BAUCE, BARBARA
 Distribuzione geografica
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Continente #
NA - Nord America 9.710
EU - Europa 2.043
AS - Asia 1.034
OC - Oceania 9
SA - Sud America 4
Continente sconosciuto - Info sul continente non disponibili 3
AF - Africa 2
Totale 12.805
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Nazione #
US - Stati Uniti d'America 9.698
IT - Italia 921
CN - Cina 541
SG - Singapore 366
SE - Svezia 362
FI - Finlandia 198
DE - Germania 156
UA - Ucraina 112
FR - Francia 100
GB - Regno Unito 92
VN - Vietnam 47
IN - India 40
GR - Grecia 33
NL - Olanda 16
TR - Turchia 15
IE - Irlanda 13
CA - Canada 11
HK - Hong Kong 9
CZ - Repubblica Ceca 6
AU - Australia 5
BE - Belgio 5
IR - Iran 5
RO - Romania 5
ES - Italia 4
NZ - Nuova Zelanda 4
PL - Polonia 4
AT - Austria 3
CH - Svizzera 3
EU - Europa 3
LB - Libano 3
BY - Bielorussia 2
HR - Croazia 2
JP - Giappone 2
RU - Federazione Russa 2
AL - Albania 1
AR - Argentina 1
BG - Bulgaria 1
CL - Cile 1
CO - Colombia 1
CR - Costa Rica 1
DZ - Algeria 1
EC - Ecuador 1
IQ - Iraq 1
KZ - Kazakistan 1
LK - Sri Lanka 1
LV - Lettonia 1
MA - Marocco 1
PK - Pakistan 1
PT - Portogallo 1
SA - Arabia Saudita 1
TW - Taiwan 1
Totale 12.805
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Città #
Fairfield 1.640
Woodbridge 1.042
Houston 928
Chandler 771
Ashburn 689
Ann Arbor 671
Seattle 581
Cambridge 557
Wilmington 522
Jacksonville 407
Singapore 274
Princeton 201
San Diego 151
Padova 135
Beijing 122
Roxbury 114
Medford 99
Helsinki 96
Nanjing 86
Des Moines 85
Milan 82
Guangzhou 54
Boardman 53
Dong Ket 47
Santa Clara 47
Rome 39
New York 33
Hebei 26
Changsha 24
Jinan 24
London 22
Shenyang 22
Norwalk 21
Redwood City 20
Turin 20
Jiaxing 19
Ogden 19
Bologna 16
Tianjin 16
Nanchang 14
Verona 13
Washington 13
Zhengzhou 13
Pune 12
Dublin 11
Istanbul 11
Venice 11
Dallas 10
Falls Church 10
Hounslow 9
Naples 9
Trieste 9
Munich 8
Treviso 8
Bari 7
Dearborn 7
Los Angeles 7
Bagnacavallo 6
Borås 6
Florence 6
Hong Kong 6
Kharkiv 6
Kilburn 6
Noale 6
Selvazzano Dentro 6
Augusta 5
Bolzano 5
Brno 5
Chicago 5
Frankfurt am Main 5
Hangzhou 5
Indiana 5
Shanghai 5
Brendola 4
Brescia 4
Cagliari 4
Genoa 4
Kunming 4
Lanzhou 4
Lappeenranta 4
Livorno 4
Napoli 4
Nürnberg 4
Palermo 4
Parma 4
Pavia 4
Ponte di Piave 4
Prescot 4
Qualiano 4
Rovellasca 4
Sassuolo 4
Stanford 4
Taizhou 4
Toronto 4
Waanrode 4
Alessandria 3
Alghero 3
Amsterdam 3
Avellino 3
Beirut 3
Totale 10.148
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Nome #
'Hot phase' clinical presentation in arrhythmogenic cardiomyopathy 241
Cardiomiopatia/displasia aritmogena del ventricolo destro 230
A targeted next-generation gene panel reveals a novel heterozygous nonsense variant in the TP63 gene in patients with arrhythmogenic cardiomyopathy 183
Morphofunctional abnormalities of mitral annulus and arrhythmic mitral valve prolapse 165
Large Genomic Rearrangements of Desmosomal Genes in Italian Arrhythmogenic Cardiomyopathy Patients 162
The 2020 “Padua Criteria” for Diagnosis and Phenotype Characterization of Arrhythmogenic Cardiomyopathy in Clinical Practice 155
Arrhythmogenic Cardiomyopathy 150
Compound and Digenic Heterozygosity Contributes to Arrhythmogenic Right Ventricular Cardiomyopathy 141
Whole-Exome Sequencing Identifies Pathogenic Variants in TJP1 Gene Associated With Arrhythmogenic Cardiomyopathy 141
Electrocardiographic Pattern in Arrhythmogenic Right Ventricular Cardiomyopathy 140
Missense mutations in desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitro. 137
Predictive value of exercise testing in athletes with ventricular ectopy evaluated by cardiac magnetic resonance 135
Ultrastructural evidence of intercalated disc remodelling in arrhythmogenic right ventricular cardiomyopathy: an electron microscopy investigation on endomyocardial biopsies. 134
Homozygous desmocollin-2 mutations and arrhythmogenic cardiomyopathy 130
Three-dimensional electroanatomical voltage mapping and histologic evaluation of myocardial substrate in right ventricular outflow tract tachycardia. 129
Follow-Up with Exercise Test of Effort-Induced Ventricular Arrhythmias Linked to Ryanodine Receptor Type 2 Gene Mutations. 127
Arrhythmogenic right ventricular cardiomyopathy type 1 (ARVD1): confirmation of locus assignment and mutation screening of four candidate genes. 127
PHENOTYPIC EXPRESSION IS A PREREQUISITE FOR MALIGNANT ARRHYTHMIC EVENTS AND SUDDEN CARDIAC DEATH IN ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 126
Arrhythmic Mitral Valve Prolapse and Sudden Cardiac Death 125
