RAMPAZZO, ALESSANDRA
 Distribuzione geografica
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Continente #
NA - Nord America 8.202
AS - Asia 3.052
EU - Europa 2.489
SA - Sud America 895
AF - Africa 748
OC - Oceania 87
Continente sconosciuto - Info sul continente non disponibili 30
Totale 15.503
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Nazione #
US - Stati Uniti d'America 7.782
SG - Singapore 1.013
IT - Italia 654
CN - Cina 638
BR - Brasile 633
HK - Hong Kong 372
DE - Germania 280
SE - Svezia 216
FI - Finlandia 186
VN - Vietnam 181
UA - Ucraina 118
FR - Francia 101
NL - Olanda 97
IN - India 86
PL - Polonia 85
GB - Regno Unito 75
RU - Federazione Russa 74
TR - Turchia 56
MX - Messico 48
AR - Argentina 43
GR - Grecia 41
AT - Austria 40
CI - Costa d'Avorio 38
BJ - Benin 36
EC - Ecuador 36
ES - Italia 33
PY - Paraguay 33
CO - Colombia 31
JO - Giordania 31
IQ - Iraq 30
KR - Corea 30
CR - Costa Rica 29
DO - Repubblica Dominicana 29
CU - Cuba 28
NP - Nepal 28
BE - Belgio 27
IE - Irlanda 27
PE - Perù 27
ZA - Sudafrica 27
AM - Armenia 26
JP - Giappone 26
CA - Canada 25
KE - Kenya 25
KZ - Kazakistan 25
LB - Libano 25
PK - Pakistan 25
SA - Arabia Saudita 25
JM - Giamaica 24
LA - Repubblica Popolare Democratica del Laos 24
MY - Malesia 24
NO - Norvegia 24
AE - Emirati Arabi Uniti 23
AU - Australia 23
CV - Capo Verde 23
GN - Guinea 23
ID - Indonesia 23
IL - Israele 23
MA - Marocco 23
MK - Macedonia 23
PH - Filippine 23
PS - Palestinian Territory 23
SI - Slovenia 23
TN - Tunisia 23
UY - Uruguay 23
DK - Danimarca 22
EE - Estonia 22
IR - Iran 22
LV - Lettonia 22
MR - Mauritania 22
PA - Panama 22
SK - Slovacchia (Repubblica Slovacca) 22
TJ - Tagikistan 22
AL - Albania 21
BA - Bosnia-Erzegovina 21
GT - Guatemala 21
KG - Kirghizistan 21
AO - Angola 20
BF - Burkina Faso 20
DZ - Algeria 20
GH - Ghana 20
LC - Santa Lucia 20
LY - Libia 20
MD - Moldavia 20
MG - Madagascar 20
NC - Nuova Caledonia 20
SN - Senegal 20
UZ - Uzbekistan 20
XK - ???statistics.table.value.countryCode.XK??? 20
AZ - Azerbaigian 19
BG - Bulgaria 19
BO - Bolivia 19
CH - Svizzera 19
EG - Egitto 19
GM - Gambi 19
ML - Mali 19
MN - Mongolia 19
MZ - Mozambico 19
VE - Venezuela 19
AF - Afghanistan, Repubblica islamica di 18
BY - Bielorussia 18
Totale 14.662
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Città #
Fairfield 1.114
Woodbridge 741
Ashburn 712
Singapore 585
Houston 583
Chandler 541
Ann Arbor 474
Seattle 412
Cambridge 373
Wilmington 365
Hong Kong 354
Jacksonville 321
Santa Clara 184
Beijing 181
Boardman 140
Princeton 137
Padova 94
Munich 90
San Diego 90
Helsinki 76
Los Angeles 70
Nanjing 69
Roxbury 69
Dong Ket 63
Milan 63
São Paulo 59
Chicago 58
Medford 57
Bytom 55
Des Moines 55
Guangzhou 49
New York 45
Ho Chi Minh City 38
Abidjan 36
Cotonou 35
Amman 31
Dallas 30
Buffalo 27
Havana 27
Rome 27
Vienna 27
Hanoi 25
Turku 25
Conakry 23
Nairobi 23
Changsha 22
Jinan 22
Panama City 22
Salt Lake City 22
Vientiane 21
Dublin 20
Dushanbe 20
Nouakchott 20
Noumea 20
Riga 20
Rio de Janeiro 20
San José 20
Shenyang 20
Tashkent 20
Villafranca Padovana 20
Baku 19
Bishkek 19
Castries 19
Dakar 19
Redwood City 19
Yerevan 19
Amsterdam 18
Hefei 18
Montevideo 18
Praia 18
Tallinn 18
Ulan Bator 18
Chennai 17
Djibouti 17
Istanbul 17
Lima 17
Luanda 17
Managua 17
Maputo 17
Verona 17
Accra 16
Andorra la Vella 16
Antananarivo 16
Bamako 16
Hebei 16
Nuremberg 16
Brooklyn 15
Jiaxing 15
Kampala 15
Kingston 15
North Bergen 15
Phnom Penh 15
Podgorica 15
Redondo Beach 15
Salvador 15
Sofia 15
Tokyo 15
Athens 14
Belo Horizonte 14
Bologna 14
Totale 9.623
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Nome #
