IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

CACCIA, SONIA
 Distribuzione geografica
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Continente #
EU - Europa 5.549
NA - Nord America 5.340
AS - Asia 4.327
SA - Sud America 439
AF - Africa 80
Continente sconosciuto - Info sul continente non disponibili 35
OC - Oceania 30
Totale 15.800
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Nazione #
US - Stati Uniti d'America 5.141
GB - Regno Unito 1.710
CN - Cina 1.463
SG - Singapore 1.132
IT - Italia 914
DE - Germania 748
SE - Svezia 405
RU - Federazione Russa 399
HK - Hong Kong 343
BR - Brasile 316
VN - Vietnam 288
IN - India 275
NL - Olanda 254
FR - Francia 228
BD - Bangladesh 199
TR - Turchia 174
FI - Finlandia 150
IE - Irlanda 128
CA - Canada 126
UA - Ucraina 126
DK - Danimarca 110
KR - Corea 108
ES - Italia 90
JP - Giappone 77
ID - Indonesia 76
EU - Europa 72
MX - Messico 44
BE - Belgio 39
CO - Colombia 38
AR - Argentina 37
AT - Austria 35
PL - Polonia 32
GR - Grecia 30
CI - Costa d'Avorio 29
PH - Filippine 29
PT - Portogallo 26
RO - Romania 23
AU - Australia 22
IR - Iran 20
CZ - Repubblica Ceca 19
TW - Taiwan 19
CH - Svizzera 16
TH - Thailandia 16
IQ - Iraq 15
ZA - Sudafrica 15
BG - Bulgaria 14
CL - Cile 14
EC - Ecuador 13
AE - Emirati Arabi Uniti 12
PK - Pakistan 11
UZ - Uzbekistan 11
RS - Serbia 10
IL - Israele 9
SA - Arabia Saudita 9
HR - Croazia 8
NZ - Nuova Zelanda 8
LT - Lituania 7
MA - Marocco 7
PE - Perù 7
VE - Venezuela 7
HU - Ungheria 5
KZ - Kazakistan 5
NP - Nepal 5
PA - Panama 5
SC - Seychelles 5
JM - Giamaica 4
JO - Giordania 4
KE - Kenya 4
LB - Libano 4
TN - Tunisia 4
AZ - Azerbaigian 3
DZ - Algeria 3
GT - Guatemala 3
MT - Malta 3
MY - Malesia 3
NI - Nicaragua 3
NO - Norvegia 3
PR - Porto Rico 3
PS - Palestinian Territory 3
PY - Paraguay 3
SI - Slovenia 3
SK - Slovacchia (Repubblica Slovacca) 3
SN - Senegal 3
SV - El Salvador 3
AL - Albania 2
AM - Armenia 2
BA - Bosnia-Erzegovina 2
BO - Bolivia 2
DO - Repubblica Dominicana 2
EG - Egitto 2
ET - Etiopia 2
GE - Georgia 2
KH - Cambogia 2
LU - Lussemburgo 2
LV - Lettonia 2
ML - Mali 2
UY - Uruguay 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AG - Antigua e Barbuda 1
AO - Angola 1
Totale 15.819
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Città #
Southend 1.498
Singapore 690
Ashburn 527
Chandler 448
Milan 379
Hong Kong 303
Beijing 277
Hanover 274
Dallas 267
San Jose 216
Wilmington 177
Fairfield 170
Seattle 169
Princeton 141
Ann Arbor 140
Los Angeles 140
Council Bluffs 133
Dearborn 129
Dublin 120
Houston 114
Redwood City 112
Woodbridge 110
Frankfurt am Main 99
Boardman 97
New York 96
Helsinki 86
Santa Clara 86
Jacksonville 81
Ho Chi Minh City 80
Bengaluru 74
Guangzhou 74
Shanghai 67
Des Moines 66
Hanoi 66
Cambridge 65
Lauterbourg 61
Nanjing 60
Mountain View 55
Buffalo 54
Hefei 54
Toronto 54
Redmond 52
Tokyo 52
Moscow 47
Munich 47
Somerville 46
Berlin 44
Mumbai 44
Shenyang 39
Jinan 38
Serra 38
Jakarta 37
Columbus 36
Istanbul 36
Putian 35
Roxbury 34
São Paulo 34
Chicago 33
Dong Ket 33
Andover 32
Barcelona 32
Brussels 31
Athens 30
Bogotá 30
Sakarya 30
Seoul 30
The Dalles 30
Abidjan 29
Rome 28
Fuzhou 26
Phoenix 26
Changsha 25
Tianjin 25
Nanchang 24
Saint Petersburg 24
Medford 23
Cangzhou 22
Bodio Lomnago 20
Fremont 20
Vienna 20
London 19
Montreal 19
Nuremberg 17
Amsterdam 16
Zhengzhou 16
Ankara 15
Atlanta 15
Chennai 15
Ottawa 15
Shenzhen 15
Chengdu 14
Falls Church 14
San Francisco 14
Warsaw 14
Lisbon 13
Odernheim 13
Rio de Janeiro 13
San Diego 13
Taipei 13
Brooklyn 12
Totale 9.486
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Nome #
Current and emerging biologics for the treatment of hereditary angioedema 765
Recombinant human C1 esterase inhibitor (Conestat alfa) for prophylaxis to prevent attacks in adult and adolescent patients with hereditary angioedema 641
The central role of endothelium in hereditary angioedema due to C1 inhibitor deficiency 557
IgM Autoantibodies to Complement Factor H in Atypical Hemolytic Uremic Syndrome 511
