RABACCHI, CLAUDIO
 Distribuzione geografica
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Continente #
NA - Nord America 5.039
EU - Europa 2.714
AS - Asia 2.073
SA - Sud America 318
Continente sconosciuto - Info sul continente non disponibili 101
AF - Africa 37
OC - Oceania 6
Totale 10.288
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Nazione #
US - Stati Uniti d'America 4.939
IT - Italia 1.201
SG - Singapore 693
CN - Cina 449
GB - Regno Unito 409
SE - Svezia 264
HK - Hong Kong 253
VN - Vietnam 230
BR - Brasile 220
DE - Germania 189
BD - Bangladesh 142
RU - Federazione Russa 123
FR - Francia 108
FI - Finlandia 101
IN - India 58
NL - Olanda 55
UA - Ucraina 55
CA - Canada 50
KR - Corea 49
IE - Irlanda 43
TR - Turchia 38
BG - Bulgaria 34
ID - Indonesia 34
AR - Argentina 33
CL - Cile 30
MX - Messico 26
IQ - Iraq 21
PK - Pakistan 20
BE - Belgio 18
CH - Svizzera 15
ES - Italia 15
PL - Polonia 15
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
MY - Malesia 8
SA - Arabia Saudita 8
MA - Marocco 7
AU - Australia 6
EC - Ecuador 6
PY - Paraguay 6
EU - Europa 5
JM - Giamaica 5
PT - Portogallo 5
SI - Slovenia 5
UZ - Uzbekistan 5
VE - Venezuela 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
BZ - Belize 3
CR - Costa Rica 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
EE - Estonia 2
GT - Guatemala 2
NI - Nicaragua 2
NO - Norvegia 2
RO - Romania 2
SK - Slovacchia (Repubblica Slovacca) 2
SV - El Salvador 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
Totale 10.189
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Città #
Ashburn 678
Singapore 440
Santa Clara 428
Fairfield 386
San Jose 273
Southend 249
Hong Kong 248
Chandler 234
Woodbridge 233
Houston 231
Nyköping 175
Seattle 153
Cambridge 143
Wilmington 136
Ann Arbor 118
Jacksonville 109
Council Bluffs 105
Milan 102
New York 98
Rome 98
London 93
Hefei 92
Modena 91
Beijing 87
Chicago 79
Helsinki 78
Dearborn 74
Los Angeles 74
Ho Chi Minh City 68
Hanoi 59
Seoul 47
Reading 45
Dublin 42
Naples 42
San Diego 41
Dallas 39
Princeton 32
Bremen 30
Munich 30
Shanghai 30
Sofia 30
The Dalles 29
São Paulo 28
Lauterbourg 27
Grafing 26
Bologna 25
Jakarta 24
Moscow 24
Salt Lake City 23
Santiago 23
Buffalo 22
Turin 22
Boardman 21
Des Moines 19
Columbus 18
Elk Grove Village 18
Eugene 18
Orem 16
Tampa 16
Frankfurt am Main 15
Rio de Janeiro 15
Da Nang 13
St Louis 13
Atlanta 12
Brussels 12
Florence 12
Izmir 12
Parma 12
Phoenix 12
Redwood City 12
Verona 12
Watertown 12
Brooklyn 11
Montreal 11
Palermo 11
Redondo Beach 11
Toronto 11
Bari 10
Baytown 10
Brescia 10
Wuhan 10
Belo Horizonte 9
Brasília 9
Denver 9
Baghdad 8
Boston 8
Haiphong 8
Mexico City 8
Nuremberg 8
Philadelphia 8
Piacenza 8
Poplar 8
Angola 7
Brno 7
Catania 7
Detroit 7
Genoa 7
Imola 7
Kassel 7
Padova 7
Totale 6.645
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Nome #
CASO CLINICO: QUANDO LA RISPOSTA ALLA DIETA IPOLIPIDEMIZZANTE DETERMINA LA DIAGNOSI 1.228
Lysosomal lipase deficiency: Molecular characterization of eleven patients with Wolman or cholesteryl ester storage disease 417
Can APOE and MTHFR polymorphisms have an influence on the severity of cardiovascular manifestations in Italian Pseudoxanthoma elasticum affected patients? 400
Functional analysis of two novel splice site mutations of APOB gene in familial hypobetalipoproteinemia 386
Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in Italy 381
A novel deletion of BRCA1 gene that eliminates the ATG initiation codon without affecting the promoter region 364
Circulating mucosal-associated invariant T cells identify patients responding to anti-PD-1 therapy 359
An apparent inconsistency in parent to offspring transmission ofpoint mutations of LDLR gene in familial hypercholesterolemia 344
Incidental finding of severe hypertriglyceridemia in children. Role of multiple rare variants in genes affecting plasma triglyceride. 338
Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 gene 334
Rearrangements of the ABCC6 gene in Italian patients with PXE 333
DIAGNOSI MOLECOLARE DELLE IPERTRIGLICERIDEMIE PRIMITIVE ATTRAVERSO “NGS” (NEXT GENERATION SEQUENCING) 310
Novel mutations in the GPIHBP1 gene identified in 2 patients with recurrent acute pancreatitis 308
Leucine 10 allelic variant in signal peptide of PCSK9 increases the LDL cholesterol-lowering effect of statins in patients with familial hypercholesterolaemia. 308
A 3-day-old neonate with severe hypertriglyceridemia from novel mutations of the GPIHBP1 gene 304
Homozygous familial hypercholesterolemia in Italy: Clinical and molecular features 303
Timely diagnosis of sitosterolemia by next generation sequencing in two children with severe hypercholesterolemia 286
Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia 281
Severe hypertriglyceridemia in a newborn with monogenic lipoprotein lipase deficiency: an unconventional therapeutic approach with exchange transfusion. 266
Phenotypic variability in 4 homozygous familial hypercholesterolemia siblings compound heterozygous for LDLR mutations 262
Characterization of new ATM deletion associated with hereditary breast cancer 261
Worldwide experience of homozygous familial hypercholesterolaemia: retrospective cohort study 250
Clinical application of NGS in the diagnosis of iron overload disorders or hyperferritinemia of genetic origin 243
In vitro functional characterization of splicing variants of the APOB gene found in familial hypobetalipoproteinemia 239
Novel mutations of SAR1B gene in four children with chylomicron retention disease 234
A man with low cholesterol and weakness of the lower limbs. 233
Hypercholesterolemia in Childhood: How the Response to Diet could Lead to Diagnosis. Lesson from a Case-Report 211
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 196
Effects of miglustat treatment in a patient affected by an atypical form of Tangier disease 194
HDL‐mediated reduction of cholesterol content inhibits the proliferation of prostate cancer cells induced by LDL: Role of ABCA1 and proteasome inhibition 191
Comparison of two polygenic risk score to identify non-monogenic primary hypocholesterolemias in a large cohort of Italian hypocholesterolemic subjects 189
Novel mutations of ABCA1 transporter in patients with Tangier disease and familial HDL deficiency. 179
The study of familial hypercholesterolemia in Italy: A narrative review. 156
Totale 10.288
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Categoria #
all - tutte 38.056
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 38.056
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022590 0 0 0 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
2026/2027707 156 181 215 155 0 0 0 0 0 0 0 0
Totale 10.288