TARUGI, Patrizia Maria
 Distribuzione geografica
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Continente #
NA - Nord America 17.713
AS - Asia 7.974
EU - Europa 7.311
SA - Sud America 1.041
Continente sconosciuto - Info sul continente non disponibili 204
AF - Africa 150
OC - Oceania 27
Totale 34.420
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Nazione #
US - Stati Uniti d'America 17.406
SG - Singapore 2.509
GB - Regno Unito 2.446
CN - Cina 2.075
IT - Italia 1.729
HK - Hong Kong 1.006
BR - Brasile 792
VN - Vietnam 782
SE - Svezia 730
DE - Germania 537
BD - Bangladesh 410
FI - Finlandia 395
UA - Ucraina 337
RU - Federazione Russa 310
FR - Francia 280
KR - Corea 223
TR - Turchia 194
IN - India 193
BG - Bulgaria 146
CA - Canada 137
ID - Indonesia 118
NL - Olanda 95
MX - Messico 80
AR - Argentina 75
IQ - Iraq 65
JP - Giappone 60
PK - Pakistan 57
BE - Belgio 51
AE - Emirati Arabi Uniti 42
ES - Italia 40
CO - Colombia 38
ZA - Sudafrica 34
EC - Ecuador 31
IE - Irlanda 31
CL - Cile 26
PL - Polonia 26
AU - Australia 25
VE - Venezuela 25
AT - Austria 24
UZ - Uzbekistan 23
KE - Kenya 21
MY - Malesia 21
CH - Svizzera 19
SA - Arabia Saudita 19
PH - Filippine 18
CR - Costa Rica 17
DZ - Algeria 17
EG - Egitto 17
JM - Giamaica 17
CZ - Repubblica Ceca 16
PE - Perù 16
TN - Tunisia 16
TW - Taiwan 16
EU - Europa 15
IR - Iran 15
KZ - Kazakistan 15
LT - Lituania 15
NP - Nepal 15
MA - Marocco 14
PY - Paraguay 14
BA - Bosnia-Erzegovina 13
BZ - Belize 13
PT - Portogallo 12
UY - Uruguay 12
JO - Giordania 11
BO - Bolivia 10
ET - Etiopia 10
HU - Ungheria 10
IL - Israele 10
TH - Thailandia 10
AZ - Azerbaigian 9
AL - Albania 8
DO - Repubblica Dominicana 8
TT - Trinidad e Tobago 8
BH - Bahrain 7
GT - Guatemala 7
OM - Oman 7
LK - Sri Lanka 6
PS - Palestinian Territory 6
DK - Danimarca 5
GE - Georgia 5
GR - Grecia 5
HN - Honduras 5
KG - Kirghizistan 5
KW - Kuwait 5
MD - Moldavia 5
SI - Slovenia 5
PR - Porto Rico 4
QA - Qatar 4
RO - Romania 4
SC - Seychelles 4
SK - Slovacchia (Repubblica Slovacca) 4
SV - El Salvador 4
BB - Barbados 3
EE - Estonia 3
KH - Cambogia 3
NI - Nicaragua 3
BY - Bielorussia 2
CG - Congo 2
GY - Guiana 2
Totale 34.195
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Città #
Southend 1.766
Ashburn 1.738
Fairfield 1.667
Singapore 1.620
Santa Clara 1.563
Woodbridge 1.149
Hong Kong 982
Houston 901
San Jose 871
Jacksonville 707
Hefei 700
Chandler 664
Seattle 640
Wilmington 616
Ann Arbor 522
Cambridge 490
Dearborn 403
Nyköping 396
Council Bluffs 391
Beijing 367
London 353
Helsinki 282
Los Angeles 275
Modena 253
Ho Chi Minh City 243
Chicago 212
Seoul 209
The Dalles 209
Milan 203
New York 191
Hanoi 175
San Diego 152
Princeton 149
Sofia 139
Columbus 132
Buffalo 130
Rome 113
Dallas 110
Eugene 110
Lauterbourg 107
Reading 101
Moscow 96
Salt Lake City 89
Shanghai 87
Jakarta 81
Izmir 74
Des Moines 69
São Paulo 66
Falls Church 61
Boardman 54
Naples 52
Grafing 51
Da Nang 46
Orem 46
Elk Grove Village 45
Munich 43
Frankfurt am Main 40
Bremen 39
Rio de Janeiro 37
Tokyo 36
Brussels 35
Toronto 35
Atlanta 34
Phoenix 34
Mexico City 33
Tampa 31
Nanjing 29
Redwood City 29
Dublin 28
Bologna 26
Brooklyn 26
Detroit 26
Miano 26
Haiphong 24
Baghdad 23
Chennai 23
Guangzhou 23
Kunming 23
Verona 23
Nuremberg 22
Turin 22
Montreal 21
Norwalk 21
Tashkent 21
Belo Horizonte 20
Palermo 19
San Mateo 19
Florence 18
Kent 18
Lahore 18
Miami 18
Padova 18
Paris 18
Philadelphia 18
San Francisco 18
Biên Hòa 17
Kilburn 17
Wuhan 17
Charlotte 16
Manchester 16
Totale 24.036
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Nome #
CASO CLINICO: QUANDO LA RISPOSTA ALLA DIETA IPOLIPIDEMIZZANTE DETERMINA LA DIAGNOSI 1.208
Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN) 534
