IRIS
CALI', IGNAZIO
 Distribuzione geografica
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Continente #
EU - Europa 262
NA - Nord America 72
AS - Asia 67
Totale 401
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Nazione #
IE - Irlanda 114
US - Stati Uniti d'America 71
IT - Italia 68
SG - Singapore 61
DE - Germania 30
CZ - Repubblica Ceca 25
FI - Finlandia 22
CN - Cina 6
FR - Francia 3
CA - Canada 1
Totale 401
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Città #
Dublin 114
Boardman 59
Delia 50
Singapore 35
Brno 25
Munich 24
Espoo 14
Milan 14
Helsinki 8
Chicago 7
Ningbo 5
Forest City 3
Rome 3
Germantown 2
Borgetto 1
Falkenstein 1
Görwihl 1
Paris 1
Totale 367
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Nome #
Synthetic amyloid fibrils generated from the N-terminal prion protein fragment 23–144 cause transmissible prion disease in mice 19
Amyloid-β pathology in iatrogenic Creutzfeldt-Jakob disease: a multi-center study 13
Atypical Case of VV1 Creutzfeldt-Jakob Disease Subtype: Case Report 13
Transmissibility and propagation of co-existing prions of sporadic Creutzfeldt-Jakob disease into humanized transgenic mice 13
A novel de novo insertional mutation in the PrP gene characterized by slowly progressive atypical dementia: Neuropathological and biochemical findings 13
Sporadic Creutzfeldt-Jakob disease 13
Efficient transmission of human prion diseases to a glycan-free prion protein-expressing host 12
Transmissibility and propagation of PrPSc from sCJDMM1-2 in humanized transgenic mice 12
Codistribution of amyloid beta plaques and spongiform degeneration in familial Creutzfeldt-Jakob disease with the E200K-129M haplotype 11
Distinct disease phenotypes and PrP type 1 variants in Creutzfeldt-Jakob disease with codon 129MM genotype 11
Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone. 11
Zoonotic Potential of CWD Prions: an update 11
Two different conformers of type 1 prion protein propagate as distinct strains in transgenic mice 10
Prion disease with insertion of two-octapeptide repeats in the PrP gene: Molecular and phenotypic determination 10
Characterization of Prion Disease Associated with a Two-Octapeptide Repeat Insertion 10
Mammalian prions generated from bacterially expressed prion protein in the absence of any mammalian cofactors 9
Transmission characteristics of variably protease-sensitive prionopathy 9
Co-occurrence of Distinct Types of Scrapie Prion Protein in Sporadic Creutzfeldt-Jakob Disease 9
Comparative Study of Prions in Iatrogenic and Sporadic Creutzfeldt-Jakob Disease 9
Human Sporadic Prion Diseases 9
Glycoform-selective prion formation in sporadic and familial forms of prion disease 9
Generation of human chronic wasting disease in transgenic mice 9
Distinct strain of Amyloid beta and pathogenic tau protein in iatrogenic Creutzfeldt-Jakob disease. 9
Variant Creutzfeldt-Jakob Disease 9
Protease-sensitive prions with 144-bp insertion mutations 9
Two distinct conformers of PrP D type 1 of sporadic Creutzfeldt-Jakob disease with codon 129VV genotype faithfully propagate in vivo 8
Human prion diseases: surgical lessons learned from iatrogenic prion transmission 8
Sporadic Creutzfeldt-Jakob disease in a native Puerto Rican patient 8
PMCA-replicated PrPD in urine of vCJD patients maintains infectivity and strain characteristics of brain PrPD: Transmission study 8
Co-existence of PrPD types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristics 8
Molecular biology and pathology of prion strains in sporadic human prion diseases 8
Amyloid fibrils from the N-terminal prion protein fragment are infectious 8
Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone 7
A novel subtype of sporadic Creutzfeldt-Jakob disease with PRNP codon 129MM genotype and PrP plaques 7
Insoluble Aggregates and Protease-resistant Conformers of Prion Protein in Uninfected Human Brains 7
Sporadic fatal insomnia in a young woman: a diagnostic challenge: case report 7
Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States 6
Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics 6
Pathologic evidence that the T188R mutation in PRNP is associated with prion disease 6
Variant Creutzfeldt-Jakob disease 6
Classification of sporadic Creutzfeldt-Jakob disease revisited 6
Glycans modulate the transmissibility of PrPSc and the sCJDMM2 and sFI phenotypes 6
Thermodynamic stabilization of the folded domain of prion protein inhibits prion infection in vivo 5
Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification 5
Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study 5
Sporadic Creutzfeldt-Jakob Disease in a Very Young Person 5
Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation cases 4
Novel histotypes of sporadic Creutzfeldt-Jakob disease linked to 129MV genotype 4
Co-occurrence of chronic traumatic encephalopathy and prion disease 4
Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion type 4
Sporadic fatal insomnia in an adolescent 4
Gerstmann-Sträussler-Scheinker disease revisited: accumulation of covalently-linked multimers of internal prion protein fragments 4
Synthetic Aβ peptides acquire prion-like properties in the brain 4
A Novel Mechanism of Phenotypic Heterogeneity in Creutzfeldt-Jakob Disease 4
Impaired transmissibility of atypical prions from genetic CJDG114V 4
Case Report: Histopathology and Prion Protein Molecular Properties in Inherited Prion Disease With a De Novo Seven-Octapeptide Repeat Insertion 4
Evaluation of the human transmission risk of an atypical bovine spongiform encephalopathy prion strain. 3
Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein 3
Variable Protease-Sensitive Prionopathy Transmission to Bank Voles 2
Totale 460
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Categoria #
all - tutte 4.053
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 4.053
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/2024166 0 0 0 0 0 0 0 0 0 0 0 166
2024/2025294 100 38 84 48 24 0 0 0 0 0 0 0
Totale 460