IRIS
CALI', IGNAZIO
 Distribuzione geografica
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Continente #
EU - Europa 342
AS - Asia 321
NA - Nord America 149
SA - Sud America 46
AF - Africa 3
Totale 861
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Nazione #
IE - Irlanda 167
HK - Hong Kong 165
SG - Singapore 146
US - Stati Uniti d'America 146
IT - Italia 89
BR - Brasile 42
DE - Germania 34
CZ - Repubblica Ceca 25
FI - Finlandia 22
CN - Cina 6
FR - Francia 3
AR - Argentina 2
IQ - Iraq 2
MX - Messico 2
BH - Bahrain 1
CA - Canada 1
EC - Ecuador 1
EG - Egitto 1
KE - Kenya 1
MA - Marocco 1
MD - Moldavia 1
PK - Pakistan 1
RU - Federazione Russa 1
VE - Venezuela 1
Totale 861
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Città #
Dublin 167
Hong Kong 165
Boardman 59
Santa Clara 59
Singapore 55
Delia 50
Munich 26
Brno 25
Espoo 14
Milan 14
Turin 9
Helsinki 8
Chicago 7
Assago 6
Ningbo 5
Forest City 3
Rio de Janeiro 3
Rome 3
Apodaca 2
Brasília 2
Campinas 2
Cleveland 2
Colombo 2
Germantown 2
Palermo 2
Pescara 2
São Paulo 2
Taboão da Serra 2
Agadir 1
Aparecida de Goiânia 1
Araguari 1
Araras 1
Ashburn 1
Barbacena 1
Basra 1
Borgetto 1
Brumadinho 1
Buíque 1
Campo Grande 1
Caracas 1
Carapicuíba 1
Catamarca 1
Catania 1
Chisinau 1
Cianorte 1
Curitiba 1
Cândido Mendes 1
Falkenstein 1
Giza 1
Guarulhos 1
Görwihl 1
Iguatu 1
Itabira 1
Itapetinga 1
Jatai 1
Joinville 1
João Monlevade 1
Loja 1
Los Polvorines 1
Manama 1
Mata de São João 1
Nairobi 1
Nova Iguaçu 1
Nova Odessa 1
Paracatu 1
Paris 1
Pintópolis 1
Porto Velho 1
Poços de Caldas 1
Rawalpindi 1
Salgueiro 1
Sarandi 1
Saratov 1
Sinop 1
Sulaymaniyah 1
Taquara 1
The Dalles 1
Vigodarzere 1
Totale 748
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Nome #
Sporadic fatal insomnia in a young woman: a diagnostic challenge: case report 29
Amyloid-β pathology in iatrogenic Creutzfeldt-Jakob disease: a multi-center study 28
Transmissibility and propagation of co-existing prions of sporadic Creutzfeldt-Jakob disease into humanized transgenic mice 26
Synthetic amyloid fibrils generated from the N-terminal prion protein fragment 23–144 cause transmissible prion disease in mice 25
Atypical Case of VV1 Creutzfeldt-Jakob Disease Subtype: Case Report 24
Comparative Study of Prions in Iatrogenic and Sporadic Creutzfeldt-Jakob Disease 24
Mammalian prions generated from bacterially expressed prion protein in the absence of any mammalian cofactors 22
Efficient transmission of human prion diseases to a glycan-free prion protein-expressing host 22
Human Sporadic Prion Diseases 21
Transmissibility and propagation of PrPSc from sCJDMM1-2 in humanized transgenic mice 20
Codistribution of amyloid beta plaques and spongiform degeneration in familial Creutzfeldt-Jakob disease with the E200K-129M haplotype 19
Distinct disease phenotypes and PrP type 1 variants in Creutzfeldt-Jakob disease with codon 129MM genotype 19
Zoonotic Potential of CWD Prions: an update 19
Two distinct conformers of PrP D type 1 of sporadic Creutzfeldt-Jakob disease with codon 129VV genotype faithfully propagate in vivo 17
Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone. 17
A novel de novo insertional mutation in the PrP gene characterized by slowly progressive atypical dementia: Neuropathological and biochemical findings 17
Sporadic fatal insomnia in an adolescent 17
Protease-sensitive prions with 144-bp insertion mutations 17
Sporadic Creutzfeldt-Jakob disease 17
Transmission characteristics of variably protease-sensitive prionopathy 16
Co-occurrence of Distinct Types of Scrapie Prion Protein in Sporadic Creutzfeldt-Jakob Disease 16
Two different conformers of type 1 prion protein propagate as distinct strains in transgenic mice 16
Prion disease with insertion of two-octapeptide repeats in the PrP gene: Molecular and phenotypic determination 16
Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics 16
A novel subtype of sporadic Creutzfeldt-Jakob disease with PRNP codon 129MM genotype and PrP plaques 16
Molecular biology and pathology of prion strains in sporadic human prion diseases 16
Gerstmann-Sträussler-Scheinker disease revisited: accumulation of covalently-linked multimers of internal prion protein fragments 16
Variant Creutzfeldt-Jakob Disease 16
Amyloid fibrils from the N-terminal prion protein fragment are infectious 16
Sporadic Creutzfeldt-Jakob disease in a native Puerto Rican patient 15
Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification 15
Distinct strain of Amyloid beta and pathogenic tau protein in iatrogenic Creutzfeldt-Jakob disease. 15
Human prion diseases: surgical lessons learned from iatrogenic prion transmission 14
Glycoform-selective prion formation in sporadic and familial forms of prion disease 14
PMCA-replicated PrPD in urine of vCJD patients maintains infectivity and strain characteristics of brain PrPD: Transmission study 14
Generation of human chronic wasting disease in transgenic mice 14
Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion type 14
Insoluble Aggregates and Protease-resistant Conformers of Prion Protein in Uninfected Human Brains 14
Characterization of Prion Disease Associated with a Two-Octapeptide Repeat Insertion 14
Case Report: Histopathology and Prion Protein Molecular Properties in Inherited Prion Disease With a De Novo Seven-Octapeptide Repeat Insertion 14
Pathologic evidence that the T188R mutation in PRNP is associated with prion disease 13
Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States 12
Co-existence of PrPD types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristics 12
Thermodynamic stabilization of the folded domain of prion protein inhibits prion infection in vivo 12
Variant Creutzfeldt-Jakob disease 12
Classification of sporadic Creutzfeldt-Jakob disease revisited 12
Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study 12
Sporadic Creutzfeldt-Jakob Disease in a Very Young Person 12
Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone 11
Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation cases 11
Co-occurrence of chronic traumatic encephalopathy and prion disease 11
Glycans modulate the transmissibility of PrPSc and the sCJDMM2 and sFI phenotypes 11
Synthetic Aβ peptides acquire prion-like properties in the brain 11
Impaired transmissibility of atypical prions from genetic CJDG114V 11
A Novel Mechanism of Phenotypic Heterogeneity in Creutzfeldt-Jakob Disease 10
Evaluation of the human transmission risk of an atypical bovine spongiform encephalopathy prion strain. 9
Novel histotypes of sporadic Creutzfeldt-Jakob disease linked to 129MV genotype 9
Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein 7
Variable Protease-Sensitive Prionopathy Transmission to Bank Voles 5
Totale 920
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Categoria #
all - tutte 7.990
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 7.990
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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
2024/2025754 100 38 84 48 89 150 58 41 135 11 0 0
Totale 920