Distribuzione geografica
Continente #
NA - Nord America 10796
EU - Europa 4517
AS - Asia 427
SA - Sud America 18
Continente sconosciuto - Info sul continente non disponibili 9
AF - Africa 2
Totale 15769
Nazione #
US - Stati Uniti d'America 10763
GB - Regno Unito 2049
SE - Svezia 718
IT - Italia 490
DE - Germania 384
UA - Ucraina 315
TR - Turchia 179
FR - Francia 171
CN - Cina 163
BG - Bulgaria 138
FI - Finlandia 123
BE - Belgio 52
IN - India 38
NL - Olanda 27
RU - Federazione Russa 22
BZ - Belize 17
IR - Iran 15
CA - Canada 13
CH - Svizzera 9
EU - Europa 8
MY - Malesia 7
JP - Giappone 6
ID - Indonesia 5
VN - Vietnam 5
AR - Argentina 4
BR - Brasile 4
BA - Bosnia-Erzegovina 3
CO - Colombia 3
ES - Italia 3
MX - Messico 3
PL - Polonia 3
EC - Ecuador 2
IE - Irlanda 2
KG - Kirghizistan 2
KR - Corea 2
PE - Perù 2
RO - Romania 2
UY - Uruguay 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AT - Austria 1
BD - Bangladesh 1
BO - Bolivia 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
EG - Egitto 1
GR - Grecia 1
HK - Hong Kong 1
HR - Croazia 1
IL - Israele 1
LK - Sri Lanka 1
NG - Nigeria 1
PT - Portogallo 1
SG - Singapore 1
Totale 15769
Città #
Southend 1865
Fairfield 1752
Woodbridge 1212
Houston 980
Chandler 750
Jacksonville 740
Ashburn 713
Seattle 680
Ann Arbor 610
Wilmington 596
Cambridge 543
Dearborn 445
Nyköping 445
Modena 197
San Diego 150
Princeton 148
Sofia 134
Eugene 115
Des Moines 89
Izmir 87
Grafing 82
Beijing 58
Falls Church 49
Brussels 44
London 39
Bremen 38
San Jose 36
Milan 28
Redwood City 28
Norwalk 26
Boardman 23
San Mateo 22
Rome 21
Nanjing 20
Helsinki 18
Belize City 17
Leawood 15
Hefei 14
Augusta 13
Indiana 13
Kunming 13
Jinan 10
Saint Louis 10
Saint Petersburg 9
San Francisco 9
Ardabil 8
Dallas 8
Fremont 8
Naples 8
Toronto 8
Auburn Hills 7
Bartlesville 7
Verona 7
Waanrode 6
Bologna 5
Chicago 5
Hebei 5
New York 5
San Giorgio Ionico 5
Xian 5
Amsterdam 4
Dong Ket 4
Hagen 4
Monmouth Junction 4
Monopoli 4
Mountain View 4
Ningbo 4
Nürnberg 4
Palermo 4
Sesto Fiorentino 4
Tulare 4
Turin 4
Atlanta 3
Buffalo 3
Catania 3
Detroit 3
Fiorano Modenese 3
Foggia 3
Guangzhou 3
Limbiate 3
Maastricht 3
Menlo Park 3
Nanchang 3
Paris 3
Parma 3
Philadelphia 3
Pontinia 3
Sarajevo 3
Avigliana 2
Benevento 2
Borås 2
Buenos Aires 2
Casalnuovo di Napoli 2
Chongqing 2
Columbus 2
Cornaredo 2
Deventer 2
Diedorf 2
Dortmund 2
Dublin 2
Totale 13123
Nome #
Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN) 324
Altered mRNA splicing in lipoprotein disorders. 196
Impact of rare variants in autosomal dominant hypercholesterolemia causing genes. 193
Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia 193
Hypertriglyceridaemia and low plasma HDL in a patient with apolipoprotein A-V deficiency due to a novel mutation in the APOA5 gene 191
Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN study 185
Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 gene 180
A novel deletion of BRCA1 gene that eliminates the ATG initiation codon without affecting the promoter region. 177
A 'de novo' point mutation of the low-density lipoprotein receptor gene in an Italian subject with primary hypercholesterolemia 175
Pseudoxanthoma elasticum and familial hypercholesterolemia: A deleterious combination of cardiovascular risk factors 175
Incidental finding of severe hypertriglyceridemia in children. Role of multiple rare variants in genes affecting plasma triglyceride. 171
Leucine 10 allelic variant in signal peptide of PCSK9 increases the LDL cholesterol-lowering effect of statins in patients with familial hypercholesterolaemia. 171
Novel mutations in SAR1B and MTTP genes in Tunisian children with chylomicron retention disease and abetalipoproteinemia. 168
Sequential expression during postnatal development of specific markers of junctional and free sarcoplasmic reticulum in chicken pectoralis muscle. 167
Evaluation of the performance of Dutch Lipid Clinic Network score in an Italian FH population: The LIPIGEN study 161
A novel sequence variant in APOA5 gene found in patients with severe hypertriglyceridemia 160
Additive effect of mutations in LDLR and PCSK9 genes on the phenotype of familial hypercholesterolemia 159
Two novel rare variants of APOA5 gene found in subjects with severe hypertriglyceridemia. 159
A study of fatty liver disease and plasma lipoproteins in a kindred with familial hypobetalipoproteinemia due to a novel truncated form of apolipoprotein B (apo B-54.5) 158
Identification and characterization of novel loss of function mutations in ATP-binding cassette transporter A1 in patients with low plasma high-density lipoprotein cholesterol. 158
