NAVA, ANDREA
 Distribuzione geografica
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Continente #
NA - Nord America 6.868
EU - Europa 936
AS - Asia 494
SA - Sud America 4
OC - Oceania 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 8.305
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Nazione #
US - Stati Uniti d'America 6.863
CN - Cina 399
IT - Italia 187
FI - Finlandia 176
DE - Germania 167
SE - Svezia 156
UA - Ucraina 146
VN - Vietnam 68
GB - Regno Unito 59
TR - Turchia 15
NL - Olanda 12
IE - Irlanda 10
FR - Francia 8
IN - India 8
CA - Canada 5
BE - Belgio 4
GR - Grecia 3
AU - Australia 2
CL - Cile 2
DK - Danimarca 2
PL - Polonia 2
BR - Brasile 1
CH - Svizzera 1
CZ - Repubblica Ceca 1
EC - Ecuador 1
EU - Europa 1
HK - Hong Kong 1
IR - Iran 1
JP - Giappone 1
MK - Macedonia 1
MO - Macao, regione amministrativa speciale della Cina 1
RU - Federazione Russa 1
Totale 8.305
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Città #
Fairfield 1.069
Woodbridge 760
Houston 673
Jacksonville 600
Ann Arbor 565
Chandler 526
Ashburn 448
Wilmington 414
Seattle 352
Cambridge 339
Princeton 210
San Diego 98
Roxbury 91
Nanjing 87
Beijing 82
Dong Ket 68
Helsinki 61
Boardman 56
Des Moines 56
Guangzhou 40
Medford 34
Hebei 28
Shenyang 28
Changsha 26
Norwalk 23
London 22
Redwood City 20
Padova 19
Jinan 17
Jiaxing 15
Nanchang 15
Tianjin 13
New York 12
Istanbul 11
Dublin 10
Indiana 7
Munich 7
Zhengzhou 7
Kharkiv 6
Milan 6
Dearborn 5
Falls Church 5
Hangzhou 5
Rome 5
Borås 4
Kilburn 4
Naples 4
Waanrode 4
Chiswick 3
Falkenstein 3
Furore 3
Grosseto 3
Hounslow 3
Kunming 3
Nürnberg 3
Pescara 3
Shanghai 3
Taizhou 3
Trieste 3
Turin 3
Venice 3
Aarhus 2
Augusta 2
Bitonto 2
Bologna 2
Cagliari 2
Camponogara 2
Chicago 2
Fuzhou 2
Geislingen an der Steige 2
Grezzana 2
Haikou 2
Lanzhou 2
Los Angeles 2
Lugo 2
Napoli 2
Ogden 2
Radomsko 2
Recanati 2
Rende 2
San Cesario Di Lecce 2
Siena 2
Stanford 2
Taiyuan 2
Tekirdağ 2
Toronto 2
Verona 2
Washington 2
Acton 1
Agro 1
Albany 1
Andover 1
Angri 1
Ardabil 1
Atlanta 1
Bari 1
Barletta 1
Bassano Del Grappa 1
Belluno 1
Berlin 1
Totale 7.062
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Nome #
Cardiomiopatia/displasia aritmogena del ventricolo destro 215
Compound and Digenic Heterozygosity Contributes to Arrhythmogenic Right Ventricular 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
Follow-Up with Exercise Test of Effort-Induced Ventricular Arrhythmias Linked to Ryanodine Receptor Type 2 Gene Mutations. 126
Myocyte necrosis underlies progressive myocardial dystrophy in mouse dsg2-related arrhythmogenic right ventricular cardiomyopathy 121
Characterization of C14orf4, a novel intronless human gene containing a polyglutamine repeat, mapped to the ARVD1 critical region 119
Signal-averaged electrocardiogram in patients with arrhythmogenic right ventricular cardiomyopathy and ventricular arrhythmias 118
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
A NEW LOCUS FOR ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY (ARVD2) MAPS TO CHROMOSOME 1q42-q43 110
Arrhythmogenic right ventricular cardiomyopathy in young versus adult patients: similarities and differences. 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
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
A CASUAL SPONTANEOUS MUTATION AS POSSIBLE CAUSE OF THE FAMILIAL FORM OF ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY (ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA) 98
Identification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathy. 97
Arrhythmogenic right ventricular cardiomyopathy - A still underrecognized clinic entity 96
Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy 95
Quantitative assessment of endomyocardial biopsy in arrhythmogenic right ventricular cardiomyopathy/dysplasia: an in vitro validation of diagnostic criteria 93
THE GENE FOR ARRHYTHMOGENIC RIGHT-VENTRICULAR CARDIOMYOPATHY MAPS TO CHROMOSOME 14Q23-Q24 93
ARVD4, a new locus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm. 92
About the histology of arrhythmogenic right ventricular dysplasia - Response 91
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
Right ventricular cardiomyopathy and sudden death in young people. 88
Diagnostic accuracy of right ventriculography in arrhythmogenic right ventricular cardiomyopathy. 88
Late potentials and ventricular arrhythmias in 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
Molecular Genetics of Arrhythmogenic Right Ventricular Cardiomyopathy 84
Late-onset arrhythmogenic right ventricular cardiomyopathy 84
Arrhythmogenic right ventricular cardiomyopathy: clinical registry and database, evaluation of therapies, pathology registry, DNA banking 83
QT-interval variability in hypertrophic cardiomyopathy patients with cardiac arrest 82
Right ventricular cardiomyopathy in identical and nonidentical young twins 82
CLINICAL PROFILE OF CONCEALED FORM OF ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY PRESENTING WITH APPARENTLY IDIOPATHIC VENTRICULAR ARRHYTHMIAS 82
Familial cardiomyopathy underlies syndrome of right bundle branch block, ST segment elevation and sudden death 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
HEART-RATE-VARIABILITY IN PATIENTS WITH ORTHOTOPIC HEART-TRANSPLANTATION - LONG-TERM FOLLOW-UP 79
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
Endomyocardial biopsy in right ventricular cardiomyopathy 79
Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the Task Force Criteria. 78
Noninvasive risk stratification in arrhythmogenic right ventricular cardiomyopathy 78
Heart rate variability in arrhythmogenic right ventricular cardiomyopathy correlation with clinical and prognostic features 77
Spectrum of clinicopathologic manifestations of arrhythmogenic right ventricular cardiomyopathy/dysplasia: a multicenter study. 77
Desmin mutations and arrhythmogenic right ventricular cardiomyopathy. 77
Homozygous SCN5A mutation in Brugada syndrome with monomorphic ventricular tachycardia and structural heart abnormalities. 77
Molecular genetics of arrhythmogenic right ventricular cardiomyopathy 75
Signal-averaged electrocardiography in familial form of arrhythmogenic right ventricular cardiomyopathy. 74
Arrhythmogenic right ventricular cardiomyopathy: current diagnostic and management strategies 74
Arrhythmogenic right ventricular cardiomyopathy 73
Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1. 73
Hypertrophic cardiomyopathy and sudden death in the young: pathologic evidence of myocardial ischemia 73
Asystole with syncope secondary to hyperventilation in three young athletes. 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
Fatal paroxysmal supraventricular tachycardia in an infant. 70
SUDDEN-DEATH IN YOUNG COMPETITIVE ATHLETES - CLINICOPATHOLOGICAL CORRELATIONS IN 22 CASES 70
Rhythm and conduction disturbances in isolated, congenitally corrected transposition of the great arteries. 69
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 pharmacological approach to the study of AV conduction in man. 68
RIGHT VENTRICULAR CARDIOMYOPATHY - IS THERE EVIDENCE OF AN INFLAMMATORY ETIOLOGY 68
A FORMAL ANALYSIS OF THE MODE OF TRANSMISSION OF RIGHT VENTRICULAR DYSPLASIA 67
Compound and Digenic Heterozygosity Contributes to Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia (vol 55, pg 587, 2010) 67
Letter regarding article by Norman et al, "Novel mutation in desmoplakin causes arrhythmogenic left ventricular cardiomyopathy" 67
Monomorphic repetitive rhythms originating from the outflow tract in patients with minor forms of right ventricular 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
Three-dimensional electroanatomic voltage mapping increases accuracy of diagnosing arrhythmogenic right ventricular cardiomyopathy/dysplasia 64
COEXISTENCE OF KENT ACCESSORY PATHWAY, ENHANCED AV NODE CONDUCTION, AND VARIOUS CONDUCTION DISTURBANCES IN A YOUNG ATHLETE WITH TRICUSPID-VALVE DYSPLASIA 61
Right bundle branch block, right precordial ST-segment elevation, and sudden death in young people 60
Gene symbol: RYR2. Disease: Effort-induced polymorphic ventricular arrhythmias. 59
Echocardiographic findings in patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia. 59
Is the cause of arrhythmogenic right ventricular cardiomyopathy congenital or acquired? 59
Familial effort polymorphic ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy map to chromosome 1q42-43. 58
Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D); Proposed Modification of the Task Force Criteria 57
Familial effort polymorphic ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy are linked to chromosome 1q42-43 55
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. 53
Multiple lesions of the conduction system in a case of cardiac rhabdomyosarcoma with complex arrhythmias. An anatomic and clinical study. 49
What is the Brugada syndrome? 48
Genetics of arrhythmogenic right ventricular cardiomyopathy 48
Arrhythmogenic right ventricular dysplasia: cardiomyopathy current opinions on diagnostic and therapeutic aspects 48
Arrhythmogenic right ventricular dysplasia/cardiomyopathy - Need for an international registry 46
A DHPLC-based approach for detecting RYR2 mutations involved in malignant arrhythmias. 45
COMPARISON OF QT DISPERSION IN HYPERTROPHIC CARDIOMYOPATHY BETWEEN PATIENTS WITH AND WITHOUT VENTRICULAR ARRHYTHMIAS AND SUDDEN DEATH 44
Spin-echo neclear magnetic resonance for tissue characterisation in arrhythmogenic right ventricular cardiomyopathy. 44
[Superior axial deviation in the young adult. An electro-vectorcardiographic study] 41
Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: Recent Advances 40
The conduction system in corrected transposition with situs inversus. 39
Is arrhythmogenic right ventricular cardiomyopathy a pediatric problem too? 38
Characterization of fibrofatty scar in arrhythmogenic right ventricular cardiomyopathy/dysplasia: Concordance between contrast-enhanced cardiac magnetic resonance and 3-D electroanatomic voltage mapping 38
Letter regarding article by Nasir et al, "Electrocardiographic features of arrhythmogenic right ventricular dysplasia/cardiomyopathy according to disease severity: a need to broaden diagnostic criteria" 37
Familial cardiomyopathy associated with right bundle branch block, ST segment elevation and sudden death - Reply 37
Totale 7.926
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Categoria #
all - tutte 26.233
article - articoli 23.808
book - libri 233
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.401
Totale 51.675
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019673 0 0 0 0 0 0 0 0 0 147 288 238
2019/20201.733 293 51 29 115 179 155 144 202 151 247 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
2023/2024317 25 74 47 33 30 58 19 10 14 7 0 0
Totale 8.363