / Hahn, A. F. et al. | 2000
- 54
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Proinflammatory Cytokines and Interleukin-9 Exacerbate Excitotoxic Lesions of the Newborn Murine NeopalliumMarie-Aliette, D. / Pathai, J. / Jean-Christophe, R. / Evrard, P. / Gressens, P. et al. | 2000
- 64
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Higher Sedentary Energy Expenditure in Patients with Huntington's DiseasePratley, R. E. / Salbe, A. D. / Ravussin, E. / Caviness, J. V. et al. | 2000
- 71
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Acute Inflammatory Demyclination in Reperfusion Nerve InjuryNukada, H. / McMorran, P. D. / Shimizu, J. et al. | 2000
- 80
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Mitochondrial Dysfunction and Free Radical Damage in the Huntington R6/2 Transgenic MouseTabrizi, S. J. / Workman, J. / Hart, P. E. / Mangiarini, L. / Mahal, A. / Bates, G. / Cooper, J. M. / Schapira, A. H. et al. | 2000
- 87
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Cross-Reactive Idiotypy in Cerebrospinal Fluid Immunoglobulins in Multiple SclerosisLaGanke, C. C. / Freeman, D. W. / Whitaker, J. N. et al. | 2000
- 93
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Assessment of Cerebral Blood Flow in Alzheimer's Disease by Spin-Labeled Magnetic Resonance ImagingAlsop, D. C. / Detre, J. A. / Grossman, M. et al. | 2000
- 101
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Hemizygous Mutation of the Peripheral Myelin Protein 22 Gene Associated with Charcot-Marie-Tooth Disease Type 1Numakura, C. / Lin, C. / Oka, N. / Akiguchi, I. / Hayasaka, K. et al. | 2000
- 104
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Clinical and Magnetic Resonance Imaging Findings in Chronic Sensory GanglionopathiesLauria, G. / Pareyson, D. / Grisoli, M. / Sghirlanzoni, A. et al. | 2000
- 109
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Atypical Refsum Disease with Pipecolic Acidemia and Abnormal Catalase DistributionBaumgartner, M. R. / Jansen, G. A. / Verhoeven, N. M. / Mooyer, P. A. / Jakobs, C. / Roels, F. / Espeel, M. / Fourmaintraux, A. / Bellet, H. / Wanders, R. J. et al. | 2000
- 113
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Diffusion-Weighted Magnetic Resonance Imaging in Boys with Neural Cell Adhesion Molecule L1 Mutations and Congenital HydrocephalusGraf, W. D. / Born, D. F. / Shaw, D. W. / Thomas, J. R. / Holloway, L. W. / Michaelis, R. C. et al. | 2000
- 117
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A Nonsense Mutation of the ATRX Gene Causing Mild Mental Retardation and EpilepsyGuerrini, R. / Shanahan, J. J. / Carrozzo, R. / Bonanni, P. / Higgs, D. R. / Gibbons, R. J. et al. | 2000
- 122
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Endothelin-1 in the Brain of Patients with Galactosialidosis: Its Abnormal Increase and Distribution PatternItoh, K. / Oyanagi, K. / Takahashi, H. / Sato, T. / Hashizume, Y. / Shimmoto, M. / Sakuraba, H. et al. | 2000
- 127
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Combination Therapy with Glatiramer Acetate (Copolymer-1) and a Type I Interferon (IFN-alpha) Does Not Improve Experimental Autoimmune EncephalomyelitisBrod, S. A. / Lindsey, J. W. / Wolinsky, J. S. et al. | 2000
- 132
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Intraoperative Unmasking of Brain Redundant Motor Sites during Resection of a Precentral Angioma: Evidence Using Direct Cortical StimulationDuffau, H. / Jean-Pierre, S. / Lehericy, S. et al. | 2000
- 136
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Recurrent Strokes after VaricellaHattori, H. / Higuchi, Y. / Tsuji, M. et al. | 2000
- 136
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Levodopa Induces a Cytoplasmic Localization of D1 Dopamine Receptors in Striatal Neurons in Parkinson's DiseaseDi Rocco, A. / Werner, P. et al. | 2000
- 137
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Cerebrospinal Fluid Interleukin-10 Levels in Primary Central Nervous System Lymphoma: A Possible Marker of Response to Treatment?Salmaggi, A. / Eoli, M. / Corsini, E. / Gelati, M. / Frigerio, S. / Silvani, A. / Boiardi, A. et al. | 2000
- 138
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Gene-Gene Interactions between Interleukin-6 and alpha~2-Macroglobulin Influences the Risk for Alzheimer's DiseaseBagli, M. / Papassotiropoulos, A. / Jessen, F. / Rao, M. J. / Maier, W. / Heun, R. et al. | 2000
- 141
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Age-Related White Matter Changes and Cognitive ImpairmentInzitari, D. et al. | 2000
- 143
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Congenital Muscular Dystrophy: An Expanding Clinical SyndromeDubowitz, V. et al. | 2000
- 145
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Cerebral White Matter Lesions and Cognitive Function: The Rotterdam Scan Studyde Groot, J. C. / Frank-Erik / de Leeuw / Oudkerk, M. / Gijn, J. v. / Hofman, A. / Jolles, J. / Breteler, M. M. et al. | 2000
- 152
