CALANDRA BUONAURA, Sebastiano
 Distribuzione geografica
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Continente #
NA - Nord America 11.367
EU - Europa 5.298
AS - Asia 1.279
SA - Sud America 24
Continente sconosciuto - Info sul continente non disponibili 9
AF - Africa 8
OC - Oceania 1
Totale 17.986
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Nazione #
US - Stati Uniti d'America 11.328
GB - Regno Unito 2.158
IT - Italia 996
SE - Svezia 732
CN - Cina 455
DE - Germania 414
UA - Ucraina 318
SG - Singapore 290
HK - Hong Kong 227
FI - Finlandia 185
FR - Francia 182
TR - Turchia 179
BG - Bulgaria 138
BE - Belgio 46
IN - India 44
IE - Irlanda 31
ID - Indonesia 29
NL - Olanda 27
RU - Federazione Russa 24
BZ - Belize 17
CA - Canada 17
IR - Iran 17
CH - Svizzera 12
BR - Brasile 10
CZ - Repubblica Ceca 9
EU - Europa 8
JP - Giappone 7
MY - Malesia 7
PL - Polonia 6
ES - Italia 5
TW - Taiwan 5
VN - Vietnam 5
AR - Argentina 4
IL - Israele 4
LT - Lituania 4
TN - Tunisia 4
BA - Bosnia-Erzegovina 3
CO - Colombia 3
MX - Messico 3
CU - Cuba 2
EC - Ecuador 2
KG - Kirghizistan 2
KR - Corea 2
PE - Perù 2
RO - Romania 2
SA - Arabia Saudita 2
UY - Uruguay 2
ZA - Sudafrica 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AT - Austria 1
AZ - Azerbaigian 1
BD - Bangladesh 1
BO - Bolivia 1
DK - Danimarca 1
EG - Egitto 1
GR - Grecia 1
HR - Croazia 1
LK - Sri Lanka 1
MD - Moldavia 1
NG - Nigeria 1
NZ - Nuova Zelanda 1
PT - Portogallo 1
TH - Thailandia 1
Totale 17.986
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Città #
Southend 1.865
Fairfield 1.752
Woodbridge 1.212
Houston 980
Ashburn 874
Chandler 750
Jacksonville 740
Seattle 688
Ann Arbor 610
Wilmington 596
Cambridge 543
Nyköping 458
Dearborn 445
Hong Kong 225
Singapore 207
Modena 203
San Diego 150
Beijing 148
Princeton 148
Sofia 134
Eugene 115
Milan 98
Des Moines 89
Izmir 87
Grafing 82
Helsinki 79
New York 74
Rome 72
London 56
Shanghai 50
Falls Church 49
Bremen 38
Brussels 38
San Jose 37
Boardman 33
Dublin 29
Los Angeles 28
Naples 28
Redwood City 28
Norwalk 26
Jakarta 24
San Mateo 22
Nanjing 20
Turin 18
Belize City 17
Dallas 16
Leawood 15
Bologna 14
Hefei 14
Kilburn 14
Augusta 13
Chiswick 13
Hounslow 13
Indiana 13
Kunming 13
Palermo 13
Parma 13
Chicago 12
Florence 10
Jinan 10
Saint Louis 10
Brescia 9
Paris 9
Reggio Emilia 9
Saint Petersburg 9
San Francisco 9
Verona 9
Acton 8
Ardabil 8
Brno 8
Fremont 8
Padova 8
Toronto 8
Auburn Hills 7
Bartlesville 7
Guangzhou 7
Islington 7
Prescot 7
Southwark 7
Washington 7
Munich 6
Waanrode 6
Atlanta 5
Catania 5
Frankfurt am Main 5
Guishan 5
Hebei 5
Piacenza 5
San Giorgio Ionico 5
Xian 5
Amsterdam 4
Benevento 4
Cagliari 4
Casalnuovo di Napoli 4
Dong Ket 4
Ferrara 4
Hagen 4
Monmouth Junction 4
Monopoli 4
Monza 4
Totale 14.414
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Nome #
CASO CLINICO: QUANDO LA RISPOSTA ALLA DIETA IPOLIPIDEMIZZANTE DETERMINA LA DIAGNOSI 745
Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN) 377
Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN study 216
Hypertriglyceridaemia and low plasma HDL in a patient with apolipoprotein A-V deficiency due to a novel mutation in the APOA5 gene 209
Altered mRNA splicing in lipoprotein disorders. 208
Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia 204
A novel deletion of BRCA1 gene that eliminates the ATG initiation codon without affecting the promoter region. 201
Impact of rare variants in autosomal dominant hypercholesterolemia causing genes. 200
A 'de novo' point mutation of the low-density lipoprotein receptor gene in an Italian subject with primary hypercholesterolemia 199
Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 gene 198
Pseudoxanthoma elasticum and familial hypercholesterolemia: A deleterious combination of cardiovascular risk factors 188
Incidental finding of severe hypertriglyceridemia in children. Role of multiple rare variants in genes affecting plasma triglyceride. 187
Leucine 10 allelic variant in signal peptide of PCSK9 increases the LDL cholesterol-lowering effect of statins in patients with familial hypercholesterolaemia. 186
Novel mutations in SAR1B and MTTP genes in Tunisian children with chylomicron retention disease and abetalipoproteinemia. 183
A novel sequence variant in APOA5 gene found in patients with severe hypertriglyceridemia 183
Evaluation of the performance of Dutch Lipid Clinic Network score in an Italian FH population: The LIPIGEN study 177
Additive effect of mutations in LDLR and PCSK9 genes on the phenotype of familial hypercholesterolemia 176
Identification and characterization of novel loss of function mutations in ATP-binding cassette transporter A1 in patients with low plasma high-density lipoprotein cholesterol. 174
