statistiche ricercatore

Continente	#
NA - Nord America	637
AS - Asia	453
EU - Europa	438
SA - Sud America	39
AF - Africa	8
OC - Oceania	3
Continente sconosciuto - Info sul continente non disponibili	1
Totale	1.579

Nome	#
PREDESTINATION: PRimary vEntricular fibrillation and suDden dEath during a firST myocardIal iNfArcTION: Genetic basis.	125
Gene symbol: KCNH2	124
A KCNH2 branch point mutation causing aberrant splicing contributes to an explanation of genotype-negative long QT syndrome.	120
Novel human pathological mutations. Gene symbol: SCN5A. Disease: Brugada Syndrome.	103
Long QT syndrome-associated mutations in intrauterine fetal death.	99
Inherited cardiac arrhythmia syndrome. Role of potassium channels	98
Cardiac potassium channel dysfunction in sudden infant death syndrome.	98
Cardiac sodium channel dysfunction in sudden infant death syndrome.	94
Arrhythmogenic disorders of genetic origin. Long QT Syndrome: from genetics to management.	94
Prevalence of the congenital long-QT syndrome.	89
KCNH2-K897T Is a Genetic Modifier of Latent Congenital Long-QT Syndrome.	87
Prevalence of long-QT syndrome gene variants in sudden infant death syndrome.	83
Propranolol prevents life-threatening arrhythmias in LQT3 transgenic mice: implications for the clinical management of LQT3 patients.	82
KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome.	80
NOS1AP Is a Genetic Modifier of the Long-QT Syndrome	79
Torsades de Pointes following Acute Myocardial Infarction: Evidence for a Deadly Link with a Common Genetic Variant.	76
Inherited cardiac arrhythmia syndrome: Role of potassium channels.	59
Totale	1.590

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	85	0	0	0	0	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	253	6	22	5	5	1	10	12	32	72	9	30	49
2025/2026	314	43	56	59	52	101	3	0	0	0	0	0	0
Totale													1.590