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Congenital Muscular Dystrophy with Rigid Spine Syndrome: A Clinical, Pathological, Radiological, and Genetic StudyFlanigan, K. M. / Kerr, L. / Bromberg, M. B. / Leonard, C. / Tsuruda, J. / Zhang, R. / Gonzalez-Gomez, I. / Cohn, R. / Campbell, K. P. / Leppert, M. et al. | 2000
- 162
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The Spectrum of Mutations Causing End-Plate Acetylcholinesterase DeficiencyOhno, K. / Engel, A. G. / Brengman, J. M. / Xin-Ming, S. / Heidenreich, F. / Vincent, A. / Milone, M. / Tan, E. / Demirci, M. / Walsh, P. et al. | 2000
- 171
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Impaired Reading in Patients with Right HemianopiaLeff, A. P. / Scott, S. K. / Crewes, H. / Hodgson, T. L. / Cowey, A. / Howard, D. / Wise, R. J. et al. | 2000
- 179
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Oxidative Phosphorylation Defect in the Brains of Carriers of the tRNA^l^e^u^(^U^U^R^) A3243G Mutation in a MELAS PedigreeDubeau, F. / De Stefano, N. / Zifkin, B. G. / Arnold, D. L. / Shoubridge, E. A. et al. | 2000
- 186
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Synergistic Neurotoxicity by Human Immunodeficiency Virus Proteins Tat and gp120: Protection by MemantineNath, A. / Haughey, N. J. / Jones, M. / Anderson, C. / Bell, J. E. / Geiger, J. D. et al. | 2000
- 195
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Prognostic Value of Proton Magnetic Resonance Spectroscopic Imaging for Surgical Outcome in Patients with Intractable Temporal Lobe Epilepsy and Bilateral Hippocampal AtrophyLi, L. M. / Cendes, F. / Antel, S. B. / Andermann, F. / Serles, W. / Dubeau, F. / Olivier, A. / Arnold, D. L. et al. | 2000
- 201
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Expression of alpha-Synuclein, Parkin, and Ubiquitin Carboxy-Terminal Hydrolase L1 mRNA in Human Brain: Genes Associated with Familial Parkinson's DiseaseSolano, S. M. / Miller, D. W. / Augood, S. J. / Young, A. B. / Penney, J. B. et al. | 2000
- 211
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Molecular Analysis of the CDR3 Encoding Region of the Immunoglobulin Heavy Chain Locus in Cerebrospinal Fluid Cells as a Diagnostic Tool in Lymphomatous MeningitisStorch-Hagenlocher, B. / Haas, J. / Vogt-Schaden, M. E. / Bentz, M. / Hoffmann, L. A. / Biessmann, A. / Wildemann, B. et al. | 2000
- 218
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Joint Position Sense Is Impaired by Parkinson's DiseaseZia, S. / Cody, F. / O'Boyle, D. et al. | 2000
- 229
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Profile of Endothelial and Leukocyte Activation in Fabry PatientsDeGraba, T. / Azhar, S. / Dignat-George, F. / Brown, E. / Boutiere, B. / Altarescu, G. / McCarron, R. / Schiffmann, R. et al. | 2000
- 234
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Heterogeneity of T-Lymphocyte Function in Primary Progressive Multiple Sclerosis: Relation to Magnetic Resonance Imaging Lesion VolumePrat, A. / Pelletier, D. / Duquette, P. / Arnold, D. L. / Antel, J. P. et al. | 2000
- 238
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No Acute Antimigraine Efficacy of CP-122,288, a Highly Potent Inhibitor of Neurogenic Inflammation: Results of Two Randomized, Double-Blind, Placebo-Controlled Clinical TrialsRoon, K. I. / Olesen, J. / Diener, H. C. / Ellis, P. / Hettiarachchi, J. / Poole, P. H. / Christianssen, I. / Kleinermans, D. / Kok, J. G. / Ferrari, M. D. et al. | 2000
- 242
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Significant Association between the tau Gene A0/A0 Genotype and Parkinson's DiseasePastor, P. / Ezquerra, M. / Munoz, E. / Marti, M. J. / Blesa, R. / Tolosa, E. / Oliva, R. et al. | 2000
- 246
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Major Depression Is a Risk Factor for Seizures in Older AdultsHesdorffer, D. C. / Hauser, W. A. / Annegers, J. F. / Cascino, G. et al. | 2000
- 249
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Novel Leu723Pro Amyloid Precursor Protein Mutation Increases Amyloid beta42(43) Peptide Levels and Induces ApoptosisKwok, J. B. / Oiao-Xin, L. / Hallupp, M. / Whyte, S. / Ames, D. / Beyreuther, K. / Masters, C. L. / Schofield, P. R. et al. | 2000
- 254
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Prenatal Testing for Late Infantile Neuronal Ceroid LipofuscinosisBerry-Kravis, E. / Sleat, D. E. / Sohar, I. / Meyer, P. / Donnelly, R. / Lobel, P. et al. | 2000
- 257
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Creutzfeld-Jakob Disease Profile in Patients Homozygous for the PRNP E200K MutationSimon, E. S. / Kahana, E. / Chapman, J. / Treyes, T. A. / Gabizon, R. / Rosenmann, H. / Zilber, N. / Korczyn, A. D. et al. | 2000
- 260
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Vitamin E Deficiency due to Chylomicron Retention Disease in Marinesco-Sjogren SyndromeAguglia, U. / Annesi, G. / Pasquinelli, G. / Spadafora, P. / Gambardella, A. / Annesi, F. / Pasqua, A. A. / Cavalcanti, F. / Crescibene, L. / Bagala, A. et al. | 2000
- 265
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Genetic and Neuroradiological Heterogeneity of Double Cortex SyndromeGleeson, J. G. / Luo, R. F. / Grant, P. E. / Guerrini, R. / Huttenlocher, P. R. / Berg, M. J. / Ricci, S. / Cusmai, R. / Wheless, J. W. / Berkovic, S. et al. | 2000
