CRIS Current Research Information System

BIAGINI, ELENA
 Distribuzione geografica
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Continente #
NA - Nord America 4.492
EU - Europa 3.170
AS - Asia 2.916
AF - Africa 220
SA - Sud America 182
OC - Oceania 4
Continente sconosciuto - Info sul continente non disponibili 1
Totale 10.985
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Nazione #
US - Stati Uniti d'America 4.455
SG - Singapore 1.001
CN - Cina 942
GB - Regno Unito 731
IT - Italia 593
DE - Germania 466
VN - Vietnam 372
SE - Svezia 360
HK - Hong Kong 220
UA - Ucraina 191
RU - Federazione Russa 163
IN - India 150
FR - Francia 140
BR - Brasile 126
IE - Irlanda 114
NL - Olanda 111
KR - Corea 88
CI - Costa d'Avorio 73
FI - Finlandia 70
EE - Estonia 61
ZA - Sudafrica 50
JP - Giappone 42
TG - Togo 39
CH - Svizzera 38
BG - Bulgaria 35
JO - Giordania 35
AR - Argentina 29
BE - Belgio 28
SC - Seychelles 26
CA - Canada 24
PL - Polonia 24
NG - Nigeria 21
ID - Indonesia 16
IR - Iran 12
AT - Austria 11
EC - Ecuador 10
ES - Italia 8
MX - Messico 7
BD - Bangladesh 6
TR - Turchia 6
GR - Grecia 5
MY - Malesia 5
AU - Australia 4
CO - Colombia 4
CZ - Repubblica Ceca 4
EG - Egitto 4
PH - Filippine 4
CL - Cile 3
LT - Lituania 3
PK - Pakistan 3
PY - Paraguay 3
RO - Romania 3
UY - Uruguay 3
UZ - Uzbekistan 3
HN - Honduras 2
IL - Israele 2
KE - Kenya 2
LB - Libano 2
MA - Marocco 2
PE - Perù 2
RS - Serbia 2
SM - San Marino 2
AM - Armenia 1
AO - Angola 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BO - Bolivia 1
BY - Bielorussia 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
GI - Gibilterra 1
HR - Croazia 1
IQ - Iraq 1
JM - Giamaica 1
KH - Cambogia 1
LA - Repubblica Popolare Democratica del Laos 1
MK - Macedonia 1
SI - Slovenia 1
SO - Somalia 1
SV - El Salvador 1
SY - Repubblica araba siriana 1
TH - Thailandia 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
VE - Venezuela 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 10.985
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Città #
Singapore 671
Southend 570
Ashburn 532
Fairfield 531
Chandler 322
Houston 290
Woodbridge 263
Hefei 225
Ann Arbor 224
Hong Kong 217
Seattle 213
Wilmington 193
Dong Ket 186
Cambridge 168
Santa Clara 159
Princeton 145
Beijing 132
Jacksonville 122
Dublin 114
Boardman 109
Seoul 84
Bologna 75
Los Angeles 75
Abidjan 73
Turin 64
Westminster 64
Munich 63
Padova 63
New York 60
Nanjing 57
Milan 55
Ho Chi Minh City 48
Helsinki 47
Enfield 44
Berlin 43
Bremen 43
Tokyo 42
Lomé 39
Frankfurt am Main 37
Jinan 37
Shenyang 37
Amman 35
Hanoi 35
Sofia 35
Dearborn 33
Saint Petersburg 32
Buffalo 31
Nanchang 29
Brussels 28
Rome 28
Bern 26
Dallas 26
Changsha 25
Bengaluru 22
San Diego 22
Redondo Beach 21
Abeokuta 20
Falkenstein 20
Mülheim 20
The Dalles 20
Turku 19
Des Moines 18
Florence 18
Hebei 17
São Paulo 17
Warsaw 17
Chicago 15
Zhengzhou 15
Guangzhou 14
Mahé 14
Haikou 13
Tianjin 13
Olalla 12
Redwood City 12
Düsseldorf 11
Shenzhen 11
London 10
Phoenix 10
Shanghai 10
Toronto 10
Yubileyny 9
Brooklyn 8
Cesena 8
Hangzhou 8
Lanzhou 8
Medford 8
Moscow 8
Verona 8
Atlanta 7
Haiphong 7
Jiaxing 7
Kunming 7
Naples 7
Ningbo 7
Redmond 7
Rio de Janeiro 7
Taiyuan 7
Taizhou 7
Zanjan 7
Brescia 6
Totale 7.468
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Nome #
Prolasso valvolare mitralico e disgiunzione mitro-anulare. La consapevolezza di un possibile substrato aritmico 294
Ventricular remodeling in Loeffler endocarditis: Implications for therapeutic decision making. 275
Acute heart failure in patients with acute aortic syndrome: Pathophysiology and clinical-prognostic implications 269
Effects of myocardial fibrosis assessed by MRI on dynamic left ventricular outflow tract obstruction in patients with hypertrophic cardiomyopathy: a retrospective database analysis. 241
Parodoxical contributions of non-compacted and compacted segments to global left ventricular dysfunction in isolated left ventriculat noncompaction 217
Amiloidosi ereditaria da mutazione della transtiretina: caratterizzazione dei casi con interessamento cardiaco esclusivo o prevalente 200
The elusive link between aortic wall histology and echocardiographic anatomy in bicuspid aortic valve: implications for prophylactic surgery 188
Skin globotriaosylceramide 3 deposits are specific to Fabry disease with classical mutations and associated with small fibre neuropathy. 187
Disease profile and differential diagnosis of hereditary transthyretin-related amyloidosis with exclusively cardiac phenotype: an Italian perspective 181
