IRIS
GALLIZZI, Romina
 Distribuzione geografica
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Continente #
EU - Europa 9.351
NA - Nord America 6.431
AS - Asia 3.829
SA - Sud America 1.402
AF - Africa 117
OC - Oceania 13
Continente sconosciuto - Info sul continente non disponibili 5
Totale 21.148
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Nazione #
US - Stati Uniti d'America 6.335
RU - Federazione Russa 3.728
IT - Italia 1.725
SG - Singapore 1.669
BR - Brasile 1.200
CN - Cina 1.059
IE - Irlanda 1.025
SE - Svezia 992
HK - Hong Kong 438
DE - Germania 366
UA - Ucraina 366
FR - Francia 308
PL - Polonia 255
VN - Vietnam 249
FI - Finlandia 189
GB - Regno Unito 175
IN - India 99
NL - Olanda 71
AR - Argentina 66
BD - Bangladesh 48
AT - Austria 41
MX - Messico 41
EC - Ecuador 37
IQ - Iraq 36
TR - Turchia 33
VE - Venezuela 30
BE - Belgio 28
MA - Marocco 27
CA - Canada 26
ZA - Sudafrica 26
UZ - Uzbekistan 25
CO - Colombia 24
PK - Pakistan 22
ID - Indonesia 20
JP - Giappone 19
TN - Tunisia 15
SA - Arabia Saudita 14
JO - Giordania 13
PY - Paraguay 13
AZ - Azerbaigian 12
CL - Cile 12
KE - Kenya 12
AU - Australia 11
CH - Svizzera 11
CZ - Repubblica Ceca 11
UY - Uruguay 10
EG - Egitto 9
OM - Oman 9
ES - Italia 8
PH - Filippine 8
DZ - Algeria 7
NP - Nepal 7
PE - Perù 7
IL - Israele 6
LT - Lituania 6
MY - Malesia 6
AE - Emirati Arabi Uniti 5
AL - Albania 5
CR - Costa Rica 5
ET - Etiopia 5
HN - Honduras 5
JM - Giamaica 5
PA - Panama 5
RO - Romania 5
AO - Angola 4
DK - Danimarca 4
DO - Repubblica Dominicana 4
EU - Europa 4
GR - Grecia 4
RS - Serbia 4
AM - Armenia 3
BG - Bulgaria 3
BN - Brunei Darussalam 3
BO - Bolivia 3
BY - Bielorussia 3
GE - Georgia 3
KZ - Kazakistan 3
LB - Libano 3
LV - Lettonia 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
GT - Guatemala 2
HR - Croazia 2
KG - Kirghizistan 2
KH - Cambogia 2
LU - Lussemburgo 2
LY - Libia 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
Totale 21.137
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Città #
Moscow 1.182
Dublin 1.021
Singapore 934
Ashburn 799
Chandler 782
Jacksonville 734
Dallas 593
Hong Kong 438
Nyköping 399
Beijing 392
Warsaw 253
Dearborn 213
The Dalles 201
Princeton 189
Medford 175
Cambridge 167
Lauterbourg 159
San Jose 158
Des Moines 143
Los Angeles 135
Boardman 123
Rome 102
Ann Arbor 95
Milan 93
São Paulo 88
Buffalo 80
Ho Chi Minh City 79
Messina 73
Tianjin 68
Wilmington 59
Woodbridge 53
New York 52
Redondo Beach 49
Munich 46
Hanoi 41
Bologna 40
Jinan 36
Frankfurt am Main 33
Rio de Janeiro 33
Vienna 33
Naples 30
Orem 30
Shenyang 29
Belo Horizonte 28
Brussels 28
San Mateo 27
Florence 25
Catania 24
Chennai 23
Curitiba 23
Dong Ket 23
Guangzhou 23
Nanjing 23
Santa Clara 23
Tashkent 23
Helsinki 22
Hyderabad 22
Washington 22
Houston 21
Shenzhen 21
Bari 20
Brasília 20
Palermo 20
Tokyo 19
Lancaster 18
Nanchang 17
Turin 17
Zhengzhou 17
Baghdad 16
Campinas 16
Haikou 16
Hebei 16
Nuremberg 16
Fortaleza 15
Johannesburg 15
London 15
Norwalk 15
Trieste 15
Chicago 14
Council Bluffs 14
Guayaquil 14
Pisa 14
Porto Alegre 14
Seattle 14
Turku 14
Brooklyn 13
Quito 13
Dhaka 12
Modena 12
Shanghai 12
Sorocaba 12
Amman 11
Baku 11
Brescia 11
Jakarta 11
Jiaxing 11
Manchester 11
Pune 11
Recife 11
Santo André 11
Totale 11.407
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Nome #
Lipodistrofia parziale tipo Dunnigan: aspetti clinici e genetici 1.089
Pericardite e piastrinosi persistente: esordio di morbo di Crohn. 311
Ipernatriemia e Febbre di ndd 231
Autoimmune liver disease in Noonan Syndrome. 229
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. 220
Juvenile Idiopathic Arthritis associated uveitis: a retrospective analysis from a centre of South Italy 213
5. Sindrome di Borjeson-Forssman-Lehmann: descrizione di un caso 211
A case of Mondor's disease in a patient with Beta Thalassemia Syndrome 199
Febbre Mediterranea Familiare e mutazioni in eterozigosi: forma di ereditarietà pseudodominante? 191
Atypical phenotypic aspects of autoimmune thyroid disorders in young patients with Turner syndrome 186
Approccio clinico-diagnostico al dolore osteo-articolare in età pediatrica 184
