IRIS
CALI', IGNAZIO
 Distribuzione geografica
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Continente #
AS - Asia 391
EU - Europa 372
NA - Nord America 241
SA - Sud America 100
AF - Africa 6
Totale 1.110
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Nazione #
US - Stati Uniti d'America 229
SG - Singapore 183
HK - Hong Kong 169
IE - Irlanda 167
IT - Italia 102
BR - Brasile 92
DE - Germania 34
CZ - Repubblica Ceca 25
FI - Finlandia 22
TR - Turchia 18
CN - Cina 6
GB - Regno Unito 5
PL - Polonia 5
AR - Argentina 4
CA - Canada 4
IN - India 4
IQ - Iraq 4
MX - Messico 4
SE - Svezia 4
EC - Ecuador 3
FR - Francia 3
BD - Bangladesh 2
DO - Repubblica Dominicana 2
KE - Kenya 2
RU - Federazione Russa 2
ZA - Sudafrica 2
AL - Albania 1
AZ - Azerbaigian 1
BH - Bahrain 1
EG - Egitto 1
HN - Honduras 1
IL - Israele 1
JP - Giappone 1
MA - Marocco 1
MD - Moldavia 1
PK - Pakistan 1
TT - Trinidad e Tobago 1
UA - Ucraina 1
VE - Venezuela 1
Totale 1.110
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Città #
Hong Kong 169
Dublin 167
Singapore 92
Santa Clara 62
Boardman 59
Delia 50
The Dalles 35
Munich 26
Brno 25
Istanbul 18
Espoo 14
Milan 14
Assago 10
Turin 9
Chicago 8
Helsinki 8
São Paulo 8
Brooklyn 5
Ningbo 5
Rio de Janeiro 5
Rome 5
Warsaw 5
Belo Horizonte 4
Curitiba 4
Stockholm 4
Ashburn 3
Brasília 3
Forest City 3
New York 3
Ancona 2
Apodaca 2
Boston 2
Campinas 2
Cleveland 2
Colombo 2
Germantown 2
Johannesburg 2
London 2
Los Angeles 2
Mentana 2
Nairobi 2
Osimo 2
Palermo 2
Pedro Leopoldo 2
Pescara 2
Taboão da Serra 2
Agadir 1
Almirante Brown 1
Annone Veneto 1
Aparecida de Goiânia 1
Aracaju 1
Araguari 1
Araras 1
Atlanta 1
Bady Bassitt 1
Baku 1
Barbacena 1
Basra 1
Belém 1
Birmingham 1
Borgetto 1
Brumadinho 1
Buffalo 1
Buíque 1
Caldas Novas 1
Camaçari 1
Campo Grande 1
Caracas 1
Caraguatatuba 1
Carapicuíba 1
Catamarca 1
Catania 1
Caxias do Sul 1
Chapecó 1
Charleston 1
Charlotte 1
Chennai 1
Chesapeake 1
Chisinau 1
Cianorte 1
Coimbatore 1
Concord 1
Concórdia 1
Cumbernauld 1
Cândido Mendes 1
Dallas 1
Delhi 1
Denver 1
Diadema 1
Duhok 1
El Progreso 1
Falkenstein 1
Giza 1
Guarulhos 1
Guayaquil 1
Görwihl 1
Iguatu 1
Imbituba 1
Inajá 1
Itabira 1
Totale 911
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Nome #
Sporadic fatal insomnia in a young woman: a diagnostic challenge: case report 39
Amyloid-β pathology in iatrogenic Creutzfeldt-Jakob disease: a multi-center study 32
Comparative Study of Prions in Iatrogenic and Sporadic Creutzfeldt-Jakob Disease 30
Transmissibility and propagation of co-existing prions of sporadic Creutzfeldt-Jakob disease into humanized transgenic mice 28
Mammalian prions generated from bacterially expressed prion protein in the absence of any mammalian cofactors 27
Atypical Case of VV1 Creutzfeldt-Jakob Disease Subtype: Case Report 27
Synthetic amyloid fibrils generated from the N-terminal prion protein fragment 23–144 cause transmissible prion disease in mice 27
Human Sporadic Prion Diseases 26
Efficient transmission of human prion diseases to a glycan-free prion protein-expressing host 25
Transmissibility and propagation of PrPSc from sCJDMM1-2 in humanized transgenic mice 25
Distinct disease phenotypes and PrP type 1 variants in Creutzfeldt-Jakob disease with codon 129MM genotype 24
Zoonotic Potential of CWD Prions: an update 24
Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics 24
Sporadic fatal insomnia in an adolescent 24
Codistribution of amyloid beta plaques and spongiform degeneration in familial Creutzfeldt-Jakob disease with the E200K-129M haplotype 23
A novel de novo insertional mutation in the PrP gene characterized by slowly progressive atypical dementia: Neuropathological and biochemical findings 23
Distinct strain of Amyloid beta and pathogenic tau protein in iatrogenic Creutzfeldt-Jakob disease. 23
Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone. 22
Prion disease with insertion of two-octapeptide repeats in the PrP gene: Molecular and phenotypic determination 22
Co-occurrence of Distinct Types of Scrapie Prion Protein in Sporadic Creutzfeldt-Jakob Disease 21
Two distinct conformers of PrP D type 1 of sporadic Creutzfeldt-Jakob disease with codon 129VV genotype faithfully propagate in vivo 21
Two different conformers of type 1 prion protein propagate as distinct strains in transgenic mice 21
Amyloid fibrils from the N-terminal prion protein fragment are infectious 21
Human prion diseases: surgical lessons learned from iatrogenic prion transmission 20
A novel subtype of sporadic Creutzfeldt-Jakob disease with PRNP codon 129MM genotype and PrP plaques 20
Variant Creutzfeldt-Jakob disease 20
Variant Creutzfeldt-Jakob Disease 20
Sporadic Creutzfeldt-Jakob disease in a native Puerto Rican patient 19
Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion type 19
Molecular biology and pathology of prion strains in sporadic human prion diseases 19
Gerstmann-Sträussler-Scheinker disease revisited: accumulation of covalently-linked multimers of internal prion protein fragments 19
Protease-sensitive prions with 144-bp insertion mutations 19
Sporadic Creutzfeldt-Jakob disease 19
Transmission characteristics of variably protease-sensitive prionopathy 18
Generation of human chronic wasting disease in transgenic mice 18
Pathologic evidence that the T188R mutation in PRNP is associated with prion disease 18
Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study 18
Glycoform-selective prion formation in sporadic and familial forms of prion disease 17
Thermodynamic stabilization of the folded domain of prion protein inhibits prion infection in vivo 17
Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification 17
Classification of sporadic Creutzfeldt-Jakob disease revisited 17
Characterization of Prion Disease Associated with a Two-Octapeptide Repeat Insertion 17
Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States 16
Co-existence of PrPD types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristics 16
Co-occurrence of chronic traumatic encephalopathy and prion disease 16
Insoluble Aggregates and Protease-resistant Conformers of Prion Protein in Uninfected Human Brains 16
Synthetic Aβ peptides acquire prion-like properties in the brain 16
Case Report: Histopathology and Prion Protein Molecular Properties in Inherited Prion Disease With a De Novo Seven-Octapeptide Repeat Insertion 16
PMCA-replicated PrPD in urine of vCJD patients maintains infectivity and strain characteristics of brain PrPD: Transmission study 15
Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone 14
Sporadic Creutzfeldt-Jakob Disease in a Very Young Person 14
Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation cases 13
Evaluation of the human transmission risk of an atypical bovine spongiform encephalopathy prion strain. 13
Glycans modulate the transmissibility of PrPSc and the sCJDMM2 and sFI phenotypes 13
Impaired transmissibility of atypical prions from genetic CJDG114V 13
Novel histotypes of sporadic Creutzfeldt-Jakob disease linked to 129MV genotype 12
A Novel Mechanism of Phenotypic Heterogeneity in Creutzfeldt-Jakob Disease 12
Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein 10
Case report: Atypical young case of MV1 Creutzfeldt-Jakob disease with unusually long survival 8
Variable Protease-Sensitive Prionopathy Transmission to Bank Voles 7
Totale 1.170
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Categoria #
all - tutte 9.321
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 9.321
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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
2024/20251.004 100 38 84 48 89 150 58 41 135 78 119 64
Totale 1.170