Risk Factors for diagnostic delay in acute aortic dissection. 180
Prognostic stratification of patients with right bundle branch block using dobutamine stress echocardiography. 178
Utility of stress perfusion-cardiac magnetic resonance in follow-up of patients undergoing percutaneous coronary interventions of the left main coronary artery 175
Accuracy of non-invasive techniques for diagnosis of coronary artery disease and prediction of cardiac events in patients with left bundle branch block: a meta-analysis. 173
Different types of cardiomyopathy associated with isolated ventricular noncompaction 172
Systemic cardiac amyloidoses: disease profiles and clinical courses of the 3 main types. 164
Clinical use of doppler echocardiography in organic mitral regurgitation: From diagnosis to patients’ management 164
Wide spectrum of presentation and variable outcomes of isolated left ventricular non-compaction 159
Prognostic implications of the Doppler restrictive filling pattern in hypertrophic cardiomyopathy 159
Long-Term Implications of Atrial Fibrillation in Patients With Degenerative Mitral Regurgitation 159
Defining the diagnosis in echocardiographically suspected senile systemic amyloidosis. 159
Development and Validation of a Diagnostic Echocardiographic Mass Score in the Approach to Cardiac Masses 157
Exercise stress echocardiography is superior to rest echocardiography in predicting left ventricular reverse remodelling and functional improvement after cardiac resynchronization therapy. 157
The residual risk of cerebral embolism after carotid stenting: the complex interplay between stent coverage and aortic arch atherosclerosis. 156
Histological and histometric characterization of myocardial fibrosis in end-stage hypertrophic cardiomyopathy. A Clinical-Pathological Study of 30 Explanted Hearts 156
Long term outcome in patients with silent versus symptomatic ischaemia during dobutamine stress echocardiography. 153
Dilated-Hypokinetic evolution of hypertrophic cardiomyopathy 153
Transesophageal echocardiography-guided algorithm for stent-graft implantation in aortic dissection 152
Correlations Between Cardiac Magnetic Resonance and Myocardial Histologic Findings in Fabry Disease 151
Frequency, determinants, and clinical relevance of acute coronary syndrome-like electrocardiographic findings in patients with acute aortic syndrome 150
Resincronizzazione cardiaca con pacing biventricolare o ventricolare sinistro: effetti a medio termine su funzione sistolica e sincronia ventricolare sinistra 149
Effects of cardiac resynchronisation therapy on dilated cardiomyopathy with isolated ventricular non-compaction. 149
Prenatal echographic recognition of hypertrophic cardiomyopathy leading to heart transplantation in the newborn. 148
Transthyretin-related amyloidoses and the heart: a clinical overview. 146
L'eziologia dell'amiloidosi condiziona i meccanismi dello scompenso cardiaco della cardiomiopatia amiloidotica 146
Long-term prediction of mortality in elderly persons by dobutamine stress echocardiography. 143
Aortic thrombosis: a shared complication of different underlying diseases 143
Circulating miR-184 is a potential predictive biomarker of cardiac damage in Anderson–Fabry disease 143
Diagnostic delay for acute aortic dissection: secular trends and risk factors 142
Electrocardiogram analysis in Anderson-Fabry disease: a valuable tool for progressive phenotypic expression tracking 141
Usefulness of 99-Tc DPD scintigraphy and identification of transthyretin-related cardiac amyloidosis 141
Significance of magnetic resonance imaging in apical hypertrophic cardiomyopathy. 140
Differences in cardiac phenotype and natural history of laminopathies with and without neuromuscular onset 139
Familial Amyloidoses and the Heart 136
Predictors of nonsimultaneous interventricular delay at cardiac resynchronization therapy optimization 135
Cambi di paradigma in tema di aorta: Implicazioni cliniche e terapeutiche La biopatologia dell'aorta [Paradigm shifts in aortic pathology: clinical and therapeutic implications. Biology and pathology of the aortic wall]. 134
Prevalence of Anderson-Fabry disease in patients with hypertrophic cardiomyopathy: the European Anderson-Fabry Disease survey. 133
Clinical presentations leading to arrhythmogenic left ventricular cardiomyopathy 128
Heart transplantation in hypertrophic cardiomyopathy. 127
Significance of sarcomere gene mutations analysis in the end-stage phase of hypertrophic cardiomyopathy 125