- 269
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Increased Numbers of CCR5+ Interferon-gamma- and Tumor Necrosis Factor-alpha-Secreting T Lymphocytes in Multiple Sclerosis PatientsStrunk, T. / Bubel, S. / Mascher, B. / Schlenke, P. / Kirchner, H. / Klaus-Peter, W. et al. | 2000
- 274
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No Cytomegalovirus DNA in Sera from Patients with Anti-MAG/SGPG Antibody-Associated NeuropathyIrie, S. / Kanazawa, N. / Ogino, M. / Saito, T. / Funato, T. et al. | 2000
- 275
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The Pocket Monsters EpisodeHarding, G. F. et al. | 2000
- 276
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Seasonal Fluctuations of Gadolinium-Enhancing Magnetic Resonance Imaging Lesions in Multiple SclerosisAuer, D. P. / Schumann, E. M. / Kumpfel, T. / Gossl, C. / Trenkwalder, C. et al. | 2000
- 277
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Intracellular Adhesion Molecule-1 Polymorphisms and Genetic Susceptibility to Multiple Sclerosis: Additional Data and Meta-AnalysisKillestein, J. / Schrijver, H. M. / Crusius, J. B. / Perez, C. / Uitdehaag, B. M. / Pena, A. S. / Polman, C. H. et al. | 2000
- 279
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Subtle Brain Abnormalities in Children with Sickle Cell Disease: Relationship to Blood HematocritRivera, J. P. et al. | 2000
- 281
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Peroxisome 1, 2, 3Rizzo, W. B. et al. | 2000
- 283
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Alzheimer's Disease Risk and the Interleukin-1 GenesTanzi, R. E. et al. | 2000
- 286
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Pharmacological Induction of Peroxisomes in Peroxisome Biogenesis DisordersWei, H. / Kemp, S. / McGuinness, M. C. / Moser, A. B. / Smith, K. D. et al. | 2000
- 297
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New Purkinje Cell Antibody (PCA-2): Marker of Lung Cancer-Related Neurological AutoimmunityVernino, S. / Lennon, V. A. et al. | 2000
- 306
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Increased Lymphoproliferative Response to Human Herpesvirus Type 6A Variant in Multiple Sclerosis PatientsSoldan, S. S. / Leist, T. P. / Juhng, K. N. / McFarland, H. F. / Jacobson, S. et al. | 2000
- 314
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Clinical Features and Response to Treatment in Guillain-Barre Syndrome Associated with Antibodies to GM1b GangliosideYuki, N. / Ang, C. W. / Koga, M. / Jacobs, B. C. / van Doorn, P. A. / Hirata, K. / van der Meche, F. G. et al. | 2000
- 322
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Sensory Tricks in Cervical Dystonia: Perceptual Dysbalance of Parietal Cortex Modulates Frontal Motor ProgrammingNaumann, M. / Magyar-Lehmann, S. / Reiners, K. / Erbguth, F. / Leenders, K. L. et al. | 2000
- 329
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Endothelin Inhibition Improves Cerebral Blood Flow and Is Neuroprotective in Pneumococcal MeningitisPfister, L. A. / Tureen, J. H. / Shaw, S. / Christen, S. / Ferriero, D. M. / Tauber, M. G. / Leib, S. L. et al. | 2000
- 336
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Prolonged Febrile Seizures in the Immature Rat Model Enhance Hippocampal Excitability Long TermDube, C. / Chen, K. / Eghbal-Ahmadi, M. / Brunson, K. / Soltesz, I. / Baram, T. Z. et al. | 2000
- 345
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Degeneration of the Centre Median-Parafascicular Complex in Parkinson's DiseaseHenderson, J. M. / Carpenter, K. / Cartwright, H. / Halliday, G. M. et al. | 2000
- 353
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Specific Changes in Somatosensory Evoked Magnetic Fields during Recovery from Sensorimotor StrokeWikstrom, H. / Roine, R. O. / Aronen, H. J. / Salonen, O. / Sinkkonen, J. / Ilmoniemi, R. J. / Huttunen, J. et al. | 2000
- 361
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Association of Early-Onset Alzheimer's Disease with an Interleukin-1alpha Gene PolymorphismGrimaldi, L. M. / Casadei, V. M. / Ferri, C. / Veglia, F. / Licastro, F. / Annoni, G. / Biunno, I. / De Bellis, G. / Sorbi, S. / Mariani, C. et al. | 2000
- 365
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Association of Interleukin-1 Gene Polymorphisms with Alzheimer's DiseaseNicoll, J. A. / Mrak, R. E. / Graham, D. I. / Stewart, J. / Wilcock, G. / MacGowan, S. / Esiri, M. M. / Murray, L. S. / Dewar, D. / Love, S. et al. | 2000
- 369
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Evaluation of the Role of the D2 Dopamine Receptor in Myoclonus DystoniaKlein, C. / Gurvich, N. / Sena-Esteves, M. / Bressman, S. / Brin, M. F. / Ebersole, B. J. / Fink, S. / Forsgren, L. / Friedman, J. / Grimes, D. et al. | 2000
- 374
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Corticobasal Degeneration Shares a Common Genetic Background with Progressive Supranuclear PalsyDi Maria, E. / Tabaton, M. / Vigo, T. / Abbruzzese, G. / Bellone, E. / Donati, C. / Frasson, E. / Marchese, R. / Montagna, P. / Munoz, D. G. et al. | 2000
