statistiche ricercatore

Nome	#
Targeted next-generation sequencing detects novel gene- phenotype associations and expands the mutational spectrum in cardiomyopathies	124
Clinical and functional characterization of a novel mutation in lamin a/C gene in a multigenerational family with arrhythmogenic cardiac laminopathy	109
Head-up tilt testing for diagnosing vasovagal syncope: a meta-analysis	107
Left ventricular hypertrophy and ventricular pre-excitation: let’s not forget Danon disease	56
VINYL: Variant prIoritizatioN by survivaL analysis	49
Screening For Sarcomere Protein Gene Mutations and Genotype-Phenotype Correlations in Patients with Hypertrophic Cardiomyopathy: experience of a Single Centre	47
Left ventricular hypertrophy: when to suspect Anderson-Fabry disease?	47
Genetic and phenotypic heterogeneity in hypertrophic cardiomyopathy: our experience by using targeted next-generation sequencing	43
Sarcomere gene mutations and clinical correlates in patients with hypertrophic cardiomyopathy	42
Left ventricular systolic dysfunction and conduction system disorders: when do you think about cardiolaminopathy?	41
null	28
A novel LMNA gene mutation in a multigenerational family with arrhythmogenic cardiac laminopathy	28
Missense and Non-Missense Lamin A/C Gene Mutations Are Similarly Associated with Major Arrhythmic Cardiac Events: A 20-Year Single-Centre Experience	11
Association of beta-adrenergic receptor polymorphisms and progression to heart failure in patients with idiopathic dilated cardiomyopathy	1
Totale	733

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	74	0	0	0	0	5	7	13	10	14	10	12	3
2020/2021	90	3	3	2	1	4	5	25	6	12	13	11	5
2021/2022	90	2	14	0	0	4	7	5	5	6	7	13	27
2022/2023	136	14	33	9	4	17	19	1	16	20	0	2	1
2023/2024	57	5	12	3	11	7	9	0	3	0	0	1	6
2024/2025	84	19	6	28	9	22	0	0	0	0	0	0	0
Totale													733