RABACCHI, CLAUDIO
 Distribuzione geografica
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Continente #
NA - Nord America 4.237
EU - Europa 2.549
AS - Asia 1.928
SA - Sud America 309
AF - Africa 37
Continente sconosciuto - Info sul continente non disponibili 9
OC - Oceania 5
Totale 9.074
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Nazione #
US - Stati Uniti d'America 4.169
IT - Italia 1.048
SG - Singapore 679
CN - Cina 440
GB - Regno Unito 408
SE - Svezia 264
HK - Hong Kong 251
VN - Vietnam 230
BR - Brasile 213
DE - Germania 188
RU - Federazione Russa 123
FR - Francia 106
FI - Finlandia 101
IN - India 58
UA - Ucraina 54
NL - Olanda 53
KR - Corea 47
IE - Irlanda 41
TR - Turchia 38
BG - Bulgaria 34
ID - Indonesia 34
AR - Argentina 33
CL - Cile 29
CA - Canada 28
BD - Bangladesh 27
MX - Messico 25
IQ - Iraq 21
BE - Belgio 18
PK - Pakistan 18
CH - Svizzera 15
ES - Italia 15
PL - Polonia 14
JP - Giappone 12
LT - Lituania 12
ZA - Sudafrica 12
AE - Emirati Arabi Uniti 10
CZ - Repubblica Ceca 10
AT - Austria 9
CO - Colombia 9
SA - Arabia Saudita 8
BA - Bosnia-Erzegovina 7
MA - Marocco 7
MY - Malesia 7
EC - Ecuador 6
PY - Paraguay 6
AU - Australia 5
EU - Europa 5
SI - Slovenia 5
UZ - Uzbekistan 5
AZ - Azerbaigian 4
DK - Danimarca 4
EG - Egitto 4
KE - Kenya 4
KZ - Kazakistan 4
NP - Nepal 4
PH - Filippine 4
PT - Portogallo 4
TW - Taiwan 4
UY - Uruguay 4
VE - Venezuela 4
BZ - Belize 3
DZ - Algeria 3
IL - Israele 3
IR - Iran 3
KG - Kirghizistan 3
PE - Perù 3
XK - ???statistics.table.value.countryCode.XK??? 3
AL - Albania 2
BH - Bahrain 2
BO - Bolivia 2
BY - Bielorussia 2
CR - Costa Rica 2
EE - Estonia 2
HN - Honduras 2
JM - Giamaica 2
NO - Norvegia 2
RO - Romania 2
SK - Slovacchia (Repubblica Slovacca) 2
TH - Thailandia 2
TT - Trinidad e Tobago 2
AM - Armenia 1
BJ - Benin 1
CW - ???statistics.table.value.countryCode.CW??? 1
DO - Repubblica Dominicana 1
ET - Etiopia 1
GR - Grecia 1
GT - Guatemala 1
JO - Giordania 1
KW - Kuwait 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
LV - Lettonia 1
MK - Macedonia 1
ML - Mali 1
MM - Myanmar 1
NI - Nicaragua 1
OM - Oman 1
PR - Porto Rico 1
PS - Palestinian Territory 1
QA - Qatar 1
Totale 9.068
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Città #
Ashburn 488
Singapore 433
Santa Clara 412
Fairfield 386
Southend 249
Hong Kong 246
Chandler 234
Woodbridge 233
Houston 227
San Jose 202
Nyköping 175
Seattle 145
Cambridge 142
Wilmington 136
Ann Arbor 118
Jacksonville 107
Hefei 92
London 92
Modena 91
Beijing 82
Helsinki 78
Rome 77
Chicago 75
Milan 75
New York 75
Dearborn 74
Ho Chi Minh City 68
Los Angeles 60
Hanoi 59
Seoul 45
San Diego 41
Dublin 40
Council Bluffs 39
Naples 32
Princeton 32
Bremen 30
Munich 30
Sofia 30
Shanghai 29
The Dalles 29
Lauterbourg 27
Dallas 26
Grafing 26
Bologna 24
Jakarta 24
Moscow 24
Salt Lake City 23
São Paulo 23
Santiago 22
Turin 21
Des Moines 19
Elk Grove Village 18
Eugene 18
Buffalo 17
Frankfurt am Main 15
Rio de Janeiro 15
Tampa 14
Da Nang 13
Orem 13
Brussels 12
Izmir 12
Parma 12
Redwood City 12
St Louis 12
Watertown 12
Redondo Beach 11
Baytown 10
Boardman 10
Florence 10
Wuhan 10
Belo Horizonte 9
Brasília 9
Brescia 9
Brooklyn 9
Palermo 9
Atlanta 8
Baghdad 8
Boston 8
Haiphong 8
Mexico City 8
Nuremberg 8
Poplar 8
Verona 8
Angola 7
Bari 7
Brno 7
Catania 7
Columbus 7
Kassel 7
Montreal 7
Padova 7
Phoenix 7
Tokyo 7
Toronto 7
Casalnuovo di Napoli 6
Denver 6
Detroit 6
Dong Ket 6
Genoa 6
Guangzhou 6
Totale 6.035
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Nome #
CASO CLINICO: QUANDO LA RISPOSTA ALLA DIETA IPOLIPIDEMIZZANTE DETERMINA LA DIAGNOSI 1.147
Lysosomal lipase deficiency: Molecular characterization of eleven patients with Wolman or cholesteryl ester storage disease 405
Can APOE and MTHFR polymorphisms have an influence on the severity of cardiovascular manifestations in Italian Pseudoxanthoma elasticum affected patients? 372