- 377
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Sensory Discrimination Capabilities in Patients with Focal Hand DystoniaBara-Jimenez, W. / Shelton, P. / Sanger, T. D. / Hallett, M. et al. | 2000
- 381
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Very Low Levels of the mtDNA A3243G Mutation Associated with Mitochondrial Dysfunction In VivoChinnery, P. F. / Taylor, D. J. / Brown, D. T. / Manners, D. / Styles, P. / Lodi, R. et al. | 2000
- 385
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Increased Bone Turnover in Epileptic Patients Treated with CarbamazepineVerrotti, A. / Greco, R. / Morgese, G. / Chiarelli, F. et al. | 2000
- 388
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De Novo Mutation in the Notch3 Gene Causing CADASILJoutel, A. / Dodick, D. D. / Parisi, J. E. / Cecillon, M. / Tournier-Lasserve, E. / Bousser, M. G. et al. | 2000
- 391
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Quantitative Pathological Evidence for Axonal Loss in Normal Appearing White Matter in Multiple SclerosisEvangelou, N. / Esiri, M. M. / Smith, S. / Palace, J. / Matthews, P. M. et al. | 2000
- 395
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Congenital Encephalomyopathy with Epilepsy, Chorioretinitis, Basal Ganglia Involvement, and Muscle MinicoresAvoni, P. / Monari, L. / Carelli, V. / Carcangiu, R. / Barboni, P. / Donati, C. / Badiali, L. / Baruzzi, A. / Montagna, P. et al. | 2000
- 399
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A Genetic Variation of Cathepsin D Is a Major Risk Factor for Alzheimer's DiseasePapassotiropoulos, A. / Bagli, M. / Kurz, A. / Kornhuber, J. / Forstl, H. / Maier, W. / Pauls, J. / Lautenschlager, N. / Heun, R. et al. | 2000
- 404
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William Osler: On Chorea: On CharcotGoetz, C. G. et al. | 2000
- 408
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Multiple Sclerosis and Chlamydia pneumoniaeTreib, J. / Haass, A. / Stille, W. / Maass, M. / Stephan, C. / Holzer, G. / Morgenthaler, M. / Woessner, R. / Grauer, M. T. et al. | 2000
- 408
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Chlamydia, Rickettsia, and Antibiotic Treatment of Multiple SclerosisHoption Cann, S. A. / van Netten, J. P. / van Netten, C. et al. | 2000
- 411
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The Contribution of HLA to Multiple Sclerosis Susceptibility in Sardinian Affected Sibling PairsMarrosu, M. G. / Fadda, E. / Mancosu, C. / Lai, M. / Cocco, E. / Pugliatti, M. et al. | 2000
- 412
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In Vivo Visualization of Human Neural Pathways by Magnetic Resonance ImagingMori, S. / Kaufmann, W. E. / Pearlson, G. D. / Crain, B. J. / Stieltjes, B. / Solaiyappan, M. / van Zijl, P. C. et al. | 2000
- 417
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"Missing" Tau Mutation IdentifiedHutton, M. et al. | 2000
- 419
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Mere Forgetfulness or Alzheimer's Disease?Rossor, M. N. / Fox, N. C. et al. | 2000
- 421
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Where in the Brain Does Alzheimer's Disease Begin?Terry, R. D. et al. | 2000
- 422
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A Novel Mutation at Position +12 in the Intron following Exon 10 of the Tau Gene in Familial Frontotemporal Dementia (FTD-Kumamoto)Yasuda, M. / Takamatsu, J. / D'Souza, I. / Crowther, R. A. / Kawamata, T. / Hasegawa, M. / Hasegawa, H. / Spillantini, M. G. / Tanimukai, S. / Poorkaj, P. et al. | 2000
- 430
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Use of Structural Magnetic Resonance Imaging to Predict Who Will Get Alzheimer's DiseaseKilliany, R. J. / Gomez-Isla, T. / Moss, M. / Kikinis, R. / Sandor, T. / Jolesz, F. / Tanzi, R. / Jones, K. / Hyman, B. T. / Albert, M. S. et al. | 2000
- 440
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Neural Consequences of Competing Stimuli in Both Visual Hemifields: A Physiological Basis for Visual ExtinctionFink, G. R. / Driver, J. / Rorden, C. / Baldeweg, T. / Dolan, R. J. et al. | 2000
- 447
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Partial Deficiency of Manganese Superoxide Dismutase Exacerbates a Transgenic Mouse Model of Amyotrophic Lateral SclerosisAndreassen, O. A. / Ferrante, R. J. / Klivenyi, P. / Klein, A. M. / Shinobu, L. A. / Epstein, C. J. / Beal, M. F. et al. | 2000
- 456
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Movement-Related Electroencephalographic Desynchronization in Patients with Hand Cramps: Evidence for Motor Cortical Involvement in Focal DystoniaToro, C. / Deuschl, G. / Hallett, M. et al. | 2000
- 462
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Thrombolytic Reversal of Acute Human Cerebral Ischemic Injury Shown by Diffusion/Perfusion Magnetic Resonance ImagingKidwell, C. S. / Saver, J. L. / Mattiello, J. / Starkman, S. / Vinuela, F. / Duckwiler, G. / Gobin, Y. P. / Jahan, R. / Vespa, P. / Kalafut, M. et al. | 2000
- 470
