PAPERS - RESEARCH FRONT: 2

TITLE 1ST AUTHOR YEAR
FROM SLOW VIRUS TO PRION - A REVIEW OF TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES LANTOS PL 1992
RECENTLY DESCRIBED SCRAPIE-LIKE ENCEPHALOPATHIES OF ANIMALS - CASE DEFINITIONS WELLS GAH 1992
IMMUNOREACTIVITY TO UBIQUITIN PROTEIN CONJUGATES IS PRESENT EARLY IN THE DISEASE PROCESS IN THE BRAINS OF SCRAPIE-INFECTED MICE LOWE J 1992
PRION PROTEIN IMMUNOCYTOCHEMISTRY HELPS TO ESTABLISH THE TRUE INCIDENCE OF PRION DISEASES LANTOS PL 1992
SYNAPTIC DEGENERATION IS THE PRIMARY NEUROPATHOLOGICAL FEATURE IN PRION DISEASE - A PRELIMINARY-STUDY CLINTON J 1993
GENETIC-CHARACTERIZATION OF A FAMILIAL NONSPECIFIC DEMENTIA ORIGINATING IN JUTLAND, DENMARK BROWN J 1993
CREUTZFELDT-JAKOB DISEASE - REPORT OF A CASE OF THE PANENCEPHALOPATHIC TYPE AND EXPERIENCES OF A TEACHING HOSPITAL IN TAIWAN SU MS 1993
ABSENCE OF PROTEASE-RESISTANT PRION PROTEIN IN DEMENTIA CHARACTERIZED BY NEURONAL LOSS AND STATUS SPONGIOSUS POLLANEN MS 1993
EXPRESSION OF POLYUBIQUITIN AND HEAT-SHOCK PROTEIN-70 GENES INCREASES IN THE LATER STAGES OF DISEASE PROGRESSION IN SCRAPIE-INFECTED MOUSE-BRAIN KENWARD N 1994
CHROMOSOME 14-ENCODED ALZHEIMERS-DISEASE - GENETIC AND CLINICOPATHOLOGICAL DESCRIPTION HALTIA M 1994
VERTICAL TRANSMISSION OF PRION DISEASE BROWN P 1994
VERTICAL TRANSFER OF PRION DISEASE - REPLY WILL RG 1994
THE NEUROPATHOLOGY AND EPIDEMIOLOGY OF BOVINE SPONGIFORM ENCEPHALOPATHY WELLS GAH 1995
ALLELIC VARIATIONS IN APOLIPOPROTEIN-E AND PRION PROTEIN GENOTYPE RELATED TO PLAQUE-FORMATION AND AGE-OF-ONSET IN SPORADIC CREUTZFELDT-JAKOB-DISEASE PICKERINGBROWN SM 1995
LIMITATIONS OF DOT-BLOT IMMUNOASSAY IN THE DIAGNOSIS OF CREUTZFELDT-JAKOB-DISEASE JEZIORE Y 1995
SPASTIC TETRAPLEGIA AS AN INITIAL MANIFESTATION OF FAMILIAL ALZHEIMERS-DISEASE SODEYAMA N 1995
Precocious loss of physiological sleep in a case of Creutzfeldt-Jakob disease: A serial polygraphic study Terzano MG 1995
Diagnosis and incidence of prion (Creutzfeldt-Jakob) disease: A retrospective archival survey with implications for future research Bruton CJ 1995
Cellular prion protein and GABA(A) receptors: No physical association? Kannenberg K 1995
Protein folding, nucleation phenomena and delayed neurodegeneration in Alzheimer's disease Fox N 1996
Neurogenetics Reichmann H 1996
A panencephalopathic type of Creutzfeldt-Jakob disease with selective lesions of the thalamic nuclei in 2 Swiss patients Carota A 1996
Hippocampal slices from prion protein null mice: Disrupted Ca2+-activated K+ currents Colling SB 1996
Creutzfeldt-Jakob disease in Austria Hainfellner JA 1996
Two cases of frontal dementia with non specific histological lesions: Nosology clinicopathological discussion Michel B 1996
Mechanochemical mechanism for peptidyl free radical generation by amyloid fibrils Kay CJ 1997
The nature of transmission in prion diseases Ridley RM 1997
Marked decrease of neuropeptide Y Y2 receptor binding sites in the hippocampus in murine prion disease Diez M 1997
Conformational change in prion protein: Testing a novel method of secondary structure prediction Yan JF 1998
MRI in sporadic Creutzfeldt-Jakob disease: Correlation with clinical and neuropathological data Urbach H 1998
Characterization of the sheep apolipoprotein E (ApoE) gene and allelic variations of the ApoE gene in scrapie Suffolk sheep Komatsu Y 1998
Neuropeptide Y: some viewpoints on a multifaceted peptide in the normal and diseased nervous system Hokfelt T 1998
Neuro-ophthalmological aspects of prion diseases Neetens A 1998
Differential expression of transforming growth factor-beta isoforms in human prion diseases Tashiro H 1998
Protein precipitation: a common etiology in neurodegenerative disorders? Kakizuka A 1998