Sequential expression during postnatal development of specific markers of junctional and free sarcoplasmic reticulum in chicken pectoralis muscle. 173
A novel homozygous mutation in CETP gene as a cause of CETP deficiency in a Caucasian kindred. 173
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) 171
Two novel rare variants of APOA5 gene found in subjects with severe hypertriglyceridemia. 170
Molecular analysis of NPC1 and NPC2 gene in 34 Niemann-Pick C Italian Patients: Identification and structural modeling of novel mutations 170
A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease 168
Functional analysis of two novel splice site mutations of APOB gene in familial hypobetalipoproteinemia. 166
Mechanisms and genetic determinants regulating sterol absorption, circulating LDL levels, and sterol elimination: implications for classification and disease risk. 164
Multiple abnormally spliced ABCA1 mRNAs caused by a novel splice site mutation of ABCA1 gene in a patient with Tangier disease. 163
A novel mutation in the sterol 27-hydroxylase gene of a woman with autosomal recessive cerebrotendinous xanthomatosis. 161
Separation of the isoprotein forms of apoprotein A-I of rat, rabbit and human HDL by combined isoelectrofocusing and SDS-polyacrylamide gel electrophoresis. 160
Abnormal apolipoprotein B pre-mRNA splicing in patients with familial hypobetalipoproteinaemia 159
Lysosomal lipase deficiency: Molecular characterization of eleven patients with Wolman or cholesteryl ester storage disease 159
Modulation of the synthesis of apolipoproteins in rat hepatoma cells. 156
Abnormal splicing of ABCA1 pre-mRNA in Tangier disease due to a IVS2+5G > C mutation in ABCA1 gene 156
Plasma and urine lipoproteins during the development of nephrotic syndrome induced in the rat by adriamycin. 156
Functional lecithin: Cholesterol acyltransferase Is not required for efficient atheroprotection in humans 155
Preemptive liver transplantation in a child with familial hypercholesterolemia 154
An apparent inconsistency in parent to offspring transmission ofpoint mutations of LDLR gene in familial hypercholesterolemia 152
Effect of the desulfation of heparin on its anticoagulant and anti-proliferative activity 152
Hypobetalipoproteinemia with an apparently recessive inheritance due to a de novo mutation of apolipoprotein B 151
Effect of ezetimibe coadministered with statins in genotype-confirmed heterozygous FH patients 151
Clinical characteristics and plasma lipids in subjects with familial combined hypolipidemia: a pooled analysis. 151
Effect of a thromboxane A2 synthase inhibitor on the dyslipoproteinemia of an inbred rat strain with spontaneous age-related nephrotic syndrome 150
Fatty liver in heterozygous hypobetalipoproteinemia caused by a novel truncated form of apolipoprotein B 149
Analysis of LDL receptor gene mutations in Italian patients with homozygous familial hypercholesterolemia 148
Inherited apolipoprotein A-V deficiency in severe hypertriglyceridemia 148
Mutations in MTP gene in abeta- and hypobeta-lipoproteinemia 146
Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in Italy 146
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 145
Adult-onset Niemann-Pick type C disease: A clinical, neuroimaging, and molecular genetic study 145
Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiency 143
Rearrangements of the ABCC6 gene in Italian patients with PXE 143
Cholesterol synthesis in isolated rat hepatocytes: effect of homologous and heterologous serum lipoproteins. 143
Isoforms of rat apolipoprotein A-I isolated from the lipoproteins of hepatic Golgi apparatus and plasma. 142
Chemical and morphological changes of rat plasma lipoproteins after a prolonged administration of diets containing olive oil and cholesterol. 142
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). 142
Severe HDL deficiency due to novel defects in the ABCA1 transporter 139
Apolipoprotein B-100 production and cholesteryl ester content in the liver of developing chick 139
A novel mutation of the apolipoprotein A-I gene in a family with familial combined hyperlipidemia 139
Autosomal recessive hypercholesterolemia (ARH) and homozygous familial hypercholesterolemia (FH): a phenotypic comparison. 139
Characterization of Three Kindreds with Familial Combined Hypolipidemia Due to Loss of Function Mutations of ANGPTL3. 138
MOLECULAR CHARACTERIZATION OF TWO PATIENTS WITH SEVERE LCAT DEFICIENCY 137
Familial HDL deficiency due to ABCA1 gene mutations with or without other genetic lipoprotein disorders 137