Mechanisms and genetic determinants regulating sterol absorption, circulating LDL levels, and sterol elimination: implications for classification and disease risk. 157
Molecular analysis of NPC1 and NPC2 gene in 34 Niemann-Pick C Italian Patients: Identification and structural modeling of novel mutations 155
Multiple abnormally spliced ABCA1 mRNAs caused by a novel splice site mutation of ABCA1 gene in a patient with Tangier disease. 154
A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease 154
A novel homozygous mutation in CETP gene as a cause of CETP deficiency in a Caucasian kindred. 151
Separation of the isoprotein forms of apoprotein A-I of rat, rabbit and human HDL by combined isoelectrofocusing and SDS-polyacrylamide gel electrophoresis. 149
Preemptive liver transplantation in a child with familial hypercholesterolemia 148
Hypobetalipoproteinemia with an apparently recessive inheritance due to a de novo mutation of apolipoprotein B 146
Effect of a thromboxane A2 synthase inhibitor on the dyslipoproteinemia of an inbred rat strain with spontaneous age-related nephrotic syndrome 145
Abnormal apolipoprotein B pre-mRNA splicing in patients with familial hypobetalipoproteinaemia 145
A novel mutation in the sterol 27-hydroxylase gene of a woman with autosomal recessive cerebrotendinous xanthomatosis. 145
Lysosomal lipase deficiency: Molecular characterization of eleven patients with Wolman or cholesteryl ester storage disease 144
Functional lecithin: Cholesterol acyltransferase Is not required for efficient atheroprotection in humans 144
Modulation of the synthesis of apolipoproteins in rat hepatoma cells. 143
Plasma and urine lipoproteins during the development of nephrotic syndrome induced in the rat by adriamycin. 142
Clinical characteristics and plasma lipids in subjects with familial combined hypolipidemia: a pooled analysis. 141
Effect of ezetimibe coadministered with statins in genotype-confirmed heterozygous FH patients 138
Fatty liver in heterozygous hypobetalipoproteinemia caused by a novel truncated form of apolipoprotein B 137
Mutations in MTP gene in abeta- and hypobeta-lipoproteinemia 137
Analysis of LDL receptor gene mutations in Italian patients with homozygous familial hypercholesterolemia 136
Functional analysis of two novel splice site mutations of APOB gene in familial hypobetalipoproteinemia. 135
Abnormal splicing of ABCA1 pre-mRNA in Tangier disease due to a IVS2+5G > C mutation in ABCA1 gene 135
An apparent inconsistency in parent to offspring transmission ofpoint mutations of LDLR gene in familial hypercholesterolemia 134
Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in Italy 134
Cholesterol synthesis in isolated rat hepatocytes: effect of homologous and heterologous serum lipoproteins. 133
Inherited apolipoprotein A-V deficiency in severe hypertriglyceridemia 133
Isoforms of rat apolipoprotein A-I isolated from the lipoproteins of hepatic Golgi apparatus and plasma. 132
Therapeutic management of a new case of LCAT deficiency with a multifactorial long-term approach based on high doses of angiotensin II receptor blockers (ARBs). 131
Autosomal recessive hypercholesterolemia (ARH) and homozygous familial hypercholesterolemia (FH): a phenotypic comparison. 131
Chemical and morphological changes of rat plasma lipoproteins after a prolonged administration of diets containing olive oil and cholesterol. 130
Rearrangements of the ABCC6 gene in Italian patients with PXE 128
Apolipoprotein B-100 production and cholesteryl ester content in the liver of developing chick 128
Adaptor protein ARH is recruited to the plasma membrane by low density lipoprotein (LDL) binding and modulates endocytosis of the LDL/LDL receptor complex in hepatocytes 126
Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiency 126
Cholesterol synthesis in freshly isolated human leukocytes. 126
Variable phenotypic expression of homozygous familial hypobetalipoproteinaemia due to novel APOB gene mutations 126
A novel mutation of the apolipoprotein A-I gene in a family with familial combined hyperlipidemia 126
Characterization of Three Kindreds with Familial Combined Hypolipidemia Due to Loss of Function Mutations of ANGPTL3. 125
Severe HDL deficiency due to novel defects in the ABCA1 transporter 124
Changes of the main isoform of human apolipoprotein A-I following incubation of plasma. 124
Adult-onset Niemann-Pick type C disease: A clinical, neuroimaging, and molecular genetic study 124