Low-density lipoprotein (LDL) receptor/transferrin fusion protein: in vivoproduction and functional evaluation as a potential therapeutic tool forlowering plasma LDL cholesterol. 498
Implementation of an NGS-based workflow for BRCA1 and BRCA2 mutation screening 473
A novel loss of function mutation of PCSK9 gene in white subjects with low-plasma low-density lipoprotein cholesterol 407
Additive effect of mutations in LDLR and PCSK9 genes on the phenotype of familial hypercholesterolemia 386
Functional analysis of two novel splice site mutations of APOB gene in familial hypobetalipoproteinemia 378
Inherited apolipoprotein A-V deficiency in severe hypertriglyceridemia 373
Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN study 368
ABCC6 mutations in Italian families affected by pseudoxanthoma elasticum(PXE). 368
Abnormal splicing of ABCA1 pre-mRNA in Tangier disease due to a IVS2+5G > C mutation in ABCA1 gene 361
Abnormal apolipoprotein B pre-mRNA splicing in patients with familial hypobetalipoproteinaemia 360
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) 358
A novel homozygous mutation in CETP gene as a cause of CETP deficiency in a caucasian kindred 355
Altered mRNA splicing in lipoprotein disorders 355
Novel mutations in SAR1B and MTTP genes in Tunisian children with chylomicron retention disease and abetalipoproteinemia. 351
Clinical characteristics and plasma lipids in subjects with familial combined hypolipidemia: a pooled analysis. 348
The Janus-faced manifestations of homozygous familial hypobetalipoproteinemia due to apolipoprotein B truncations 342
Incidental finding of severe hypertriglyceridemia in children. Role of multiple rare variants in genes affecting plasma triglyceride. 332
Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 gene 331
Threshold Effects of Circulating Angiopoietin-Like 3 Levels on Plasma Lipoproteins. 328
Absence of apolipoprotein B-48 in the chick, Gallus domesticus 327
A novel sequence variant in APOA5 gene found in patients with severe hypertriglyceridemia 327
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. 326
Pseudoxanthoma elasticum and familial hypercholesterolemia: A deleterious combination of cardiovascular risk factors 321
Impact of rare variants in autosomal dominant hypercholesterolemia causing genes. 317
Identification of patients with abetalipoproteinemia and homozygous familial hypobetalipoproteinemia in Tunisia 316
APOA5 and trigliceride metabolism, lesson from human APOA5 deficiency. 316
Association between familial hypobetalipoproteinemia and the risk of diabetes. Is this the other side of the cholesterol–diabetes connection? A systematic review of literature 316
Molecular diagnosis of hypobetalipoproteinemia: an ENID Review 316
Plasma and urine lipoproteins during the development of nephrotic syndrome induced in the rat by adriamycin. 314
Structure-function analyses of microsomal triglyceride transfer protein missense mutations in abetalipoproteinemia and hypobetalipoproteinemia subjects 307
Hypobetalipoproteinemia with an apparently recessive inheritance due to a de novo mutation of apolipoprotein B 306
Homozygous familial hypobetalipoproteinemia: A Turkish case carrying a missense mutation in apolipoprotein B 305
Improvement in the high-performance liquid chromatography malondialdehyde level determination in normal human plasma 302
DIAGNOSI MOLECOLARE DELLE IPERTRIGLICERIDEMIE PRIMITIVE ATTRAVERSO “NGS” (NEXT GENERATION SEQUENCING) 302
Novel mutations in the GPIHBP1 gene identified in 2 patients with recurrent acute pancreatitis 301
Separation of the isoprotein forms of apoprotein A-I of rat, rabbit and human HDL by combined isoelectrofocusing and SDS-polyacrylamide gel electrophoresis. 297
