IRIS
GALLIZZI, Romina
 Distribuzione geografica
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Continente #
EU - Europa 9.351
NA - Nord America 6.992
AS - Asia 3.840
SA - Sud America 1.372
Continente sconosciuto - Info sul continente non disponibili 168
AF - Africa 114
OC - Oceania 13
Totale 21.850
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Nazione #
US - Stati Uniti d'America 6.871
RU - Federazione Russa 3.677
IT - Italia 1.796
SG - Singapore 1.659
BR - Brasile 1.169
CN - Cina 1.071
IE - Irlanda 1.009
SE - Svezia 986
HK - Hong Kong 433
DE - Germania 366
UA - Ucraina 365
FR - Francia 307
PL - Polonia 254
VN - Vietnam 243
FI - Finlandia 186
GB - Regno Unito 175
IN - India 99
NL - Olanda 76
AR - Argentina 62
BD - Bangladesh 61
AT - Austria 41
CA - Canada 41
MX - Messico 41
EC - Ecuador 37
IQ - Iraq 36
TR - Turchia 33
VE - Venezuela 31
BE - Belgio 28
MA - Marocco 27
CO - Colombia 25
UZ - Uzbekistan 25
ZA - Sudafrica 25
ID - Indonesia 22
PK - Pakistan 21
JP - Giappone 19
CL - Cile 14
SA - Arabia Saudita 14
JO - Giordania 13
PY - Paraguay 13
TN - Tunisia 13
AZ - Azerbaigian 12
KE - Kenya 12
AU - Australia 11
CH - Svizzera 11
CZ - Repubblica Ceca 11
ES - Italia 11
EG - Egitto 10
PH - Filippine 10
UY - Uruguay 10
NP - Nepal 9
OM - Oman 9
CR - Costa Rica 7
DZ - Algeria 7
MY - Malesia 7
PE - Perù 7
HN - Honduras 6
IL - Israele 6
JM - Giamaica 6
LT - Lituania 6
AE - Emirati Arabi Uniti 5
AL - Albania 5
DO - Repubblica Dominicana 5
ET - Etiopia 5
PA - Panama 5
RO - Romania 5
RS - Serbia 5
AO - Angola 4
DK - Danimarca 4
EU - Europa 4
GR - Grecia 4
GT - Guatemala 4
KZ - Kazakistan 4
AM - Armenia 3
BG - Bulgaria 3
BN - Brunei Darussalam 3
BO - Bolivia 3
BY - Bielorussia 3
GE - Georgia 3
LB - Libano 3
PS - Palestinian Territory 3
SM - San Marino 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
QA - Qatar 2
SN - Senegal 2
TH - Thailandia 2
BB - Barbados 1
BH - Bahrain 1
EE - Estonia 1
GD - Grenada 1
Totale 21.672
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Città #
Moscow 1.165
Dublin 1.005
Singapore 931
Ashburn 872
Chandler 779
Jacksonville 734
Dallas 593
Hong Kong 433
Nyköping 396
Beijing 388
Council Bluffs 259
Warsaw 252
San Jose 238
Dearborn 213
The Dalles 198
Princeton 186
Medford 172
Cambridge 164
Lauterbourg 157
Des Moines 140
Los Angeles 138
Boardman 123
Rome 110
Milan 101
Ann Arbor 95
São Paulo 84
Buffalo 79
Messina 76
Ho Chi Minh City 73
Tianjin 67
Wilmington 59
New York 57
Woodbridge 53
Redondo Beach 48
Munich 46
Hanoi 44
Santa Clara 42
Bologna 40
Jinan 36
Orem 33
Rio de Janeiro 33
Vienna 33
Frankfurt am Main 32
Naples 31
Shenyang 29
Belo Horizonte 28
Brussels 28
Columbus 27
Florence 26
San Mateo 26
Catania 24
Chennai 23
Curitiba 23
Dong Ket 23
Guangzhou 23
Nanjing 23
Tashkent 23
Helsinki 22
Hyderabad 22
Washington 22
Bari 21
Shenzhen 21
Houston 20
Palermo 20
Brasília 19
Tokyo 19
Turin 19
Lancaster 18
Chicago 17
Nanchang 17
Zhengzhou 17
Campinas 16
Haikou 16
Hebei 16
Nuremberg 16
Baghdad 15
Fortaleza 15
Johannesburg 15
London 15
Norwalk 15
Porto Alegre 15
Trieste 15
Guayaquil 14
Pisa 14
Seattle 14
Turku 14
Brooklyn 13
Quito 13
Brescia 12
Dhaka 12
Manchester 12
Modena 12
Shanghai 12
Sorocaba 12
Amman 11
Baku 11
Jakarta 11
Jiaxing 11
Mascali 11
Recife 11
Totale 11.797
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Nome #
Lipodistrofia parziale tipo Dunnigan: aspetti clinici e genetici 1.150
Pericardite e piastrinosi persistente: esordio di morbo di Crohn. 331
Ipernatriemia e Febbre di ndd 235
Autoimmune liver disease in Noonan Syndrome. 235
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. 225
Juvenile Idiopathic Arthritis associated uveitis: a retrospective analysis from a centre of South Italy 219
5. Sindrome di Borjeson-Forssman-Lehmann: descrizione di un caso 213
A case of Mondor's disease in a patient with Beta Thalassemia Syndrome 205
Febbre Mediterranea Familiare e mutazioni in eterozigosi: forma di ereditarietà pseudodominante? 205
A national cohort study on pediatric Behcet's disease: Cross-sectional data from an Italian registry 192