Familial HDL deficiency due to ABCA1 gene mutations with or without other genetic lipoprotein disorders 124
Isolation of a cDNA clone for chick intestinal apolipoprotein AI (Apo-AI) and its use for detecting apo-AI mRNA expression in several chick tissues. 122
Experimental nephrotic syndrome in the rat induced by puromycin aminonucleoside: hepatic synthesis of lipoproteins and apolipoproteins. 122
Plasma lecithin: cholesterol acyltransferase activity in liver disease. 122
Plasma lipoproteins in rats with experimental biliary obstruction. I. A chemical study. 122
Synthesis and secretion of apolipoprotein A-I by chick skin. 120
Changes in apolipoprotein A-I mRNA level in the liver of rats with experimental nephrotic syndrome 119
Plasma and urinary lipids and lipoproteins during the development of nephrotic syndrome induced in the rat by puromycin aminonucleoside. 119
Lung involvement in Niemann-Pick disease type C1: improvement with bronchoalveolar lavage 118
Effect of the desulfation of heparin on its anticoagulant and anti-proliferative activity 118
Effect of prostaglandin E1 on cholesterol biosynthesis in rat liver. 118
Characterization of three mutations of the low density lipoprotein receptor gene in Italian patients with familial hypercholesterolemia. 118
Effect of heparin derived fractions on the proliferation and protein synthesis of cells in culture. 118
The relation between plasma cholesterol and cholesterol synthesis in rats with experimental biliary obstruction. 118
Secretion of lipoproteins, apolipoprotein A-I and apolipoprotein E by isolated and perfused liver of rat with experimental nephrotic syndrome. 117
Pravastatin in heterozygous familial hypercholesterolemia: low-density lipoprotein (LDL) cholesterol-lowering effect and LDL receptor activity on skin fibroblastS. 117
The ultrastructure of rat plasma lipoproteins. 117
Genetic polymorphisms affecting the phenotypic expression of familial hypercholesterolemia 117
Heavy metals and experimental atherosclerosis. Effect of lead intoxication on rabbit plasma lipoproteins. 116
Partial duplication of the EGF precursor homology domain of the LDL receptor protein causing familial hypercholesterolemia (FH-Salerno) 116
The complete sequence of chick apolipoprotein AI mRNA and its expression in the developing chick 114
Genetics and molecular biology: proprotein convertase subtilisin/kexin type 9 and LDL receptor--an intriguing story. 113
Cholesteryl Ester Storage Disease (CESD) due to novel mutations in the LIPA gene. 110
Effect of cholesterol feeding on cholesterol biosynthesis in maternal and foetal rat liver. 110
Secretion of apoB- and apoA-I-containing lipoproteins by chick kidney 109
Experimental nephrotic syndrome in the rat induced by puromycin aminonucleoside. Plasma and urinary lipoproteins 109
Molecular diagnosis of hypobetalipoproteinemia: an ENID Review 109
Plasma lipoproteins in rats with experimental biliary obstruction. II. An ultrastructural study. 108
Synthesis and secretion of B-100 and A-I apolipoproteins in response to the changes of intracellular cholesteryl ester content in chick liver 107
Duplication of exons 13, 14 and 15 of the LDL-receptor gene in a patients with heterozygous familial hypercholesterolemia 107
Recurrent mutations of the apolipoprotein A-I gene in three kindreds with severe HDL deficiency 107
Quantitative polymerase chain reaction and microchip electrophoresis to detect major rearrangements of the low-density lipoprotein receptor gene causing familial hypercholesterolemia 106
The molecular basis of lecithin:cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian families. 105
The type of LDLR gene mutationpredicts cardiovascular risk in children with familial hypercholesterolemia. 104
Beta-thalassemia is a modifying factor of the clinical expression of familial hypercholesterolemia 100
Plasma lipoproteins, tissue cholesterol overload, and skeletal muscle apolipoprotein A-I synthesis in the developing chick. 100
APOA5 and trigliceride metabolism, lesson from human APOA5 deficiency. 97
Totale 13896
Categoria #
all - tutte 30599
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 30599

Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2017/2018179 0000 00 00 22417145
2018/20192292 6312863120 141137 13627 104276522575
2019/20204158 379226159287 489644 746390 351141186160
2020/20213121 26889199280 351267 432341 138349257150
2021/20222677 109307317155 55210 204103 284178494261
2022/20232083 258267163197 285383 41221 268000
Totale 15912