Acute haemorrhagic oedema of infancy: A condition that is not always benign 184
A national cohort study on pediatric Behcet's disease: Cross-sectional data from an Italian registry 183
Congenital hypopituitarism: How to select the patients for genetic analyses 178
Approccio clinico-diagnostico al dolore osteo-articolare in età pediatrica. 172
Catastrophic antiphospholipid syndrome in a 4-year old child 172
Clinical significance of NOD2/CARD15 and Toll-like receptor 4 gene single nucleotide polymorphisms in inflammatory bowel disease. 172
Indeterminate colitis: a distinctive clinical pattern of inflammatory bowel disease in children 169
Intestinal and neurological involvement in Behcet disease: A clinical case 168
Pontine Tegmental Cap Dysplasia: developmental and cognitive outcome in three adolescent patients 165
Apparent third patient with cutaneous mastocytosis, microcephaly, conductive hearing loss, and microtia 165
UNO STRANO VOMITO.. 161
Febbri ricorrenti ed eredità oligogenica 161
Anakinra drug retention rate and predictive factors of long-term response in systemic juvenile idiopathic arthritis and adult onset still disease 160
Incidenza, sintomatologia, anomalie associate 159
Familial Mediterranean Fever: Clinical And Genetic Characterization In A Southern Italy Population 156
Familial mediterranean fever in a sicilian family: genotype-phenotype correlation and intrafamilial variability 155
Familial Mediterranean Fever AND Multiple sclerosis: first case report in Italy. 155
Paraplegia agli arti inferiori dopo intervento di coartazione aortica 154
Porpora di Schonlein Henoch e Febbre Mediterranea Familiare: descrizione di un caso clinico con mutazione del gene MEFV 151
LA SINDROME DI DIGEORGE: PECULIARITÀ CLINICHE E GENETICHE 147
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 147
Oxidative stress in children with Down's syndrome 146
Autoimmune diseases and HLA 144
Mutations in TMEM216 cause Joubert (JBTS2), Meckel (MKS2) and related syndromes 144
Familial Mediterranean Fever in a sicilian family: genotype-phenotype correlation and intrafamilial variability 143
Contenuto di omega-6 omega-3 nel latte di donne siciliane. Indagine preliminare. 143
Blefarofimosi e sindromi correlateBlepharophimosis and related Syndromes 142
Artrite idiopatica giovanile: aspetti immunologici e geneticiJuvenile idiopathic arthritis: immunological and genetic factors 140
Cutaneous small-vessel vasculitis associated with paediatric ulcerative colitis: A case study and literature review 140
Genetica, immunologia e clinica dell’infezione da HIV in età pediatricaGenetics, immunology and clinical management of HIV infection in children 138
SU UN CASO DI SINDROME DI SHWACHMAN-DIAMOND 137
Intestinal Behcet and Crohn's disease: Two sides of the same coin 137
Development of the autoinflammatory disease damage index (ADDI) 137
Su un caso di torcicollo parossistico benigno 132
Febbri ricorrenti a trasmissione oligogenica? 132
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 132
Disease status, reasons for discontinuation and adverse events in 1038 Italian children with juvenile idiopathic arthritis treated with etanercept 131
Heterozygous mutation in MEFV have a potential triallelic effect on patients with two mutations in MVK gene? 130
Giant Arachnoid Granulation (GAG) in a child with acute headache 130
Febbre Mediterranea Familiare (FMF) in una famiglia siciliana: variabilità fenotipica 129
Ipercalcemia grave con nefrocalcinosi da sovradosaggio di vitamina D. Descrizione di un caso 129
Approccio clinico alla malattia di Kawasaki 128
Management of pediatric rheumatological diseases during the outbreak of COVID-19: Our experience 128
Un caso severo di Dermatomiosite Giovanile 126
APLV E DERMATITE ATOPICA: RISULTATI TERAPEUTICI PRELIMINARI CON BECLOMETASONE DIPROPIONATO PER OS 126
Apparent third patient with cutaneous mastocytosis, microcephaly, conductive hearing loss, and microtia (OMIM 248910) 126
Deficit di sottoclassi di IgG: tra storia e attualità 124
Gene-environment interaction in childhood asthma 123
