CALANDRA BUONAURA, Sebastiano
 Distribuzione geografica
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Continente #
NA - Nord America 18.324
AS - Asia 8.826
EU - Europa 7.535
SA - Sud America 1.262
AF - Africa 176
OC - Oceania 15
Continente sconosciuto - Info sul continente non disponibili 13
Totale 36.151
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Nazione #
US - Stati Uniti d'America 18.033
SG - Singapore 3.228
GB - Regno Unito 2.552
CN - Cina 2.176
IT - Italia 1.637
HK - Hong Kong 975
BR - Brasile 968
VN - Vietnam 820
SE - Svezia 773
DE - Germania 560
BD - Bangladesh 434
FI - Finlandia 371
FR - Francia 348
UA - Ucraina 342
RU - Federazione Russa 329
KR - Corea 221
TR - Turchia 215
IN - India 205
BG - Bulgaria 141
CA - Canada 128
ID - Indonesia 114
NL - Olanda 110
AR - Argentina 95
MX - Messico 83
IE - Irlanda 72
IQ - Iraq 68
JP - Giappone 54
BE - Belgio 52
ZA - Sudafrica 50
PK - Pakistan 49
PL - Polonia 47
EC - Ecuador 41
AE - Emirati Arabi Uniti 39
CL - Cile 39
CO - Colombia 39
ES - Italia 39
AT - Austria 26
CZ - Repubblica Ceca 26
SA - Arabia Saudita 23
KE - Kenya 22
MA - Marocco 21
VE - Venezuela 21
EG - Egitto 20
TN - Tunisia 20
UZ - Uzbekistan 20
MY - Malesia 19
PY - Paraguay 18
BZ - Belize 17
CH - Svizzera 17
DZ - Algeria 17
IR - Iran 17
LT - Lituania 16
PE - Perù 16
UY - Uruguay 16
JO - Giordania 14
AU - Australia 13
BA - Bosnia-Erzegovina 13
PH - Filippine 13
JM - Giamaica 12
PT - Portogallo 12
TW - Taiwan 12
OM - Oman 11
AZ - Azerbaigian 10
CR - Costa Rica 10
KZ - Kazakistan 10
NP - Nepal 10
TH - Thailandia 10
RO - Romania 9
BH - Bahrain 8
BO - Bolivia 8
DO - Repubblica Dominicana 8
EU - Europa 8
IL - Israele 8
TT - Trinidad e Tobago 7
AL - Albania 6
ET - Etiopia 6
KG - Kirghizistan 6
KW - Kuwait 6
SK - Slovacchia (Repubblica Slovacca) 6
DK - Danimarca 5
HU - Ungheria 5
LB - Libano 5
PR - Porto Rico 5
GR - Grecia 4
GT - Guatemala 4
HN - Honduras 4
SV - El Salvador 4
SY - Repubblica araba siriana 4
XK - ???statistics.table.value.countryCode.XK??? 4
BB - Barbados 3
EE - Estonia 3
GE - Georgia 3
HR - Croazia 3
LK - Sri Lanka 3
NG - Nigeria 3
PS - Palestinian Territory 3
QA - Qatar 3
RS - Serbia 3
SN - Senegal 3
AO - Angola 2
Totale 36.111
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Città #
Singapore 2.111
Southend 1.865
Ashburn 1.850
Fairfield 1.752
Santa Clara 1.660
Woodbridge 1.212
Houston 1.005
Hong Kong 957
San Jose 890
Hefei 769
Chandler 751
Jacksonville 745
Seattle 700
Wilmington 615
Ann Arbor 610
Cambridge 560
Nyköping 458
Dearborn 445
London 372
Beijing 332
Ho Chi Minh City 271
Los Angeles 271
Council Bluffs 269
Helsinki 253
Seoul 218
The Dalles 216
Modena 209
Milan 206
Chicago 198
New York 197
Hanoi 192
San Diego 153
Princeton 148
Sofia 134
Reading 129
Lauterbourg 118
Rome 116
Buffalo 115
Eugene 115
Moscow 104
Shanghai 96
Dallas 94
São Paulo 91
Des Moines 90
Izmir 88
Columbus 87
Grafing 82
Salt Lake City 79
Jakarta 78
Dublin 70
Munich 59
Naples 59
Da Nang 56
Orem 54
Falls Church 49
Rio de Janeiro 45
Boardman 44
Brussels 41
Tokyo 41
Atlanta 40
Bologna 38
Bremen 38
Elk Grove Village 38
Tampa 38
Frankfurt am Main 33
Toronto 33
Warsaw 33
Mexico City 28
Phoenix 28
Redwood City 28
Belo Horizonte 27
Montreal 27
Norwalk 27
Brooklyn 26
Guangzhou 26
Nuremberg 26
Santiago 26
Chennai 25
Turin 24
Baghdad 23
Nanjing 23
Haiphong 22
Johannesburg 22
San Mateo 22
Detroit 21
San Francisco 21
Brno 20
Kent 20
Miano 20
St Louis 20
Boston 19
Manchester 19
Newark 19
Palermo 19
Poplar 19
Kunming 18
Tashkent 18
Verona 18
Amsterdam 17
Augusta 17
Totale 25.620
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Nome #
CASO CLINICO: QUANDO LA RISPOSTA ALLA DIETA IPOLIPIDEMIZZANTE DETERMINA LA DIAGNOSI 1.190
Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN) 531
Lysosomal lipase deficiency: Molecular characterization of eleven patients with Wolman or cholesteryl ester storage disease 406
A 'de novo' point mutation of the low-density lipoprotein receptor gene in an Italian subject with primary hypercholesterolemia 386
Additive effect of mutations in LDLR and PCSK9 genes on the phenotype of familial hypercholesterolemia 378
Functional analysis of two novel splice site mutations of APOB gene in familial hypobetalipoproteinemia 374
Inherited apolipoprotein A-V deficiency in severe hypertriglyceridemia 367
Hypertriglyceridaemia and low plasma HDL in a patient with apolipoprotein A-V deficiency due to a novel mutation in the APOA5 gene 366
Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN study 361
A novel deletion of BRCA1 gene that eliminates the ATG initiation codon without affecting the promoter region 357
Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in Italy 357
Abnormal splicing of ABCA1 pre-mRNA in Tangier disease due to a IVS2+5G > C mutation in ABCA1 gene 356
