RABACCHI, CLAUDIO
 Distribuzione geografica
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Continente #
NA - Nord America 4.609
EU - Europa 2.669
AS - Asia 2.060
SA - Sud America 311
Continente sconosciuto - Info sul continente non disponibili 101
AF - Africa 37
OC - Oceania 6
Totale 9.793
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Nazione #
US - Stati Uniti d'America 4.519
IT - Italia 1.161
SG - Singapore 691
CN - Cina 447
GB - Regno Unito 408
SE - Svezia 264
HK - Hong Kong 252
VN - Vietnam 230
BR - Brasile 214
DE - Germania 188
BD - Bangladesh 137
RU - Federazione Russa 123
FR - Francia 107
FI - Finlandia 101
IN - India 58
UA - Ucraina 55
NL - Olanda 54
KR - Corea 49
CA - Canada 44
IE - Irlanda 43
TR - Turchia 38
BG - Bulgaria 34
ID - Indonesia 34
AR - Argentina 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
BA - Bosnia-Erzegovina 8
SA - Arabia Saudita 8
MA - Marocco 7
MY - Malesia 7
AU - Australia 6
EC - Ecuador 6
PY - Paraguay 6
EU - Europa 5
PT - Portogallo 5
SI - Slovenia 5
UZ - Uzbekistan 5
AZ - Azerbaigian 4
DK - Danimarca 4
EG - Egitto 4
JM - Giamaica 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
HN - Honduras 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
GT - Guatemala 2
NI - Nicaragua 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
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
OM - Oman 1
PR - Porto Rico 1
PS - Palestinian Territory 1
QA - Qatar 1
Totale 9.694
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Città #
Ashburn 552
Singapore 439
Santa Clara 425
Fairfield 386
Southend 249
Hong Kong 247
Chandler 234
Woodbridge 233
Houston 229
San Jose 218
Nyköping 175
Seattle 145
Cambridge 143
Wilmington 136
Ann Arbor 118
Jacksonville 109
New York 97
Milan 93
Hefei 92
London 92
Modena 91
Beijing 86
Rome 81
Chicago 78
Helsinki 78
Dearborn 74
Los Angeles 70
Council Bluffs 69
Ho Chi Minh City 68
Hanoi 59
Seoul 47
Reading 45
Dublin 42
Naples 41
San Diego 41
Dallas 34
Princeton 32
Bremen 30
Munich 30
Shanghai 30
Sofia 30
The Dalles 29
Lauterbourg 27
Grafing 26
Bologna 25
Jakarta 24
Moscow 24
Salt Lake City 23
Santiago 23
São Paulo 23
Buffalo 22
Turin 22
Des Moines 19
Elk Grove Village 18
Eugene 18
Tampa 16
Frankfurt am Main 15
Orem 15
Rio de Janeiro 15
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
Brescia 10
Columbus 10
Montreal 10
Toronto 10
Wuhan 10
Atlanta 9
Bari 9
Belo Horizonte 9
Brasília 9
Brooklyn 9
Denver 9
Baghdad 8
Boston 8
Haiphong 8
Mexico City 8
Nuremberg 8
Phoenix 8
Poplar 8
Angola 7
Brno 7
Catania 7
Genoa 7
Kassel 7
Padova 7
Tokyo 7
Tuzla 7
Bergamo 6
Casalnuovo di Napoli 6
Totale 6.335
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Nome #
CASO CLINICO: QUANDO LA RISPOSTA ALLA DIETA IPOLIPIDEMIZZANTE DETERMINA LA DIAGNOSI 1.197
Lysosomal lipase deficiency: Molecular characterization of eleven patients with Wolman or cholesteryl ester storage disease 407
Can APOE and MTHFR polymorphisms have an influence on the severity of cardiovascular manifestations in Italian Pseudoxanthoma elasticum affected patients? 387
Functional analysis of two novel splice site mutations of APOB gene in familial hypobetalipoproteinemia 375
Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in Italy 359
A novel deletion of BRCA1 gene that eliminates the ATG initiation codon without affecting the promoter region 357
Circulating mucosal-associated invariant T cells identify patients responding to anti-PD-1 therapy 346
An apparent inconsistency in parent to offspring transmission ofpoint mutations of LDLR gene in familial hypercholesterolemia 334
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
Novel mutations in the GPIHBP1 gene identified in 2 patients with recurrent acute pancreatitis 298
DIAGNOSI MOLECOLARE DELLE IPERTRIGLICERIDEMIE PRIMITIVE ATTRAVERSO “NGS” (NEXT GENERATION SEQUENCING) 296
Leucine 10 allelic variant in signal peptide of PCSK9 increases the LDL cholesterol-lowering effect of statins in patients with familial hypercholesterolaemia. 289
A 3-day-old neonate with severe hypertriglyceridemia from novel mutations of the GPIHBP1 gene 286
Rearrangements of the ABCC6 gene in Italian patients with PXE 282
Homozygous familial hypercholesterolemia in Italy: Clinical and molecular features 279
Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia 277
Timely diagnosis of sitosterolemia by next generation sequencing in two children with severe hypercholesterolemia 268
Characterization of new ATM deletion associated with hereditary breast cancer 247
Severe hypertriglyceridemia in a newborn with monogenic lipoprotein lipase deficiency: an unconventional therapeutic approach with exchange transfusion. 244
Phenotypic variability in 4 homozygous familial hypercholesterolemia siblings compound heterozygous for LDLR mutations 243
Clinical application of NGS in the diagnosis of iron overload disorders or hyperferritinemia of genetic origin 233
Worldwide experience of homozygous familial hypercholesterolaemia: retrospective cohort study 233
In vitro functional characterization of splicing variants of the APOB gene found in familial hypobetalipoproteinemia 223
A man with low cholesterol and weakness of the lower limbs. 213
Novel mutations of SAR1B gene in four children with chylomicron retention disease 208
Hypercholesterolemia in Childhood: How the Response to Diet could Lead to Diagnosis. Lesson from a Case-Report 200
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 188
Effects of miglustat treatment in a patient affected by an atypical form of Tangier disease 188
HDL‐mediated reduction of cholesterol content inhibits the proliferation of prostate cancer cells induced by LDL: Role of ABCA1 and proteasome inhibition 184
Comparison of two polygenic risk score to identify non-monogenic primary hypocholesterolemias in a large cohort of Italian hypocholesterolemic subjects 175
Novel mutations of ABCA1 transporter in patients with Tangier disease and familial HDL deficiency. 171
The study of familial hypercholesterolemia in Italy: A narrative review. 152
Totale 9.793
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Categoria #
all - tutte 36.168
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 36.168
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022679 0 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
2025/20263.218 210 114 219 322 541 264 367 192 281 314 196 198
2026/2027212 156 56 0 0 0 0 0 0 0 0 0 0
Totale 9.793