IRIS
GALLIZZI, Romina
 Distribuzione geografica
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Continente #
EU - Europa 9.456
NA - Nord America 8.003
AS - Asia 3.846
SA - Sud America 1.378
Continente sconosciuto - Info sul continente non disponibili 178
AF - Africa 115
OC - Oceania 13
Totale 22.989
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Nazione #
US - Stati Uniti d'America 7.798
RU - Federazione Russa 3.683
IT - Italia 1.876
SG - Singapore 1.659
BR - Brasile 1.174
CN - Cina 1.071
IE - Irlanda 1.009
SE - Svezia 987
HK - Hong Kong 433
DE - Germania 367
UA - Ucraina 365
FR - Francia 307
PL - Polonia 254
VN - Vietnam 243
FI - Finlandia 186
GB - Regno Unito 183
IN - India 99
NL - Olanda 76
CA - Canada 69
AR - Argentina 62
BD - Bangladesh 61
AT - Austria 41
MX - Messico 41
EC - Ecuador 37
IQ - Iraq 36
TR - Turchia 34
VE - Venezuela 31
BE - Belgio 28
MA - Marocco 27
CO - Colombia 26
UZ - Uzbekistan 25
ZA - Sudafrica 25
ID - Indonesia 22
PK - Pakistan 21
JP - Giappone 19
PR - Porto Rico 16
CL - Cile 14
SA - Arabia Saudita 14
CR - Costa Rica 13
GT - Guatemala 13
HN - Honduras 13
JO - Giordania 13
PY - Paraguay 13
TN - Tunisia 13
AZ - Azerbaigian 12
ES - Italia 12
KE - Kenya 12
AU - Australia 11
CH - Svizzera 11
CZ - Repubblica Ceca 11
CW - ???statistics.table.value.countryCode.CW??? 10
EG - Egitto 10
PH - Filippine 10
UY - Uruguay 10
IL - Israele 9
NP - Nepal 9
OM - Oman 9
JM - Giamaica 8
MY - Malesia 8
DZ - Algeria 7
EE - Estonia 7
PE - Perù 7
LT - Lituania 6
SV - El Salvador 6
AE - Emirati Arabi Uniti 5
AL - Albania 5
DO - Repubblica Dominicana 5
ET - Etiopia 5
KZ - Kazakistan 5
NI - Nicaragua 5
PA - Panama 5
RO - Romania 5
RS - Serbia 5
SM - San Marino 5
AO - Angola 4
DK - Danimarca 4
EU - Europa 4
GR - Grecia 4
TT - Trinidad e Tobago 4
AM - Armenia 3
BG - Bulgaria 3
BN - Brunei Darussalam 3
BO - Bolivia 3
BY - Bielorussia 3
GE - Georgia 3
GP - Guadalupe 3
LB - Libano 3
PS - Palestinian Territory 3
BA - Bosnia-Erzegovina 2
BW - Botswana 2
CI - Costa d'Avorio 2
CY - Cipro 2
GA - Gabon 2
HR - Croazia 2
KG - Kirghizistan 2
KH - Cambogia 2
LU - Lussemburgo 2
LV - Lettonia 2
NZ - Nuova Zelanda 2
PT - Portogallo 2
Totale 22.803
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Città #
Moscow 1.165
Ashburn 1.070
Dublin 1.005
Singapore 931
Chandler 779
Jacksonville 737
Dallas 597
Hong Kong 433
Nyköping 396
Beijing 388
San Jose 383
Council Bluffs 323
Warsaw 253
Dearborn 213
The Dalles 198
Princeton 187
Medford 172
Cambridge 164
Lauterbourg 157
Los Angeles 143
Des Moines 140
Boardman 123
Rome 116
Milan 102
Ann Arbor 95
São Paulo 84
Buffalo 79
Messina 76
Ho Chi Minh City 73
Tianjin 67
Wilmington 64
New York 59
Woodbridge 53
Santa Clara 52
Redondo Beach 48
Munich 46
Hanoi 44
Bologna 42
Naples 37
Jinan 36
Orem 35
Frankfurt am Main 33
Rio de Janeiro 33
Vienna 33
Columbus 29
Shenyang 29
Belo Horizonte 28
Brussels 28
Catania 28
Florence 28
San Mateo 26
Houston 25
Turin 24
Chennai 23
Curitiba 23
Dong Ket 23
Guangzhou 23
Nanjing 23
Palermo 23
Tashkent 23
Washington 23
Bari 22
Brasília 22
Helsinki 22
Hyderabad 22
Chicago 21
Shenzhen 21
Lancaster 19
Tokyo 19
Brooklyn 17
London 17
Nanchang 17
Norwalk 17
Zhengzhou 17
Campinas 16
Haikou 16
Hebei 16
Montreal 16
Nuremberg 16
Trieste 16
Baghdad 15
Fortaleza 15
Johannesburg 15
Porto Alegre 15
Seattle 15
Atlanta 14
Guayaquil 14
Phoenix 14
