BAUCE, BARBARA
 Distribuzione geografica
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Continente #
NA - Nord America 9.520
EU - Europa 1.753
AS - Asia 610
OC - Oceania 9
SA - Sud America 4
Continente sconosciuto - Info sul continente non disponibili 3
AF - Africa 2
Totale 11.901
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Nazione #
US - Stati Uniti d'America 9.512
IT - Italia 735
CN - Cina 486
SE - Svezia 362
FI - Finlandia 198
DE - Germania 151
UA - Ucraina 112
GB - Regno Unito 92
VN - Vietnam 47
IN - India 39
GR - Grecia 33
FR - Francia 16
TR - Turchia 15
NL - Olanda 14
IE - Irlanda 13
CA - Canada 8
HK - Hong Kong 7
AU - Australia 5
BE - Belgio 5
IR - Iran 5
RO - Romania 5
NZ - Nuova Zelanda 4
CH - Svizzera 3
EU - Europa 3
LB - Libano 3
PL - Polonia 3
BY - Bielorussia 2
ES - Italia 2
JP - Giappone 2
RU - Federazione Russa 2
AR - Argentina 1
AT - Austria 1
BG - Bulgaria 1
CL - Cile 1
CO - Colombia 1
CZ - Repubblica Ceca 1
DZ - Algeria 1
EC - Ecuador 1
HR - Croazia 1
IQ - Iraq 1
LK - Sri Lanka 1
MA - Marocco 1
PK - Pakistan 1
PT - Portogallo 1
SA - Arabia Saudita 1
SG - Singapore 1
TW - Taiwan 1
Totale 11.901
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Città #
Fairfield 1.640
Woodbridge 1.042
Houston 928
Chandler 771
Ashburn 685
Ann Arbor 671
Seattle 581
Cambridge 557
Wilmington 522
Jacksonville 407
Princeton 201
San Diego 151
Padova 129
Beijing 120
Roxbury 114
Medford 99
Helsinki 96
Nanjing 86
Des Moines 85
Milan 68
Guangzhou 53
Boardman 52
Dong Ket 47
New York 33
Hebei 26
Changsha 24
Jinan 24
Rome 23
London 22
Shenyang 22
Norwalk 21
Redwood City 20
Jiaxing 19
Ogden 19
Tianjin 16
Nanchang 14
Zhengzhou 13
Pune 12
Verona 12
Bologna 11
Dublin 11
Istanbul 11
Venice 11
Falls Church 10
Washington 10
Hounslow 9
Naples 9
Dearborn 7
Turin 7
Borås 6
Hong Kong 6
Kharkiv 6
Kilburn 6
Los Angeles 6
Noale 6
Selvazzano Dentro 6
Treviso 6
Augusta 5
Bolzano 5
Frankfurt am Main 5
Hangzhou 5
Indiana 5
Trieste 5
Bari 4
Brendola 4
Cagliari 4
Chicago 4
Genoa 4
Kunming 4
Lanzhou 4
Lappeenranta 4
Napoli 4
Nürnberg 4
Pavia 4
Ponte di Piave 4
Prescot 4
Sassuolo 4
Shanghai 4
Stanford 4
Taizhou 4
Waanrode 4
Avellino 3
Beirut 3
Bengaluru 3
Blacksburg 3
Cachan 3
Camponogara 3
Castellarano 3
Chiswick 3
Detroit 3
Essen 3
Faenza 3
Furore 3
Grosseto 3
Haikou 3
Kharar 3
Legnaro 3
Marcallo con Casone 3
Modena 3
Munich 3
Totale 9.728
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Nome #
Cardiomiopatia/displasia aritmogena del ventricolo destro 215
'Hot phase' clinical presentation in arrhythmogenic cardiomyopathy 195
A targeted next-generation gene panel reveals a novel heterozygous nonsense variant in the TP63 gene in patients with arrhythmogenic cardiomyopathy 175
Morphofunctional abnormalities of mitral annulus and arrhythmic mitral valve prolapse 154
Large Genomic Rearrangements of Desmosomal Genes in Italian Arrhythmogenic Cardiomyopathy Patients 151
Arrhythmogenic Cardiomyopathy 144
Electrocardiographic Pattern in Arrhythmogenic Right Ventricular Cardiomyopathy 138
Compound and Digenic Heterozygosity Contributes to Arrhythmogenic Right Ventricular Cardiomyopathy 136
Whole-Exome Sequencing Identifies Pathogenic Variants in TJP1 Gene Associated With Arrhythmogenic Cardiomyopathy 136
Ultrastructural evidence of intercalated disc remodelling in arrhythmogenic right ventricular cardiomyopathy: an electron microscopy investigation on endomyocardial biopsies. 133
Missense mutations in desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitro. 131
Homozygous desmocollin-2 mutations and arrhythmogenic cardiomyopathy 129
Three-dimensional electroanatomical voltage mapping and histologic evaluation of myocardial substrate in right ventricular outflow tract tachycardia. 128
Follow-Up with Exercise Test of Effort-Induced Ventricular Arrhythmias Linked to Ryanodine Receptor Type 2 Gene Mutations. 126
Predictive value of exercise testing in athletes with ventricular ectopy evaluated by cardiac magnetic resonance 125
Arrhythmogenic right ventricular cardiomyopathy type 1 (ARVD1): confirmation of locus assignment and mutation screening of four candidate genes. 124
PHENOTYPIC EXPRESSION IS A PREREQUISITE FOR MALIGNANT ARRHYTHMIC EVENTS AND SUDDEN CARDIAC DEATH IN ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 124
Arrhythmic Mitral Valve Prolapse and Sudden Cardiac Death 122
Myocyte necrosis underlies progressive myocardial dystrophy in mouse dsg2-related arrhythmogenic right ventricular cardiomyopathy 121
Nonischemic left ventricular scar as a substrate of life-threatening ventricular arrhythmias and sudden cardiac death in competitive athletes 121
Arrhythmogenic cardiomyopathy 121
