IORIO, RAFFAELE
 Distribuzione geografica
Continente #
AS - Asia 8.384
NA - Nord America 7.642
EU - Europa 5.310
SA - Sud America 956
Continente sconosciuto - Info sul continente non disponibili 229
AF - Africa 221
OC - Oceania 11
Totale 22.753
Nazione #
US - Stati Uniti d'America 7.358
SG - Singapore 3.943
RU - Federazione Russa 2.382
CN - Cina 1.615
VN - Vietnam 1.328
IT - Italia 964
BR - Brasile 753
HK - Hong Kong 648
UA - Ucraina 354
DE - Germania 341
FR - Francia 284
FI - Finlandia 281
NL - Olanda 221
GB - Regno Unito 163
CA - Canada 159
BD - Bangladesh 130
IN - India 130
JP - Giappone 120
AR - Argentina 78
CI - Costa d'Avorio 74
KR - Corea 74
MX - Messico 72
TH - Thailandia 57
IE - Irlanda 56
PL - Polonia 56
IQ - Iraq 47
SE - Svezia 44
ZA - Sudafrica 43
TR - Turchia 35
ES - Italia 34
ID - Indonesia 33
EC - Ecuador 32
PH - Filippine 32
AT - Austria 24
PK - Pakistan 24
SA - Arabia Saudita 21
VE - Venezuela 21
CO - Colombia 20
LT - Lituania 19
TW - Taiwan 19
MA - Marocco 18
EG - Egitto 15
MY - Malesia 14
PY - Paraguay 14
TN - Tunisia 14
JO - Giordania 13
PS - Palestinian Territory 13
UY - Uruguay 13
CL - Cile 12
JM - Giamaica 12
KE - Kenya 11
BE - Belgio 10
PE - Perù 10
BG - Bulgaria 9
CZ - Repubblica Ceca 9
NP - Nepal 8
AE - Emirati Arabi Uniti 7
AL - Albania 7
LB - Libano 7
CR - Costa Rica 6
DZ - Algeria 6
KZ - Kazakistan 6
NO - Norvegia 6
UZ - Uzbekistan 6
DO - Repubblica Dominicana 5
IL - Israele 5
LV - Lettonia 5
MN - Mongolia 5
PT - Portogallo 5
AO - Angola 4
AU - Australia 4
AZ - Azerbaigian 4
DK - Danimarca 4
EU - Europa 4
GT - Guatemala 4
HN - Honduras 4
IR - Iran 4
KH - Cambogia 4
MK - Macedonia 4
MW - Malawi 4
NI - Nicaragua 4
NZ - Nuova Zelanda 4
OM - Oman 4
QA - Qatar 4
SY - Repubblica araba siriana 4
TT - Trinidad e Tobago 4
XK - ???statistics.table.value.countryCode.XK??? 4
AM - Armenia 3
BO - Bolivia 3
CG - Congo 3
CV - Capo Verde 3
ET - Etiopia 3
GR - Grecia 3
PA - Panama 3
TL - Timor Orientale 3
BH - Bahrain 2
CH - Svizzera 2
CU - Cuba 2
CY - Cipro 2
DM - Dominica 2
Totale 22.466
Città #
Singapore 1.855
San Jose 1.244
Hong Kong 624
Chandler 605
Ashburn 599
Moscow 589
Beijing 445
Hefei 366
Ho Chi Minh City 360
Jacksonville 346
Santa Clara 325
Hanoi 296
Naples 230
The Dalles 219
Los Angeles 205
Lauterbourg 201
Amsterdam 171
Princeton 168
Millbury 165
Boston 155
Munich 146
Dallas 129
Nanjing 106
Tokyo 103
New York 97
Buffalo 93
Wilmington 77
Napoli 76
Haiphong 71
São Paulo 71
Redondo Beach 66
Da Nang 60
Seoul 60
Turku 59
Orem 58
Council Bluffs 53
Chicago 48
Helsinki 48
Seattle 48
Ottawa 47
Houston 45
Rome 43
Atlanta 40
Montreal 40
Nanchang 39
Frankfurt am Main 38
Warsaw 37
Milan 36
Denver 35
Des Moines 35
San Francisco 34
Brooklyn 33
Phoenix 31
Poplar 31
Chennai 29
Hebei 28
Mexico City 28
Norwalk 27
Shenyang 27
Toronto 26
Boardman 23
Hải Dương 23
London 23
Rio de Janeiro 23
Bangkok 22
Lawrence 22
Baghdad 21
Dublin 19
Tianjin 19
Washington 19
Ankara 18
Johannesburg 18
Afragola 17
Jiaxing 17
Stockholm 17
Charlotte 16
Palermo 16
Biên Hòa 15
Changsha 15
Dhaka 15
Falls Church 15
Vienna 15
Woodbridge 15
Belo Horizonte 14
Brasília 14
Campinas 14
Lappeenranta 14
Manchester 13
Mumbai 13
Nuremberg 13
Quito 13
Bắc Giang 12
Cairo 12
Falkenstein 12
Guarulhos 12
Kronberg 12
Philadelphia 12
Querétaro 12
Amman 11
Bari 11
Totale 12.003
Nome #
Wilson's disease caused by alternative splicing and Alu exonization due to a homozygous 3039-bp deletion spanning from intron 1 to exon 2 of the ATP7B gene 215
Assessment of non-motor and autonomic symptoms in Wilson's disease patients 197
Tubercular hemoptysis in a young liver transplanted patient: Case report 182
È tempo di ridefinire gli intervalli di riferimento e terapeutici della cupruria nella malattia di Wilson? 180
Paediatric liver ultrasound: a pictorial essay 179
A retrospective evaluation of the association of celiac disease and growth hormone deficiency: More than a casual association? 167
Activation of autophagy, observed in liver tissues from patients with Wilson disease and from Atp7b-deficient animals, protects hepatocytes from copper-induced apoptosis 163
Randomised Clinical Trial: Calorie Restriction Regimen with Tomato Juice Supplementation Ameliorates Oxidative Stress and Preserves a Proper Immune Surveillance Modulating Mitochondrial Bioenergetics of T-Lymphocytes in Obese Children Affected by Non-Alcoholic Fatty Liver Disease (NAFLD) 162
Reproductive function of long-term treated patients with hepatic onset of Wilson's disease: a prospective study 161