Immunoglobulin injection for the treatment of multiple oral ulcers in Stevens-Johnson syndrome 123
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family 121
MARKERS DI STRESS OSSIDATIVO IN BAMBINI CON SINDROME DI DOWN 120
Thyroid function test evolution in children with Hashimoto's thyroiditis is closely conditioned by the biochemical picture at diagnosis 120
The Italian version of the Juvenile Arthritis Multidimensional Assessment Report (JAMAR) 119
Management of pernio-like cutaneous manifestations in children during the outbreak of COVID-19 118
Onset of pyoderma gangrenosum after tocilizumab therapy for Takayasu arteritis: A new undescribed paradoxical reaction 118
Extracapillary glomerulonephritis during etanercept treatment for juvenile psoriatic arthritis 117
SINDROME DA ATTIVAZIONE MACROFAGICA: DESCRIZIONE DI UN CASO 116
Linfoistiocitosi Emofagocitica e sindrome di Down: descrizione di un caso clinicoHemophagocytic lymphohistiocytosis and Down syndrome: description of a clinical case 114
Subclinical hypothyroidism in children: is it always subclinical? 114
PRELIMINARY EVIDENCE THAT ETANERCEPT MAY REDUCE RADIOGRAPHIC PROGRESSION IN JUVENILE IDIOPATHIC ARTHRITIS. 113
Neurofibromatosi di tipo 1: aspetti genetici e clinici 113
Le sindromi febbrili ereditarie potrebbero essere a trasmissione oligogenica 113
Mutations in TMEM216 cause Joubert (JBTS2), Meckel (MKS2) and related syndromes 113
sindrome da shock tossico con ARDS: descrizione di un caso 112
Familial Mediterranean fever: genetic and immunological aspects 112
Speckle tracking echocardiography as a new diagnostic tool for an assessment of cardiovascular disease in rheumatic patients 112
Drug retention rate and predictive factors of drug survival for interleukin-1 inhibitors in systemic juvenile idiopathic arthritis 112
Sindrome “catastrofica” da anticorpi antifosfolipidi: caso clinico 110
TINU Syndrome: descrizione di un caso 108
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 107
Pericardite ricorrente in età pediatrica. Descrizione di un caso di difficile inquadramento eziopatogenetico 106
Persistent pericarditis and thrombocytosis as presenting manifestations of Crohn disease 105
Mevalonico aciduria 105
Celiachia: una malattia da disregolazione immunologica 103
Livelli di leptina, grelina e obestatina in una popolazione siciliana di madri e neonati: dati preliminari 103
Safety profile of the interleukin-1 inhibitors anakinra and canakinumab in real-life clinical practice: a nationwide multicenter retrospective observational study 102
Un caso di priapismo in paziente affetto da drepanocitosi 101
Linfangioma cistico:descrizione di un caso 100
Su un caso di ACG sistemica di difficile diagnosi 100
Descrizione di un raro caso di policistosi renale e displasia renale multicistica sx in un lattante 99
Juvenile idiopathic arthritis: immunological and genetic factors 98
Sindrome di Noonan: un caso di Epatite Autoimmune 98
Dalla Schönlein-Henoch allo scorbuto: un difficile percorso diagnostico 97
Clinical impact of MEFV mutations in children with periodic fever in a prevalent western European Caucasian population. 97
Sindrome di munchausen:casistica degli ultimi sei anni 96
Un caso di collagenopatia:dopo 5 anni la diagnosi definitiva 96
Mastocitosi, bassa statura, microtia e ipoacusia conduttiva (OMIM 248910): descrizione del terzo caso 96
NGAL as an early biomarker of kidney disease in Joubert syndrome: three brothers compared. 96
Phenotypic variability and disparities in treatment and outcomes of childhood arthritis throughout the world: an observational cohort study 96
Totale 14.734
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Categoria #
all - tutte 65.059
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 65.059
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021356 0 0 0 0 0 0 0 0 0 176 80 100
2021/20221.297 11 78 11 60 33 14 112 71 29 267 182 429
2022/20233.146 257 206 154 245 252 308 48 180 1.269 34 137 56
2023/2024942 80 133 67 107 109 122 42 67 31 47 34 103
2024/20253.366 52 77 109 200 185 94 66 782 875 177 213 536
2025/20268.410 387 647 606 619 727 2.005 1.102 1.022 990 305 0 0
Totale 21.313