CALANDRA BUONAURA, Sebastiano
 Distribuzione geografica
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Continente #
NA - Nord America 20.878
AS - Asia 8.896
EU - Europa 7.675
SA - Sud America 1.291
AF - Africa 180
Continente sconosciuto - Info sul continente non disponibili 167
OC - Oceania 17
Totale 39.104
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Nazione #
US - Stati Uniti d'America 20.480
SG - Singapore 3.240
GB - Regno Unito 2.573
CN - Cina 2.191
IT - Italia 1.727
BR - Brasile 990
HK - Hong Kong 983
VN - Vietnam 821
SE - Svezia 773
DE - Germania 562
BD - Bangladesh 453
FI - Finlandia 371
FR - Francia 352
UA - Ucraina 347
RU - Federazione Russa 335
KR - Corea 221
TR - Turchia 217
IN - India 207
CA - Canada 183
BG - Bulgaria 141
ID - Indonesia 118
NL - Olanda 113
AR - Argentina 96
MX - Messico 85
IE - Irlanda 72
IQ - Iraq 68
JP - Giappone 55
BE - Belgio 52
PK - Pakistan 51
PL - Polonia 50
ZA - Sudafrica 50
CO - Colombia 42
EC - Ecuador 41
AE - Emirati Arabi Uniti 40
CL - Cile 39
ES - Italia 39
CZ - Repubblica Ceca 27
AT - Austria 26
SA - Arabia Saudita 24
VE - Venezuela 24
KE - Kenya 22
CR - Costa Rica 21
JM - Giamaica 21
MA - Marocco 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
AU - Australia 15
PH - Filippine 15
BA - Bosnia-Erzegovina 14
JO - Giordania 14
TT - Trinidad e Tobago 14
PT - Portogallo 12
TW - Taiwan 12
OM - Oman 11
AZ - Azerbaigian 10
KZ - Kazakistan 10
NP - Nepal 10
TH - Thailandia 10
NI - Nicaragua 9
PR - Porto Rico 9
RO - Romania 9
SV - El Salvador 9
BH - Bahrain 8
BO - Bolivia 8
DO - Repubblica Dominicana 8
EU - Europa 8
IL - Israele 8
GT - Guatemala 7
AL - Albania 6
EE - Estonia 6
ET - Etiopia 6
HN - Honduras 6
KG - Kirghizistan 6
KW - Kuwait 6
SK - Slovacchia (Repubblica Slovacca) 6
DK - Danimarca 5
HU - Ungheria 5
LB - Libano 5
SC - Seychelles 5
GR - Grecia 4
HR - Croazia 4
SY - Repubblica araba siriana 4
XK - ???statistics.table.value.countryCode.XK??? 4
BB - Barbados 3
GE - Georgia 3
LK - Sri Lanka 3
NG - Nigeria 3
PS - Palestinian Territory 3
QA - Qatar 3
RS - Serbia 3
Totale 38.906
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Città #
Ashburn 2.436
Singapore 2.117
Southend 1.865
Fairfield 1.753
Santa Clara 1.694
Woodbridge 1.212
San Jose 1.205
Houston 1.010
Hong Kong 963
Hefei 769
Chandler 751
Jacksonville 748
Seattle 713
Wilmington 619
Ann Arbor 616
Council Bluffs 575
Cambridge 560
Nyköping 458
Dearborn 445
London 376
Beijing 342
Los Angeles 296
Ho Chi Minh City 272
Helsinki 253
Milan 234
New York 220
The Dalles 220
Seoul 218
Modena 209
Chicago 208
Hanoi 192
San Diego 158
Columbus 155
Princeton 148
Sofia 134
Reading 129
Rome 127
Buffalo 126
Dallas 120
Lauterbourg 118
Eugene 115
São Paulo 105
Moscow 104
Shanghai 97
Des Moines 90
Izmir 88
Grafing 82
Salt Lake City 79
Jakarta 78
Boardman 73
Dublin 70
Naples 61
Munich 59
Orem 57
Da Nang 56
Phoenix 55
Atlanta 54
Washington 52
Falls Church 49
Toronto 48
Rio de Janeiro 46
Tokyo 42
Brussels 41
Bologna 39
Bremen 38
Brooklyn 38
Elk Grove Village 38
Tampa 38
Montreal 37
Warsaw 36
Frankfurt am Main 34
Newark 32
North Bergen 29
Franklin 28
Mexico City 28
Redwood City 28
Belo Horizonte 27
Norwalk 27
Philadelphia 27
Guangzhou 26
Nuremberg 26
Santiago 26
Chennai 25
Turin 25
Baghdad 23
Manchester 23
Nanjing 23
Saint Augustine 23
Denver 22
Detroit 22
Haiphong 22
Johannesburg 22
San Francisco 22
San Mateo 22
St Louis 22
Boston 21
Miami 21
Brno 20
Kent 20
Miano 20
Totale 27.365
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Nome #
CASO CLINICO: QUANDO LA RISPOSTA ALLA DIETA IPOLIPIDEMIZZANTE DETERMINA LA DIAGNOSI 1.230
Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN) 545
Lysosomal lipase deficiency: Molecular characterization of eleven patients with Wolman or cholesteryl ester storage disease 419
Additive effect of mutations in LDLR and PCSK9 genes on the phenotype of familial hypercholesterolemia 412
A 'de novo' point mutation of the low-density lipoprotein receptor gene in an Italian subject with primary hypercholesterolemia 408
Hypertriglyceridaemia and low plasma HDL in a patient with apolipoprotein A-V deficiency due to a novel mutation in the APOA5 gene 402
Functional analysis of two novel splice site mutations of APOB gene in familial hypobetalipoproteinemia 393
Inherited apolipoprotein A-V deficiency in severe hypertriglyceridemia 382
Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in Italy 382
Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN study 374
Abnormal splicing of ABCA1 pre-mRNA in Tangier disease due to a IVS2+5G > C mutation in ABCA1 gene 373
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) 371
A novel deletion of BRCA1 gene that eliminates the ATG initiation codon without affecting the promoter region 371
