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Scrapie removal using Planova((R)) virus removal filters
BIOLOGICALS
Detection of a coronary arterial thrombus by indium-111-oxine-labeled platelet scintigraphy
ANNALS OF NUCLEAR MEDICINE
Transient increase in plasma brain (B-type) natriuretic peptide after percutaneous transluminal coronary angioplasty
CLINICAL CARDIOLOGY
Gerstmann-Straussler-Scheinker disease - The dilemma of molecular and clinical correlations
CLINICAL NEUROPATHOLOGY
Infectious and sporadic prion diseases
PRION BIOLOGY AND DISEASES
Clinical course of patients with coronary ectasia
CARDIOLOGY
ABNORMAL CYTOARCHITECTURE OF CORTICAL DYSPLASIA VERIFIED BY IMMUNOHISTOCHEMISTRY
Clinical neuropathology
CODON-219 LYS ALLELE OF PRNP IS NOT FOUND IN SPORADIC CREUTZFELDT-JAKOB-DISEASE
Annals of neurology
ACCUMULATION OF INDIUM-111-OXINE LABELED LEUKOCYTE WITH AORTIC-ANEURYSMS
The Journal of nuclear medicine
PROTECTIVE PRION PROTEIN POLYMORPHISMS AGAINST SPORADIC CREUTZFELDT-JAKOB-DISEASE
Lancet
CORRELATION BETWEEN INITIAL POTENTIALS ON A SIGNAL-AVERAGED P-WAVE AND INDICE OF ELECTROPHYSIOLOGIC MEASUREMENTS IN THE RIGHT ATRIUM
Japanese Circulation Journal
A COMPARATIVE-STUDY OF ABNORMAL PRION PROTEIN ISOFORMS BETWEEN GERSTMANN-STRAUSSLER-SCHEINKER SYNDROME AND CREUTZFELDT-JAKOB-DISEASE
Journal of the neurological sciences
THE HUMAN PRION DISEASES - FROM NEUROPATHOLOGY TO PATHOBIOLOGY AND MOLECULAR-GENETICS - FINAL REPORT OF AN EU CONCERTED ACTION
Neuropathology and applied neurobiology
AMYLOID BETA-PROTEIN (A-BETA) 1-40 BUT NOT A-BETA-1-42 CONTRIBUTES TOTHE EXPERIMENTAL FORMATION OF ALZHEIMER-DISEASE AMYLOID FIBRILS IN FAAT BRAIN
The Journal of neuroscience
CREUTZFELDT-JAKOB-DISEASE WITH FLORID PLAQUES AFTER CADAVERIC DURAL GRAFT IN A JAPANESE WOMAN
Lancet
A COMPARATIVE-STUDY OF EMBEDDED NERVE-TISSUE IN 6 NF2-ASSOCIATED SCHWANNOMAS AND 17 NONASSOCIATED NF2 SCHWANNOMAS
Surgical neurology
MEDICINAL AND OTHER PRODUCTS AND HUMAN AND ANIMAL TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES - MEMORANDUM FROM A WHO MEETING
Bulletin of the World Health Organization
TYPING PRION ISOFORMS
Nature
FIBRINOLYTIC-ACTIVITY IS INHIBITED BY BOTH OF HEPARIN AND THROMBIN INHIBITOR, ARGATOROBAN, DURING CORONARY ANGIOGRAPHY
The American journal of cardiology
EXPRESSION OF NEUROFIBROMATOSIS-2 PROTEIN IN HUMAN BRAIN-TUMORS - AN IMMUNOHISTOCHEMICAL STUDY
Acta Neuropathologica
LESER-TRELAT SIGN WITH ANAPLASTIC EPENDYMOMA - AN AUTOPSY CASE
Acta Neuropathologica
MICRO-ANATOMICAL STUDY OF THE CAROTID CAVE
Acta neurochirurgica
