CALI', IGNAZIO
 Distribuzione geografica
Continente #
NA - Nord America 1.418
AS - Asia 817
EU - Europa 489
SA - Sud America 243
Continente sconosciuto - Info sul continente non disponibili 64
AF - Africa 21
Totale 3.052
Nazione #
US - Stati Uniti d'America 1.385
SG - Singapore 411
BR - Brasile 203
HK - Hong Kong 181
IE - Irlanda 167
IT - Italia 157
CN - Cina 58
VN - Vietnam 49
BD - Bangladesh 45
DE - Germania 42
CZ - Repubblica Ceca 25
FI - Finlandia 23
TR - Turchia 22
FR - Francia 17
GB - Regno Unito 16
AR - Argentina 14
IN - India 12
MX - Messico 12
IQ - Iraq 11
PL - Polonia 11
CA - Canada 10
EC - Ecuador 8
ZA - Sudafrica 8
SE - Svezia 7
JP - Giappone 6
CL - Cile 5
ID - Indonesia 5
CO - Colombia 4
ES - Italia 4
HN - Honduras 4
PK - Pakistan 4
RU - Federazione Russa 4
SA - Arabia Saudita 4
CI - Costa d'Avorio 3
IL - Israele 3
KE - Kenya 3
LT - Lituania 3
NL - Olanda 3
PE - Perù 3
TT - Trinidad e Tobago 3
BE - Belgio 2
DK - Danimarca 2
DO - Repubblica Dominicana 2
EG - Egitto 2
ET - Etiopia 2
MA - Marocco 2
TH - Thailandia 2
UY - Uruguay 2
VE - Venezuela 2
AE - Emirati Arabi Uniti 1
AL - Albania 1
AZ - Azerbaigian 1
BH - Bahrain 1
BY - Bielorussia 1
JM - Giamaica 1
MD - Moldavia 1
NG - Nigeria 1
NI - Nicaragua 1
PT - Portogallo 1
PY - Paraguay 1
RO - Romania 1
SR - Suriname 1
UA - Ucraina 1
UZ - Uzbekistan 1
Totale 2.988
Città #
Dallas 392
San Jose 263
Singapore 204
Hong Kong 181
Dublin 167
Ashburn 161
Santa Clara 80
The Dalles 76
Chicago 72
Boardman 59
Delia 50
Beijing 26
Munich 26
Brno 25
Milan 21
Phoenix 20
São Paulo 19
Istanbul 18
New York 18
Espoo 14
Rome 14
Los Angeles 12
Turin 12
Hanoi 11
Ho Chi Minh City 11
Assago 10
Brooklyn 10
Warsaw 9
Helsinki 8
Curitiba 7
Johannesburg 7
Stockholm 7
Bari 6
Buffalo 6
London 6
Rio de Janeiro 6
Tokyo 6
Belo Horizonte 5
Catania 5
Ningbo 5
Palermo 4
San Francisco 4
Abidjan 3
Aracaju 3
Baghdad 3
Boston 3
Brasília 3
Charlotte 3
Chennai 3
Council Bluffs 3
Da Nang 3
Forest City 3
Frankfurt am Main 3
Limburg an der Lahn 3
Manchester 3
Mexico City 3
Montreal 3
Nairobi 3
North Kansas City 3
Orem 3
Riyadh 3
Taboão da Serra 3
Thái Bình 3
Vilnius 3
Ancona 2
Ankara 2
Apodaca 2
Atlanta 2
Barra de São Francisco 2
Camaçari 2
Campinas 2
Can Tho 2
Caracas 2
Caxias do Sul 2
Cleveland 2
Colombo 2
Delhi 2
Denver 2
Des Moines 2
Dhaka 2
Florence 2
Germantown 2
Giza 2
Hillsboro 2
Houston 2
Hải Dương 2
Jakarta 2
Joinville 2
João Monlevade 2
Karachi 2
Karbala 2
La Concordia 2
La Plata 2
Lima 2
Mentana 2
Mumbai 2
Osimo 2
Ourinhos 2
Pedro Leopoldo 2
Pescara 2
Totale 2.201
Nome #
Sporadic fatal insomnia in a young woman: a diagnostic challenge: case report 141
Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein 95
Case report: Atypical young case of MV1 Creutzfeldt-Jakob disease with unusually long survival 68
Gerstmann-Sträussler-Scheinker disease revisited: accumulation of covalently-linked multimers of internal prion protein fragments 64
Amyloid-β pathology in iatrogenic Creutzfeldt-Jakob disease: a multi-center study 62
Sporadic Creutzfeldt-Jakob disease 62
Comparative Study of Prions in Iatrogenic and Sporadic Creutzfeldt-Jakob Disease 60
Atypical Case of VV1 Creutzfeldt-Jakob Disease Subtype: Case Report 59
Codistribution of amyloid beta plaques and spongiform degeneration in familial Creutzfeldt-Jakob disease with the E200K-129M haplotype 58
Mammalian prions generated from bacterially expressed prion protein in the absence of any mammalian cofactors 57
Two distinct conformers of PrP D type 1 of sporadic Creutzfeldt-Jakob disease with codon 129VV genotype faithfully propagate in vivo 56
Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification 56
Synthetic amyloid fibrils generated from the N-terminal prion protein fragment 23–144 cause transmissible prion disease in mice 56
Efficient transmission of human prion diseases to a glycan-free prion protein-expressing host 55
Impaired transmissibility of atypical prions from genetic CJDG114V 55
Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics 53
Classification of sporadic Creutzfeldt-Jakob disease revisited 53
Variable Protease-Sensitive Prionopathy Transmission to Bank Voles 53