Nonischemic left ventricular scar as a substrate of life-threatening ventricular arrhythmias and sudden cardiac death in competitive athletes 124
Arrhythmogenic cardiomyopathy 123
Myocyte necrosis underlies progressive myocardial dystrophy in mouse dsg2-related arrhythmogenic right ventricular cardiomyopathy 122
Treatment of arrhythmogenic right ventricular cardiomyopathy/dysplasia: An international task force consensus statement 121
Imaging Study of Ventricular Scar in Arrhythmogenic Right Ventricular Cardiomyopathy: Comparison of 3D Standard Electroanatomical Voltage Mapping and Contrast-Enhanced Cardiac Magnetic Resonance. 120
Signal-averaged electrocardiogram in patients with arrhythmogenic right ventricular cardiomyopathy and ventricular arrhythmias 119
The p.A897KfsX4 frameshift variation in desmocollin-2 is not a causative mutation in arrhythmogenic right ventricular cardiomyopathy 117
Mutations in the area composita protein alphaT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy 116
Relationship between electrocardiographic findings and cardiac magnetic resonance phenotypes in arrhythmogenic cardiomyopathy 116
Three-Dimensional Electroanatomical Voltage Mapping and Histologic Evaluation of Myocardial Substrate in Right Ventricular Outflow Tract Tachycardia 113
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? 110
Juvenile sudden death in a family with polymorphic ventricular arrhythmias caused by a novel RyR2 gene mutation: evidence of specific morphological substrates. 109
Electrocardiographic predictors of electroanatomic scar size in arrhythmogenic right ventricular cardiomyopathy: implications for arrhythmic risk stratification. 108
Clinical phenotype and diagnosis of arrhythmogenic right ventricular cardiomyopathy in pediatric patients carrying desmosomal gene mutations. 107
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2) 106
Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia 106
Subcutaneous implantable cardioverter defibrillator in patients with arrhythmogenic right ventricular cardiomyopathy: Results from an Italian multicenter registry 106
Imaging study of ventricular scar in arrhythmogenic right ventricular cardiomyopathy/dysplasia: comparison of three-dimensional electroanatomic voltage mapping and contrast-enhanced cardiac magnetic resonance 105
Differences and similarities between arrhythmogenic right ventricular cardiomyopathy and athlete's heart adaptations 103
Denaturing HPLC-based approach for detecting RYR2 mutations involved in malignant arrhythmias 103
Arrhythmogenic cardiomyopathy: natural history and risk stratification 102
TAIL1: an isthmin-like gene, containing type 1 thrombospondin-repeat and AMOP domain, mapped to ARVD1 critical region. 101
Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy 101
Response to Letters Regarding Article, "Arrhythmic Mitral Valve Prolapse and Sudden Cardiac Death" 101
Exercise-Induced Normalization of Right Precordial Negative T Waves in Arrhythmogenic Right Ventricular Cardiomyopathy. 101
Identification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathy. 100
Compound and digenic heterozygosity predicts lifetime arrhythmic outcome and sudden cardiac death in desmosomal gene-related arrhythmogenic right ventricular cardiomyopathy. 100
Definition and treatment of arrhythmogenic cardiomyopathy: an updated expert panel report 99
Implantable Cardioverter-Defibrillator Therapy in Athletes 98
Evolution of focal moderate (International Society for Heart and Lung Transplantation grade 2) rejection of the cardiac allograft 95
Quantitative assessment of endomyocardial biopsy in arrhythmogenic right ventricular cardiomyopathy/dysplasia: an in vitro validation of diagnostic criteria 94
Arrhythmogenic Right Ventricular Cardiomyopathy 94
Arrhythmogenic Right Ventricular Cardiomyopathy: Characterization of Left Ventricular Phenotype and Differential Diagnosis With Dilated Cardiomyopathy 94
Pregnancy in women with arrhythmogenic right ventricular cardiomyopathy/dysplasia. 93
Gender differences and role of pregnancy in the history of post-surgical women affected by tetralogy of Fallot. 92
Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutations. 91
Response to letters regarding article, "arrhythmic mitral valve prolapse and sudden cardiac death" 91
Dispersion of ventricular depolarization-repolarization: a noninvasive marker for risk stratification in arrhythmogenic right ventricular cardiomyopathy. 90
Prognostic value of endocardial voltage mapping in patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia. 90
Pharmacotherapy and other therapeutic modalities for managing arrhythmogenic right ventricular cardiomyopathy. 90