ADVANCED GLYCOSYLATION END-PRODUCTS AND HEAT-SHOCK PROTEINS ACCUMULATE IN THE BASOPHILIC DEGENERATION OF THE MYOCARDIUM AND THE CORPORA-AMYLACEA OF THE GLIA
Pathology international
TRANSMISSION OF HUMAN PRION DISEASES TO RODENTS
Seminars in virology
INACTIVATION OF THE CAUSAL AGENTS OF CREUTZFELDT-JAKOB-DISEASE AND OTHER HUMAN PRION DISEASES - REPLY
Brain pathology
IMMUNOHISTOLOGICAL EVALUATION OF CREUTZFELDT-JAKOB-DISEASE WITH REFERENCE TO THE TYPE PRPRES DEPOSITION
Clinical neuropathology
TISSUE HANDLING IN SUSPECTED CREUTZFELDT- JAKOB-DISEASE (CJD) AND OTHER HUMAN SPONGIFORM ENCEPHALOPATHIES (PRION DISEASES)
Der Pathologe
EXPERIMENTAL TRANSMISSION OF CREUTZFELDT-JAKOB-DISEASE AND RELATED DISEASES TO RODENTS
Neurology
VASCULAR VARIANT OF PRION PROTEIN CEREBRAL AMYLOIDOSIS WITH TAU-POSITIVE NEUROFIBRILLARY TANGLES - THE PHENOTYPE OF THE STOP CODON-145 MUTATION IN PRNP
Proceedings of the National Academy of Sciences of the United Statesof America
A JAPANESE CASE OF CREUTZFELDT-JAKOB-DISEASE WITH A POINT MUTATION INTHE PRION PROTEIN GENE AT CODON-210
Journal of the neurological sciences
DISTINCTIVE IMMUNOHISTOCHEMICAL PROFILES OF SMELL HEAT-SHOCK PROTEINS(HEAT-SHOCK-PROTEIN-27 AND ALPHA-B-CRYSTALLIN) IN HUMAN BRAIN-TUMORS
Cancer
HUMANIZED PRION PROTEIN KNOCK-IN BY CRE-INDUCED SITE-SPECIFIC RECOMBINATION IN THE MOUSE
Biochemical and biophysical research communications
DIAGNOSTIC-CRITERIA FOR SPORADIC CREUTZFELDT-JAKOB-DISEASE
Archives of neurology
MUTATION IN THE PRION PROTEIN GENE AT CODON-232 IN JAPANESE PATIENTS WITH CREUTZFELDT-JAKOB-DISEASE - A CLINICOPATHOLOGICAL, IMMUNOHISTOCHEMICAL AND TRANSMISSION STUDY
Acta Neuropathologica
PROLIFERATIVE ACTIVITY AND APOPTOSIS OF LANGERHANS HISTIOCYTES IN EOSINOPHILIC GRANULOMAS AS EVALUATED BY MIB-1 AND TUNEL METHODS
JCP. Clinical molecular pathology
NEUROPATHOLOGICAL DIAGNOSTIC-CRITERIA FOR CREUTZFELDT-JAKOB-DISEASE (CJD) AND OTHER HUMAN SPONGIFORM ENCEPHALOPATHIES (PRION DISEASES)
Brain pathology
THE ORIGINAL GERSTMANN-STRAUSSLER-SCHEINKER FAMILY OF AUSTRIA - DIVERGENT CLINICOPATHOLOGICAL PHENOTYPES BUT CONSTANT PRP GENOTYPE
Brain pathology
TISSUE HANDLING IN SUSPECTED CREUTZFELDT-JAKOB-DISEASE (CJD) AND OTHER HUMAN SPONGIFORM ENCEPHALOPATHIES (PRION DISEASES)
Brain pathology
INHERITED PRION DISEASES AND TRANSMISSION TO RODENTS
Brain pathology
PRION DISEASES
Microbiology and immunology
INHIBITION OF ARTERIOLE ALPHA(2)-ADRENOCEPTOR BUT NOT ALPHA(1)-ADRENOCEPTOR CONSTRICTION BY ACIDOSIS AND HYPOXIA IN-VITRO
American journal of physiology. Heart and circulatory physiology