Pisa 14
Turku 14
Brescia 13
Modena 13
Quito 13
San Francisco 13
Denver 12
Dhaka 12
Manchester 12
Shanghai 12
Sorocaba 12
Amman 11
Totale 12.310
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Nome #
Lipodistrofia parziale tipo Dunnigan: aspetti clinici e genetici 1.158
Pericardite e piastrinosi persistente: esordio di morbo di Crohn. 341
Autoimmune liver disease in Noonan Syndrome. 251
Ipernatriemia e Febbre di ndd 239
Epidemiological and clinical aspects of autoimmune thyroid diseases in children with Down's syndrome. Ital J Pediatr. 2018 Mar 21;44(1):39. doi: 10.1186/s13052-018-0478-9. 231
Juvenile Idiopathic Arthritis associated uveitis: a retrospective analysis from a centre of South Italy 227
5. Sindrome di Borjeson-Forssman-Lehmann: descrizione di un caso 219
Febbre Mediterranea Familiare e mutazioni in eterozigosi: forma di ereditarietà pseudodominante? 215
A case of Mondor's disease in a patient with Beta Thalassemia Syndrome 213
A national cohort study on pediatric Behcet's disease: Cross-sectional data from an Italian registry 200
Acute haemorrhagic oedema of infancy: A condition that is not always benign 198
Approccio clinico-diagnostico al dolore osteo-articolare in età pediatrica 194
Indeterminate colitis: a distinctive clinical pattern of inflammatory bowel disease in children 192
Atypical phenotypic aspects of autoimmune thyroid disorders in young patients with Turner syndrome 192
Congenital hypopituitarism: How to select the patients for genetic analyses 190
Clinical significance of NOD2/CARD15 and Toll-like receptor 4 gene single nucleotide polymorphisms in inflammatory bowel disease. 189
Approccio clinico-diagnostico al dolore osteo-articolare in età pediatrica. 183
Anakinra drug retention rate and predictive factors of long-term response in systemic juvenile idiopathic arthritis and adult onset still disease 180
Catastrophic antiphospholipid syndrome in a 4-year old child 179
Pontine Tegmental Cap Dysplasia: developmental and cognitive outcome in three adolescent patients 178
Intestinal and neurological involvement in Behcet disease: A clinical case 177
Apparent third patient with cutaneous mastocytosis, microcephaly, conductive hearing loss, and microtia 176
Familial Mediterranean Fever: Clinical And Genetic Characterization In A Southern Italy Population 170
Incidenza, sintomatologia, anomalie associate 170
UNO STRANO VOMITO.. 169
Febbri ricorrenti ed eredità oligogenica 168
Familial mediterranean fever in a sicilian family: genotype-phenotype correlation and intrafamilial variability 166
Familial Mediterranean Fever AND Multiple sclerosis: first case report in Italy. 165
Paraplegia agli arti inferiori dopo intervento di coartazione aortica 162
Porpora di Schonlein Henoch e Febbre Mediterranea Familiare: descrizione di un caso clinico con mutazione del gene MEFV 162
A snapshot on the on-label and off-label use of the interleukin-1 inhibitors in Italy among rheumatologists and pediatric rheumatologists: A nationwide multi-center retrospective observational study 162
2016 Classification Criteria for Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis: A European League Against Rheumatism/American College of Rheumatology/Paediatric Rheumatology International Trials Organisation Collaborative Initiative 161
