statistiche ricercatore

Nome	#
Identification and characterization of novel loss of function mutations in ATP-binding cassette transporter A1 in patients with low plasma high-density lipoprotein cholesterol.	193
A novel loss of function mutation of PCSK9 gene in white subjects with low-plasma low-density lipoprotein cholesterol	187
Multiple abnormally spliced ABCA1 mRNAs caused by a novel splice site mutation of ABCA1 gene in a patient with Tangier disease.	183
Lysosomal lipase deficiency: Molecular characterization of eleven patients with Wolman or cholesteryl ester storage disease	178
Functional lecithin: Cholesterol acyltransferase Is not required for efficient atheroprotection in humans	175
Effect of ezetimibe coadministered with statins in genotype-confirmed heterozygous FH patients	170
Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiency	168
Severe HDL deficiency due to novel defects in the ABCA1 transporter	158
Totale	1.412

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	172	0	0	0	0	0	0	62	31	37	12	15	15
2020/2021	196	14	11	19	18	33	7	19	29	5	25	11	5
2021/2022	191	4	37	36	8	6	3	12	11	17	6	35	16
2022/2023	171	18	22	8	9	30	27	1	15	22	1	4	14
2023/2024	89	4	6	8	12	17	6	13	5	3	0	2	13
2024/2025	168	6	1	10	23	65	63	0	0	0	0	0	0
Totale													1.412