IRIS
GALLIZZI, Romina
 Distribuzione geografica
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Continente #
EU - Europa 9.312
NA - Nord America 6.601
AS - Asia 3.801
SA - Sud America 1.366
AF - Africa 114
OC - Oceania 13
Continente sconosciuto - Info sul continente non disponibili 5
Totale 21.212
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Nazione #
US - Stati Uniti d'America 6.498
RU - Federazione Russa 3.677
IT - Italia 1.766
SG - Singapore 1.656
BR - Brasile 1.168
CN - Cina 1.055
IE - Irlanda 1.009
SE - Svezia 986
HK - Hong Kong 430
UA - Ucraina 365
DE - Germania 364
FR - Francia 306
PL - Polonia 254
VN - Vietnam 241
FI - Finlandia 186
GB - Regno Unito 175
IN - India 99
NL - Olanda 73
AR - Argentina 61
BD - Bangladesh 57
AT - Austria 41
MX - Messico 39
EC - Ecuador 37
IQ - Iraq 35
CA - Canada 33
TR - Turchia 30
VE - Venezuela 30
BE - Belgio 28
MA - Marocco 27
UZ - Uzbekistan 25
ZA - Sudafrica 25
CO - Colombia 24
PK - Pakistan 21
ID - Indonesia 20
JP - Giappone 19
SA - Arabia Saudita 14
JO - Giordania 13
PY - Paraguay 13
TN - Tunisia 13
AZ - Azerbaigian 12
CL - Cile 12
KE - Kenya 12
AU - Australia 11
CH - Svizzera 11
CZ - Repubblica Ceca 11
EG - Egitto 10
UY - Uruguay 10
ES - Italia 9
OM - Oman 9
NP - Nepal 8
PH - Filippine 8
DZ - Algeria 7
PE - Perù 7
CR - Costa Rica 6
IL - Israele 6
LT - Lituania 6
MY - Malesia 6
AE - Emirati Arabi Uniti 5
AL - Albania 5
DO - Repubblica Dominicana 5
ET - Etiopia 5
HN - Honduras 5
JM - Giamaica 5
PA - Panama 5
RO - Romania 5
AO - Angola 4
DK - Danimarca 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
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
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
HU - Ungheria 1
Totale 21.200
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Città #
Moscow 1.165
Dublin 1.005
Singapore 928
Ashburn 852
Chandler 779
Jacksonville 732
Dallas 592
Hong Kong 430
Nyköping 396
Beijing 387
Warsaw 252
Dearborn 213
San Jose 211
The Dalles 198
Princeton 186
Medford 172
Cambridge 164
Lauterbourg 157
Des Moines 140
Los Angeles 136
Boardman 123
Rome 107
Ann Arbor 95
Milan 94
São Paulo 84
Buffalo 79
Messina 76
Ho Chi Minh City 73
Tianjin 67
Wilmington 59
New York 56
Woodbridge 53
Redondo Beach 48
Munich 46
Council Bluffs 42
Hanoi 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
Santa Clara 28
San Mateo 26
Florence 25
Catania 24
Chennai 23
Curitiba 23
Dong Ket 23
Guangzhou 23
Nanjing 23
Tashkent 23
Helsinki 22
Hyderabad 22
Washington 22
Shenzhen 21
Bari 20
Houston 20
Palermo 20
Brasília 19
Tokyo 19
Turin 19
Lancaster 18
Nanchang 17
Zhengzhou 17
Campinas 16
Chicago 16
Haikou 16
Hebei 16
Nuremberg 16
Baghdad 15
Fortaleza 15
Johannesburg 15
London 15
Norwalk 15
Trieste 15
Guayaquil 14
Pisa 14
Porto Alegre 14
Seattle 14
Turku 14
Brooklyn 13
Quito 13
Brescia 12
Dhaka 12
Modena 12
Shanghai 12
Sorocaba 12
Amman 11
Baku 11
Jakarta 11
Jiaxing 11
Manchester 11
Mascali 11
Recife 11
Caracas 10
Totale 11.472
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Nome #
Lipodistrofia parziale tipo Dunnigan: aspetti clinici e genetici 1.120
Pericardite e piastrinosi persistente: esordio di morbo di Crohn. 325
Ipernatriemia e Febbre di ndd 232
Autoimmune liver disease in Noonan Syndrome. 230
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. 224
Juvenile Idiopathic Arthritis associated uveitis: a retrospective analysis from a centre of South Italy 215
5. Sindrome di Borjeson-Forssman-Lehmann: descrizione di un caso 212
Febbre Mediterranea Familiare e mutazioni in eterozigosi: forma di ereditarietà pseudodominante? 204
A case of Mondor's disease in a patient with Beta Thalassemia Syndrome 201
A national cohort study on pediatric Behcet's disease: Cross-sectional data from an Italian registry 189
Atypical phenotypic aspects of autoimmune thyroid disorders in young patients with Turner syndrome 186
Approccio clinico-diagnostico al dolore osteo-articolare in età pediatrica 185
Acute haemorrhagic oedema of infancy: A condition that is not always benign 184
Congenital hypopituitarism: How to select the patients for genetic analyses 179
Clinical significance of NOD2/CARD15 and Toll-like receptor 4 gene single nucleotide polymorphisms in inflammatory bowel disease. 176
Approccio clinico-diagnostico al dolore osteo-articolare in età pediatrica. 173
Catastrophic antiphospholipid syndrome in a 4-year old child 173
Indeterminate colitis: a distinctive clinical pattern of inflammatory bowel disease in children 171
Intestinal and neurological involvement in Behcet disease: A clinical case 170
Pontine Tegmental Cap Dysplasia: developmental and cognitive outcome in three adolescent patients 168