Variable phenotypic expression of homozygous familial hypobetalipoproteinaemia due to novel APOB gene mutations 136
Changes of the main isoform of human apolipoprotein A-I following incubation of plasma. 134
Cholesterol synthesis in freshly isolated human leukocytes. 134
Plasma and urinary lipids and lipoproteins during the development of nephrotic syndrome induced in the rat by puromycin aminonucleoside. 134
Plasma lipoproteins in rats with experimental biliary obstruction. I. A chemical study. 131
Lung involvement in Niemann-Pick disease type C1: improvement with bronchoalveolar lavage 130
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. 130
Experimental nephrotic syndrome in the rat induced by puromycin aminonucleoside: hepatic synthesis of lipoproteins and apolipoproteins. 129
Synthesis and secretion of apolipoprotein A-I by chick skin. 129
The relation between plasma cholesterol and cholesterol synthesis in rats with experimental biliary obstruction. 129
Heavy metals and experimental atherosclerosis. Effect of lead intoxication on rabbit plasma lipoproteins. 128
Effect of heparin derived fractions on the proliferation and protein synthesis of cells in culture. 128
Characterization of three mutations of the low density lipoprotein receptor gene in Italian patients with familial hypercholesterolemia. 127
Plasma lecithin: cholesterol acyltransferase activity in liver disease. 127
Effect of prostaglandin E1 on cholesterol biosynthesis in rat liver. 126
Partial duplication of the EGF precursor homology domain of the LDL receptor protein causing familial hypercholesterolemia (FH-Salerno) 125
Genetic polymorphisms affecting the phenotypic expression of familial hypercholesterolemia 125
Pravastatin in heterozygous familial hypercholesterolemia: low-density lipoprotein (LDL) cholesterol-lowering effect and LDL receptor activity on skin fibroblastS. 124
Changes in apolipoprotein A-I mRNA level in the liver of rats with experimental nephrotic syndrome 124
Secretion of lipoproteins, apolipoprotein A-I and apolipoprotein E by isolated and perfused liver of rat with experimental nephrotic syndrome. 123
The complete sequence of chick apolipoprotein AI mRNA and its expression in the developing chick 123
The ultrastructure of rat plasma lipoproteins. 122
Molecular diagnosis of hypobetalipoproteinemia: an ENID Review 122
Secretion of apoB- and apoA-I-containing lipoproteins by chick kidney 121
Effect of cholesterol feeding on cholesterol biosynthesis in maternal and foetal rat liver. 121
Genetics and molecular biology: proprotein convertase subtilisin/kexin type 9 and LDL receptor--an intriguing story. 120
Recurrent mutations of the apolipoprotein A-I gene in three kindreds with severe HDL deficiency 120
Cholesteryl Ester Storage Disease (CESD) due to novel mutations in the LIPA gene. 119
Duplication of exons 13, 14 and 15 of the LDL-receptor gene in a patients with heterozygous familial hypercholesterolemia 118
Experimental nephrotic syndrome in the rat induced by puromycin aminonucleoside. Plasma and urinary lipoproteins 117
APOA5 and trigliceride metabolism, lesson from human APOA5 deficiency. 116
Quantitative polymerase chain reaction and microchip electrophoresis to detect major rearrangements of the low-density lipoprotein receptor gene causing familial hypercholesterolemia 115
Synthesis and secretion of B-100 and A-I apolipoproteins in response to the changes of intracellular cholesteryl ester content in chick liver 115
Plasma lipoproteins in rats with experimental biliary obstruction. II. An ultrastructural study. 115
The molecular basis of lecithin: Cholesterol acyltransferase deficiency syndromes: A comprehensive study of molecular and biochemical findings in 13 unrelated Italian families 115
A point mutation in the lariat branch point of intron 6 of NPC1 as the cause of abnormal pre-mRNA splicing in Niemann-Pick type C disease. 112
Plasma lipoproteins, tissue cholesterol overload, and skeletal muscle apolipoprotein A-I synthesis in the developing chick. 111
β-thalassemia is a modifying factor of the clinical expression of familial hypercholesterolemia 109
Totale 15.586
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Categoria #
all - tutte 81.321
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 81.321
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20203.553 0 0 159 287 489 644 746 390 351 141 186 160
2020/20213.121 268 89 199 280 351 267 432 341 138 349 257 150
2021/20222.677 109 307 317 155 55 210 204 103 284 178 494 261
2022/20232.390 258 267 163 197 285 383 37 213 324 53 99 111
2023/20241.564 66 78 144 141 292 162 150 162 56 90 40 183
2024/2025354 196 53 105 0 0 0 0 0 0 0 0 0
Totale 18.137