NAVA, ANDREA
 Distribuzione geografica
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Continente #
NA - Nord America 7.345
EU - Europa 1.139
AS - Asia 1.117
SA - Sud America 109
AF - Africa 35
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 2
Totale 9.750
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Nazione #
US - Stati Uniti d'America 7.331
CN - Cina 475
SG - Singapore 455
DE - Germania 217
IT - Italia 204
FI - Finlandia 182
SE - Svezia 156
UA - Ucraina 146
BR - Brasile 101
HK - Hong Kong 72
FR - Francia 70
VN - Vietnam 68
GB - Regno Unito 60
RU - Federazione Russa 56
CI - Costa d'Avorio 25
TR - Turchia 19
NL - Olanda 14
IE - Irlanda 10
CA - Canada 9
AT - Austria 8
IN - India 8
BE - Belgio 4
DZ - Algeria 4
ID - Indonesia 4
AR - Argentina 3
AU - Australia 3
GR - Grecia 3
IQ - Iraq 3
PL - Polonia 3
BD - Bangladesh 2
CL - Cile 2
DK - Danimarca 2
JM - Giamaica 2
MA - Marocco 2
MX - Messico 2
OM - Oman 2
TN - Tunisia 2
UZ - Uzbekistan 2
AL - Albania 1
CH - Svizzera 1
CO - Colombia 1
CZ - Repubblica Ceca 1
EC - Ecuador 1
EU - Europa 1
IR - Iran 1
JP - Giappone 1
LB - Libano 1
MK - Macedonia 1
MO - Macao, regione amministrativa speciale della Cina 1
NG - Nigeria 1
NI - Nicaragua 1
NP - Nepal 1
PE - Perù 1
PK - Pakistan 1
QA - Qatar 1
XK - ???statistics.table.value.countryCode.XK??? 1
ZA - Sudafrica 1
Totale 9.750
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Città #
Fairfield 1.069
Woodbridge 760
Houston 673
Jacksonville 600
Ann Arbor 565
Chandler 526
Ashburn 456
Wilmington 414
Seattle 352
Cambridge 339
Princeton 210
Singapore 193
Santa Clara 186
Boardman 168
San Diego 98
Roxbury 91
Nanjing 87
Beijing 84
Hong Kong 70
Dong Ket 68
Helsinki 67
Des Moines 56
Guangzhou 43
Medford 34
Shenyang 29
Hebei 28
Changsha 27
Abidjan 25
London 23
Norwalk 23
Munich 21
Redwood City 20
Padova 19
Jinan 17
Jiaxing 15
Nanchang 15
North Bergen 15
New York 13
Tianjin 13
Istanbul 12
Nuremberg 12
São Paulo 12
Dublin 10
Zhengzhou 10
Shanghai 9
Rome 8
Indiana 7
Milan 7
Hangzhou 6
Kharkiv 6
Los Angeles 6
Dearborn 5
Falkenstein 5
Falls Church 5
Rio de Janeiro 5
Borås 4
Chicago 4
Kilburn 4
Naples 4
Waanrode 4
Belo Horizonte 3
Campinas 3
Chiswick 3
Dallas 3
Furore 3
Fuzhou 3
Grosseto 3
Hounslow 3
Kunming 3
Nürnberg 3
Pescara 3
Shenzhen 3
Taizhou 3
Toronto 3
Trieste 3
Turin 3
Venice 3
Washington 3
Aarhus 2
Augusta 2
Aulla 2
Baghdad 2
Barge 2
Betim 2
Bitonto 2
Bologna 2
Cagliari 2
Camaçari 2
Camponogara 2
Curitiba 2
Frankfurt am Main 2
Geislingen an der Steige 2
Grezzana 2
Haikou 2
Lanzhou 2
Lugo 2
Montreal 2
Muscat 2
Napoli 2
Ningbo 2
Totale 7.755
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Nome #
Cardiomiopatia/displasia aritmogena del ventricolo destro 239
Missense mutations in desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitro. 175
Ultrastructural evidence of intercalated disc remodelling in arrhythmogenic right ventricular cardiomyopathy: an electron microscopy investigation on endomyocardial biopsies. 152
Compound and Digenic Heterozygosity Contributes to Arrhythmogenic Right Ventricular Cardiomyopathy 149
A NEW LOCUS FOR ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY (ARVD2) MAPS TO CHROMOSOME 1q42-q43 141
Follow-Up with Exercise Test of Effort-Induced Ventricular Arrhythmias Linked to Ryanodine Receptor Type 2 Gene Mutations. 136
Arrhythmogenic right ventricular cardiomyopathy in young versus adult patients: similarities and differences. 134
Characterization of C14orf4, a novel intronless human gene containing a polyglutamine repeat, mapped to the ARVD1 critical region 133
Signal-averaged electrocardiogram in patients with arrhythmogenic right ventricular cardiomyopathy and ventricular arrhythmias 130
Myocyte necrosis underlies progressive myocardial dystrophy in mouse dsg2-related arrhythmogenic right ventricular cardiomyopathy 129
Mutations in the area composita protein alphaT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy 126
The p.A897KfsX4 frameshift variation in desmocollin-2 is not a causative mutation in arrhythmogenic right ventricular cardiomyopathy 124
Clinical phenotype and diagnosis of arrhythmogenic right ventricular cardiomyopathy in pediatric patients carrying desmosomal gene mutations. 123
ARVD4, a new locus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm. 122
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? 117
Arrhythmogenic right ventricular cardiomyopathy - A still underrecognized clinic entity 115
Juvenile sudden death in a family with polymorphic ventricular arrhythmias caused by a novel RyR2 gene mutation: evidence of specific morphological substrates. 114
