SCHWARTZ, PETER
 Distribuzione geografica
Continente #
EU - Europa 118
NA - Nord America 51
AS - Asia 11
OC - Oceania 1
Totale 181
Nazione #
IT - Italia 94
US - Stati Uniti d'America 47
GB - Regno Unito 8
IN - India 6
CZ - Repubblica Ceca 3
FR - Francia 3
BY - Bielorussia 2
CA - Canada 2
DE - Germania 2
PH - Filippine 2
AU - Australia 1
CH - Svizzera 1
HT - Haiti 1
IR - Iran 1
JP - Giappone 1
MX - Messico 1
NL - Olanda 1
RO - Romania 1
RS - Serbia 1
SE - Svezia 1
SY - Repubblica araba siriana 1
UA - Ucraina 1
Totale 181
Città #
Pavia 31
Palermo 9
Fleming Island 6
Milan 5
Kolkata 4
Boardman 3
Bologna 3
Cerro Maggiore 3
Galveston 3
Paris 3
Prato 3
Spilimbergo 3
Turin 3
Albany 2
Brooklyn 2
Chieri 2
Council Bluffs 2
Genoa 2
Lehigh Acres 2
Minsk 2
Naples 2
Perth 2
Port Leyden 2
Portland 2
Rome 2
Sabbioneta 2
San Jose 2
York 2
Albignasego 1
Amsterdam 1
Anaheim 1
Aosta 1
Arco 1
Ashland 1
Ayr 1
Bari 1
Bengaluru 1
Berlin 1
Bucharest 1
Cadoneghe 1
Cagayan de Oro 1
Canterbury 1
Capaci 1
Castellammare di Stabia 1
Cerritos 1
Chennai 1
Davis 1
El Paso 1
Haar 1
Ilford 1
Inverigo 1
League City 1
Manduria 1
Mason City 1
Meda 1
Mexicali 1
New Palestine 1
Odesa 1
Ozark 1
Port Coquitlam 1
Port-au-Prince 1
Quezon City 1
Rochester 1
Sacramento 1
Salem 1
Salerno 1
San Genesio Ed Uniti 1
Santa Clara 1
Shell Rock 1
Shinkocho 1
St. Catharines 1
Stockholm 1
Sudbury 1
Watford 1
Wednesbury 1
Zurich 1
Totale 157
Nome #
Mortality in the Survival With ORal D-sotalol (SWORD) trial: why did patients die?, file e1f104fa-132f-8c6e-e053-1005fe0aa0dd 45
Linee Guida. Task Force sulla Morte Cardiaca Improvvisa, Società Europea di Cardiologia. Riassunto delle raccomandazioni, file e1f104fa-0f43-8c6e-e053-1005fe0aa0dd 36
How really rare are rare diseases?: the intriguing case of independent compound mutations in the long QT syndrome., file e1f104fa-1149-8c6e-e053-1005fe0aa0dd 8
Quantitative analysis of T wave abnormalities and their prognostic implications in the idiopathic long QT syndrome., file e1f104fa-104c-8c6e-e053-1005fe0aa0dd 5
Efficacy of permanent pacing in the management of high-risk patients with long QT syndrome., file e1f104fa-132e-8c6e-e053-1005fe0aa0dd 5
Genotype-Phenotype correlation in the Long QT Syndrome. Gene-specific triggers for life-threatening arrhythmias, file e1f104fa-05f4-8c6e-e053-1005fe0aa0dd 4
Effect of ventricular fibrillation complicating acute myocardial infarction on long-term prognosis: importance of the site of infarction., file e1f104fa-103a-8c6e-e053-1005fe0aa0dd 4
Comparison of baroreflex sensitivity and heart period variability after myocardial infarction., file e1f104fa-1042-8c6e-e053-1005fe0aa0dd 4
Gender and the relationship between ventricular repolarization and cardiac cycle length during 24-h Holter recordings., file e1f104fa-10c2-8c6e-e053-1005fe0aa0dd 4
Electrocardiography first for reducing cot death., file e1f104fa-10cc-8c6e-e053-1005fe0aa0dd 4
Pathophysiology and prevention of atrial fibrillation., file e1f104fa-10d1-8c6e-e053-1005fe0aa0dd 3
Genetic and molecular basis of cardiac arrhythmias: impact on clinical management.Parts I and II, file e1f104fa-12bc-8c6e-e053-1005fe0aa0dd 3
null, file e1f104fb-71c6-8c6e-e053-1005fe0aa0dd 3
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi005-A from a patient carrying the KCNQ1-R190W mutation, file e1f104fc-377d-8c6e-e053-1005fe0aa0dd 3