Human neuroserpin : structure and time-dependent inhibition 365
A transcriptomics study of hereditary angioedema attacks 355
Acid Sphingomyelinase Downregulation Enhances Mitochondrial Fusion and Promotes Oxidative Metabolism in a Mouse Model of Melanoma 350
Remittent C1-inhibitor deficiency due to Arg378Cys mutation 334
Intermittent C1-Inhibitor Deficiency Associated with Recessive Inheritance: Functional and Structural Insight 325
Embelin binds to human neuroserpin and impairs its polymerisation 318
Molecular bases of neuroserpin function and pathology 300
Gene regulation in the pathogenesis of angioedema due to inherited c1 inhibitor deficiency (hereditary angioedema) 299
Antibodies to tissue-type plasminogen activator (tPA) in patients with antiphospholipid syndrome : evidence of interaction between the antibodies and the catalytic domain of tPA in 2 patients 281
Molecular mechanism for the pathogenicity of the human C1-inhibitor Arg378Cys variant 267
Structural and functional characterization of mutations in C1-ihn responsible for hereditary angioedema 266
Identification of novel deafness-causing variants in the tmprss3 gene by whole-exome sequencing 250
Effects of mutations within the coding region of C1-INH gene on disease manifestation and protein function in families with HAE 244
Mutation screening of C1 inhibitor gene in 108 unrelated families with hereditary angioedema : functional and structural correlates 244
The kinetics of the reaction between NO and O2 as studied by a novel approach 242
Modulation of the association reaction between hemoglobin and carbon monoxide by proton and chloride 239
Gene regulation in the pathogenesis of inherited C1-inhibitor deficiency (Hereditary Angioedema) 236
Diagnosis, Course, and Management of Angioedema in Patients With Acquired C1-Inhibitor Deficiency 232
The anticoagulant thrombin mutant W215A/E217A has a collapsed primary specificity pocket 229
Effect of mutations within the coding region of C1-INH gene on protein function in families with HAE 228
Molecular dissection of Na+ binding to thrombin 228
A SERPING1 variant that causes C1-inhibitor deficiency without hereditary angioedema 226
Exome sequencing identifies PRPS1 as a major locus for X-linked nonsyndromic hearing loss in the Italian population 223
Antibodies to tissue-type plasminogen activator (t-PA) in patients with inflammatory bowel disease : high prevalence, interactions with functional domains of t-PA and possible implications in thrombosis 218
Identification of variables causing different clinical expression of inherited c1-inh deficiency (hereditary angioedema) 218
Circulating endothelial progenitors are increased in Covid‐19 patients and correlate with SARS‐CoV‐2 RNA in severe cases 217
Identification by exome sequencing and functional characterization of novel deafness-causing mutations in PRPS1 212
Congenital hypofibrinogenemia associated with a novel heterozygous nonsense mutation in the globular C-terminal domain of the γ-chain (p.Glu275Stop) 210
Identification of novel NSHL-causing mutations by whole exome sequencing 208
Genetic variants in the fgb and fgg genes mapping in the beta and gamma nodules of the fibrinogen molecule in congenital quantitative fibrinogen disorders associated with a thrombotic phenotype 207
C1-inhibitor deficiency and angioedema : molecular mechanisms and clinical progress 206
Analysis of the structural effects of four novel and a previously known mutations causing factor XI deficiency 205
Cleaved human neuroserpin 204
Thrombomodulin changes the molecular surface of interaction and the rate of complex formation between thrombin and protein C 202
The use of plasma-derived C1 inhibitor in the treatment of hereditary angioedema 202
Alpha-synuclein dynamics bridge Type-I Interferon response and SARS-CoV-2 replication in peripheral cells 200
Patterns of C1-Inhibitor Plasma Levels and Kinin–Kallikrein System Activation in Relation to COVID-19 Severity 194
