statistiche ricercatore

Continente	#
NA - Nord America	469
EU - Europa	341
AS - Asia	247
OC - Oceania	3
Continente sconosciuto - Info sul continente non disponibili	1
Totale	1.061

Nome	#
PREDESTINATION: PRimary vEntricular fibrillation and suDden dEath during a firST myocardIal iNfArcTION: Genetic basis.	96
A KCNH2 branch point mutation causing aberrant splicing contributes to an explanation of genotype-negative long QT syndrome.	86
Gene symbol: KCNH2	85
Novel human pathological mutations. Gene symbol: SCN5A. Disease: Brugada Syndrome.	75
Cardiac sodium channel dysfunction in sudden infant death syndrome.	67
Inherited cardiac arrhythmia syndrome. Role of potassium channels	65
Cardiac potassium channel dysfunction in sudden infant death syndrome.	65
Prevalence of the congenital long-QT syndrome.	65
Arrhythmogenic disorders of genetic origin. Long QT Syndrome: from genetics to management.	63
Long QT syndrome-associated mutations in intrauterine fetal death.	61
KCNH2-K897T Is a Genetic Modifier of Latent Congenital Long-QT Syndrome.	57
Prevalence of long-QT syndrome gene variants in sudden infant death syndrome.	57
Propranolol prevents life-threatening arrhythmias in LQT3 transgenic mice: implications for the clinical management of LQT3 patients.	55
Torsades de Pointes following Acute Myocardial Infarction: Evidence for a Deadly Link with a Common Genetic Variant.	51
NOS1AP Is a Genetic Modifier of the Long-QT Syndrome	46
KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome.	41
Inherited cardiac arrhythmia syndrome: Role of potassium channels.	37
Totale	1.072

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	88	0	0	0	0	0	16	3	15	2	17	33	2
2020/2021	130	16	10	5	14	0	15	3	23	4	20	16	4
2021/2022	89	2	1	3	2	2	1	3	4	4	1	14	52
2022/2023	311	30	39	2	16	27	31	0	19	138	1	7	1
2023/2024	92	12	24	1	4	12	13	0	7	1	8	6	4
2024/2025	49	6	22	5	5	1	10	0	0	0	0	0	0
Totale													1.072