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Verbal Fluency Activates the Left Medial Temporal Lobe: A Functional Magnetic Resonance Imaging StudyPihlajamaki, M. / Tanila, H. / Hanninen, T. / Kononen, M. / Laakso, M. / Partanen, K. / Soininen, H. / Aronen, H. J. et al. | 2000
- 477
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Thalamic Involvement in Neurofibromatosis type 1: Evaluation with Proton Magnetic Resonance Spectroscopic ImagingWang, P. Y. / Kaufmann, W. E. / Koth, C. W. / Denckla, M. B. / Barker, P. B. et al. | 2000
- 485
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Penumbral Tissue Alkalosis in Focal Cerebral Ischemia: Relationship to Energy Metabolism, Blood Flow, and Steady PotentialBack, T. / Hoehn, M. / Mies, G. / Busch, E. / Schmitz, B. / Kohno, K. / Konstantin-Alexander, H. et al. | 2000
- 493
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In Vivo Positron Emission Tomographic Evidence for Compensatory Changes in Presynaptic Dopaminergic Nerve Terminals in Parkinson's DiseaseLee, C. S. / Samii, A. / Sossi, V. / Ruth, T. J. / Schulzer, M. / Holden, J. E. / Wudel, J. / Pal, P. K. / de la Fuente-Fernandez, R. / Calne, D. B. et al. | 2000
- 504
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IgG from "Seronegative" Myasthenia Gravis Patients Binds to a Myasthenia Gravis Patients Binds to a Muscle Cell Line, TE671, but Not to Human Acetylcholine ReceptorBlaes, F. / Beeson, D. / Plested, P. / Lang, B. / Vincent, A. et al. | 2000
- 511
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Reversible Brain Creatine Deficiency in Two Sisters with Normal Blood Creatine LevelBianchi, M. C. / Tosetti, M. / Fornai, F. / Alessandri, G. / Cipriani, P. / De Vito, G. / Canapicchi, R. et al. | 2000
- 514
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Sonic Hedgehog Signal Peptide Mutation in a Patient with HoloprosencephalyKato, M. / Nanba, E. / Akaboshi, S. / Shiihara, T. / Ito, A. / Honma, T. / Tsuburaya, K. / Hayasaka, K. et al. | 2000
- 517
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Dopa-Responsive Dystonia due to a Large Deletion in the GTP Cyclohydrolase I GeneFurukawa, Y. / Guttman, M. / Sparagana, S. P. / Trugman, J. M. / Hyland, K. / Wyatt, P. / Lang, A. E. / Rouleau, G. A. / Shimadzu, M. / Kish, S. J. et al. | 2000
- 521
-
Synphilin-1 Is Present in Lewy Bodies in Parkinson's DiseaseWakabayashi, K. / Engelender, S. / Yoshimoto, M. / Tsuji, S. / Ross, C. A. / Takahashi, H. et al. | 2000
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Nitration of Manganese Superoxide Dismutase in Cerebrospinal Fluids Is a Marker for Peroxynitrite-Mediated Oxidative Stress in Neurodegenerative DiseasesAoyama, K. / Matsubara, K. / Fujikawa, Y. / Nagahiro, Y. / Shimizu, K. / Umegae, N. / Hayase, N. / Shiono, H. / Kobayashi, S. et al. | 2000
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A Single Nucleotide Polymorphism of Dopamine Transporter Gene Is Associated with Parkinson's DiseaseMorino, H. / Kawarai, T. / Izumi, Y. / Kazuta, T. / Oda, M. / Komure, O. / Udaka, F. / Kameyama, M. / Nakamura, S. / Kawakami, H. et al. | 2000
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A Novel Congenital Myopathy with Apoptotic ChangesIkezoe, K. / Yan, C. / Momoi, T. / Imoto, C. / Minami, N. / Ariga, M. / Nihei, K. / Nonaka, I. et al. | 2000
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Novel Missense Mutations in the Glycogen-Branching Enzyme Gene in Adult Polyglucosan Body DiseaseZiemssen, F. / Sindern, E. / Schroder, J. M. / Shin, Y. S. / Zange, J. / Kilimann, M. W. / Jean-Pierre, M. / Vorgerd, M. et al. | 2000
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Mental Retardation and Behavioral Problems as Presenting Signs of a Creatine Synthesis Defectvan der Knaap, M. S. / Verhoeven, N. M. / Maaswinkel-Mooij, P. / Pouwels, P. J. / Onkenhout, W. / Peeters, E. A. / Stockler-Ipsiroglu, S. / Jakobs, C. et al. | 2000
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Inclusion Body Myositis, Muscle Blood Vessel and Cardiac Amyloidosis, and Transthyretin Val122Ile AlleleAskanas, V. / Engel, W. K. / Alvarez, R. B. / Frangione, B. / Ghiso, J. / Vidal, R. et al. | 2000
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Neuronal Intranuclear Inclusions in Spinocerebellar Ataxia Type 2Koyano, S. / Uchihara, T. / Fujigasaki, H. / Nakamura, A. / Yagishita, S. / Iwabuchi, K. et al. | 2000
- 550
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Valproate for Girls with EpilepsyBalen, A. H. / Genton, P. et al. | 2000
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Simvastin and Plasma Very-Long-Chain Fatty Acids in X-Linked AdrenoleukodystrophyVerrips, A. / Willemsen, M. A. / Rubino-Gozalbo, E. / De Jong, J. / Smeitink, J. A. et al. | 2000
- 553
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Mirror Agnosia: The Ramachandran SignAltschuler, E. L. et al. | 2000
- 557
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The Hippocampal Sclerosis Whodunit: Enter the GenesBerkovic, S. F. / Jackson, G. D. et al. | 2000
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New Magnetic Resonance Imaging Methods for Cerebrovascular Disease: Emerging Clinical ApplicationsNeumann-Haefelin, T. / Moseley, M. E. / Albers, G. W. et al. | 2000