Functional analysis of two novel splice site mutations of APOB gene in familial hypobetalipoproteinemia 359
A novel deletion of BRCA1 gene that eliminates the ATG initiation codon without affecting the promoter region 349
Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in Italy 337
An apparent inconsistency in parent to offspring transmission ofpoint mutations of LDLR gene in familial hypercholesterolemia 319
Circulating mucosal-associated invariant T cells identify patients responding to anti-PD-1 therapy 316
Incidental finding of severe hypertriglyceridemia in children. Role of multiple rare variants in genes affecting plasma triglyceride. 311
Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 gene 307
DIAGNOSI MOLECOLARE DELLE IPERTRIGLICERIDEMIE PRIMITIVE ATTRAVERSO “NGS” (NEXT GENERATION SEQUENCING) 285
Novel mutations in the GPIHBP1 gene identified in 2 patients with recurrent acute pancreatitis 274
Rearrangements of the ABCC6 gene in Italian patients with PXE 272
Leucine 10 allelic variant in signal peptide of PCSK9 increases the LDL cholesterol-lowering effect of statins in patients with familial hypercholesterolaemia. 272
Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia 270
A 3-day-old neonate with severe hypertriglyceridemia from novel mutations of the GPIHBP1 gene 258
Timely diagnosis of sitosterolemia by next generation sequencing in two children with severe hypercholesterolemia 248
Homozygous familial hypercholesterolemia in Italy: Clinical and molecular features 246
Clinical application of NGS in the diagnosis of iron overload disorders or hyperferritinemia of genetic origin 229
Characterization of new ATM deletion associated with hereditary breast cancer 229
Phenotypic variability in 4 homozygous familial hypercholesterolemia siblings compound heterozygous for LDLR mutations 223
Severe hypertriglyceridemia in a newborn with monogenic lipoprotein lipase deficiency: an unconventional therapeutic approach with exchange transfusion. 209
A man with low cholesterol and weakness of the lower limbs. 199
Worldwide experience of homozygous familial hypercholesterolaemia: retrospective cohort study 192
Hypercholesterolemia in Childhood: How the Response to Diet could Lead to Diagnosis. Lesson from a Case-Report 190
In vitro functional characterization of splicing variants of the APOB gene found in familial hypobetalipoproteinemia 181
Effects of miglustat treatment in a patient affected by an atypical form of Tangier disease 178
Identification and Molecular Characterization of a Novel Large-Scale Variant (Exons 4_18 Loss) in the LDLR Gene as a Cause of Familial Hypercholesterolaemia in an Italian Family 173
HDL‐mediated reduction of cholesterol content inhibits the proliferation of prostate cancer cells induced by LDL: Role of ABCA1 and proteasome inhibition 170
Novel mutations of SAR1B gene in four children with chylomicron retention disease 168
Comparison of two polygenic risk score to identify non-monogenic primary hypocholesterolemias in a large cohort of Italian hypocholesterolemic subjects 168
Novel mutations of ABCA1 transporter in patients with Tangier disease and familial HDL deficiency. 161
The study of familial hypercholesterolemia in Italy: A narrative review. 149
Totale 9.166
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Categoria #
all - tutte 33.127
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 33.127
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021264 0 0 0 0 0 0 0 0 0 101 108 55
2021/2022707 28 34 55 21 21 78 51 36 95 63 141 84
2022/2023903 118 108 67 61 117 104 35 71 90 31 54 47
2023/2024751 41 35 77 74 98 82 49 102 29 47 40 77
2024/20251.721 72 23 66 102 300 246 208 96 152 66 142 248
2025/20262.803 210 114 219 322 541 264 367 192 281 293 0 0
Totale 9.166