Treatment of arrhythmogenic right ventricular cardiomyopathy/dysplasia: An international task force consensus statement 120
Signal-averaged electrocardiogram in patients with arrhythmogenic right ventricular cardiomyopathy and ventricular arrhythmias 118
Imaging Study of Ventricular Scar in Arrhythmogenic Right Ventricular Cardiomyopathy: Comparison of 3D Standard Electroanatomical Voltage Mapping and Contrast-Enhanced Cardiac Magnetic Resonance. 116
The p.A897KfsX4 frameshift variation in desmocollin-2 is not a causative mutation in arrhythmogenic right ventricular cardiomyopathy 116
Mutations in the area composita protein alphaT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy 113
Three-Dimensional Electroanatomical Voltage Mapping and Histologic Evaluation of Myocardial Substrate in Right Ventricular Outflow Tract Tachycardia 112
Relationship between electrocardiographic findings and cardiac magnetic resonance phenotypes in arrhythmogenic cardiomyopathy 109
Juvenile sudden death in a family with polymorphic ventricular arrhythmias caused by a novel RyR2 gene mutation: evidence of specific morphological substrates. 106
Clinical phenotype and diagnosis of arrhythmogenic right ventricular cardiomyopathy in pediatric patients carrying desmosomal gene mutations. 105
Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia 105
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2) 104
Electrocardiographic predictors of electroanatomic scar size in arrhythmogenic right ventricular cardiomyopathy: implications for arrhythmic risk stratification. 104
Differences and similarities between arrhythmogenic right ventricular cardiomyopathy and athlete's heart adaptations 102
Arrhythmogenic right ventricular cardiomyopathy is a life-threatening disease at high risk for cardiac arrest during effort. Minor forms are as dangerous as major forms? 101
Denaturing HPLC-based approach for detecting RYR2 mutations involved in malignant arrhythmias 101
Imaging study of ventricular scar in arrhythmogenic right ventricular cardiomyopathy/dysplasia: comparison of three-dimensional electroanatomic voltage mapping and contrast-enhanced cardiac magnetic resonance 100
TAIL1: an isthmin-like gene, containing type 1 thrombospondin-repeat and AMOP domain, mapped to ARVD1 critical region. 99
Subcutaneous implantable cardioverter defibrillator in patients with arrhythmogenic right ventricular cardiomyopathy: Results from an Italian multicenter registry 99
Compound and digenic heterozygosity predicts lifetime arrhythmic outcome and sudden cardiac death in desmosomal gene-related arrhythmogenic right ventricular cardiomyopathy. 99
Response to Letters Regarding Article, "Arrhythmic Mitral Valve Prolapse and Sudden Cardiac Death" 98
Identification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathy. 97
Exercise-Induced Normalization of Right Precordial Negative T Waves in Arrhythmogenic Right Ventricular Cardiomyopathy. 97
Definition and treatment of arrhythmogenic cardiomyopathy: an updated expert panel report 97
The 2020 “Padua Criteria” for Diagnosis and Phenotype Characterization of Arrhythmogenic Cardiomyopathy in Clinical Practice 96
Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy 95
Implantable Cardioverter-Defibrillator Therapy in Athletes 94
Evolution of focal moderate (International Society for Heart and Lung Transplantation grade 2) rejection of the cardiac allograft 93
Quantitative assessment of endomyocardial biopsy in arrhythmogenic right ventricular cardiomyopathy/dysplasia: an in vitro validation of diagnostic criteria 93
Arrhythmogenic cardiomyopathy: natural history and risk stratification 93
Arrhythmogenic Right Ventricular Cardiomyopathy 92
Gender differences and role of pregnancy in the history of post-surgical women affected by tetralogy of Fallot. 90
Arrhythmogenic Right Ventricular Cardiomyopathy: Characterization of Left Ventricular Phenotype and Differential Diagnosis With Dilated Cardiomyopathy 90
Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutations. 89
Dispersion of ventricular depolarization-repolarization: a noninvasive marker for risk stratification in arrhythmogenic right ventricular cardiomyopathy. 88
Pathophysiology of arrhythmogenic cardiomyopathy 88
Prognostic value of endocardial voltage mapping in patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia. 87
Pharmacotherapy and other therapeutic modalities for managing arrhythmogenic right ventricular cardiomyopathy. 87
Comparison of clinical features of arrhythmogenic right ventricular cardiomyopathy in men versus women 86
Pregnancy in women with arrhythmogenic right ventricular cardiomyopathy/dysplasia. 86
Differential diagnosis between early repolarization of athlete's heart and coved-type Brugada electrocardiogram. 85