Mutations in TMEM216 cause Joubert (JBTS2), Meckel (MKS2) and related syndromes 157
Development of the autoinflammatory disease damage index (ADDI) 157
Blefarofimosi e sindromi correlateBlepharophimosis and related Syndromes 156
LA SINDROME DI DIGEORGE: PECULIARITÀ CLINICHE E GENETICHE 155
Autoimmune diseases and HLA 155
Contenuto di omega-6 omega-3 nel latte di donne siciliane. Indagine preliminare. 154
Familial Mediterranean Fever in a sicilian family: genotype-phenotype correlation and intrafamilial variability 152
Cutaneous small-vessel vasculitis associated with paediatric ulcerative colitis: A case study and literature review 152
Artrite idiopatica giovanile: aspetti immunologici e geneticiJuvenile idiopathic arthritis: immunological and genetic factors 151
Disease status, reasons for discontinuation and adverse events in 1038 Italian children with juvenile idiopathic arthritis treated with etanercept 151
Oxidative stress in children with Down's syndrome 150
SU UN CASO DI SINDROME DI SHWACHMAN-DIAMOND 148
Intestinal Behcet and Crohn's disease: Two sides of the same coin 147
Management of pediatric rheumatological diseases during the outbreak of COVID-19: Our experience 146
Su un caso di torcicollo parossistico benigno 143
Genetica, immunologia e clinica dell’infezione da HIV in età pediatricaGenetics, immunology and clinical management of HIV infection in children 142
Immunoglobulin injection for the treatment of multiple oral ulcers in Stevens-Johnson syndrome 142
Apparent third patient with cutaneous mastocytosis, microcephaly, conductive hearing loss, and microtia (OMIM 248910) 139
Giant Arachnoid Granulation (GAG) in a child with acute headache 139
Febbre Mediterranea Familiare (FMF) in una famiglia siciliana: variabilità fenotipica 138
Febbri ricorrenti a trasmissione oligogenica? 138
Heterozygous mutation in MEFV have a potential triallelic effect on patients with two mutations in MVK gene? 138
Ipercalcemia grave con nefrocalcinosi da sovradosaggio di vitamina D. Descrizione di un caso 137
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family 136
Un caso severo di Dermatomiosite Giovanile 135
Approccio clinico alla malattia di Kawasaki 135
APLV E DERMATITE ATOPICA: RISULTATI TERAPEUTICI PRELIMINARI CON BECLOMETASONE DIPROPIONATO PER OS 134
Speckle tracking echocardiography as a new diagnostic tool for an assessment of cardiovascular disease in rheumatic patients 134
Management of pernio-like cutaneous manifestations in children during the outbreak of COVID-19 133
PRELIMINARY EVIDENCE THAT ETANERCEPT MAY REDUCE RADIOGRAPHIC PROGRESSION IN JUVENILE IDIOPATHIC ARTHRITIS. 132
The Italian version of the Juvenile Arthritis Multidimensional Assessment Report (JAMAR) 131
Deficit di sottoclassi di IgG: tra storia e attualità 130
Onset of pyoderma gangrenosum after tocilizumab therapy for Takayasu arteritis: A new undescribed paradoxical reaction 130
MARKERS DI STRESS OSSIDATIVO IN BAMBINI CON SINDROME DI DOWN 128
Linfoistiocitosi Emofagocitica e sindrome di Down: descrizione di un caso clinicoHemophagocytic lymphohistiocytosis and Down syndrome: description of a clinical case 128
Extracapillary glomerulonephritis during etanercept treatment for juvenile psoriatic arthritis 127
Le sindromi febbrili ereditarie potrebbero essere a trasmissione oligogenica 127
Subclinical hypothyroidism in children: is it always subclinical? 127
