statistiche ricercatore

Continente	#
EU - Europa	795
Totale	795

Nazione	#
IT - Italia	795
Totale	795

Nome	#
Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia	142
A complex phenotype in a child with familial HDL deficiency due to a novel frameshift mutation in APOA1 gene (apoA-IGuastalla)	127
Cholesteryl Ester Storage Disease (CESD) due to novel mutations in the LIPA gene.	126
Additive effect of mutations in LDLR and PCSK9 genes on the phenotype of familial hypercholesterolemia	126
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.	105
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	32
Effect of a common missense variant in LIPA gene on fatty liver disease and lipid phenotype: New perspectives from a single-center observational study	28
Hypoalpha-hypobetalipoproteinemia (Familial Combined Hypolipidemia) caused by loss of function mutations of ANGPTL3 gene.	8
Totale	816

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2018/2019	67	0	0	0	0	0	0	0	0	0	13	28	26
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	69	4	9	1	14	8	28	1	3	1	0	0	0
Totale													816