CALANDRA BUONAURA, Sebastiano
 Distribuzione geografica
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Continente #
NA - Nord America 15.597
EU - Europa 6.639
AS - Asia 6.609
SA - Sud America 1.009
AF - Africa 91
Continente sconosciuto - Info sul continente non disponibili 11
OC - Oceania 9
Totale 29.965
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Nazione #
US - Stati Uniti d'America 15.437
SG - Singapore 2.614
GB - Regno Unito 2.518
CN - Cina 1.984
IT - Italia 1.265
HK - Hong Kong 870
BR - Brasile 829
SE - Svezia 768
DE - Germania 527
VN - Vietnam 346
UA - Ucraina 332
RU - Federazione Russa 320
FI - Finlandia 230
FR - Francia 204
TR - Turchia 196
KR - Corea 174
BG - Bulgaria 138
IN - India 103
NL - Olanda 99
ID - Indonesia 92
AR - Argentina 64
CA - Canada 62
MX - Messico 51
BE - Belgio 49
JP - Giappone 40
BD - Bangladesh 39
PL - Polonia 37
ZA - Sudafrica 33
IE - Irlanda 32
EC - Ecuador 27
PK - Pakistan 26
CL - Cile 24
AT - Austria 23
ES - Italia 22
IQ - Iraq 21
CO - Colombia 20
BZ - Belize 17
IR - Iran 17
LT - Lituania 15
PY - Paraguay 14
CZ - Repubblica Ceca 13
CH - Svizzera 12
TN - Tunisia 12
EG - Egitto 10
MA - Marocco 10
KE - Kenya 9
PE - Perù 9
UY - Uruguay 9
EU - Europa 8
UZ - Uzbekistan 8
VE - Venezuela 8
AU - Australia 7
DZ - Algeria 7
MY - Malesia 7
RO - Romania 7
AE - Emirati Arabi Uniti 6
SA - Arabia Saudita 6
AZ - Azerbaigian 5
BO - Bolivia 5
DO - Repubblica Dominicana 5
IL - Israele 5
KG - Kirghizistan 5
NP - Nepal 5
TT - Trinidad e Tobago 5
TW - Taiwan 5
AL - Albania 4
BA - Bosnia-Erzegovina 4
JM - Giamaica 4
JO - Giordania 4
LB - Libano 4
BB - Barbados 3
DK - Danimarca 3
HR - Croazia 3
KZ - Kazakistan 3
PH - Filippine 3
PT - Portogallo 3
SY - Repubblica araba siriana 3
CR - Costa Rica 2
CU - Cuba 2
GE - Georgia 2
GR - Grecia 2
HN - Honduras 2
KW - Kuwait 2
MD - Moldavia 2
NI - Nicaragua 2
NZ - Nuova Zelanda 2
OM - Oman 2
PS - Palestinian Territory 2
RS - Serbia 2
SN - Senegal 2
SV - El Salvador 2
XK - ???statistics.table.value.countryCode.XK??? 2
YE - Yemen 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AM - Armenia 1
AO - Angola 1
BH - Bahrain 1
BY - Bielorussia 1
CG - Congo 1
DJ - Gibuti 1
Totale 29.947
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Città #
Southend 1.865
Fairfield 1.752
Singapore 1.725
Santa Clara 1.562
Ashburn 1.313
Woodbridge 1.212
Houston 1.000
Hong Kong 863
Hefei 769
Chandler 751
Jacksonville 744
Seattle 696
Wilmington 615
Ann Arbor 610
Cambridge 559
Nyköping 458
Dearborn 445
London 366
Beijing 256
Los Angeles 215
Modena 208
Chicago 182
Seoul 172
San Diego 150
Princeton 148
New York 141
Sofia 134
Milan 122
Ho Chi Minh City 121
The Dalles 118
Eugene 115
Helsinki 112
Moscow 102
Rome 96
Buffalo 92
Shanghai 92
Des Moines 89
Izmir 88
Grafing 82
Hanoi 79
Salt Lake City 79
São Paulo 75
Council Bluffs 74
Dallas 69
Jakarta 68
Columbus 66
San Jose 65
Munich 59
Falls Church 49
Naples 42
Brussels 41
Bremen 38
Elk Grove Village 38
Boardman 37
Tampa 37
Rio de Janeiro 36
Atlanta 32
Dublin 30
Tokyo 30
Redwood City 28
Warsaw 28
Norwalk 27
Guangzhou 26
Brooklyn 25
Belo Horizonte 24
Bologna 24
Nuremberg 24
Nanjing 22
Orem 22
San Mateo 22
Turin 22
Frankfurt am Main 21
Montreal 21
Santiago 21
Kent 20
Mexico City 20
Poplar 19
Boston 18
Detroit 18
Kunming 18
Toronto 18
Belize City 17
San Francisco 17
St Louis 17
Augusta 16
Brasília 16
Johannesburg 15
Leawood 15
Phoenix 15
Chennai 14
Da Nang 14
Jinan 14
Kilburn 14
Lancaster 14
Padova 14
Redondo Beach 14
Reggio Emilia 14
Chiswick 13
Denver 13
Florence 13
Totale 21.951
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Nome #
CASO CLINICO: QUANDO LA RISPOSTA ALLA DIETA IPOLIPIDEMIZZANTE DETERMINA LA DIAGNOSI 1.079
Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN) 474
Lysosomal lipase deficiency: Molecular characterization of eleven patients with Wolman or cholesteryl ester storage disease 380
A 'de novo' point mutation of the low-density lipoprotein receptor gene in an Italian subject with primary hypercholesterolemia 343
Functional analysis of two novel splice site mutations of APOB gene in familial hypobetalipoproteinemia 334
Inherited apolipoprotein A-V deficiency in severe hypertriglyceridemia 332
A novel deletion of BRCA1 gene that eliminates the ATG initiation codon without affecting the promoter region 312
Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN study 310
Altered mRNA splicing in lipoprotein disorders 308
Hypertriglyceridaemia and low plasma HDL in a patient with apolipoprotein A-V deficiency due to a novel mutation in the APOA5 gene 307
Abnormal apolipoprotein B pre-mRNA splicing in patients with familial hypobetalipoproteinaemia 301
A novel homozygous mutation in CETP gene as a cause of CETP deficiency in a caucasian kindred 299
Additive effect of mutations in LDLR and PCSK9 genes on the phenotype of familial hypercholesterolemia 297
MOLECULAR CHARACTERIZATION OF TWO PATIENTS WITH SEVERE LCAT DEFICIENCY 281
An apparent inconsistency in parent to offspring transmission ofpoint mutations of LDLR gene in familial hypercholesterolemia 280
Incidental finding of severe hypertriglyceridemia in children. Role of multiple rare variants in genes affecting plasma triglyceride. 280
Impact of rare variants in autosomal dominant hypercholesterolemia causing genes. 279
A novel sequence variant in APOA5 gene found in patients with severe hypertriglyceridemia 279
Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in Italy 278
Clinical characteristics and plasma lipids in subjects with familial combined hypolipidemia: a pooled analysis. 277
Identification and characterization of novel loss of function mutations in ATP-binding cassette transporter A1 in patients with low plasma high-density lipoprotein cholesterol. 276
Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 gene 276
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 275
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) 272
Pseudoxanthoma elasticum and familial hypercholesterolemia: A deleterious combination of cardiovascular risk factors 270
Novel mutations in SAR1B and MTTP genes in Tunisian children with chylomicron retention disease and abetalipoproteinemia. 270
Preemptive liver transplantation in a child with familial hypercholesterolemia 263
Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiency 260
Effect of ezetimibe coadministered with statins in genotype-confirmed heterozygous FH patients 259
Sequential expression during postnatal development of specific markers of junctional and free sarcoplasmic reticulum in chicken pectoralis muscle. 257
APOA5 and trigliceride metabolism, lesson from human APOA5 deficiency. 256
Abnormal splicing of ABCA1 pre-mRNA in Tangier disease due to a IVS2+5G > C mutation in ABCA1 gene 256
A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease 251
Multiple abnormally spliced ABCA1 mRNAs caused by a novel splice site mutation of ABCA1 gene in a patient with Tangier disease. 250
Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia 247
Rearrangements of the ABCC6 gene in Italian patients with PXE 246
Absence of apolipoprotein B-48 in the chick, Gallus domesticus 246
Modulation of the synthesis of apolipoproteins in rat hepatoma cells. 246
Two novel rare variants of APOA5 gene found in subjects with severe hypertriglyceridemia. 245