The long QT syndrome. Prospective longitudinal study of 328 families., file e1f104fa-1046-8c6e-e053-1005fe0aa0dd 2
Counting heart beats: a peephole into prediction of sudden and nonsudden cardiac death., file e1f104fa-1138-8c6e-e053-1005fe0aa0dd 2
Delayed after depolarizations elicited in vivo by left stellate ganglion stimulation., file e1f104fa-11aa-8c6e-e053-1005fe0aa0dd 2
Torsades de Pointes following Acute Myocardial Infarction: Evidence for a Deadly Link with a Common Genetic Variant., file e1f104fa-11c9-8c6e-e053-1005fe0aa0dd 2
Calmodulin mutations associated with recurrent cardiac arrest in infants., file e1f104fa-99b8-8c6e-e053-1005fe0aa0dd 2
Ranolazine in the treatment of atrial fibrillation: Results of the dose-ranging RAFFAELLO (ranolazine in atrial fibrillation following an electrical cardioversion) study, file e1f104fa-f0fc-8c6e-e053-1005fe0aa0dd 2
Cardiac sympathetic denervation 100years later: Jonnesco would have never believed it, file e1f104fb-389e-8c6e-e053-1005fe0aa0dd 2
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi004-A from a carrier of the KCNQ1-R594Q mutation, file e1f104fc-2b7d-8c6e-e053-1005fe0aa0dd 2
Identification of a targeted and testable antiarrhythmic therapy for long-QT syndrome type 2 using a patient-specific cellular model, file e1f104fc-31e0-8c6e-e053-1005fe0aa0dd 2
Generation of two human induced pluripotent stem cell (hiPSC) lines from a long QT syndrome South African founder population, file e1f104fc-3e0f-8c6e-e053-1005fe0aa0dd 2
Precision Medicine and cardiac channelopathies: when dreams meet reality, file 0caf473c-0be2-45ea-a6ff-b90a5e603af5 1
Use of hiPSC-Derived Cardiomyocytes to Rule Out Proarrhythmic Effects of Drugs: The Case of Hydroxychloroquine in COVID-19, file 79c99d8b-17ba-4b5b-af38-d5beec2a998d 1
Cost-effectiveness of Neonatal ECG as a Screening for Long QT-syndrome: A Decision Analysis Approach., file e1f104fa-0132-8c6e-e053-1005fe0aa0dd 1
Homozygous Deletion in KVLQT1 Associated With Jervell and Lange-Nielsen Syndrome., file e1f104fa-0e33-8c6e-e053-1005fe0aa0dd 1
Unexpected interaction between beta-adrenergic blockade and heart rate variability before and after myocardial infarction. A longitudinal study in dogs at high and low risk for sudden death., file e1f104fa-10b7-8c6e-e053-1005fe0aa0dd 1
Depressed heart rate variability identifies postinfarction patients who might benefit from prophylactic treatment with amiodarone: a substudy of EMIAT (The European Myocardial Infarct Amiodarone Trial)., file e1f104fa-10cb-8c6e-e053-1005fe0aa0dd 1
Influence of the genotype on the clinical course of the Long QT Syndrome., file e1f104fa-12b5-8c6e-e053-1005fe0aa0dd 1
Protective effect of vagal stimulation on reperfusion arrhythmias in cats., file e1f104fa-1327-8c6e-e053-1005fe0aa0dd 1
The Jervell and Lange-Nielsen syndrome: natural history, molecular basis, and clinical outcome., file e1f104fa-1331-8c6e-e053-1005fe0aa0dd 1
KCNH2-K897T Is a Genetic Modifier of Latent Congenital Long-QT Syndrome., file e1f104fa-14f9-8c6e-e053-1005fe0aa0dd 1
Effects of unilateral stellate ganglion blockade on the arrhythmias associated with coronary occlusion., file e1f104fa-159e-8c6e-e053-1005fe0aa0dd 1
Real-life observations of clinical outcomes with rhythm- and rate-control therapies for atrial fibrillation RECORDAF (Registry on Cardiac Rhythm Disorders Assessing the Control of Atrial Fibrillation)., file e1f104fa-1afb-8c6e-e053-1005fe0aa0dd 1