Sequential expression during postnatal development of specific markers of junctional and free sarcoplasmic reticulum in chicken pectoralis muscle. 292
Homozygous familial hypercholesterolemia in Italy: Clinical and molecular features 292
Mutations in MTP gene in abeta- and hypobeta-lipoproteinemia 288
Molecular analysis of NPC1 and NPC2 gene in 34 Niemann-Pick C Italian Patients: Identification and structural modeling of novel mutations 282
Familial HDL deficiency due to ABCA1 gene mutations with or without other genetic lipoprotein disorders 280
Pediatric gallstone disease in familial hypobetalipoproteinemia 279
Isoforms of rat apolipoprotein A-I isolated from the lipoproteins of hepatic Golgi apparatus and plasma. 279
Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia 279
Clinical and biochemical characteristics of individuals with low cholesterol syndromes: A comparison between familial hypobetalipoproteinemia and familial combined hypolipidemia. 277
Adult-onset Niemann-Pick type C disease: A clinical, neuroimaging, and molecular genetic study 277
Cholesterol synthesis in isolated rat hepatocytes: effect of homologous and heterologous serum lipoproteins. 271
Apolipoprotein B-100 production and cholesteryl ester content in the liver of developing chick 270
Variable phenotypic expression of homozygous familial hypobetalipoproteinaemia due to novel APOB gene mutations 269
Effect of a thromboxane A2 synthase inhibitor on the dyslipoproteinemia of an inbred rat strain with spontaneous age-related nephrotic syndrome 268
Flow-mediated dilation, carotid wall thickness and HDL function in subjects with hyperalphalipoproteinemia 266
Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin:cholesterol acyltransferase deficiency and hypobetalipoproteinemia. 264
A novel APOB mutation identified by exome sequencing cosegregates with steatosis, liver cancer, and hypocholesterolemia. 263
A 54-year-old diabetic man with low serum cholesterol. 263
Fatty liver in heterozygous hypobetalipoproteinemia caused by a novel truncated form of apolipoprotein B 261
Plasma non-cholesterol sterols in primary hypobetalipoproteinemia. 259
Mechanisms and genetic determinants regulating sterol absorption, circulating LDL levels, and sterol elimination: implications for classification and disease risk. 259
Evaluation of the performance of Dutch Lipid Clinic Network score in an Italian FH population: The LIPIGEN study 256
Novel mutations of CETP gene in Italian subjects with hyeralphalipoproteinemia 253
Characterization of Three Kindreds with Familial Combined Hypolipidemia Due to Loss of Function Mutations of ANGPTL3. 253
PCSK9 dominant negative mutant results in increased LDL catabolic rate and familial hypobetalipoproteinemia 252
Influence of chondroitin sulfate charge density, sulfate group position, and molecular mass on Cu2+-mediated oxidation of human low-density lipoproteins: Effect of normal human plasma-derived chondroitin sulfate 249
Phenotypic variability in 4 homozygous familial hypercholesterolemia siblings compound heterozygous for LDLR mutations 247
Microsomal Triglyceride Transfer Protein Transfers and Determines Plasma Concentrations of Ceramide and Sphingomyelin but Not Glycosylceramide 246
Prevalence of ANGPTL3 and APOB Gene Mutations in Subjects With Combined Hypolipidemia. 245
β-thalassemia is a modifying factor of the clinical expression of familial hypercholesterolemia 244
Secretion of apoB- and apoA-I-containing lipoproteins by chick kidney 241
The C-terminal domain of apolipoprotein A-I is involved in ABCA1-driven phospholipid and cholesterol efflux 241