TOXIC MYOCARDIAL DAMAGE DUE TO INTRAVENOUS PHENYTOIN ADMINISTRATION
Histopathology
NEURODEGENERATION IN THE LIMBIC AND PARALIMBIC SYSTEM IN PROGRESSIVE SUPRANUCLEAR PALSY
Neuropathology and applied neurobiology
ALLELIC VARIATION OF APOLIPOPROTEIN-E IN JAPANESE SPORADIC CREUTZFELDT-JAKOB-DISEASE PATIENTS
Neuroscience letters
NEW VARIANT PRION PROTEIN IN A JAPANESE FAMILY WITH GERSTMANN-STRAUSSLER SYNDROME
Molecular brain research
APOLIPOPROTEIN-E IN CREUTZFELDT-JAKOB-DISEASE
Lancet
SERIAL MRI IN EARLY CREUTZFELDT-JACOB DISEASE WITH A POINT MUTATION OF PRION PROTEIN AT CODON-180
Neuroradiology
FIRST EXPERIMENTAL TRANSMISSION OF FATAL FAMILIAL INSOMNIA
Nature
APOLIPOPROTEIN-E MESSENGER-RNA IN THE BRAINS OF PATIENTS WITH ALZHEIMERS-DISEASE
Journal of the neurological sciences
PRION PROTEIN AMYLOID ANGIOPATHY AND ALZHEIMER NEUROFIBRILLARY TANGLES IN PRNP STOP CODON-145
Journal of neuropathology and experimental neurology
ATP-SENSITIVE K-ADRENERGIC RECEPTOR CONTRACTION OF ARTERIOLAR SMOOTH-MUSCLE AND REVERSAL OF CONTRACTION BY HYPOXIA( CHANNELS MEDIATE ALPHA(2D))
Circulation research
ALPHA-B-CRYSTALLIN IN C6 GLIOMA-CELLS SUPPORTS THEIR SURVIVAL IN ELEVATED EXTRACELLULAR K- THE IMPLICATION OF A PROTECTIVE ROLE OF ALPHA-B-CRYSTALLIN ACCUMULATION IN REACTIVE GLIA( )
Brain research
PRION DISEASE WITH 144-BASE-PAIR INSERTION IN A JAPANESE FAMILY LINE
Acta Neuropathologica
HUMAN PRION DISEASES WITH VARIANT PRION PROTEIN
Philosophical transactions-Royal Society of London. Biological sciences
INHIBITION OF ARTERIOLE ALPHA-2A-ADRENOCEPTOR (AR) CONSTRICTION BY HYPOXIA AND ACIDOSIS DOES NOT INVOLVE CALCIUM-CHANNEL (CC) BLOCKADE
The FASEB journal
INHIBITION OF ARTERIOLE ALPHA-2A-ADRENOCEPTOR (AR) CONSTRICTION BY HYPOXIA AND ACIDOSIS DOES NOT INVOLVE CALCIUM-CHANNEL (CC) BLOCKADE
The FASEB journal
SEQUENCE HETEROGENEITY OF HTLV-I PROVIRAL DNA IN THE CENTRAL-NERVOUS-SYSTEM OF PATIENTS WITH HTLV-I-ASSOCIATED MYELOPATHY
Annals of neurology
PRP GENE-MUTATIONS AND SUBTYPES OF HEREDITARY PRION
Neurobiology of aging
CREUTZFELDT-JAKOB-DISEASE TRANSMITTED BY A CADAVERIC DURA-MATER GRAFT
Neurosurgery
JAPANESE FAMILY WITH CREUTZFELDT-JAKOB-DISEASE WITH CODON-200 POINT MUTATION OF THE PRION PROTEIN GENE
Neurology
A VARIANT OF GERSTMANN-STRAUSSLER-SCHEINKER-DISEASE CARRYING CODON-105 MUTATION WITH CODON-129 POLYMORPHISM OF THE PRION PROTEIN GENE - A CLINICOPATHOLOGICAL STUDY
Journal of the neurological sciences
SENSE AND ANTISENSE MODIFICATION OF GLIAL ALPHA-B-CRYSTALLIN PRODUCTION RESULTS IN ALTERATIONS OF STRESS FIBER FORMATION AND THERMORESISTANCE
The Journal of cell biology