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Interleukin (IL)-1beta, IL-1alpha, and IL-1 Receptor Antagonist Gene Polymorphisms in Patients with Temporal Lobe EpilepsyKanemoto, K. / Kawasaki, J. / Miyamoto, T. / Obayashi, H. / Nishimura, M. et al. | 2000
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Diagnosis of New Variant Creutzfeldt-Jakob DiseaseWill, R. G. / Zeidler, M. / Stewart, G. E. / Macleod, M. A. / Ironside, J. W. / Cousens, S. N. / Mackenzie, J. / Estibeiro, K. / Green, A. J. / Knight, R. S. et al. | 2000
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Fumaric Aciduria: Clinical and Imaging FeaturesKerrigan, J. F. / Aleck, K. A. / Tarby, T. J. / Bird, C. R. / Heidenreich, R. A. et al. | 2000
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Differential Features of Patients with Mutations in Two COX Assembly Genes, SURF-1 and SCO2Sue, C. M. / Karadimas, C. / Checcarelli, N. / Tanji, K. / Papadopoulou, L. C. / Pallotti, F. / Guo, F. L. / Shanske, S. / Hirano, M. / De Vivo, D. C. et al. | 2000
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Functional Motor Unit Failure Precedes Neuromuscular Degeneration in Canine Motor Neuron DiseaseBalice-Gordon, R. J. / Smith, D. B. / Goldman, J. / Cork, L. C. / Shirley, A. / Cope, T. C. / Pinter, M. J. et al. | 2000
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The Motor Cortex Shows Adaptive Functional Changes to Brain Injury from Multiple SclerosisLee, M. / Reddy, H. / Johansen-Berg, H. / Pendlebury, S. / Jenkinson, M. / Smith, S. / Palace, D. J. / Matthews, P. M. et al. | 2000
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An Association between Migraine and Cutaneous AllodyniaBurstein, R. / Yarnitsky, D. / Goor-Aryeh, I. / Ransil, B. J. / Bajwa, Z. H. et al. | 2000
- 624
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Three Novel Mutations (G27E, insAAC, R179X) in the ORNT1 Gene of Japanese Patients with Hyperornithinemia, Hyperammonemia, and Homocitrullinuria SyndromeTsujino, S. / Kanazawa, N. / Ohashi, T. / Eto, Y. / Saito, T. / Jun-ichi, K. / Yamada, T. et al. | 2000
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alpha-Synuclein and Parkinson's Disease: Selective Neurodegenerative Effect of alpha-Synuclein Fragment on Dopaminergic Neurons In Vitro and In VivoForloni, G. / Bertani, I. / Calella, A. M. / Thaler, F. / Invernizzi, R. et al. | 2000
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Glutamate Uptake Is Decreased in Platelets from Alzheimer's Disease PatientsFerrarese, C. / Begni, B. / Canevari, C. / Zoia, C. / Piolti, R. / Frigo, M. / Appollonio, I. / Frattola, L. et al. | 2000
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Benzodiazepine Receptor Binding in Huntington's Disease: [^1^1C]Flumazenil Uptake Measured Using Positron Emission TomographyKiinig, G. / Leenders, K. L. / Sanchez-Pernaute, R. / Antonini, A. / Vontobel, P. / Verhagen, A. / Gunther, I. et al. | 2000
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Serum Elastase Activity Is Elevated in MigraineTzourio, C. / Amrani, M. E. / Robert, L. / Alperovitch, A. et al. | 2000
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Evidence for Infection with Chlamydia pneumoniae in a Subgroup of Patients with Multiple SclerosisLayh-Schmitt, G. / Bendl, C. / IIildt, U. / Dong-Si, T. / Juttler, E. / Schnitzler, P. / Grond-Ginsbach, C. / Grau, A. J. et al. | 2000
- 655
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Levodopa-Induced Dyskinesias in Parkinson's Disease: Is Sensitization Reversible?Boulos-Paul, B. / Arnulf, I. / Demeret, S. / Damier, P. / Anne-Marie, B. / Jean-Luc, H. / Agid, Y. et al. | 2000
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Increased Serum Transferrin Receptor Concentrations in Friedreich AtaxiaWilson, R. B. / Lynch, D. R. / Farmer, J. M. / Brooks, D. G. / Fischbeck, K. H. et al. | 2000
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Motor Benefit from Levodopa in Spastic Quadriplegic Cerebral PalsyBrunstrom, J. E. / Bastian, A. J. / Wong, M. / Mink, J. W. et al. | 2000
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X-Linked Vacuolar Myopathies: Two Separate Loci and Refined Genetic MappingAuranen, M. / Villanova, M. / Muntoni, F. / Fardean, M. / Scherer, S. W. / Kalino, H. / Minassian, B. A. et al. | 2000
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Influence of Mutation Type and X Chromosome Inactivation on Rett Syndrome PhenotypesAmir, R. E. / Van de Veyver, I. B. / Schultz, R. / Malicki, D. M. / Tran, C. Q. / Dahle, E. J. / Timar, L. / Philippi, A. / Percy, A. K. / Motil, K. J. et al. | 2000
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In Vitro Glatiramer Acetate Treatment of Brain Endothelium Does Not Reduce Adhesion PhenomenaDufour, A. / Corsini, E. / Gelati, M. / Massa, G. / Tarcic, N. / Salmaggi, A. et al. | 2000
- 682
-
The Role of Inheritance in Sporadic Parkinson's DiseaseHawkes, C. et al. | 2000