Leucine 10 allelic variant in signal peptide of PCSK9 increases the LDL cholesterol-lowering effect of statins in patients with familial hypercholesterolaemia. 245
Separation of the isoprotein forms of apoprotein A-I of rat, rabbit and human HDL by combined isoelectrofocusing and SDS-polyacrylamide gel electrophoresis. 244
Severe HDL deficiency due to novel defects in the ABCA1 transporter 243
Hypobetalipoproteinemia with an apparently recessive inheritance due to a de novo mutation of apolipoprotein B 242
A novel mutation in the sterol 27-hydroxylase gene of a woman with autosomal recessive cerebrotendinous xanthomatosis. 239
Plasma and urine lipoproteins during the development of nephrotic syndrome induced in the rat by adriamycin. 236
Molecular analysis of NPC1 and NPC2 gene in 34 Niemann-Pick C Italian Patients: Identification and structural modeling of novel mutations 236
Adult-onset Niemann-Pick type C disease: A clinical, neuroimaging, and molecular genetic study 236
Effect of a thromboxane A2 synthase inhibitor on the dyslipoproteinemia of an inbred rat strain with spontaneous age-related nephrotic syndrome 234
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. 234
A novel mutation of the apolipoprotein A-I gene in a family with familial combined hyperlipidemia 233
Fatty liver in heterozygous hypobetalipoproteinemia caused by a novel truncated form of apolipoprotein B 232
Functional lecithin: Cholesterol acyltransferase Is not required for efficient atheroprotection in humans 231
Genetic polymorphisms affecting the phenotypic expression of familial hypercholesterolemia 230
Molecular diagnosis of hypobetalipoproteinemia: an ENID Review 228
Familial HDL deficiency due to ABCA1 gene mutations with or without other genetic lipoprotein disorders 228
Effect of the desulfation of heparin on its anticoagulant and anti-proliferative activity 227
A 3-day-old neonate with severe hypertriglyceridemia from novel mutations of the GPIHBP1 gene 226
Autosomal recessive hypercholesterolemia (ARH) and homozygous familial hypercholesterolemia (FH): A phenotypic comparison 224
Analysis of LDL receptor gene mutations in Italian patients with homozygous familial hypercholesterolemia 223
Cholesterol synthesis in isolated rat hepatocytes: effect of homologous and heterologous serum lipoproteins. 221
Isoforms of rat apolipoprotein A-I isolated from the lipoproteins of hepatic Golgi apparatus and plasma. 220
Mutations in MTP gene in abeta- and hypobeta-lipoproteinemia 219
Apolipoprotein B-100 production and cholesteryl ester content in the liver of developing chick 219
Mechanisms and genetic determinants regulating sterol absorption, circulating LDL levels, and sterol elimination: implications for classification and disease risk. 219
Quantitative polymerase chain reaction and microchip electrophoresis to detect major rearrangements of the low-density lipoprotein receptor gene causing familial hypercholesterolemia 218
Evaluation of the performance of Dutch Lipid Clinic Network score in an Italian FH population: The LIPIGEN study 216
Characterization of Three Kindreds with Familial Combined Hypolipidemia Due to Loss of Function Mutations of ANGPTL3. 214
Lung involvement in Niemann-Pick disease type C1: improvement with bronchoalveolar lavage 213
Plasma lipoproteins in rats with experimental biliary obstruction. II. An ultrastructural study. 213
Variable phenotypic expression of homozygous familial hypobetalipoproteinaemia due to novel APOB gene mutations 208
Characterization of three mutations of the low density lipoprotein receptor gene in Italian patients with familial hypercholesterolemia. 206