AN EXON-8-SPLICED OUT TRANSCRIPT OF NEUROFIBROMATOSIS-2 GENE IS CONSTITUTIVELY EXPRESSED IN VARIOUS HUMAN TISSUES
Journal of Biochemistry
ALPHA-2A-ADRENOCEPTOR CONTRACTION OF ARTERIOLAR SMOOTH-MUSCLE AND SELECTIVE-INHIBITION BY HYPOXIA ARE MEDIATED BY COUPLING TO K(ATP) CHANNELS
Circulation
ALPHA-2A-ADRENOCEPTOR CONTRACTION OF ARTERIOLAR SMOOTH-MUSCLE AND SELECTIVE-INHIBITION BY HYPOXIA ARE MEDIATED BY COUPLING TO K(ATP) CHANNELS
Circulation
MIB1 STAINING INDEX AND SCORING OF HISTOLOGIC FEATURES IN MENINGIOMA - INDICATORS FOR THE PREDICTION OF BIOLOGIC POTENTIAL AND POSTOPERATIVE MANAGEMENT
Cancer
AN IMMUNOHISTOCHEMICAL STUDY OF TISSUE TRANSGLUTAMINASE IN GLIOMAS WITH REFERENCE TO THEIR CELL DYING PROCESSES
The American journal of pathology
CYTOPLASMIC INCLUSIONS OF ASTROCYTIC ELEMENTS OF GLIAL TUMORS - SPECIAL REFERENCE TO ROUND GRANULATED BODY AND EOSINOPHILIC HYALINE DROPLETS
Acta Neuropathologica
DISTRIBUTION OF PRION PROTEIN IN GERMAN PATIENTS WITH CREUTZFELDT-JAKOB-DISEASE IS DIFFERENT FROM THAT IN JAPANESE PATIENTS
Acta Neuropathologica
A NEW INHERITED PRION DISEASE (PRP-P105L MUTATION) SHOWING SPASTIC PARAPARESIS
Annals of neurology
ALZHEIMERS AMYLOID PRECURSOR PROTEIN MESSENGER-RNA WITHOUT EXON-15 ISUBIQUITOUSLY EXPRESSED EXCEPT IN THE RAT CENTRAL-NERVOUS-SYSTEM
Molecular brain research
IMMUNOHISTOCHEMICAL DISTRIBUTION OF AMYLOID PRECURSOR PROTEIN DURING NORMAL RAT DEVELOPMENT
Developmental brain research
A MISSENSE MUTATION AT CODON-105 WITH CODON-129 POLYMORPHISM OF THE PRION PROTEIN GENE IN A NEW VARIANT OF GERSTMANN-STRAUSSLER-SCHEINKER DISEASE
Neurology
SPECIES BARRIER PREVENTS AN ABNORMAL ISOFORM OF PRION PROTEIN FROM ACCUMULATING IN FOLLICULAR DENDRITIC CELLS OF MICE WITH CREUTZFELDT-JAKOB-DISEASE
Journal of virology
THE RAT CENTRAL-NERVOUS-SYSTEM EXPRESSES ALZHEIMERS AMYLOID PRECURSORPROTEIN APP(695), BUT NOT APP(677) (L-APP FORM)
Journal of neurochemistry
DEVELOPMENTS IN DIAGNOSIS FOR PRION DISEASES
British Medical Bulletin
AN AMBER MUTATION OF PRION PROTEIN IN GERSTMANN-STRAUSSLER SYNDROME WITH MUTANT PRP PLAQUES
Biochemical and biophysical research communications
ACCUMULATION OF ABNORMAL PRION PROTEIN IN MICE INFECTED WITH CREUTZFELDT-JAKOB-DISEASE VIA INTRAPERITONEAL ROUTE - A SEQUENTIAL STUDY
The American journal of pathology
ALPHA-B-CRYSTALLIN AND 27-KD HEAT-SHOCK PROTEIN ARE REGULATED BY STRESS CONDITIONS IN THE CENTRAL-NERVOUS-SYSTEM AND ACCUMULATE IN ROSENTHAL FIBERS
The American journal of pathology
WIDESPREAD DISTRIBUTION OF TAU IN THE ASTROCYTIC ELEMENTS OF GLIAL TUMORS
Acta Neuropathologica