'Hot phase' clinical presentation in arrhythmogenic cardiomyopathy 423
A targeted next-generation gene panel reveals a novel heterozygous nonsense variant in the TP63 gene in patients with arrhythmogenic cardiomyopathy 293
Cardiomiopatia/displasia aritmogena del ventricolo destro 286
Large Genomic Rearrangements of Desmosomal Genes in Italian Arrhythmogenic Cardiomyopathy Patients 241
Whole-Exome Sequencing Identifies Pathogenic Variants in TJP1 Gene Associated With Arrhythmogenic Cardiomyopathy 233
Ultrastructural evidence of intercalated disc remodelling in arrhythmogenic right ventricular cardiomyopathy: an electron microscopy investigation on endomyocardial biopsies. 221
Arrhythmogenic Cardiomyopathy 221
Missense mutations in desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitro. 219
Phenotype and Clinical Outcomes in Desmin-Related Arrhythmogenic Cardiomyopathy 216
Advances in Genetics: Dominant Forms 216
ARVD4, a new locus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm. 216
Compound and Digenic Heterozygosity Contributes to Arrhythmogenic Right Ventricular Cardiomyopathy 209
The novel S59P mutation in the TNFRSF1A gene identified in an adult onset TNF receptor associated periodic syndrome (TRAPS) constitutively activates NF-κB pathway. 208
A NEW LOCUS FOR ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY (ARVD2) MAPS TO CHROMOSOME 1q42-q43 204
Homozygous desmocollin-2 mutations and arrhythmogenic cardiomyopathy 202
Arrhythmogenic right ventricular cardiomyopathy type 1 (ARVD1): confirmation of locus assignment and mutation screening of four candidate genes. 201
Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy 198
Follow-Up with Exercise Test of Effort-Induced Ventricular Arrhythmias Linked to Ryanodine Receptor Type 2 Gene Mutations. 197
New FIG4 gene mutations causing aggressive ALS 196
The p.A897KfsX4 frameshift variation in desmocollin-2 is not a causative mutation in arrhythmogenic right ventricular cardiomyopathy 189
Mutations in the area composita protein alphaT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy 188
A founder MYBPC3 mutation results in HCM with a high risk of sudden death after the fourth decade of life 186
Clinical phenotype and diagnosis of arrhythmogenic right ventricular cardiomyopathy in pediatric patients carrying desmosomal gene mutations. 183
PHENOTYPIC EXPRESSION IS A PREREQUISITE FOR MALIGNANT ARRHYTHMIC EVENTS AND SUDDEN CARDIAC DEATH IN ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 181
Arrhythmogenic cardiomyopathy: a disease of intercalated discs. 181
Identification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathy. 179
Wnt/b-catenin pathway in arrhythmogenic cardiomyopathy 177
A novel murine model for arrhythmogenic cardiomyopathy points to a pathogenic role of Wnt signaling and miRNA dysregulation. 177
Transcriptomic Characterization of a Human In Vitro Model of Arrhythmogenic Cardiomyopathy Under Topological and Mechanical Stimuli 177
Compound and digenic heterozygosity predicts lifetime arrhythmic outcome and sudden cardiac death in desmosomal gene-related arrhythmogenic right ventricular cardiomyopathy. 177
Characterization of C14orf4, a novel intronless human gene containing a polyglutamine repeat, mapped to the ARVD1 critical region 172
Arrhythmogenic right ventricular cardiomyopathy - A still underrecognized clinic entity 172
Co-inheritance of mutations associated with arrhythmogenic cardiomyopathy and hypertrophic cardiomyopathy 172
Molecular genetics of arrhythmogenic right ventricular cardiomyopathy 169
LGI1 microdeletion in autosomal dominant lateral temporal epilepsy. 168