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2) 114
Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia 113
Differences and similarities between arrhythmogenic right ventricular cardiomyopathy and athlete's heart adaptations 112
Identification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathy. 111
A CASUAL SPONTANEOUS MUTATION AS POSSIBLE CAUSE OF THE FAMILIAL FORM OF ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY (ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA) 110
Denaturing HPLC-based approach for detecting RYR2 mutations involved in malignant arrhythmias 108
Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy 107
Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutations. 105
About the histology of arrhythmogenic right ventricular dysplasia - Response 105
Arrhythmogenic right ventricular cardiomyopathy: clinical registry and database, evaluation of therapies, pathology registry, DNA banking 104
Right ventricular cardiomyopathy and sudden death in young people. 103
Quantitative assessment of endomyocardial biopsy in arrhythmogenic right ventricular cardiomyopathy/dysplasia: an in vitro validation of diagnostic criteria 102
Diagnostic accuracy of right ventriculography in arrhythmogenic right ventricular cardiomyopathy. 102
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2) 102
THE GENE FOR ARRHYTHMOGENIC RIGHT-VENTRICULAR CARDIOMYOPATHY MAPS TO CHROMOSOME 14Q23-Q24 101
Comparison of clinical features of arrhythmogenic right ventricular cardiomyopathy in men versus women 99
Late-onset arrhythmogenic right ventricular cardiomyopathy 99
QT-interval variability in hypertrophic cardiomyopathy patients with cardiac arrest 98
Pregnancy in women with arrhythmogenic right ventricular cardiomyopathy/dysplasia. 98
Arrhythmogenic right ventricular cardiomyopathy: current diagnostic and management strategies 98
Dispersion of ventricular depolarization-repolarization: a noninvasive marker for risk stratification in arrhythmogenic right ventricular cardiomyopathy. 96
Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy 94
Late potentials and ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy. 93
Molecular Genetics of Arrhythmogenic Right Ventricular Cardiomyopathy 93
CLINICAL PROFILE OF CONCEALED FORM OF ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY PRESENTING WITH APPARENTLY IDIOPATHIC VENTRICULAR ARRHYTHMIAS 92
Homozygous SCN5A mutation in Brugada syndrome with monomorphic ventricular tachycardia and structural heart abnormalities. 92
HEART-RATE-VARIABILITY IN PATIENTS WITH ORTHOTOPIC HEART-TRANSPLANTATION - LONG-TERM FOLLOW-UP 89
Right ventricular cardiomyopathy in identical and nonidentical young twins 89
Asystole with syncope secondary to hyperventilation in three young athletes. 89
Desmin mutations and arrhythmogenic right ventricular cardiomyopathy. 89
Gene symbol: RYR2. Disease: Arrhythmogenic right ventricular cardiomyopathy type 2. 88
Arrhythmogenic right ventricular cardiomyopathy 88
Familial cardiomyopathy underlies syndrome of right bundle branch block, ST segment elevation and sudden death 88
Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the Task Force Criteria. 87
Molecular genetics of arrhythmogenic right ventricular cardiomyopathy 87
Clinical profile and long-term follow-up of 37 families with arrhythmogenic right ventricular cardiomyopathy. 87
Endomyocardial biopsy in right ventricular cardiomyopathy 87
Mutation screening in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2) 86
Heart rate variability in arrhythmogenic right ventricular cardiomyopathy correlation with clinical and prognostic features 86
A pharmacological approach to the study of AV conduction in man. 86
A FORMAL ANALYSIS OF THE MODE OF TRANSMISSION OF RIGHT VENTRICULAR DYSPLASIA 85
Spectrum of clinicopathologic manifestations of arrhythmogenic right ventricular cardiomyopathy/dysplasia: a multicenter study. 85
Fatal paroxysmal supraventricular tachycardia in an infant. 84
Noninvasive risk stratification in arrhythmogenic right ventricular cardiomyopathy 84
Signal-averaged electrocardiography in familial form of arrhythmogenic right ventricular cardiomyopathy. 83
Genotype–Phenotype Correlations 82
IDENTIFICATION OF MUTATIONS IN THE CARDIAC RYANODINE RECEPTOR GENE IN FAMILIES AFFECTED WITH ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 81
Rhythm and conduction disturbances in isolated, congenitally corrected transposition of the great arteries. 81
Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death: early diagnosis of asymptomatic carriers. 81
Compound and Digenic Heterozygosity Contributes to Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia (vol 55, pg 587, 2010) 80
Hypertrophic cardiomyopathy and sudden death in the young: pathologic evidence of myocardial ischemia 80
Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1. 79
RIGHT VENTRICULAR CARDIOMYOPATHY - IS THERE EVIDENCE OF AN INFLAMMATORY ETIOLOGY 79
SUDDEN-DEATH IN YOUNG COMPETITIVE ATHLETES - CLINICOPATHOLOGICAL CORRELATIONS IN 22 CASES 79
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 77
Monomorphic repetitive rhythms originating from the outflow tract in patients with minor forms of right ventricular cardiomyopathy 77
Long-term follow-up of the signal-averaged ECG in arrhythmogenic right ventricular cardiomyopathy: correlation with arrhythmic events and echocardiographic findings 76
Letter regarding article by Norman et al, "Novel mutation in desmoplakin causes arrhythmogenic left ventricular cardiomyopathy" 73
Is the cause of arrhythmogenic right ventricular cardiomyopathy congenital or acquired? 72
Gene symbol: RYR2. Disease: Effort-induced polymorphic ventricular arrhythmias. 71
A DHPLC-based approach for detecting RYR2 mutations involved in malignant arrhythmias. 69
Three-dimensional electroanatomic voltage mapping increases accuracy of diagnosing arrhythmogenic right ventricular cardiomyopathy/dysplasia 68
Arrhythmogenic right ventricular dysplasia/cardiomyopathy - Need for an international registry 67
COEXISTENCE OF KENT ACCESSORY PATHWAY, ENHANCED AV NODE CONDUCTION, AND VARIOUS CONDUCTION DISTURBANCES IN A YOUNG ATHLETE WITH TRICUSPID-VALVE DYSPLASIA 67
[Superior axial deviation in the young adult. An electro-vectorcardiographic study] 67
Right bundle branch block, right precordial ST-segment elevation, and sudden death in young people 66
Fine mapping and genomic structure of ACTN2, the human gene coding for the sarcomeric fisoform of alpha-Actinin-2, expressed in skeletal and cardiac muscle. 66
Familial effort polymorphic ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy map to chromosome 1q42-43. 66
Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D); Proposed Modification of the Task Force Criteria 65
Echocardiographic findings in patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia. 64
Genetics of arrhythmogenic right ventricular cardiomyopathy 64
Familial effort polymorphic ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy are linked to chromosome 1q42-43 64
Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: Recent Advances 59
Arrhythmogenic right ventricular dysplasia: cardiomyopathy current opinions on diagnostic and therapeutic aspects 59
Multiple lesions of the conduction system in a case of cardiac rhabdomyosarcoma with complex arrhythmias. An anatomic and clinical study. 57
[Termination of idiopathic ventricular tachycardia with QRS morphology of right bundle branch block and anterior fascicular hemiblock (fascicular tachycardia) by vagal maneuvers. Presentation of 4 cases]. 55
[Arrhythmogenic right ventricular dysplasia. Study of a selected population]. 55
What is the Brugada syndrome? 54
[Contribution of electrovectorcardiography in the diagnosis of hypertrophic cardiomyopathy. Comparative study with an echocardiographic score]. 52
Spin-echo neclear magnetic resonance for tissue characterisation in arrhythmogenic right ventricular cardiomyopathy. 51
COMPARISON OF QT DISPERSION IN HYPERTROPHIC CARDIOMYOPATHY BETWEEN PATIENTS WITH AND WITHOUT VENTRICULAR ARRHYTHMIAS AND SUDDEN DEATH 50
Characterization of fibrofatty scar in arrhythmogenic right ventricular cardiomyopathy/dysplasia: Concordance between contrast-enhanced cardiac magnetic resonance and 3-D electroanatomic voltage mapping 48
Is arrhythmogenic right ventricular cardiomyopathy a pediatric problem too? 46
Totale 9.204
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Categoria #
all - tutte 35.963
article - articoli 32.452
book - libri 381
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 2.018
Totale 70.814
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020414 0 0 0 0 0 0 0 0 0 247 75 92
2020/20211.310 41 91 26 93 189 128 23 134 188 96 180 121
2021/20221.465 47 178 153 109 51 121 72 139 77 35 196 287
2022/20231.114 231 148 18 130 185 149 4 69 117 7 39 17
2023/2024435 25 74 47 33 30 58 19 10 14 9 62 54
2024/20251.327 1 147 106 96 290 104 116 217 220 30 0 0
Totale 9.808