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Association of Primary Central Nervous System Lymphoma with Long-Term Azathioprine Therapy for Myasthenia Gravis?Herrlinger, U. / Weller, M. / Dichgans, J. / Melms, A. et al. | 2000
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-
14-3-3 Cerebrospinal Fluid Protein and Creutzfeldt-Jakob DiseaseZeidler, M. et al. | 2000
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Circulating Antiganglioside Antibodies Are Not Associated with the Development of Progressive Disease or Cerebral Atrophy in Patients with Multiple SclerosisGiovannoni, G. / Morris, P. R. / Keir, G. et al. | 2000
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-
Effect of Glatiramer Acetate (Copaxone) Given Orally in Human Patients: Interleukin-10 Production During a Phase 1 Trialde Seze, J. / Edan, G. / Labalette, M. / Dessaint, J. P. / Vermersch, P. et al. | 2000
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-
No Association between the NOS3 Codon 298 Polymorphism and Alzheimer's Disease in a Sample from the United StatesCrawford, F. / Freeman, M. / Abdullah, L. / Schinka, J. / Gold, M. / Duara, R. / Mullan, M. et al. | 2000
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-
Mutations in the Neuroserpin Gene Are Rare in Familial Dementia| 2000
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-
Understanding Multiple Sclerosis: Lessons from PathologyLudwin, S. K. et al. | 2000
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-
The Role of B Cells and Autoantibodies in Multiple SclerosisArchelos, J. J. / Maria, K. S. / Hans-Peter, H. et al. | 2000
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Heterogeneity of Multiple Sclerosis Lesions: Implications for the Pathogenesis of DemyelinationLucchinetti, C. / Bruck, W. / Parisi, J. / Scheithauer, B. / Rodriguez, M. / Lassman, H. et al. | 2000
- 718
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Regional Brain Atrophy in Progressive Supranuclear Palsy and Lewy Body DiseaseCordato, N. J. / Halliday, G. M. / Harding, A. J. / Hely, M. A. / Morris, J. G. L. et al. | 2000
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Neonatal Seizures Induced Persistent Changes in Intrinsic Properties of CA1 Rat Hippocampal CellsVilleneuve, N. / Ben-Ari, Y. / Holmes, G. L. / Gaiarsa, J.-L. et al. | 2000
- 739
-
Apolipoprotein E Facilitates Neuritic and Cerebrovascular Plaque Formation in an Alzheimer's Disease ModelHoltzman, D. M. / Fagan, A. M. / Mackey, B. / Tenkova, T. / Sartorius, L. / Paul, S. M. / Bales, K. / Ashe, K. H. / Irizarry, M. C. / Hyman, B. T. et al. | 2000
- 748
-
Hemorrhagic Complications in Vein of Galen MalformationsMeyers, P. M. / Van Halbach, V. / Phatouros, C. P. / Dowd, C. F. / Malek, A. M. / Lempert, T. E. / Lefler, J. E. / Higashida, R. T. et al. | 2000
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Fukutin Protein Is Expressed in Neurons of the Normal Developing Human Brain but Is Reduced in Fukuyama-Type Congenital Muscular Dystrophy BrainSaito, Y. / Mizuguchi, M. / Oka, A. / Takashima, S. et al. | 2000
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Passive Transfer of Demyelination by Serum or IgG from Chronic Inflammatory Demyelinating Polyneuropathy PatientsYan, W. X. / Taylor, J. / Andrias-Kauba, S. / Pollard, J. D. et al. | 2000
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-
Clinical and Biochemical Characteristics of Congenital Disorder of Glycosylation Type Ic, the First Recognized Endoplasmic Reticulum Defect in N-Glycan SynthesisGrunewald, S. / Imbach, T. / Huijben, K. / Rubio-Gozalbo, M. F. / Verrips, A. / de Klerk, J. B. C. / Stroink, H. / Rijk-van Andel, J. F. d. / Van Hove, J. L. K. / Wendel, U. et al. | 2000
- 782
-
Mice Overexpressing Rat Heat Shock Protein 70 Are Protected against Cerebral InfarctionRajdev, S. / Hara, K. / Kokubo, Y. / Mestril, R. / Dillmann, W. / Weinstein, P. R. / Sharp, F. R. et al. | 2000
- 792
-
Mitochondrial Neurogastrointestinal Encephalomyopathy: An Autosomal Recessive Disorder due to Thymidine Phosphorylase MutationsNishino, I. / Spinazzola, A. / Papadimitriou, A. / Hammans, S. / Steiner, I. / Hahn, C. D. / Connolly, A. M. / Verloes, A. / Guimaraes, J. / Maillard, I. et al. | 2000
- 801
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Decreased Cerebrospinal Fluid Levels of beta-Phenylethylamine in Patients with Rett SyndromeSatoi, M. / Matsuishi, T. / Yamada, S. / Yamashita, Y. / Ohtaki, E. / Mori, K. / Riikonen, R. / Kato, H. / Percy, A. K. et al. | 2000
- 804
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Progression in Parkinson's Disease: A Positron Emission Tomography Study with a Dopamine Transporter Ligand [^1^8F]CFTNurmi, E. / Ruottinen, H. M. / Kaasinen, V. / Bergman, J. / Haaparanta, M. / Solin, O. / Rinne, J. O. et al. | 2000
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Myelin Widenings and MGUS-IgA: An Immunoelectron Microscopic StudyVallat, J.-M. / Tabaraud, F. / Sindou, P. / Preux, P.-M. / Vandenberghe, A. / Steck, A. et al. | 2000
- 811
-
Partial Laminin alpha2 Chain Deficiency in a Patient with Myopathy Resembling Inclusion Body MyositisDi Blasi, C. / Mora, M. / Pareyson, D. / Farina, L. / Sghirlanzoni, A. / Vignier, N. / Blasevich, F. / Cornelio, F. / Guicheney, P. / Morandi, L. et al. | 2000
