IRIS
CALI', IGNAZIO
 Distribuzione geografica
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Continente #
EU - Europa 120
AS - Asia 36
NA - Nord America 6
Totale 162
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Nazione #
IT - Italia 53
SG - Singapore 30
IE - Irlanda 26
CZ - Repubblica Ceca 25
DE - Germania 11
CN - Cina 6
US - Stati Uniti d'America 5
FR - Francia 3
FI - Finlandia 2
CA - Canada 1
Totale 162
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Città #
Delia 50
Dublin 26
Brno 25
Singapore 17
Munich 8
Ningbo 5
Forest City 3
Rome 3
Germantown 2
Helsinki 2
Görwihl 1
Paris 1
Totale 143
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Nome #
Variant Creutzfeldt-Jakob Disease 8
Synthetic amyloid fibrils generated from the N-terminal prion protein fragment 23–144 cause transmissible prion disease in mice 8
Transmissibility and propagation of co-existing prions of sporadic Creutzfeldt-Jakob disease into humanized transgenic mice 7
Amyloid-β pathology in iatrogenic Creutzfeldt-Jakob disease: a multi-center study 6
Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone. 6
Generation of human chronic wasting disease in transgenic mice 6
A novel de novo insertional mutation in the PrP gene characterized by slowly progressive atypical dementia: Neuropathological and biochemical findings 6
Sporadic Creutzfeldt-Jakob disease 6
Comparative Study of Prions in Iatrogenic and Sporadic Creutzfeldt-Jakob Disease 5
Codistribution of amyloid beta plaques and spongiform degeneration in familial Creutzfeldt-Jakob disease with the E200K-129M haplotype 5
Distinct disease phenotypes and PrP type 1 variants in Creutzfeldt-Jakob disease with codon 129MM genotype 5
Human Sporadic Prion Diseases 5
Co-existence of PrPD types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristics 5
Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics 5
Variant Creutzfeldt-Jakob disease 5
Insoluble Aggregates and Protease-resistant Conformers of Prion Protein in Uninfected Human Brains 5
Sporadic fatal insomnia in a young woman: a diagnostic challenge: case report 5
Atypical Case of VV1 Creutzfeldt-Jakob Disease Subtype: Case Report 4
Efficient transmission of human prion diseases to a glycan-free prion protein-expressing host 4
Co-occurrence of Distinct Types of Scrapie Prion Protein in Sporadic Creutzfeldt-Jakob Disease 4
Two different conformers of type 1 prion protein propagate as distinct strains in transgenic mice 4
Transmissibility and propagation of PrPSc from sCJDMM1-2 in humanized transgenic mice 4
Thermodynamic stabilization of the folded domain of prion protein inhibits prion infection in vivo 4
Zoonotic Potential of CWD Prions: an update 4
Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone 4
A novel subtype of sporadic Creutzfeldt-Jakob disease with PRNP codon 129MM genotype and PrP plaques 4
Classification of sporadic Creutzfeldt-Jakob disease revisited 4
Protease-sensitive prions with 144-bp insertion mutations 4
Sporadic Creutzfeldt-Jakob Disease in a Very Young Person 4
Amyloid fibrils from the N-terminal prion protein fragment are infectious 4
Mammalian prions generated from bacterially expressed prion protein in the absence of any mammalian cofactors 3
Transmission characteristics of variably protease-sensitive prionopathy 3
Two distinct conformers of PrP D type 1 of sporadic Creutzfeldt-Jakob disease with codon 129VV genotype faithfully propagate in vivo 3
Glycoform-selective prion formation in sporadic and familial forms of prion disease 3
PMCA-replicated PrPD in urine of vCJD patients maintains infectivity and strain characteristics of brain PrPD: Transmission study 3
Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States 3
Prion disease with insertion of two-octapeptide repeats in the PrP gene: Molecular and phenotypic determination 3
Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation cases 3
Novel histotypes of sporadic Creutzfeldt-Jakob disease linked to 129MV genotype 3
Distinct strain of Amyloid beta and pathogenic tau protein in iatrogenic Creutzfeldt-Jakob disease. 3
Sporadic fatal insomnia in an adolescent 3
Molecular biology and pathology of prion strains in sporadic human prion diseases 3
Gerstmann-Sträussler-Scheinker disease revisited: accumulation of covalently-linked multimers of internal prion protein fragments 3
Glycans modulate the transmissibility of PrPSc and the sCJDMM2 and sFI phenotypes 3
A Novel Mechanism of Phenotypic Heterogeneity in Creutzfeldt-Jakob Disease 3
Case Report: Histopathology and Prion Protein Molecular Properties in Inherited Prion Disease With a De Novo Seven-Octapeptide Repeat Insertion 3
Human prion diseases: surgical lessons learned from iatrogenic prion transmission 2
Sporadic Creutzfeldt-Jakob disease in a native Puerto Rican patient 2
Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification 2
Evaluation of the human transmission risk of an atypical bovine spongiform encephalopathy prion strain. 2
Co-occurrence of chronic traumatic encephalopathy and prion disease 2
Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion type 2
Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study 2
Synthetic Aβ peptides acquire prion-like properties in the brain 2
Impaired transmissibility of atypical prions from genetic CJDG114V 2
Characterization of Prion Disease Associated with a Two-Octapeptide Repeat Insertion 2
Pathologic evidence that the T188R mutation in PRNP is associated with prion disease 1
Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein 1
Variable Protease-Sensitive Prionopathy Transmission to Bank Voles 1
Totale 221
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Categoria #
all - tutte 1.172
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 1.172
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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
2024/202555 55 0 0 0 0 0 0 0 0 0 0 0
Totale 221