IRIS
CERRONE, MARINA
 Distribuzione geografica
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Continente #
NA - Nord America 396
EU - Europa 340
AS - Asia 240
Totale 976
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Nazione #
US - Stati Uniti d'America 395
CN - Cina 212
IE - Irlanda 124
FI - Finlandia 54
IT - Italia 46
UA - Ucraina 38
DE - Germania 25
SE - Svezia 19
JP - Giappone 18
GB - Regno Unito 12
RU - Federazione Russa 9
SG - Singapore 9
PL - Polonia 6
FR - Francia 3
GR - Grecia 2
BE - Belgio 1
CA - Canada 1
IL - Israele 1
NO - Norvegia 1
Totale 976
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Città #
Dublin 124
Chandler 115
Jacksonville 57
Nanjing 42
Beijing 38
Nanchang 29
Boardman 26
Ashburn 23
Helsinki 22
Hebei 21
Princeton 19
Lawrence 18
Tokyo 18
Wilmington 15
Changsha 14
Shanghai 13
Medford 12
Shenyang 12
Hangzhou 11
Jiaxing 11
Tianjin 10
Melito di Napoli 8
Milan 6
Rzeszów 6
Verona 5
Singapore 4
Woodbridge 4
Ann Arbor 3
Fairfield 3
Falls Church 3
Kunming 3
Norwalk 3
Ponticelli 3
Rome 3
Seattle 3
Casapulla 2
Genova 2
Jinan 2
Montemesola 2
New York 2
San Genesio Ed Uniti 2
Taizhou 2
Turin 2
Athens 1
Brussels 1
Campi Bisenzio 1
Changchun 1
Frankfurt am Main 1
Guangzhou 1
Kemerovo 1
London 1
Los Angeles 1
Naples 1
Oslo 1
Perm 1
Qingdao 1
Ripi 1
St Petersburg 1
Tel Aviv 1
Toronto 1
Vallanzengo 1
Velikiy Novgorod 1
Volgograd 1
Washington 1
Yekaterinburg 1
Totale 745
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Nome #
La Sindrome di Brugada: aspetti clinici, criteri diagnostici, stratificazione prognostica. 83
Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice 81
La Sindrome di Brugada 73
Long QT syndrome and catecholaminergic VT 70
Arrhythmogenic mechanisms in a mouse model of Catecholaminergic Polymorphic Ventricular Tachycardia. 70
Molecular genetics: is it making an impact in the management of inherited arrhythmogenic syndromes? 57
Genetics of ion-channel disorders 56
La Sindrome di Brugada 54
Genetics of sudden death: focus on inherited channelopathies 51
Molecular Bases of Juvenile Sudden Cardiac Death. 50
Ion Channel Diseases and Sudden Cardiac Death 50
Bidirectional Ventricular Tachycardia and Fibrillation Elicited in a Knock-In Mouse Model Carrier of a Mutation in the Cardiac Ryanodine Receptor (RyR2) 48
Routine electrocardiogram and medical history in syncope: a simple approach can identify most high-risk patients 43
Implantable Loop Recorder in Inherited Arrhythmia Diseases: A Critical Tool for Symptom Diagnosis and Advanced Risk Stratification 43
Genetically engineered SCN5A mutant pig hearts exhibit conduction defects and arrhythmias 40
KCNJ2 mutation in short QT syndrome 3 results in atrial fibrillation and ventricular proarrhythmia. 40
A clinical approach to inherited arrhythmias 38
Management of congenital long-QT syndrome: Commentary from the experts 25
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility 13
Totale 985
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Categoria #
all - tutte 3.734
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 3.734
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202075 0 0 0 7 0 7 3 10 0 10 38 0
2020/202181 7 7 3 7 0 11 0 12 5 16 10 3
2021/202263 0 0 0 0 3 2 1 2 7 3 10 35
2022/2023309 24 20 14 13 29 29 0 21 144 3 9 3
2023/2024135 9 36 4 12 12 15 5 6 0 4 10 22
2024/202561 10 29 14 8 0 0 0 0 0 0 0 0
Totale 985