Phenotypic variability in fatal familial insomnia (D178N-129M) genotype Zerr I 1998
Genetic classification of primary neurodegenerative disease Hardy J 1998
Conformation and neurotoxicity: relationship between Alzheimer's disease and prion disease Kawahara M 1998
The genetics of disorders with synuclein pathology and parkinsonism Farrer M 1999
Risk of prion disease transmission from ocular donor tissue transplantation Hogan RN 1999
Possible retroviral origin of prion disease: could prion disease be reconsidered as a preleukemia syndrome? Labat ML 1999
Neuropathological study of cerebellar degeneration in prion disease Yang Q 1999
Prion infections in Creutzfeldt-Jakob disease and its variants Parker JC 1999
Early induction of protein nexin-I in scrapie Cavallaro S 1999
The role of copper in neurodegenerative disease Waggoner DJ 1999
Intrinsic physiological and morphological properties of principal cells of the hippocampus and neocortex in hamsters infected with scrapie Barrow PA 1999
How to improve the clinical diagnosis of Creutzfeldt-Jakob disease Poser S 1999
Novel PRNP sequence variant associated with familial encephalopathy Cervenakova L 1999
Pathways to primary neurodegenerative disease Hardy J 2000
High frequency of mutations in four different disease genes in early-onset dementia Finckh U 2000
The diagnosis of human prion diseases Kordek R 2000
High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genes Finckh U 2000
Amyotrophy in prion diseases Worrall BB 2000
Familial Creutzfeldt-Jakob disease: A neuropsychological case study Gass CS 2000
Major hypercorticism is an endocrine feature of ewes with naturally occurring scrapie Gayrard V 2000
Heat shock modulates prion protein expression in human NT-2 cells Shyu WC 2000
Naturally occurring scrapie is associated with a lower CBG binding capacity in ewes Picard-Hagen N 2000
Recent advances in the pre-mortem diagnosis of Creutzfeldt-Jakob disease Collins S 2000
Amyloid in the central nervous system Ortega-Aznar A 2000
Apolipoprotein E includes a binding site which is recognized by several amyloidogenic polypeptides Baumann MH 2000
Inherited prion encephalopathy associated with the novel PRNP H187R mutation - A clinical study Butefisch CM 2000
Copper-dependent oxidative stress and neurodegeneration Rotilio G 2000
Neuronal apoptosis as a therapeutic target in neurodegenerative disease Larner AJ 2000
Molecular mechanism of neurodegeneration induced by Alzheimer's beta-amyloid protein: Channel formation and disruption of calcium homeostasis Kawahara M 2000
Creutzfeldt-Jakob disease: heat shock protein 70 mRNA levels in mononuclear blood cells and clinical study Shyu WC 2000
Genetic dissection of neurodegenerative disease Hardy J 2001
Spatial pattern of prion protein deposits in patients with sporadic Creutzfeldt-Jakob disease Armstrong RA 2001
Serotonergic nuclei of the raphe are not affected in human ageing Kloppel S 2001
Human single-chain Fv intrabodies counteract in situ huntingtin aggregation in cellular models of Huntington's disease Lecerf JM 2001
Inherited prion disease with A117V mutation of the prion protein gene: a novel Hungarian family Kovacs GG 2001
The impact of the introduction of the 14-3-3 protein assay in the surveillance of sporadic Creutzfeldt-Jakob disease in Catalonia Saiz A 2001
A new PRNP mutation (G131V) associated with Gerstmann-Straussler-Scheinker disease Panegyres PK 2001
Morvan's syndrome: peripheral and central nervous system and cardiac involvement with antibodies to voltage-gated potassium channels Liguori R 2001
Immunohistochemistry for the prion protein: Comparison of different monoclonal antibodies in human prion disease subtypes Kovacs GG 2002