Distinct disease phenotypes and PrP type 1 variants in Creutzfeldt-Jakob disease with codon 129MM genotype 52
Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone. 52
Zoonotic Potential of CWD Prions: an update 52
Transmissibility and propagation of co-existing prions of sporadic Creutzfeldt-Jakob disease into humanized transgenic mice 51
Transmissibility and propagation of PrPSc from sCJDMM1-2 in humanized transgenic mice 51
Molecular biology and pathology of prion strains in sporadic human prion diseases 51
Insoluble Aggregates and Protease-resistant Conformers of Prion Protein in Uninfected Human Brains 51
Amyloid fibrils from the N-terminal prion protein fragment are infectious 50
Distinct strain of Amyloid beta and pathogenic tau protein in iatrogenic Creutzfeldt-Jakob disease. 49
Protease-sensitive prions with 144-bp insertion mutations 49
A novel de novo insertional mutation in the PrP gene characterized by slowly progressive atypical dementia: Neuropathological and biochemical findings 48
Human prion diseases: surgical lessons learned from iatrogenic prion transmission 47
A novel subtype of sporadic Creutzfeldt-Jakob disease with PRNP codon 129MM genotype and PrP plaques 47
Co-occurrence of chronic traumatic encephalopathy and prion disease 47
Characterization of Prion Disease Associated with a Two-Octapeptide Repeat Insertion 47
Transmission characteristics of variably protease-sensitive prionopathy 46
Co-occurrence of Distinct Types of Scrapie Prion Protein in Sporadic Creutzfeldt-Jakob Disease 46
Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States 46
Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone 46
Novel histotypes of sporadic Creutzfeldt-Jakob disease linked to 129MV genotype 46
Pathologic evidence that the T188R mutation in PRNP is associated with prion disease 46
Sporadic fatal insomnia in an adolescent 46
Glycoform-selective prion formation in sporadic and familial forms of prion disease 45
Co-existence of PrPD types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristics 45
Thermodynamic stabilization of the folded domain of prion protein inhibits prion infection in vivo 44
Evaluation of the human transmission risk of an atypical bovine spongiform encephalopathy prion strain. 44
Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study 44
Human Sporadic Prion Diseases 43
Two different conformers of type 1 prion protein propagate as distinct strains in transgenic mice 43
PMCA-replicated PrPD in urine of vCJD patients maintains infectivity and strain characteristics of brain PrPD: Transmission study 43
Prion disease with insertion of two-octapeptide repeats in the PrP gene: Molecular and phenotypic determination 43
Synthetic Aβ peptides acquire prion-like properties in the brain 43
Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation cases 41
Sporadic Creutzfeldt-Jakob disease in a native Puerto Rican patient 40
Case Report: Histopathology and Prion Protein Molecular Properties in Inherited Prion Disease With a De Novo Seven-Octapeptide Repeat Insertion 40
Sporadic Creutzfeldt-Jakob Disease in a Very Young Person 38
Glycans modulate the transmissibility of PrPSc and the sCJDMM2 and sFI phenotypes 37
Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion type 36
A Novel Mechanism of Phenotypic Heterogeneity in Creutzfeldt-Jakob Disease 36
Generation of human chronic wasting disease in transgenic mice 35
Variant Creutzfeldt-Jakob disease 35
Variant Creutzfeldt-Jakob Disease 33
Variably protease-sensitive prionopathy: mass spectrometry analysis of the pathogenic prion protein provides a new perspective 6
The Phenotypic Spectrum of Sporadic Creutzfeldt‐Jakob Disease Cortical Subtype 4
Genetic Creutzfeldt-Jakob disease linked to the E200K mutation: a large cohort study 4
Understanding the Phenotypic Heterogeneity Within the Sporadic Creutzfeldt–Jakob Disease MV1 Subtype 1
Totale 3.052
Categoria #
all - tutte 18.822
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 18.822


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
2025/20261.789 135 400 177 187 35 69 271 154 137 103 55 66
2026/202793 20 47 26 0 0 0 0 0 0 0 0 0
Totale 3.052