Prevalence and features of non-motor symptoms in Wilson's disease 159
Il fruttosio prima del divezzamento: Quali i motivi per evitarne l'assunzione? 158
Case report: Horse or zebra, ascites or pseudo-ascites? Care for pictural details! 154
Characterization of liver involvement in defects of cholesterol biosynthesis: Long-term follow-up and review 153
Characterization of the most frequent ATP7B mutation causing Wilson disease in hepatocytes from patient induced pluripotent stem cells 153
Subclinical neurological involvement does not develop if Wilson's disease is treated early 151
Ultrasound Scanning in Infants with Biliary Atresia: The Different Implications of Biliary Tract Features and Liver Echostructure. 149
Steroid therapy for a case of severe drug-induced cholestasis. 148
Zinc monotherapy is effective in Wilson's disease patients with mild liver disease diagnosed in childhood: a retrospective study. 148
Long-term outcome of children with chronic hepatitis B: a 24-year observation period. 145
Ultrasound findings in paediatric cholestasis: how to image the patient and what to look for 145
Primary sclerosing cholangitis preceding Crohn's disease in a child with Down's syndrome. 144
Autoimmune Hepatitis Type 2 Arising in PFAPA Syndrome: Coincidences or Possible Correlations? 143
Oral health conditions in Wilson's disease patients: A clinical diagnostic study 143
Is HCV infection associated with liver steatosis also in children? 142
Cholestasis in neonatal intensive care unit: incidence, aetiology and management 142
Un'ipertransaminasemia urso-dipendente 142
Daily Fructose Traces Intake and Liver Injury in Children with Hereditary Fructose Intolerance 142
Hypertransaminasemia in childhood as a marker of genetic liver disorders. 140
Epidemiological profile of 806 Italian children with hepatitis C virus infection over a 15-year period. 139
Machine learning evaluation of biliary atresia patients to predict long-term outcome after the kasai procedure 139
Prevalence and Long-term corse of macro-aspartate aminotransferase in children 137
Different cortical excitability profiles in hereditary brain iron and copper accumulation 137
Lack of benefit of gluten-free diet on autoimmune hepatitis in a boy with celiac disease. 136
Clinical utility of electrophysiological evaluation in Crigler-Najjar syndrome. 136
SCYL1 variants cause a syndrome with low γ-glutamyl-transferase cholestasis, acute liver failure, and neurodegeneration (CALFAN) 136
DNA and RNA studies for molecular characterization of a gross deletion detected in homozygosity in the NH2-terminal region of the ATP7B gene in a Wilson disease patient. 135
Post-transplant erythrocytosis may affect also liver recipients. 133
Infantile hepatic hemangioendothelioma:outcomes' spectra. 131
Successful use of ursodeoxycholic acid in nodular regenerative hyperplasia of the liver. 131
Hepatic steatosis is uncommon in children with chronic hepatitis B 130
Penicillamine-Induced Elastosis Perforans Serpiginosa in Wilson's Disease: is Useful Switching to Zinc? 130
Imaging prediction with ultrasound and MRI of long-term medical outcome in native liver survivor patients with biliary atresia after kasai portoenterostomy: a pilot study 129
Hyper-gamma-glutamyltransferase is commonly present in non-breast-fed infants with biliary atresia successfully treated with portoenterostomy. 128
Colestasi neonatale: la grande simulatrice 127
Ultrasound, shear-wave elastography, and magnetic resonance imaging in native liver survivor patients with biliary atresia after Kasai portoenterostomy: correlation with medical outcome after treatment 127
Re-evaluation of thediagnostic criteria for Wilson disease in children with mild liver disease. 126
Fulminant autoimmune hepatitis in a girl with 22q13 deletion syndrome: a previously unreported association 126
A promising medium-term follow-up of pediatric sclerosing cholangitis: Mild phenotype or early diagnosis? 126
Diagnostic Approach to Acute Liver Failure in Children: A Position Paper by the SIGENP Liver Disease Working Group 125
Autoantibody prevalence in children with liver disease due to chronic hepatitis C virus (HCV) infection. 125
Is alpha-interferon usefull in children with nonB, non C chronic hepatitis ? 125
Atresia delle vie biliari: quali insidie per il pediatra? 125
Epilessia da deficit di PNPO: follow-up di 5 anni. 125
Treatment of chronic hepatitis C in children with pegylated interferon and ribavirin : the impact of dose 124