Disordered proteins in dementia Ingelsson M 2002
beta-CIT SPECT demonstrates reduced availability of serotonin transporters in patients with Fatal Familial Insomnia Kloppel S 2002
A marked disparity between the expression of prion protein and its message by neurones of the CNS Ford MJ 2002
Prion diseases. An overview Dalsgaard NJ 2002
Poly(ADP-ribose) polymerase inhibitors in the prevention of neuronal cell death Larner AJ 2002
Multiplicative genetic effects in scrapie disease susceptibility Dubois MA 2002
Creutzfeldt-Jakob disease. Lack of correlation between cerebral cortical histology and clinical course of the disease in 22 autopsy cases Geiger KD 2002
Sporadic and familial cerebral amyloid angiopathies Revesz T 2002
Distribution of intraneuronal immunoreactivity for the prion protein in human prion diseases Kovacs GG 2002
Amyloidogenic unfolding intermediates differentiate sheep prion protein variants Rezaei H 2002
The expanding role of imaging in prion disease Taber KH 2002
Mechanistic studies of the process of amyloid fibrils formation by the use of peptide fragments and, analogues: Implications for the design of fibrillization inhibitors Gazit E 2002
Identification and characterization of a novel molecular-recognition and self-assembly domain within the islet amyloid polypeptide Mazor Y 2002
Folding pathways of prion and doppel Settanni G 2002
Diffusion-weighted sequence on MRI for the diagnosis of Creutzfeldt-Jakob disease Pereira E 2002
Basic and clinical aspects of copper Harris ED 2003
Distinctive cerebellar immunoreactivity for the prion protein in familial (E200K) Creutzfeldt-Jakob disease Jarius C 2003
Bovine spongiform encephalopathy in Israel: Implications for human health Nitzan-Kaluski D 2003
Gerstmann-Straussler-Scheinker disease with P102L-V129 mutation: a case with psychiatric manifestations at onset Bianca M 2003
Aluminum-induced conformational changes of beta-amyloid protein and the pathogenesis of Alzheimer's disease Kawahara M 2003
Transforming growth factor-beta 1-mediated neuroprotection against excitotoxic injury in vivo Boche D 2003
Microglial activation with atypical proinflammatory cytokine expression in a rat model of Parkinson's disease Depino AM 2003
Cerebrospinal fluid tau and beta-amyloid - How well do these biomarkers reflect autopsy-confirmed dementia diagnoses? Clark CM 2003
Current concepts and future prospects for Alzheimer disease vaccines Heppner FL 2004
Biomarkers in non-Alzheimer dementias Galasko D 2004
Quantitative study of spongiform change in putamen of 24 cases of Creutzfeldt-Jakob disease Truchot L 2004
The influence of systemic inflammation on inflammation in the brain: implications for chronic neurodegenerative disease Perry VH 2004
Expression of excitatory amino acid transporter-1 (EAAT-1) in brain macrophages and microglia of patients with prion diseases Chretien F 2004
Loss of glycosylation associated with the T183A mutation in human prion disease Grasbon-Frodl E 2004
Mannose receptor expression specifically reveals perivascular macrophages in normal, injured, and diseased mouse brain Galea I 2005
Polygenic variation and transmission factors involved in the resistance/susceptibility to scrapie in a Romanov flock Diaz C 2005
Rapid formation of amyloid from alpha-monomeric recombinant human PrP in vitro Tahiri-Alaoui A 2005
Diffusion-weighted MRI in familial Creutzfeldt-Jakob disease with the codon 200 mutation in the prion protein gene Tsuboi Y 2005
Asymmetric cortical high signal on diffusion weighted-MRI in a case of Creutzfeldt-Jakob disease Nitrini R 2005
Role of inflammation in neurodegenerative diseases Minghetti L 2005
Overlap between neurodegenerative disorders Armstrong RA 2005