Vagus nerve stimulation: from pre-clinical to clinical application: challenges and future directions., file e1f104fa-1b02-8c6e-e053-1005fe0aa0dd 1
QTc behavior during exercise and genetic testing for the long-QT syndrome., file e1f104fa-1b08-8c6e-e053-1005fe0aa0dd 1
Spectrum and prevalence of mutations involving BrS1-12 susceptibility genes in a cohort of unrelated patients referred for Brugada Syndrome genetic testing: implications for genetic testing., file e1f104fa-2cda-8c6e-e053-1005fe0aa0dd 1
Clinical management of catecholaminergic polymorphic ventricular tachycardia the role of left cardiac sympathetic denervation, file e1f104fa-f0ff-8c6e-e053-1005fe0aa0dd 1
Left cardiac sympathetic denervation in patients with heart failure: A new indication for an old intervention?, file e1f104fa-f413-8c6e-e053-1005fe0aa0dd 1
Vox clamantis in deserto. We spoke but nobody was listening: echocardiography can help risk stratification of the long-QT syndrome., file e1f104fa-f504-8c6e-e053-1005fe0aa0dd 1
Autonomic Modulation for the Management of Patients with Chronic Heart Failure, file e1f104fa-f6e7-8c6e-e053-1005fe0aa0dd 1
Rapid recovery of baroreceptor reflexes in acute myocardial infarction is a marker of effective tissue reperfusion, file e1f104fa-facc-8c6e-e053-1005fe0aa0dd 1
Genetic Modifiers for the Long-QT Syndrome: How Important Is the Role of Variants in the 3′ Untranslated Region of KCNQ1?, file e1f104fb-1eb9-8c6e-e053-1005fe0aa0dd 1
The KCNH2-IVS9-28A/G mutation causes aberrant isoform expression and hERG trafficking defect in cardiomyocytes derived from patients affected by Long QT Syndrome type 2, file e1f104fb-20c1-8c6e-e053-1005fe0aa0dd 1
Elucidating arrhythmogenic mechanisms of long-QT syndrome CALM1-F142L mutation in patient-specific induced pluripotent stem cell-derived cardiomyocytes, file e1f104fb-25fb-8c6e-e053-1005fe0aa0dd 1
Clinical Aspects of Type 3 Long-QT Syndrome: An International Multicenter Study., file e1f104fb-3c3d-8c6e-e053-1005fe0aa0dd 1
Multiscale complexity analysis of the cardiac control identifies asymptomatic and symptomatic patients in long QT syndrome type 1., file e1f104fb-4295-8c6e-e053-1005fe0aa0dd 1
Identification of Cadherin 2 (CDH2) Mutations in Arrhythmogenic Right Ventricular Cardiomyopathy., file e1f104fb-4434-8c6e-e053-1005fe0aa0dd 1
Genotype-Phenotype Correlation in Induced Pluripotent Stem Cell (iPSC) Derived Cardiomyocytes Carrying Calmodulin Mutations, file e1f104fb-4f9c-8c6e-e053-1005fe0aa0dd 1
From patient-specific induced pluripotent stem cells to clinical translation in long QT syndrome Type 2, file e1f104fc-2b04-8c6e-e053-1005fe0aa0dd 1
Long QT Syndrome modelling with cardiomyocytes derived from human-induced pluripotent stem cells, file e1f104fc-3588-8c6e-e053-1005fe0aa0dd 1
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi007-A from a Long QT Syndrome type 1 patient carrier of two common variants in the NOS1AP gene, file e1f104fc-38b5-8c6e-e053-1005fe0aa0dd 1
Totale 181
Categoria #
all - tutte 1043
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 1043


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2017/20183 0000 00 00 0300
2019/202010 9001 00 00 0000
2022/2023148 1111013 149 2636 28000
Totale 181