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.	170
A novel loss of function mutation of PCSK9 gene in white subjects with low-plasma low-density lipoprotein cholesterol	164
Multiple abnormally spliced ABCA1 mRNAs caused by a novel splice site mutation of ABCA1 gene in a patient with Tangier disease.	162
Lysosomal lipase deficiency: Molecular characterization of eleven patients with Wolman or cholesteryl ester storage disease	158
Functional lecithin: Cholesterol acyltransferase Is not required for efficient atheroprotection in humans	153
Effect of ezetimibe coadministered with statins in genotype-confirmed heterozygous FH patients	149
Severe HDL deficiency due to novel defects in the ABCA1 transporter	137
Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiency	136
Totale	1.229

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2018/2019	82	0	0	0	0	0	0	0	0	0	0	43	39
2019/2020	358	29	24	11	26	42	54	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	74	4	6	8	12	17	6	13	5	3	0	0	0
Totale													1.229