- 816
-
Rapid Clearance of Human Immunodeficiency Virus Type 1 from Ventricular Cerebrospinal Fluid during Antiretroviral TreatmentEggers, C. / Stuerenburg, H. J. / Schafft, T. / Zollner, B. / Feucht, H. H. / Stellbrink, H. J. / van Lunzen, J. et al. | 2000
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-
A Common Mechanism for the Control of Eye and Head Movements in HumansGaymard, B. / Siegler, I. / Rivaud-Pechoux, S. / Israel, I. / Pierrot-Deseilligny, C. / Berthoz, A. et al. | 2000
- 822
-
A Novel Mutation of KCNQ3 (c.925T→C) in a Japanese Family with Benign Familial Neonatal ConvulsionsHirose, S. / Zenri, F. / Akiyoshi, H. / Fukuma, G. / Iwata, H. / Inoue, T. / Yonetani, M. / Tsutsumi, M. / Muranaka, H. / Kurokawa, T. et al. | 2000
- 827
-
Changes of Copper-Transporting Proteins and Ceruloplasmin in the Lentiform Nuclei in Primary Adult-Onset DystoniaBerg, D. / Weishaupt, A. / Francis, M. J. / Miura, N. / Yang, X.-L. / Goodyer, I. D. / Naumann, M. / Koltzenburg, M. / Reiners, K. / Becker, G. et al. | 2000
- 831
-
Diagnostic Criteria for Primary Progressive Multiple Sclerosis: A Position PaperThompson, A. J. / Montalban, X. / Barkhof, F. / Brochet, B. / Filippi, M. / Miller, D. H. / Polman, C. H. / Stevenson, V. L. / McDonald, W. I. et al. | 2000
- 836
-
Rapid Diagnosis of Peroxisome Biogenesis Disorders through Immunofluorescence Staining of Buccal SmearsZhang, Z. / Suzuki, Y. / Shimozawa, N. / Kondo, N. et al. | 2000
- 836
-
Spanish Families with Cerebral Cavernous Angioma Do Not Bear the 742C→T Hispanic American Mutation of the KRIT1 GeneLucas, M. / Solano, F. / Zayas, M. D. / Garcia-Moreno, J. M. / Gamero, M. A. / Costa, A. F. / Izquierdo, G. et al. | 2000
- 837
-
Topiramate and Essential TremorGalvez-Jimenez, N. / Hargreave, M. et al. | 2000
- 838
-
Magnetic Resonance Spectroscopy of Episodic Ataxia Type 2 and MigraineMontagna, P. / Cortelli, P. / Lodi, R. / Barbiroli, B. et al. | 2000
- 839
-
ReplySappey-Marinier, D. / Broussolle, E. / Vighetto, A. et al. | 2000
- 840
-
Clinical Heterogenity in Pedigrees with 2q-Linked Febrile SeizuresMoulard, B. / Chaigne, D. / Malafosse, A. et al. | 2000
- 840
-
Locus for Febrile SeizuresScheffer, I. E. / Wallace, R. H. / Mulley, J. C. / Berkovic, S. F. et al. | 2000
- S2
-
The Specturm of Levodopa-Induced DyskinesiasFahn, S. et al. | 2000
- S12
-
Dopamine Receptors and Locomotor Responses: Molecular AspectsSealfon, S. C. et al. | 2000
- S22
-
Pathophysiology of Levodopa-Induced Dyskinesias in Parkinson's Disease: Problems with the Current ModelObeso, J. A. / Rodriguez-Oroz, M. C. / Rodriguez, M. / DeLong, M. R. / Olanow, C. W. et al. | 2000
- S35
-
Physiologic Basis of DyskinesiaFilion, M. et al. | 2000
- S42
-
Dopamine-Mediated Gene Regulation in Models of Parkinson's DiseaseGerfen, C. R. et al. | 2000
- S53
-
Patterns of Gene Expression and Behavior Induced by Chronic Dopamine TreatmentsCanales, J. J. / Graybiel, A. M. et al. | 2000
- S60
-
Levodopa-Induced Dyskinesia: A Pathological Form of Striatal Synaptic Plasticity?Calabresi, P. / Giacomini, P. / Centonze, D. / Bernardi, G. et al. | 2000
- S70
-
Molecular Basis of Levodopa-Induced DyskinesiasCalon, F. / Grondin, R. / Morissette, M. / Goulet, M. / Blanchet, P. J. / Di Paolo, T. / Bedard, P. J. et al. | 2000
- S79
-
Investigating Levodopa-Induced Dyskinesias in the Parkinsonian PrimateLangston, J. W. / Quik, M. / Petzinger, G. / Jakowec, M. / Di Monte, D. A. et al. | 2000
- S90
-
Factors Influencing the Onset and Persistence of Dyskinesia in MPTP-Treated PrimatesJenner, P. et al. | 2000
- S105
-
The Neural Mechanisms Underlying Levodopa-Induced Dyskinesia in Parkinson's DiseaseBrotchie, J. M. et al. | 2000
- S115
-
Nigrostriatal System Plasticity in Parkison's Disease: Effect of Dopaminergic Denervation and TreatmentHirsch, E. C. et al. | 2000
- S122
-
Striatal Mechanisms and Pathogenesis of Parkinsonian Signs and Motor ComplicationsChase, T. N. / Oh, J. D. et al. | 2000
- S131
-
Physiology of Hypokinetic and Hyperkinetic Movement Disorders: Model for DyskinesiaVitek, J. L. / Giroux, M. et al. | 2000
- S141
-
Neuronal Recordings in Parkinson's Disease Patients with Dyskinesias Induced by ApomorphineLozano, A. M. / Lang, A. E. / Levy, R. / Hutchison, W. / Dostrovsky, J. et al. | 2000
- S147
-
Clinical Physiology of Dopa DyskinesiaHallett, M. et al. | 2000
- S154
-
Neuroimaging of DyskinesiaBrooks, D. J. / Piccini, P. / Turjanski, N. / Samuel, M. et al. | 2000
- S160
-
Clinical Pharmacology of Levodopa-Induced DyskinesiaNutt, J. G. et al. | 2000
- S167
-
Preventing Levodopa-Induced DyskinesiasOlanow, C. W. / Obeso, J. A. et al. | 2000
- S179
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Medical Treatment of Levodopa-Induced DyskinesiasRascol, O. et al. | 2000
- S189
-
Dyskinesias and the Subthalamic NucleusBenabid, A. L. / Benazzouz, A. / Limousin, P. / Koudsie, A. / Krack, P. / Piallat, B. / Pollak, P. et al. | 2000
- S193
-
Surgery for Levodopa-Induced DyskinesiasLang, A. F. et al. | 2000