Abnormal apolipoprotein B pre-mRNA splicing in patients with familial hypobetalipoproteinaemia 370
Novel mutations in SAR1B and MTTP genes in Tunisian children with chylomicron retention disease and abetalipoproteinemia. 367
Altered mRNA splicing in lipoprotein disorders 366
A novel homozygous mutation in CETP gene as a cause of CETP deficiency in a caucasian kindred 364
Clinical characteristics and plasma lipids in subjects with familial combined hypolipidemia: a pooled analysis. 357
Rearrangements of the ABCC6 gene in Italian patients with PXE 352
An apparent inconsistency in parent to offspring transmission ofpoint mutations of LDLR gene in familial hypercholesterolemia 345
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 344
Absence of apolipoprotein B-48 in the chick, Gallus domesticus 343
APOA5 and trigliceride metabolism, lesson from human APOA5 deficiency. 342
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. 342
Incidental finding of severe hypertriglyceridemia in children. Role of multiple rare variants in genes affecting plasma triglyceride. 342
A novel sequence variant in APOA5 gene found in patients with severe hypertriglyceridemia 339
MOLECULAR CHARACTERIZATION OF TWO PATIENTS WITH SEVERE LCAT DEFICIENCY 337
Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 gene 337
Pseudoxanthoma elasticum and familial hypercholesterolemia: A deleterious combination of cardiovascular risk factors 334
Impact of rare variants in autosomal dominant hypercholesterolemia causing genes. 332
Identification and characterization of novel loss of function mutations in ATP-binding cassette transporter A1 in patients with low plasma high-density lipoprotein cholesterol. 331
Molecular diagnosis of hypobetalipoproteinemia: an ENID Review 331
A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease 327
Hypobetalipoproteinemia with an apparently recessive inheritance due to a de novo mutation of apolipoprotein B 326
A novel mutation in the sterol 27-hydroxylase gene of a woman with autosomal recessive cerebrotendinous xanthomatosis. 322
Plasma and urine lipoproteins during the development of nephrotic syndrome induced in the rat by adriamycin. 322
Effect of ezetimibe coadministered with statins in genotype-confirmed heterozygous FH patients 321
Functional lecithin: Cholesterol acyltransferase Is not required for efficient atheroprotection in humans 321
Modulation of the synthesis of apolipoproteins in rat hepatoma cells. 320
Multiple abnormally spliced ABCA1 mRNAs caused by a novel splice site mutation of ABCA1 gene in a patient with Tangier disease. 319
Separation of the isoprotein forms of apoprotein A-I of rat, rabbit and human HDL by combined isoelectrofocusing and SDS-polyacrylamide gel electrophoresis. 318
Autosomal recessive hypercholesterolemia (ARH) and homozygous familial hypercholesterolemia (FH): A phenotypic comparison 313
A 3-day-old neonate with severe hypertriglyceridemia from novel mutations of the GPIHBP1 gene 312
Two novel rare variants of APOA5 gene found in subjects with severe hypertriglyceridemia. 310
Leucine 10 allelic variant in signal peptide of PCSK9 increases the LDL cholesterol-lowering effect of statins in patients with familial hypercholesterolaemia. 310
Preemptive liver transplantation in a child with familial hypercholesterolemia 307
Sequential expression during postnatal development of specific markers of junctional and free sarcoplasmic reticulum in chicken pectoralis muscle. 306
Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiency 305
Homozygous familial hypercholesterolemia in Italy: Clinical and molecular features 304
Molecular analysis of NPC1 and NPC2 gene in 34 Niemann-Pick C Italian Patients: Identification and structural modeling of novel mutations 302
Mutations in MTP gene in abeta- and hypobeta-lipoproteinemia 300
Effect of the desulfation of heparin on its anticoagulant and anti-proliferative activity 300
Severe HDL deficiency due to novel defects in the ABCA1 transporter 299
Cholesteryl Ester Storage Disease (CESD) due to novel mutations in the LIPA gene 297
Analysis of LDL receptor gene mutations in Italian patients with homozygous familial hypercholesterolemia 296
Familial HDL deficiency due to ABCA1 gene mutations with or without other genetic lipoprotein disorders 295
Isoforms of rat apolipoprotein A-I isolated from the lipoproteins of hepatic Golgi apparatus and plasma. 293
Cholesterol synthesis in isolated rat hepatocytes: effect of homologous and heterologous serum lipoproteins. 293
Variable phenotypic expression of homozygous familial hypobetalipoproteinaemia due to novel APOB gene mutations 288
Adult-onset Niemann-Pick type C disease: A clinical, neuroimaging, and molecular genetic study 287