Characterization of a novel human gene containing ANK repeats and ARM domains 166
Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia 165
Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutations. 164
Novel Missense Variant in MYL2 Gene Associated with Hypertrophic Cardiomyopathy Showing High Incidence of Restrictive Physiology 163
Juvenile sudden death in a family with polymorphic ventricular arrhythmias caused by a novel RyR2 gene mutation: evidence of specific morphological substrates. 161
Pathogenic Potential of Hic1-Expressing Cardiac Stromal Progenitors 161
Identification and characterization of heart-specific splicing of human Neurexin3 mRNA (NRXN3) 159
Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy 158
R25C mutation in the NKX2.5 gene in Italian patients affected with non-syndromic and syndromic congenital heart disease 156
Arrhythmogenic right ventricular cardiomyopathy: evaluation of the current diagnostic criteria and differential diagnosis 156
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2) 154
Desmin mutations and arrhythmogenic right ventricular cardiomyopathy. 152
Comparison of clinical features of arrhythmogenic right ventricular cardiomyopathy in men versus women 149
TAIL1: an isthmin-like gene, containing type 1 thrombospondin-repeat and AMOP domain, mapped to ARVD1 critical region. 149
Arrhythmogenic Ventricular Cardiomyopathy Associated With Fibromuscular Dysplasia of Ostial Right Main Coronary Artery. 147
Diagnosis of arrhythmogenic cardiomyopathy: The Padua criteria 147
Denaturing HPLC-based approach for detecting RYR2 mutations involved in malignant arrhythmias 146
Intercalated discs and arrhythmogenic cardiomyopathy. 144
Arrhythmogenic right-ventricular cardiomyopathy: Molecular genetics into clinical practice in the era of next generation sequencing 144
Clinical and Functional Characterization of a Novel Mutation in Lamin A/C Gene in a Multigenerational Family with Arrhythmogenic Cardiac Laminopathy 144
Homozygous SCN5A mutation in Brugada syndrome with monomorphic ventricular tachycardia and structural heart abnormalities. 141
Hypertrophic Cardiomyopathy and Primary Restrictive Cardiomyopathy: Similarities, Differences and Phenocopies 141
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2) 140
Compound and Digenic Heterozygosity Contributes to Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia (vol 55, pg 587, 2010) 137
THE GENE FOR ARRHYTHMOGENIC RIGHT-VENTRICULAR CARDIOMYOPATHY MAPS TO CHROMOSOME 14Q23-Q24 133
Clinical profile and long-term follow-up of 37 families with arrhythmogenic right ventricular cardiomyopathy. 132
Clinical profile and long-term follow-up of a cohort of patients with desmoplakin cardiomyopathy 132
Modeling Cardiovascular Diseases with hiPSC-Derived Cardiomyocytes in 2D and 3D Cultures 130
Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1. 129
Molecular Genetics of Arrhythmogenic Right Ventricular Cardiomyopathy 125
Evolving Diagnostic Criteria for Arrhythmogenic Cardiomyopathy 123
Is beta-catenin signalling involved in the molecular pathogenesis of arrhythmogenic right ventricular cardiomyopathy? Study on DSG2 transgenic mice 122
Gene symbol: RYR2. Disease: Arrhythmogenic right ventricular cardiomyopathy type 2. 119
Mutation screening in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2) 119
Genetics of Arrhythmogenic Right Ventricular Cardiomyopathy 119
Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death: early diagnosis of asymptomatic carriers. 117
Study of the molecular pathogenesis of arrhythmogenic cardiomyopathy due to Desmoglein-2 mutations: the zebrafish helps the mouse 116