Pravastatin in heterozygous familial hypercholesterolemia: low-density lipoprotein (LDL) cholesterol-lowering effect and LDL receptor activity on skin fibroblastS. 204
Changes of the main isoform of human apolipoprotein A-I following incubation of plasma. 203
Homozygous familial hypercholesterolemia in Italy: Clinical and molecular features 202
Secretion of apoB- and apoA-I-containing lipoproteins by chick kidney 201
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). 200
β-thalassemia is a modifying factor of the clinical expression of familial hypercholesterolemia 199
Genetics and molecular biology: proprotein convertase subtilisin/kexin type 9 and LDL receptor--an intriguing story. 198
Heavy metals and experimental atherosclerosis. Effect of lead intoxication on rabbit plasma lipoproteins. 198
A large deletion in the LDL receptor gene--the cause of familial hypercholesterolemia in three Italian families: a study that dates back to the 17th century (FH-Pavia 198
Synthesis and secretion of B-100 and A-I apolipoproteins in response to the changes of intracellular cholesteryl ester content in chick liver 197
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. 197
Partial duplication of the EGF precursor homology domain of the LDL receptor protein causing familial hypercholesterolemia (FH-Salerno) 196
Cholesteryl Ester Storage Disease (CESD) due to novel mutations in the LIPA gene 192
Duplication of exons 13, 14 and 15 of the LDL-receptor gene in a patients with heterozygous familial hypercholesterolemia 192
Plasma and urinary lipids and lipoproteins during the development of nephrotic syndrome induced in the rat by puromycin aminonucleoside. 191
Secretion of lipoproteins, apolipoprotein A-I and apolipoprotein E by isolated and perfused liver of rat with experimental nephrotic syndrome. 189
Chemical and morphological changes of rat plasma lipoproteins after a prolonged administration of diets containing olive oil and cholesterol. 188
Experimental nephrotic syndrome in the rat induced by puromycin aminonucleoside: hepatic synthesis of lipoproteins and apolipoproteins. 186
Cholesterol synthesis in freshly isolated human leukocytes. 185
Changes in apolipoprotein A-I mRNA level in the liver of rats with experimental nephrotic syndrome 184
Synthesis and secretion of apolipoprotein A-I by chick skin. 184
Plasma lecithin: cholesterol acyltransferase activity in liver disease. 184
Plasma lipoproteins in rats with experimental biliary obstruction. I. A chemical study. 183
Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genes 181
The relation between plasma cholesterol and cholesterol synthesis in rats with experimental biliary obstruction. 181
The molecular basis of lecithin: Cholesterol acyltransferase deficiency syndromes: A comprehensive study of molecular and biochemical findings in 13 unrelated Italian families 180
The ultrastructure of rat plasma lipoproteins. 178
The complete sequence of chick apolipoprotein AI mRNA and its expression in the developing chick 177
Experimental nephrotic syndrome in the rat induced by puromycin aminonucleoside. Plasma and urinary lipoproteins 175
Totale 24.731
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Categoria #
all - tutte 121.348
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 121.348
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.934 0 0 0 0 0 267 432 341 138 349 257 150
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
2024/20256.147 196 52 118 406 1.129 968 592 340 534 191 712 909
2025/20266.188 788 548 973 1.144 1.925 810 0 0 0 0 0 0
Totale 30.118