Thyroid function test evolution in children with Hashimoto's thyroiditis is closely conditioned by the biochemical picture at diagnosis 127
Drug retention rate and predictive factors of drug survival for interleukin-1 inhibitors in systemic juvenile idiopathic arthritis 125
sindrome da shock tossico con ARDS: descrizione di un caso 122
Familial Mediterranean fever: genetic and immunological aspects 122
SINDROME DA ATTIVAZIONE MACROFAGICA: DESCRIZIONE DI UN CASO 121
Neurofibromatosi di tipo 1: aspetti genetici e clinici 121
Development and Initial Validation of the Macrophage Activation Syndrome/Primary Hemophagocytic Lymphohistiocytosis Score, a Diagnostic Tool that Differentiates Primary Hemophagocytic Lymphohistiocytosis from Macrophage Activation Syndrome 121
Sindrome “catastrofica” da anticorpi antifosfolipidi: caso clinico 120
Mutations in TMEM216 cause Joubert (JBTS2), Meckel (MKS2) and related syndromes 120
Persistent pericarditis and thrombocytosis as presenting manifestations of Crohn disease 117
Clinical impact of MEFV mutations in children with periodic fever in a prevalent western European Caucasian population. 117
Phenotypic variability and disparities in treatment and outcomes of childhood arthritis throughout the world: an observational cohort study 117
Descrizione di un raro caso di policistosi renale e displasia renale multicistica sx in un lattante 114
Un caso di priapismo in paziente affetto da drepanocitosi 114
TINU Syndrome: descrizione di un caso 113
Transitional care of young people with juvenile idiopathic arthritis in Italy: results of a Delphi consensus survey 113
Safety profile of the interleukin-1 inhibitors anakinra and canakinumab in real-life clinical practice: a nationwide multicenter retrospective observational study 113
Pericardite ricorrente in età pediatrica. Descrizione di un caso di difficile inquadramento eziopatogenetico 112
Juvenile idiopathic arthritis: immunological and genetic factors 112
Mevalonico aciduria 112
Celiachia: una malattia da disregolazione immunologica 111
Livelli di leptina, grelina e obestatina in una popolazione siciliana di madri e neonati: dati preliminari 110
Linfangioma cistico:descrizione di un caso 109
Su un caso di ACG sistemica di difficile diagnosi 109
Dalla Schönlein-Henoch allo scorbuto: un difficile percorso diagnostico 109
NGAL as an early biomarker of kidney disease in Joubert syndrome: three brothers compared. 108
Dissecting the heterogeneity of macrophage activation syndrome complicating systemic juvenile idiopathic arthritis 108
Un caso di collagenopatia:dopo 5 anni la diagnosi definitiva 106
Scurvy may occur even in children with no underlying risk factors: A case report 106
Sindrome di Noonan: un caso di Epatite Autoimmune 105
Totale 15.965
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Categoria #
all - tutte 74.608
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 74.608
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.184 0 0 0 59 33 14 112 71 29 264 179 423
2022/20233.120 254 204 153 245 252 306 48 180 1.252 34 137 55
2023/2024935 80 133 67 107 108 121 41 67 31 47 32 101
2024/20253.313 51 77 109 199 183 92 63 761 863 176 211 528
2025/20268.630 378 638 592 600 717 1.976 1.089 1.005 974 339 155 167
2026/20271.587 165 375 388 659 0 0 0 0 0 0 0 0
Totale 22.989