Abnormal apolipoprotein B pre-mRNA splicing in patients with familial hypobetalipoproteinaemia 354
Altered mRNA splicing in lipoprotein disorders 351
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) 350
A novel homozygous mutation in CETP gene as a cause of CETP deficiency in a caucasian kindred 350
Novel mutations in SAR1B and MTTP genes in Tunisian children with chylomicron retention disease and abetalipoproteinemia. 346
Clinical characteristics and plasma lipids in subjects with familial combined hypolipidemia: a pooled analysis. 340
An apparent inconsistency in parent to offspring transmission ofpoint mutations of LDLR gene in familial hypercholesterolemia 333
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 328
Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 gene 327
Incidental finding of severe hypertriglyceridemia in children. Role of multiple rare variants in genes affecting plasma triglyceride. 327
A novel sequence variant in APOA5 gene found in patients with severe hypertriglyceridemia 323
MOLECULAR CHARACTERIZATION OF TWO PATIENTS WITH SEVERE LCAT DEFICIENCY 320
Identification and characterization of novel loss of function mutations in ATP-binding cassette transporter A1 in patients with low plasma high-density lipoprotein cholesterol. 319
Absence of apolipoprotein B-48 in the chick, Gallus domesticus 319
Pseudoxanthoma elasticum and familial hypercholesterolemia: A deleterious combination of cardiovascular risk factors 317
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. 317
Impact of rare variants in autosomal dominant hypercholesterolemia causing genes. 312
APOA5 and trigliceride metabolism, lesson from human APOA5 deficiency. 309
A novel mutation in the sterol 27-hydroxylase gene of a woman with autosomal recessive cerebrotendinous xanthomatosis. 306
Effect of ezetimibe coadministered with statins in genotype-confirmed heterozygous FH patients 303
Plasma and urine lipoproteins during the development of nephrotic syndrome induced in the rat by adriamycin. 303
Multiple abnormally spliced ABCA1 mRNAs caused by a novel splice site mutation of ABCA1 gene in a patient with Tangier disease. 302
A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease 302
Hypobetalipoproteinemia with an apparently recessive inheritance due to a de novo mutation of apolipoprotein B 299
Functional lecithin: Cholesterol acyltransferase Is not required for efficient atheroprotection in humans 298
Two novel rare variants of APOA5 gene found in subjects with severe hypertriglyceridemia. 294
Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiency 293
Preemptive liver transplantation in a child with familial hypercholesterolemia 291
Modulation of the synthesis of apolipoproteins in rat hepatoma cells. 289
Leucine 10 allelic variant in signal peptide of PCSK9 increases the LDL cholesterol-lowering effect of statins in patients with familial hypercholesterolaemia. 289
Separation of the isoprotein forms of apoprotein A-I of rat, rabbit and human HDL by combined isoelectrofocusing and SDS-polyacrylamide gel electrophoresis. 287
Molecular diagnosis of hypobetalipoproteinemia: an ENID Review 286
Autosomal recessive hypercholesterolemia (ARH) and homozygous familial hypercholesterolemia (FH): A phenotypic comparison 286
Severe HDL deficiency due to novel defects in the ABCA1 transporter 285
Sequential expression during postnatal development of specific markers of junctional and free sarcoplasmic reticulum in chicken pectoralis muscle. 283
Mutations in MTP gene in abeta- and hypobeta-lipoproteinemia 283
A 3-day-old neonate with severe hypertriglyceridemia from novel mutations of the GPIHBP1 gene 283
Rearrangements of the ABCC6 gene in Italian patients with PXE 280
Effect of the desulfation of heparin on its anticoagulant and anti-proliferative activity 280
Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia 277
Homozygous familial hypercholesterolemia in Italy: Clinical and molecular features 276
Isoforms of rat apolipoprotein A-I isolated from the lipoproteins of hepatic Golgi apparatus and plasma. 275
Molecular analysis of NPC1 and NPC2 gene in 34 Niemann-Pick C Italian Patients: Identification and structural modeling of novel mutations 275
Familial HDL deficiency due to ABCA1 gene mutations with or without other genetic lipoprotein disorders 275
Analysis of LDL receptor gene mutations in Italian patients with homozygous familial hypercholesterolemia 271
Adult-onset Niemann-Pick type C disease: A clinical, neuroimaging, and molecular genetic study 271
A novel mutation of the apolipoprotein A-I gene in a family with familial combined hyperlipidemia 269
Genetic polymorphisms affecting the phenotypic expression of familial hypercholesterolemia 268
Apolipoprotein B-100 production and cholesteryl ester content in the liver of developing chick 266