Arrhythmogenic Right Ventricular Cardiomyopathy: Risk Stratification and Indications for Defibrillator Therapy 85
Late-onset arrhythmogenic right ventricular cardiomyopathy 84
Response to letters regarding article, "arrhythmic mitral valve prolapse and sudden cardiac death" 83
AUTONOMIC PROFILE AND ARRHYTHMIC RISK STRATIFICATION AFTER SURGICAL REPAIR OF TETRALOGY OF FALLOT. 81
Prevalence of cardiomyopathy in Italian asymptomatic children with electrocardiographic T-wave inversion at preparticipation screening. 81
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2) 81
Gene symbol: RYR2. Disease: Arrhythmogenic right ventricular cardiomyopathy type 2. 80
Mutation screening in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2) 79
Clinical profile and long-term follow-up of 37 families with arrhythmogenic right ventricular cardiomyopathy. 79
Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the Task Force Criteria. 78
Noninvasive cardiac screening in young athletes with ventricular arrhythmias. 78
The electrocardiographic "triangular QRS-ST-T waveform" pattern in patients with ST-segment elevation myocardial infarction: Incidence, pathophysiology and clinical implications 78
Diagnostic Criteria, Genetics, and Molecular Basis of Arrhythmogenic Cardiomyopathy 78
Heart rate variability in arrhythmogenic right ventricular cardiomyopathy correlation with clinical and prognostic features 77
Desmin mutations and arrhythmogenic right ventricular cardiomyopathy. 77
Co-inheritance of mutations associated with arrhythmogenic cardiomyopathy and hypertrophic cardiomyopathy 77
Homozygous SCN5A mutation in Brugada syndrome with monomorphic ventricular tachycardia and structural heart abnormalities. 77
529Relationship between ventricular mechanics and fibro-fatty replacement on cardiac magnetic resonance in arrhythmogenic cardiomyopathy 77
Nonischemic Left Ventricular Scar: Sporadic or Familial? Screen the Genes, Scan the Mutation Carriers 76
Treatment of arrhythmogenic right ventricular cardiomyopathy/dysplasia: An international task force consensus statement 75
Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1. 73
Anchoring Vignettes in EQ-5D-5L Questionnaire: Validation of a New Instrument 73
Arrhythmogenic Right Ventricular Cardiomyopathy. 72
Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy 72
Genotype–Phenotype Correlations 72
Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death early diagnosis of asymptomatic carriers - Early diagnosis of asymptomatic carriers 70
Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death: early diagnosis of asymptomatic carriers. 69
A microRNA expression profile as non-invasive biomarker in a large arrhythmogenic cardiomyopathy cohort 69
Is Internet use associated with anxiety in patients with and at risk for cardiomyopathy? 68
Role of cardiac magnetic resonance in patients with chest pain and pulmonary aneurysm 68
Compound and Digenic Heterozygosity Contributes to Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia (vol 55, pg 587, 2010) 67
Novel pathogenic role for galectin-3 in early disease stages of arrhythmogenic cardiomyopathy. 67
IDENTIFICATION OF MUTATIONS IN THE CARDIAC RYANODINE RECEPTOR GENE IN FAMILIES AFFECTED WITH ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 66
Long-term follow-up of the signal-averaged ECG in arrhythmogenic right ventricular cardiomyopathy: correlation with arrhythmic events and echocardiographic findings 66
Relationship Between Arrhythmogenic Right Ventricular Cardiomyopathy and Brugada Syndrome: New Insights From Molecular Biology and Clinical Implications 65
Primary Prevention of Sudden Death in Young Competitive Athletes by Preparticipation Screening 65
Three-dimensional electroanatomic voltage mapping increases accuracy of diagnosing arrhythmogenic right ventricular cardiomyopathy/dysplasia 64
P1596Tissue characterization in Arrhythmogenic Cardiomyopathy: diagnostic impact of combined endomyocardial biopsy and cardiac magnetic resonance approach 64
Management of arrhythmogenic right ventricular cardiomyopathy 61
Totale 9.771
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Categoria #
all - tutte 42.307
article - articoli 39.170
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.718
Totale 83.195
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019603 0 0 0 0 0 0 0 0 0 0 328 275
2019/20202.196 302 65 28 166 241 209 189 247 225 283 132 109
2020/20212.350 67 127 86 131 201 230 77 207 344 418 332 130
2021/20222.319 97 257 317 129 127 187 114 239 149 60 200 443
2022/20231.688 309 202 53 184 246 199 20 135 198 27 75 40
2023/2024898 36 150 108 96 83 121 82 64 69 55 34 0
Totale 12.149