Approccio clinico-diagnostico al dolore osteo-articolare in età pediatrica 189
Atypical phenotypic aspects of autoimmune thyroid disorders in young patients with Turner syndrome 188
Acute haemorrhagic oedema of infancy: A condition that is not always benign 188
Congenital hypopituitarism: How to select the patients for genetic analyses 183
Clinical significance of NOD2/CARD15 and Toll-like receptor 4 gene single nucleotide polymorphisms in inflammatory bowel disease. 181
Approccio clinico-diagnostico al dolore osteo-articolare in età pediatrica. 176
Catastrophic antiphospholipid syndrome in a 4-year old child 175
Indeterminate colitis: a distinctive clinical pattern of inflammatory bowel disease in children 175
Apparent third patient with cutaneous mastocytosis, microcephaly, conductive hearing loss, and microtia 173
Pontine Tegmental Cap Dysplasia: developmental and cognitive outcome in three adolescent patients 172
Intestinal and neurological involvement in Behcet disease: A clinical case 172
Incidenza, sintomatologia, anomalie associate 167
Familial Mediterranean Fever: Clinical And Genetic Characterization In A Southern Italy Population 165
Anakinra drug retention rate and predictive factors of long-term response in systemic juvenile idiopathic arthritis and adult onset still disease 165
Febbri ricorrenti ed eredità oligogenica 164
Familial mediterranean fever in a sicilian family: genotype-phenotype correlation and intrafamilial variability 162
UNO STRANO VOMITO.. 162
Familial Mediterranean Fever AND Multiple sclerosis: first case report in Italy. 159
Paraplegia agli arti inferiori dopo intervento di coartazione aortica 157
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 157
Porpora di Schonlein Henoch e Febbre Mediterranea Familiare: descrizione di un caso clinico con mutazione del gene MEFV 153
LA SINDROME DI DIGEORGE: PECULIARITÀ CLINICHE E GENETICHE 151
Mutations in TMEM216 cause Joubert (JBTS2), Meckel (MKS2) and related syndromes 150
Oxidative stress in children with Down's syndrome 148
Familial Mediterranean Fever in a sicilian family: genotype-phenotype correlation and intrafamilial variability 148
Autoimmune diseases and HLA 147
Contenuto di omega-6 omega-3 nel latte di donne siciliane. Indagine preliminare. 146
Artrite idiopatica giovanile: aspetti immunologici e geneticiJuvenile idiopathic arthritis: immunological and genetic factors 146
Cutaneous small-vessel vasculitis associated with paediatric ulcerative colitis: A case study and literature review 146
Development of the autoinflammatory disease damage index (ADDI) 145
Blefarofimosi e sindromi correlateBlepharophimosis and related Syndromes 144
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 143
SU UN CASO DI SINDROME DI SHWACHMAN-DIAMOND 142
Disease status, reasons for discontinuation and adverse events in 1038 Italian children with juvenile idiopathic arthritis treated with etanercept 141
Genetica, immunologia e clinica dell’infezione da HIV in età pediatricaGenetics, immunology and clinical management of HIV infection in children 140
Intestinal Behcet and Crohn's disease: Two sides of the same coin 140
Su un caso di torcicollo parossistico benigno 138
Heterozygous mutation in MEFV have a potential triallelic effect on patients with two mutations in MVK gene? 135
Febbri ricorrenti a trasmissione oligogenica? 133
Apparent third patient with cutaneous mastocytosis, microcephaly, conductive hearing loss, and microtia (OMIM 248910) 133
Immunoglobulin injection for the treatment of multiple oral ulcers in Stevens-Johnson syndrome 133
Febbre Mediterranea Familiare (FMF) in una famiglia siciliana: variabilità fenotipica 132
Management of pediatric rheumatological diseases during the outbreak of COVID-19: Our experience 132
Ipercalcemia grave con nefrocalcinosi da sovradosaggio di vitamina D. Descrizione di un caso 131
Giant Arachnoid Granulation (GAG) in a child with acute headache 131
Un caso severo di Dermatomiosite Giovanile 130
Approccio clinico alla malattia di Kawasaki 130
APLV E DERMATITE ATOPICA: RISULTATI TERAPEUTICI PRELIMINARI CON BECLOMETASONE DIPROPIONATO PER OS 128