Dilated-hypokinetic evolution of hypertrophic cardiomyopathy: Incidence, risk factors, and prognostic implications in pediatric and adult patients at a nontertiary cardiological center 124
Syncope and risk of sudden death in hypertrophic cardiomyopathy 122
Seven-year follow-up after dobutamine stress echocardiography: impact of gender on prognosis. 122
Kidney transplant in fabry disease: A revision of the literature 121
Risk of sudden death and outcome in patients with hypertrophic cardiomyopathy with benign presentation and without risk factors 119
Left ventricular function after ST-elevation myocardial infarction in patients treated with primary percutaneous coronary intervention and abciximab or tirofiban (from the Facilitated Angioplasty with tirofiban or Abciximab [FATA] trial) 118
Comparison of all-cause mortality in women with known or suspected coronary artery disease referred for dobutamine stress echocardiography with normal versus abnormal test results. 118
A novel clinical risk prediction model for sudden cardiac death in hypertrophic cardiomyopathy (HCM risk-SCD). 118
Prognostic value of quantitative contrast-enhanced cardiovascular magnetic resonance for the evaluation of sudden death risk in patients with hypertrophic cardiomyopathy 111
Isolated ventricular non-compaction with restrictive cardiomyopathy. 109
Cambi di paradigma in tema di aorta: Implicazioni cliniche e terapeutiche - Imaging clinico nelle sindromi croniche ed acute. L'aorta come causa di malattia cardiaca 109
Screening approaches to cardiac amyloidosis in different clinical settings: Current practice and future perspectives 106
Patisiran for the treatment of patients with p.Ile88Leu hereditary transthyretin amyloidosis: an Italian real-life experience 105
Effetto donna" nelle cardiomiopatie Gender effect on cardiomyopathy 104
Pacemaker stress echocardiography predicts cardiac events in patients with permanent pacemaker. 103
Echocardiographic clues to diagnosis of dystrophin related dilated cardiomyopathy. 103
Prognostic significance of left anterior hemiblock in patients with suspected coronary artery disease. 101
Left ventricular versus biventricular pacing: a randomized comparative study evaluating mid-term electromechanical and clinical effects. 100
Incidence and predictors of sudden death in patients with cardiac amyloidosis 99
Exploring the gap between National Cholesterol Education Program guidelines and clinical practice in secondary care: results of a cross-sectional study involving over 10 000 patients followed in different specialty settings across Italy 99
null 99
Reply to della corte et al comment on "The elusive link between aortic wall histology and echocardio- graphic anatomy in bicuspid aortic valve: implications for pro-phylactic surgery" 96
Risk stratification of patients with classic angina pectoris and no history of coronary artery disease by dobutamine stress echocardiography 94
Diagnosis of idiopathic restrictive cardiomyopathy at a glance. J Cardiovasc Med (Hagerstown). 2007 Sep;8(9):758. No abstract available. 93
Guidelines for the diagnosis and treatment of non-ST-segment elevation acute coronary syndromes: the task force for the diagnosis and treatment of non-ST-segment elevation acute coronary syndromes of the European Society of Cardiology. 91
Arrhythmic risk stratification in patients with left ventricular ring-like scar 88
Histopathological comparison of intramural coronary artery remodeling and myocardial fibrosis in obstructive versus end-stage hypertrophic cardiomyopathy 75
Heart transplantation in infants with idiopathic hypertrophic cardiomyopathy 61
Temporal implementation of a regional referral pathway in transthyretin cardiac amyloidosis: Emilia-Romagna experience 54
Cocaine-Induced Sudden Cardiac Death Unravelling a SCN5A-Related Disease 53
Electrocardiogram evolution in Anderson-Fabry disease patients during follow-up in relation to specific treatment and cardiac disease progression 42
Survival loss linked to guideline-based indications for degenerative mitral regurgitation surgery 32
Totale 11.156
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Categoria #
all - tutte 29.619
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 29.619
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021571 0 0 0 0 0 51 9 65 97 42 59 248
2021/20221.269 129 53 75 149 110 61 28 71 53 60 265 215
2022/20231.620 137 170 79 239 109 122 41 85 289 43 216 90
2023/2024550 31 78 27 35 44 132 39 32 21 42 32 37
2024/20251.840 83 230 146 163 262 108 99 65 34 155 98 397
2025/20262.100 369 411 371 342 494 113 0 0 0 0 0 0
Totale 11.156