Is the cause of arrhythmogenic right ventricular cardiomyopathy congenital or acquired? 116
Circulating miR-185-5p as a Potential Biomarker for Arrhythmogenic Right Ventricular Cardiomyopathy 116
IDENTIFICATION OF MUTATIONS IN THE CARDIAC RYANODINE RECEPTOR GENE IN FAMILIES AFFECTED WITH ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 115
A DHPLC-based approach for detecting RYR2 mutations involved in malignant arrhythmias. 113
Comparison of knock-in mouse and hiPSC-based models of arrhythmogenic cardiomyopathy carrying the DSG2 p.Q558* mutation 112
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 112
Genetics meets epigenetics: Genetic variants that modulate noncoding RNA in cardiovascular diseases 112
Familial effort polymorphic ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy are linked to chromosome 1q42-43 111
Artificial Intelligence Advancements in Cardiomyopathies: Implications for Diagnosis and Management of Arrhythmogenic Cardiomyopathy 110
Genetic bases of arrhythmogenic right ventricular cardiomyopathy. 110
Gene symbol: RYR2. Disease: Effort-induced polymorphic ventricular arrhythmias. 108
From molecular mechanisms of cardiac development to genetic substrate of congenital heart diseases. 106
Diagnosis of arrhythmogenic cardiomyopathy: The Padua criteria 104
Familial effort polymorphic ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy map to chromosome 1q42-43. 104
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. 103
Recent advances in crispr/cas9-based genome editing tools for cardiac diseases 103
Occurrence of two different intragenic deletions in two male relatives affected with Duchenne muscular dystrophy. 99
Animal Models and Molecular Pathogenesis of Arrhythmogenic Cardiomyopathy Associated with Pathogenic Variants in Intercalated Disc Genes 97
Heart transcriptome profile of a novel transgenic mouse model for arrhythmogenic cardiomyopathy 94
Generation of a human induced pluripotent stem cell line UGENTi002-A from an arrhythmogenic cardiomyopathy patient carrying the c.817C>T DSP heterozygous variant and isogenic control using CRISPR/Cas9 editing 94
A first insight into molecular genetics of arrhythmogenic right ventricular cardiomyopathy. 94
Pathogenic variants in plakophilin-2 gene (PKP2) are associated with better survival in arrhythmogenic right ventricular cardiomyopathy 93
Regulatory mutations in transforming growth factor-beta 3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1 92
Genetics of arrhythmogenic right ventricular cardiomyopathy 90
Regulatory mutations in transforming growth factor-β3 gene involved in arrhythmogenic right ventricular cardiomyopathy 89
Mutations of the same sequence of the myelin PO gene causing two different phenotypes 81
Progress in molecular genetics of arrhythmogenic cardiomyopathy of the left ventricle. 75
Genotype-phenotype correlation in arrhythmogenic right-ventricular cardiomyopathy linked to desmoplakin mutation (ARVD8) 75
Totale 15.336
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Categoria #
all - tutte 47.263
article - articoli 42.095
book - libri 264
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 2.664
Totale 92.286
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.269 0 0 0 0 197 94 60 171 165 268 207 107
2021/20221.483 51 192 165 108 86 96 75 159 103 27 157 264
2022/20231.127 202 146 24 125 186 135 8 89 142 17 36 17
2023/2024675 34 88 67 65 59 90 35 8 26 57 74 72
2024/20252.776 15 156 105 110 299 116 216 262 217 127 487 666
2025/20264.499 557 877 1.292 1.668 105 0 0 0 0 0 0 0
Totale 15.657