RABACCHI, CLAUDIO
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 4.406
EU - Europa 2.634
AS - Asia 2.009
SA - Sud America 310
AF - Africa 37
Continente sconosciuto - Info sul continente non disponibili 9
OC - Oceania 5
Totale 9.410
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 4.333
IT - Italia 1.129
SG - Singapore 686
CN - Cina 441
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
BD - Bangladesh 98
IN - India 58
NL - Olanda 54
UA - Ucraina 54
KR - Corea 49
IE - Irlanda 43
TR - Turchia 38
BG - Bulgaria 34
ID - Indonesia 34
AR - Argentina 33
CA - Canada 33
CL - Cile 30
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
PT - Portogallo 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
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 9.404
Salva come PNG Salva come JPEG
Città #
Ashburn 527
Singapore 437
Santa Clara 416
Fairfield 386
Southend 249
Hong Kong 246
Chandler 234
Woodbridge 233
Houston 229
San Jose 209
Nyköping 175
Seattle 145
Cambridge 142
Wilmington 136
Ann Arbor 118
Jacksonville 109
Hefei 92
London 92
Milan 92
Modena 91
New York 89
Beijing 83
Rome 80
Helsinki 78
Chicago 77
Dearborn 74
Ho Chi Minh City 68
Council Bluffs 64
Los Angeles 64
Hanoi 59
Seoul 47
Dublin 42
San Diego 41
Naples 39
Princeton 32
Bremen 30
Dallas 30
Munich 30
Sofia 30
Shanghai 29
The Dalles 29
Lauterbourg 27
Grafing 26
Bologna 25
Jakarta 24
Moscow 24
Salt Lake City 23
Santiago 23
São Paulo 23
Turin 22
Des Moines 19
Buffalo 18
Elk Grove Village 18
Eugene 18
Frankfurt am Main 15
Rio de Janeiro 15
Tampa 15
Orem 14
Boardman 13
Da Nang 13
St Louis 13
Brussels 12
Florence 12
Izmir 12
Parma 12
Redwood City 12
Verona 12
Watertown 12
Palermo 11
Redondo Beach 11
Baytown 10
Toronto 10
Wuhan 10
Belo Horizonte 9
Brasília 9
Brescia 9
Brooklyn 9
Atlanta 8
Baghdad 8
Boston 8
Haiphong 8
Mexico City 8
Nuremberg 8
Phoenix 8
Poplar 8
Angola 7
Bari 7
Brno 7
Catania 7
Columbus 7
Genoa 7
Kassel 7
Montreal 7
Padova 7
Tokyo 7
Casalnuovo di Napoli 6
Denver 6
Detroit 6
Dong Ket 6
Guangzhou 6
Totale 6.197
Salva come PNG Salva come JPEG
Nome #
CASO CLINICO: QUANDO LA RISPOSTA ALLA DIETA IPOLIPIDEMIZZANTE DETERMINA LA DIAGNOSI 1.172
Lysosomal lipase deficiency: Molecular characterization of eleven patients with Wolman or cholesteryl ester storage disease 406
Can APOE and MTHFR polymorphisms have an influence on the severity of cardiovascular manifestations in Italian Pseudoxanthoma elasticum affected patients? 378
Functional analysis of two novel splice site mutations of APOB gene in familial hypobetalipoproteinemia 366
A novel deletion of BRCA1 gene that eliminates the ATG initiation codon without affecting the promoter region 351
Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in Italy 348
An apparent inconsistency in parent to offspring transmission ofpoint mutations of LDLR gene in familial hypercholesterolemia 325
Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 gene 321
Circulating mucosal-associated invariant T cells identify patients responding to anti-PD-1 therapy 321
Incidental finding of severe hypertriglyceridemia in children. Role of multiple rare variants in genes affecting plasma triglyceride. 320
Novel mutations in the GPIHBP1 gene identified in 2 patients with recurrent acute pancreatitis 293
DIAGNOSI MOLECOLARE DELLE IPERTRIGLICERIDEMIE PRIMITIVE ATTRAVERSO “NGS” (NEXT GENERATION SEQUENCING) 290
Leucine 10 allelic variant in signal peptide of PCSK9 increases the LDL cholesterol-lowering effect of statins in patients with familial hypercholesterolaemia. 281
Rearrangements of the ABCC6 gene in Italian patients with PXE 279
Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia 275
A 3-day-old neonate with severe hypertriglyceridemia from novel mutations of the GPIHBP1 gene 275
Timely diagnosis of sitosterolemia by next generation sequencing in two children with severe hypercholesterolemia 257
Homozygous familial hypercholesterolemia in Italy: Clinical and molecular features 256
Characterization of new ATM deletion associated with hereditary breast cancer 240
Severe hypertriglyceridemia in a newborn with monogenic lipoprotein lipase deficiency: an unconventional therapeutic approach with exchange transfusion. 237
Phenotypic variability in 4 homozygous familial hypercholesterolemia siblings compound heterozygous for LDLR mutations 233
Clinical application of NGS in the diagnosis of iron overload disorders or hyperferritinemia of genetic origin 231
Worldwide experience of homozygous familial hypercholesterolaemia: retrospective cohort study 229
A man with low cholesterol and weakness of the lower limbs. 204
Hypercholesterolemia in Childhood: How the Response to Diet could Lead to Diagnosis. Lesson from a Case-Report 195
Novel mutations of SAR1B gene in four children with chylomicron retention disease 194
In vitro functional characterization of splicing variants of the APOB gene found in familial hypobetalipoproteinemia 187
Effects of miglustat treatment in a patient affected by an atypical form of Tangier disease 186
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 183
HDL‐mediated reduction of cholesterol content inhibits the proliferation of prostate cancer cells induced by LDL: Role of ABCA1 and proteasome inhibition 178
Comparison of two polygenic risk score to identify non-monogenic primary hypocholesterolemias in a large cohort of Italian hypocholesterolemic subjects 173
Novel mutations of ABCA1 transporter in patients with Tangier disease and familial HDL deficiency. 166
The study of familial hypercholesterolemia in Italy: A narrative review. 152
Totale 9.502
Salva come PNG Salva come JPEG
Categoria #
all - tutte 34.690
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 34.690
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202155 0 0 0 0 0 0 0 0 0 0 0 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
2025/20263.139 210 114 219 322 541 264 367 192 281 314 196 119
Totale 9.502