Pathophysiology of arrhythmogenic cardiomyopathy 89
Arrhythmogenic Right Ventricular Cardiomyopathy: Risk Stratification and Indications for Defibrillator Therapy 88
Comparison of clinical features of arrhythmogenic right ventricular cardiomyopathy in men versus women 87
Late-onset arrhythmogenic right ventricular cardiomyopathy 87
Differential diagnosis between early repolarization of athlete's heart and coved-type Brugada electrocardiogram. 86
Co-inheritance of mutations associated with arrhythmogenic cardiomyopathy and hypertrophic cardiomyopathy 86
529Relationship between ventricular mechanics and fibro-fatty replacement on cardiac magnetic resonance in arrhythmogenic cardiomyopathy 86
AUTONOMIC PROFILE AND ARRHYTHMIC RISK STRATIFICATION AFTER SURGICAL REPAIR OF TETRALOGY OF FALLOT. 85
Prevalence of cardiomyopathy in Italian asymptomatic children with electrocardiographic T-wave inversion at preparticipation screening. 84
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2) 84
Gene symbol: RYR2. Disease: Arrhythmogenic right ventricular cardiomyopathy type 2. 82
The electrocardiographic "triangular QRS-ST-T waveform" pattern in patients with ST-segment elevation myocardial infarction: Incidence, pathophysiology and clinical implications 81
Mutation screening in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2) 80
Heart rate variability in arrhythmogenic right ventricular cardiomyopathy correlation with clinical and prognostic features 80
Clinical profile and long-term follow-up of 37 families with arrhythmogenic right ventricular cardiomyopathy. 80
Diagnostic Criteria, Genetics, and Molecular Basis of Arrhythmogenic Cardiomyopathy 80
Homozygous SCN5A mutation in Brugada syndrome with monomorphic ventricular tachycardia and structural heart abnormalities. 80
Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the Task Force Criteria. 79
Desmin mutations and arrhythmogenic right ventricular cardiomyopathy. 79
Noninvasive cardiac screening in young athletes with ventricular arrhythmias. 78
Nonischemic Left Ventricular Scar: Sporadic or Familial? Screen the Genes, Scan the Mutation Carriers 78
A microRNA expression profile as non-invasive biomarker in a large arrhythmogenic cardiomyopathy cohort 78
Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy 77
Anchoring Vignettes in EQ-5D-5L Questionnaire: Validation of a New Instrument 77
Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death: early diagnosis of asymptomatic carriers. 76
Genotype–Phenotype Correlations 76
Treatment of arrhythmogenic right ventricular cardiomyopathy/dysplasia: An international task force consensus statement 76
Arrhythmogenic Right Ventricular Cardiomyopathy. 75
Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1. 73
Role of cardiac magnetic resonance in patients with chest pain and pulmonary aneurysm 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
Management of arrhythmogenic right ventricular cardiomyopathy 70
Is Internet use associated with anxiety in patients with and at risk for cardiomyopathy? 70
Novel pathogenic role for galectin-3 in early disease stages of arrhythmogenic cardiomyopathy. 70
IDENTIFICATION OF MUTATIONS IN THE CARDIAC RYANODINE RECEPTOR GENE IN FAMILIES AFFECTED WITH ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 69
Compound and Digenic Heterozygosity Contributes to Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia (vol 55, pg 587, 2010) 68
Long-term follow-up of the signal-averaged ECG in arrhythmogenic right ventricular cardiomyopathy: correlation with arrhythmic events and echocardiographic findings 68
Relationship Between Arrhythmogenic Right Ventricular Cardiomyopathy and Brugada Syndrome: New Insights From Molecular Biology and Clinical Implications 67
Primary Prevention of Sudden Death in Young Competitive Athletes by Preparticipation Screening 67
P1596Tissue characterization in Arrhythmogenic Cardiomyopathy: diagnostic impact of combined endomyocardial biopsy and cardiac magnetic resonance approach 66
Three-dimensional electroanatomic voltage mapping increases accuracy of diagnosing arrhythmogenic right ventricular cardiomyopathy/dysplasia 65
Totale 10.218
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Categoria #
all - tutte 49.248
article - articoli 45.549
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 2.027
Totale 96.824
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.801 0 0 0 166 241 209 189 247 225 283 132 109
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
2023/20241.153 36 150 108 96 83 121 82 64 69 55 156 133
2024/2025655 31 279 198 147 0 0 0 0 0 0 0 0
Totale 13.059