Heavy metals and experimental atherosclerosis. Effect of lead intoxication on rabbit plasma lipoproteins. 241
Worldwide experience of homozygous familial hypercholesterolaemia: retrospective cohort study 239
Lung involvement in Niemann-Pick disease type C1: improvement with bronchoalveolar lavage 238
Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genes 238
Genetics and molecular biology: proprotein convertase subtilisin/kexin type 9 and LDL receptor--an intriguing story. 238
Nonsynonymous mutations within APOB in human familial hypobetalipoproteinemia: evidence for feedback inhibition of lipogenesis and postendoplasmic reticulum degradation of apolipoprotein B. 238
The protective effect on Cu2+- and AAPH-mediated oxidation of human low-density lipoproteins depends on glycosaminoglycan structure 234
Microsomal triglyceride transfer protein gene mutations in Turkish children: A novel mutation and clinical follow up. 233
In vitro functional characterization of splicing variants of the APOB gene found in familial hypobetalipoproteinemia 231
Synthesis and secretion of apolipoprotein A-I by chick skin. 229
Characterization of a mutant form of human apolipoprotein B (Thr26_Tyr27del) associated with familial hypobetalipoproteinemia 229
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. 226
Angiopoietin-like protein 3 (ANGPTL3) deficiency and familial combined hypolipidemia 224
Changes in apolipoprotein A-I mRNA level in the liver of rats with experimental nephrotic syndrome 223
Dyslipoproteinemia in an inbred rat strain with spontaneous chronic progressive nephrotic syndrome 222
Synthesis and secretion of B-100 and A-I apolipoproteins in response to the changes of intracellular cholesteryl ester content in chick liver 220
Novel Abetalipoproteinemia Missense Mutation Highlights the Importance of the N-Terminal β-Barrel in Microsomal Triglyceride Transfer Protein Function 219
Exome Sequencing in Suspected Monogenic Dyslipidemias 218
The complete sequence of chick apolipoprotein AI mRNA and its expression in the developing chick 218
Cholesterol synthesis in freshly isolated human leukocytes. 217
Phenotypic expression of heterozygous familial hypobetalipoproteinemia in three kindreds with novel mutations of apolipoprotein B gene 217
Novel mutations of SAR1B gene in four children with chylomicron retention disease 215
Familial hypobetalipoproteinemia: analysis of three Spanish cases with two new mutations in the APOB gene. 214
Chemical and morphological changes of rat plasma lipoproteins after a prolonged administration of diets containing olive oil and cholesterol. 213
Recurrent mutations of the apolipoprotein A-I gene in three kindreds with severe HDL deficiency 213
Hypobetalipoproteinemia: genetics, biochemistry, and clinical spectrum. 210
Mutation screening of the Otop1 gene in familial benign positional paroxysmal vertigo 209
Dyslipidemia in rats with hypothyroidism 208
Hypercholesterolemia in Childhood: How the Response to Diet could Lead to Diagnosis. Lesson from a Case-Report 207
Abetalipoproteinemia in an infant with severe clinical phenotype and a novel mutation 205
Totale 29.281
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Categoria #
all - tutte 136.005
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 136.005
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20222.138 0 0 219 191 56 213 151 106 282 215 454 251
2022/20232.204 257 218 159 179 252 351 40 196 294 46 131 81
2023/20241.654 73 83 149 147 301 148 131 187 74 120 49 192
2024/20255.494 184 50 118 376 1.049 849 444 333 501 241 612 737
2025/202610.645 726 466 932 1.027 1.527 741 1.346 553 951 1.019 749 608
2026/20271.244 449 630 165 0 0 0 0 0 0 0 0 0
Totale 34.420