Deficit di sottoclassi di IgG: tra storia e attualità 127
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family 127
The Italian version of the Juvenile Arthritis Multidimensional Assessment Report (JAMAR) 125
MARKERS DI STRESS OSSIDATIVO IN BAMBINI CON SINDROME DI DOWN 122
Management of pernio-like cutaneous manifestations in children during the outbreak of COVID-19 122
Thyroid function test evolution in children with Hashimoto's thyroiditis is closely conditioned by the biochemical picture at diagnosis 122
Linfoistiocitosi Emofagocitica e sindrome di Down: descrizione di un caso clinicoHemophagocytic lymphohistiocytosis and Down syndrome: description of a clinical case 121
Onset of pyoderma gangrenosum after tocilizumab therapy for Takayasu arteritis: A new undescribed paradoxical reaction 121
Extracapillary glomerulonephritis during etanercept treatment for juvenile psoriatic arthritis 119
SINDROME DA ATTIVAZIONE MACROFAGICA: DESCRIZIONE DI UN CASO 118
Le sindromi febbrili ereditarie potrebbero essere a trasmissione oligogenica 118
Subclinical hypothyroidism in children: is it always subclinical? 118
Speckle tracking echocardiography as a new diagnostic tool for an assessment of cardiovascular disease in rheumatic patients 118
Neurofibromatosi di tipo 1: aspetti genetici e clinici 117
Familial Mediterranean fever: genetic and immunological aspects 117
PRELIMINARY EVIDENCE THAT ETANERCEPT MAY REDUCE RADIOGRAPHIC PROGRESSION IN JUVENILE IDIOPATHIC ARTHRITIS. 116
Mutations in TMEM216 cause Joubert (JBTS2), Meckel (MKS2) and related syndromes 116
Drug retention rate and predictive factors of drug survival for interleukin-1 inhibitors in systemic juvenile idiopathic arthritis 116
Sindrome “catastrofica” da anticorpi antifosfolipidi: caso clinico 115
sindrome da shock tossico con ARDS: descrizione di un caso 113
Persistent pericarditis and thrombocytosis as presenting manifestations of Crohn disease 112
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 111
TINU Syndrome: descrizione di un caso 110
Pericardite ricorrente in età pediatrica. Descrizione di un caso di difficile inquadramento eziopatogenetico 108
Descrizione di un raro caso di policistosi renale e displasia renale multicistica sx in un lattante 107
Celiachia: una malattia da disregolazione immunologica 107
Safety profile of the interleukin-1 inhibitors anakinra and canakinumab in real-life clinical practice: a nationwide multicenter retrospective observational study 107
Mevalonico aciduria 106
Phenotypic variability and disparities in treatment and outcomes of childhood arthritis throughout the world: an observational cohort study 106
Clinical impact of MEFV mutations in children with periodic fever in a prevalent western European Caucasian population. 105
Juvenile idiopathic arthritis: immunological and genetic factors 104
Livelli di leptina, grelina e obestatina in una popolazione siciliana di madri e neonati: dati preliminari 104
Un caso di priapismo in paziente affetto da drepanocitosi 104
Linfangioma cistico:descrizione di un caso 103
NGAL as an early biomarker of kidney disease in Joubert syndrome: three brothers compared. 103
Su un caso di ACG sistemica di difficile diagnosi 102
Dalla Schönlein-Henoch allo scorbuto: un difficile percorso diagnostico 101
Transitional care of young people with juvenile idiopathic arthritis in Italy: results of a Delphi consensus survey 101
Sindrome di Noonan: un caso di Epatite Autoimmune 100
Sindrome di munchausen:casistica degli ultimi sei anni 99
Un caso di collagenopatia:dopo 5 anni la diagnosi definitiva 99
Dissecting the heterogeneity of macrophage activation syndrome complicating systemic juvenile idiopathic arthritis 99
Totale 15.242
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Categoria #
all - tutte 70.179
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 70.179
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.273 0 78 11 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
2026/2027448 165 283 0 0 0 0 0 0 0 0 0 0
Totale 21.850