statistiche ricercatore

Continente	#
EU - Europa	910
Totale	910

Nazione	#
IT - Italia	910
Totale	910

Nome	#
Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia	160
Cholesteryl Ester Storage Disease (CESD) due to novel mutations in the LIPA gene.	141
A complex phenotype in a child with familial HDL deficiency due to a novel frameshift mutation in APOA1 gene (apoA-IGuastalla)	140
Additive effect of mutations in LDLR and PCSK9 genes on the phenotype of familial hypercholesterolemia	138
Effect of ezetimibe coadministered with statins in genotype-confirmed heterozygous FH patients.	134
Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in Italy.	113
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	46
Effect of a common missense variant in LIPA gene on fatty liver disease and lipid phenotype: New perspectives from a single-center observational study	44
Hypoalpha-hypobetalipoproteinemia (Familial Combined Hypolipidemia) caused by loss of function mutations of ANGPTL3 gene.	17
Totale	933

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	160	0	0	0	0	0	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	96	8	11	6	25	18	28	0	0	0	0	0	0
Totale													933