Cholesteryl Ester Storage Disease (CESD) due to novel mutations in the LIPA gene 265
Effect of a thromboxane A2 synthase inhibitor on the dyslipoproteinemia of an inbred rat strain with spontaneous age-related nephrotic syndrome 264
Variable phenotypic expression of homozygous familial hypobetalipoproteinaemia due to novel APOB gene mutations 263
Quantitative polymerase chain reaction and microchip electrophoresis to detect major rearrangements of the low-density lipoprotein receptor gene causing familial hypercholesterolemia 262
Cholesterol synthesis in isolated rat hepatocytes: effect of homologous and heterologous serum lipoproteins. 262
Characterization of three mutations of the low density lipoprotein receptor gene in Italian patients with familial hypercholesterolemia. 256
Mechanisms and genetic determinants regulating sterol absorption, circulating LDL levels, and sterol elimination: implications for classification and disease risk. 255
Fatty liver in heterozygous hypobetalipoproteinemia caused by a novel truncated form of apolipoprotein B 253
Evaluation of the performance of Dutch Lipid Clinic Network score in an Italian FH population: The LIPIGEN study 252
Characterization of Three Kindreds with Familial Combined Hypolipidemia Due to Loss of Function Mutations of ANGPTL3. 249
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 248
Changes of the main isoform of human apolipoprotein A-I following incubation of plasma. 244
Pravastatin in heterozygous familial hypercholesterolemia: low-density lipoprotein (LDL) cholesterol-lowering effect and LDL receptor activity on skin fibroblastS. 243
Severe hypertriglyceridemia in a newborn with monogenic lipoprotein lipase deficiency: an unconventional therapeutic approach with exchange transfusion. 242
β-thalassemia is a modifying factor of the clinical expression of familial hypercholesterolemia 241
Secretion of apoB- and apoA-I-containing lipoproteins by chick kidney 239
Partial duplication of the EGF precursor homology domain of the LDL receptor protein causing familial hypercholesterolemia (FH-Salerno) 239
Plasma lipoproteins in rats with experimental biliary obstruction. II. An ultrastructural study. 237
Lung involvement in Niemann-Pick disease type C1: improvement with bronchoalveolar lavage 236
Genetics and molecular biology: proprotein convertase subtilisin/kexin type 9 and LDL receptor--an intriguing story. 234
Heavy metals and experimental atherosclerosis. Effect of lead intoxication on rabbit plasma lipoproteins. 234
Duplication of exons 13, 14 and 15 of the LDL-receptor gene in a patients with heterozygous familial hypercholesterolemia 234
Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genes 231
Worldwide experience of homozygous familial hypercholesterolaemia: retrospective cohort study 231
Secretion of lipoproteins, apolipoprotein A-I and apolipoprotein E by isolated and perfused liver of rat with experimental nephrotic syndrome. 230
Experimental nephrotic syndrome in the rat induced by puromycin aminonucleoside: hepatic synthesis of lipoproteins and apolipoproteins. 226
Plasma and urinary lipids and lipoproteins during the development of nephrotic syndrome induced in the rat by puromycin aminonucleoside. 226
Synthesis and secretion of apolipoprotein A-I by chick skin. 225
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). 221
The molecular basis of lecithin: Cholesterol acyltransferase deficiency syndromes: A comprehensive study of molecular and biochemical findings in 13 unrelated Italian families 220
Angiopoietin-like protein 3 (ANGPTL3) deficiency and familial combined hypolipidemia 220
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. 219
Changes in apolipoprotein A-I mRNA level in the liver of rats with experimental nephrotic syndrome 218
Synthesis and secretion of B-100 and A-I apolipoproteins in response to the changes of intracellular cholesteryl ester content in chick liver 217
Plasma lecithin: cholesterol acyltransferase activity in liver disease. 217
Cholesterol synthesis in freshly isolated human leukocytes. 213
The complete sequence of chick apolipoprotein AI mRNA and its expression in the developing chick 213
Phenotypic expression of heterozygous familial hypobetalipoproteinemia in three kindreds with novel mutations of apolipoprotein B gene 211
Recurrent mutations of the apolipoprotein A-I gene in three kindreds with severe HDL deficiency 209
Totale 29.415
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Categoria #
all - tutte 138.786
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 138.786
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2025/202611.918 788 548 973 1.144 1.925 810 1.520 595 993 1.195 758 669
2026/2027457 457 0 0 0 0 0 0 0 0 0 0 0
Totale 36.305