Characterization of three mutations of the low density lipoprotein receptor gene in Italian patients with familial hypercholesterolemia. 284
A novel mutation of the apolipoprotein A-I gene in a family with familial combined hyperlipidemia 283
Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia 282
Genetic polymorphisms affecting the phenotypic expression of familial hypercholesterolemia 281
Quantitative polymerase chain reaction and microchip electrophoresis to detect major rearrangements of the low-density lipoprotein receptor gene causing familial hypercholesterolemia 279
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 277
Apolipoprotein B-100 production and cholesteryl ester content in the liver of developing chick 276
Effect of a thromboxane A2 synthase inhibitor on the dyslipoproteinemia of an inbred rat strain with spontaneous age-related nephrotic syndrome 275
Fatty liver in heterozygous hypobetalipoproteinemia caused by a novel truncated form of apolipoprotein B 272
Severe hypertriglyceridemia in a newborn with monogenic lipoprotein lipase deficiency: an unconventional therapeutic approach with exchange transfusion. 272
Pravastatin in heterozygous familial hypercholesterolemia: low-density lipoprotein (LDL) cholesterol-lowering effect and LDL receptor activity on skin fibroblastS. 270
Mechanisms and genetic determinants regulating sterol absorption, circulating LDL levels, and sterol elimination: implications for classification and disease risk. 266
Plasma lipoproteins in rats with experimental biliary obstruction. II. An ultrastructural study. 265
Characterization of Three Kindreds with Familial Combined Hypolipidemia Due to Loss of Function Mutations of ANGPTL3. 263
Evaluation of the performance of Dutch Lipid Clinic Network score in an Italian FH population: The LIPIGEN study 262
Secretion of lipoproteins, apolipoprotein A-I and apolipoprotein E by isolated and perfused liver of rat with experimental nephrotic syndrome. 260
Changes of the main isoform of human apolipoprotein A-I following incubation of plasma. 259
β-thalassemia is a modifying factor of the clinical expression of familial hypercholesterolemia 257
Experimental nephrotic syndrome in the rat induced by puromycin aminonucleoside: hepatic synthesis of lipoproteins and apolipoproteins. 257
The molecular basis of lecithin: Cholesterol acyltransferase deficiency syndromes: A comprehensive study of molecular and biochemical findings in 13 unrelated Italian families 253
Worldwide experience of homozygous familial hypercholesterolaemia: retrospective cohort study 253
Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genes 252
Partial duplication of the EGF precursor homology domain of the LDL receptor protein causing familial hypercholesterolemia (FH-Salerno) 252
Genetics and molecular biology: proprotein convertase subtilisin/kexin type 9 and LDL receptor--an intriguing story. 251
Heavy metals and experimental atherosclerosis. Effect of lead intoxication on rabbit plasma lipoproteins. 250
Secretion of apoB- and apoA-I-containing lipoproteins by chick kidney 249
Duplication of exons 13, 14 and 15 of the LDL-receptor gene in a patients with heterozygous familial hypercholesterolemia 248
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). 246
Lung involvement in Niemann-Pick disease type C1: improvement with bronchoalveolar lavage 245
Synthesis and secretion of apolipoprotein A-I by chick skin. 245
Synthesis and secretion of B-100 and A-I apolipoproteins in response to the changes of intracellular cholesteryl ester content in chick liver 244
Plasma lecithin: cholesterol acyltransferase activity in liver disease. 241
Plasma and urinary lipids and lipoproteins during the development of nephrotic syndrome induced in the rat by puromycin aminonucleoside. 241
In vitro functional characterization of splicing variants of the APOB gene found in familial hypobetalipoproteinemia 240
Novel mutations of SAR1B gene in four children with chylomicron retention disease 238
A man with low cholesterol and weakness of the lower limbs. 236
Angiopoietin-like protein 3 (ANGPTL3) deficiency and familial combined hypolipidemia 234
The type of LDLR gene mutationpredicts cardiovascular risk in children with familial hypercholesterolemia. 231
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. 231
Experimental nephrotic syndrome in the rat induced by puromycin aminonucleoside. Plasma and urinary lipoproteins 230
Totale 31.500
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Categoria #
all - tutte 149.446
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 149.446
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.944 0 0 0 155 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
2026/20273.256 528 675 892 1.161 0 0 0 0 0 0 0 0
Totale 39.104