Wilson disease: A matter of copper, but also of zinc 124
MRI Liver Imaging Integrated with Texture Analysis in Native Liver Survivor Patients with Biliary Atresia after Kasai Portoenterostomy: Correlation with Medical Outcome after Surgical Treatment 123
Food allergy in liver transplanted children. 123
Is resistin a link between highly active antiretroviral therapy and fat redistribution in HIV-infected children? 123
MARCATORI BIOCHIMICI DEL METABOLISMO DEL RAME IN SOGGETTI PORTATORI DI MALATTIA DI WILSON 123
Neuroradiological findings in Alagille syndrome 122
An epidemiological survey of hepatitis C virus infection in Italian children in the decade 1990-1999. 121
Obese children with fatty liver: Between reality and disease mongering 119
Aberrance of serum zinc and free copper level in wilson disease 119
Diagnostic role of US for biliary atresia 118
Ursodeoxycholic acid for treatment of cholestasis in children on long-term total parenteral nutrition: a pilot study. 117
An adolescent with multinodular liver at ultrasound scanning 117
Long term effect of alpha interferon in children with chronic hepatitis B. 117
Case Report: Neonatal Cholestasis as Early Manifestation of Primary Adrenal Insufficiency 117
Association of Very Rare NOTCH2 Variants with Clinical Features of Alagille Syndrome 116
Wilson's disease: Prospective developments towards new therapies 116
The canine copper toxicosis gene MURR1 is not implicated in the pathogenesis of Wilson disease. 115
Lymphoblastoid alpha-interferon therapy in chronic hepatitis-C 115
Early occurrence of hypertransaminasemia in a 13-month-old child with Wilson disease. 115
Italian children seem to be spared from the mysterious severe acute hepatitis outbreak: A report by SIGENP Acute Hepatitis Group 114
Children with chronic hepatitis C: what future? 114
Efficacy of Sofosbuvir/Ledipasvir in Adolescents With Chronic Hepatitis C Genotypes 1, 3, and 4: A Real-world Study 112
Serum Transaminases in Children with Wilson's Disease 112
Predictive value of Epstein-Barr virus genome copy number and BZLF1 expression in blood lymphocytes of transplant recipients at risk for lymphoproliferative disease. 112
Management of cholelithiasis in Italian children: A national multicenter study. 109
Disease burden and management of Crigler-Najjar syndrome: Report of a world registry 108
RNA analysis of consensus sequence splicing mutations: implications for the diagnosis of Wilson disease. 108
Twenty-four novel mutations in Wilson disease patients of predominantly Italian origin 107
A post-transplant complication also in liver recipents? 107
LKM1 antibody and interferon therapy in children with chronic hepatitis C. 106
Mimicry between the hepatitis C virus polyprotein and antigenic targets of nuclear and smooth muscle antibodies in chronic hepatitis C virus infection. 106
Fulminant hepatic failure requiring liver transplantation in 22q13.3 deletion syndrome. 106
Is HCV infection associated with liver steatosis also in children? 106
Rare variants in PKHD1 associated with Caroli syndrome: Two case reports 105
Macroenzyme investigation and monitoring in children with persistent increase of aspartate aminotransferase of unexplained origin 105
Recurrent de novo missense variants in GNB2 can cause syndromic intellectual disability 105
Treatment of pediatric hepatitis C: results and perspectives 104
Self-concept and psychopatological risk in liver transplantated children. 104
Low virological response to interferon in children with chronic hepatitis C. 103
Cryptogenic chronic hepatitis in childwood is unrelated to hepatitis G virus 103
Mauriac syndrome still exists. 102
Side effects of ALPHA-interferon therapy and impact on health-related quality of life in children with chronic viral hepatitis 101
Le vaccinazioni opportune: epatite A 101
Penicillamine-related neurological syndrome in a child affected by Wilson disease with hepatic presentation 99
Biliary lithiasis in children 99
Jagged-1 mutations in italian patients with alagille syndrome 98
Totale 12.911
Categoria #
all - tutte 77.186
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 77.186


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022822 0 3 4 20 8 20 17 32 62 49 200 407
2022/20231.488 204 129 51 84 157 163 68 144 241 158 73 16
2023/20241.073 36 154 205 67 46 74 30 138 30 19 200 74
2024/20255.684 305 318 19 64 140 311 592 322 594 537 1.986 496
2025/202611.463 1.230 955 1.034 1.195 2.076 398 1.245 611 1.395 707 300 317
2026/2027360 324 36 0 0 0 0 0 0 0 0 0 0
Totale 22.753