A case of remittent C1-inhibitor deficiency 190
Structure/function correlates in variables causing hereditary angioedema 188
Identification of variables causing different clinical expression of inherited c1-inh deficiency (hereditary angioedema) 187
Novelties in the diagnosis and treatment of angioedema 186
Unexpected crucial role of residue 225 in serine proteases 184
Anti-C1-Inhibitor Autoantibody Detection by ELISA 181
Novel SERPING1 mutations in bulgarian patients revealed by a targeted next generation sequencing platform 178
Hereditary angioedema due to C1 inhibitor deficiency in Belarus : epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene 178
Interaction of C1 inhibitor with thrombin on the endothelial surface 176
The stability and activity of human neuroserpin are modulated by a salt bridge that stabilises the reactive centre loop 176
C1 esterase inhibitor and the kinin-kallikrein system in COVID-19 176
The expanding spectrum of PRPS1-associated phenotypes: three novel mutations segregating with X-linked hearing loss and mild peripheral neuropathy 170
First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian family 166
Studi preliminari per l'introduzione di un sito di modulazione sodio-specifico nel tPA 165
Modulation of the Association Reaction between Hemoglobin and Carbon Monoxide by Proton and Chloride 158
Hereditary angioedema in a Jordanian family with a novel missense mutation in the C1-inhibitor N-terminal domain 153
Donor complement gene abnormalities cause transplant associated microangiopathy after allogeneic bone marrow transplantation 144
Structure of native human neuroserpin 132
Platelet Microvesicles, Inflammation, and Coagulation Markers: A Pilot Study 128
Structure of human alpha-thrombin Y225I mutant bound to D-PHE-PRO-ARG-chloromethylketone 125
Crystal structure of the potent anticoagulant thrombin mutant W215A/E217A in free form 125
Efficacy of Lanadelumab in angioedema due to acquired C1 inhibitor deficiency 121
Hepatic fibrinogen storage disease: identification of two novel mutations (p.Asp316Asn, fibrinogen Pisa and p.Gly366Ser, fibrinogen Beograd) impacting on the fibrinogen γ-module 120
Pathophysiology of hereditary angioedema 119
Hereditary Deficiency of C1 Inhibitor and Angioedema 118
Structural and functional characterization of mutations in C1-inh responsible for hereditary angioedema 117
Structure of human alpha-thrombin Y225P mutant bound to D-PHE-PRO-ARG-chloromethylketone 114
Fast form of thrombin mutant R(77a)A bound to PPACK 114
The spectrum of factor XI deficiency in Italy 113
An atypical case of idiopathic nonhistaminergic angioedema with anti-C1-INH antibodies 111
Structure of human alpha-thrombin Y225F mutant bound to D-PHE-PRO-ARG-chloromethylketone 107
A novel pathogenic variant in the fibrinogen gamma chain gene p.Glu275Lys causes congenital hypofibrinogenemia 84
Elevated serum levels of interleukin-18 discriminate Still's disease from other autoinflammatory conditions: results from the European ImmunAID cohort 67
Distinct Natural Killer Cell Signature in Still Disease: Insights From a Multinational Immunome Project Consortium for Autoinflammatory Disorders 7
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Adult patients with autoinflammation of unknown origin partially phenocopy the immune presentation of Still's disease 1
Inflammatory profile of lower risk myelodysplastic syndromes 1
Totale 16.444
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Categoria #
all - tutte 41.599
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 41.599
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021113 0 0 0 0 0 0 0 0 0 0 0 113
2021/20221.632 120 74 72 63 149 96 143 124 228 177 128 258
2022/20231.363 158 168 139 158 125 230 30 87 142 19 86 21
2023/2024940 29 87 58 75 179 122 45 76 28 40 82 119
2024/20252.245 83 200 59 189 122 123 116 231 189 286 236 411
2025/20264.508 456 319 535 397 410 332 558 205 400 336 442 118
Totale 16.444