statistiche ricercatore

Continente	#
EU - Europa	822
Totale	822

Nazione	#
IT - Italia	822
Totale	822

Nome	#
Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia	149
A complex phenotype in a child with familial HDL deficiency due to a novel frameshift mutation in APOA1 gene (apoA-IGuastalla)	132
Additive effect of mutations in LDLR and PCSK9 genes on the phenotype of familial hypercholesterolemia	130
Cholesteryl Ester Storage Disease (CESD) due to novel mutations in the LIPA gene.	127
Effect of ezetimibe coadministered with statins in genotype-confirmed heterozygous FH patients.	122
Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in Italy.	106
Evaluation of the efficacy of plant sterols supplement sterolip® ESI in patients with type IIA hypercholesterolemia in relation to Genetic variants modulating intestinal absorption of cholesterol	39
Effect of a common missense variant in LIPA gene on fatty liver disease and lipid phenotype: New perspectives from a single-center observational study	30
Hypoalpha-hypobetalipoproteinemia (Familial Combined Hypolipidemia) caused by loss of function mutations of ANGPTL3 gene.	10
Totale	845

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	236	34	5	7	12	18	19	31	34	22	29	22	3
2020/2021	72	8	3	13	2	6	6	2	7	5	7	6	7
2021/2022	113	3	3	18	8	3	13	7	21	11	9	5	12
2022/2023	107	10	6	3	11	19	17	0	8	21	1	9	2
2023/2024	90	4	9	1	14	8	28	1	3	1	0	8	13
2024/2025	8	8	0	0	0	0	0	0	0	0	0	0	0
Totale													845