Apparent third patient with cutaneous mastocytosis, microcephaly, conductive hearing loss, and microtia 166
Incidenza, sintomatologia, anomalie associate 164
Febbri ricorrenti ed eredità oligogenica 163
Familial mediterranean fever in a sicilian family: genotype-phenotype correlation and intrafamilial variability 161
UNO STRANO VOMITO.. 161
Anakinra drug retention rate and predictive factors of long-term response in systemic juvenile idiopathic arthritis and adult onset still disease 161
Familial Mediterranean Fever: Clinical And Genetic Characterization In A Southern Italy Population 159
Familial Mediterranean Fever AND Multiple sclerosis: first case report in Italy. 158
Paraplegia agli arti inferiori dopo intervento di coartazione aortica 155
Porpora di Schonlein Henoch e Febbre Mediterranea Familiare: descrizione di un caso clinico con mutazione del gene MEFV 152
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 150
LA SINDROME DI DIGEORGE: PECULIARITÀ CLINICHE E GENETICHE 147
Mutations in TMEM216 cause Joubert (JBTS2), Meckel (MKS2) and related syndromes 147
Oxidative stress in children with Down's syndrome 146
Familial Mediterranean Fever in a sicilian family: genotype-phenotype correlation and intrafamilial variability 146
Autoimmune diseases and HLA 146
Contenuto di omega-6 omega-3 nel latte di donne siciliane. Indagine preliminare. 145
Blefarofimosi e sindromi correlateBlepharophimosis and related Syndromes 143
Cutaneous small-vessel vasculitis associated with paediatric ulcerative colitis: A case study and literature review 143
Artrite idiopatica giovanile: aspetti immunologici e geneticiJuvenile idiopathic arthritis: immunological and genetic factors 142
Genetica, immunologia e clinica dell’infezione da HIV in età pediatricaGenetics, immunology and clinical management of HIV infection in children 139
Intestinal Behcet and Crohn's disease: Two sides of the same coin 139
Development of the autoinflammatory disease damage index (ADDI) 139
SU UN CASO DI SINDROME DI SHWACHMAN-DIAMOND 138
Disease status, reasons for discontinuation and adverse events in 1038 Italian children with juvenile idiopathic arthritis treated with etanercept 138
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 136
Su un caso di torcicollo parossistico benigno 133
Heterozygous mutation in MEFV have a potential triallelic effect on patients with two mutations in MVK gene? 133
Febbri ricorrenti a trasmissione oligogenica? 132
Febbre Mediterranea Familiare (FMF) in una famiglia siciliana: variabilità fenotipica 131
Management of pediatric rheumatological diseases during the outbreak of COVID-19: Our experience 131
Giant Arachnoid Granulation (GAG) in a child with acute headache 130
Approccio clinico alla malattia di Kawasaki 129
Ipercalcemia grave con nefrocalcinosi da sovradosaggio di vitamina D. Descrizione di un caso 129
Immunoglobulin injection for the treatment of multiple oral ulcers in Stevens-Johnson syndrome 129
Un caso severo di Dermatomiosite Giovanile 128
Apparent third patient with cutaneous mastocytosis, microcephaly, conductive hearing loss, and microtia (OMIM 248910) 127
APLV E DERMATITE ATOPICA: RISULTATI TERAPEUTICI PRELIMINARI CON BECLOMETASONE DIPROPIONATO PER OS 126
Deficit di sottoclassi di IgG: tra storia e attualità 125
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family 124
MARKERS DI STRESS OSSIDATIVO IN BAMBINI CON SINDROME DI DOWN 121
Thyroid function test evolution in children with Hashimoto's thyroiditis is closely conditioned by the biochemical picture at diagnosis 121
Management of pernio-like cutaneous manifestations in children during the outbreak of COVID-19 120
The Italian version of the Juvenile Arthritis Multidimensional Assessment Report (JAMAR) 119
Onset of pyoderma gangrenosum after tocilizumab therapy for Takayasu arteritis: A new undescribed paradoxical reaction 119
Extracapillary glomerulonephritis during etanercept treatment for juvenile psoriatic arthritis 118
SINDROME DA ATTIVAZIONE MACROFAGICA: DESCRIZIONE DI UN CASO 117
Le sindromi febbrili ereditarie potrebbero essere a trasmissione oligogenica 117
Linfoistiocitosi Emofagocitica e sindrome di Down: descrizione di un caso clinicoHemophagocytic lymphohistiocytosis and Down syndrome: description of a clinical case 116
Subclinical hypothyroidism in children: is it always subclinical? 115
Speckle tracking echocardiography as a new diagnostic tool for an assessment of cardiovascular disease in rheumatic patients 115
Drug retention rate and predictive factors of drug survival for interleukin-1 inhibitors in systemic juvenile idiopathic arthritis 115
PRELIMINARY EVIDENCE THAT ETANERCEPT MAY REDUCE RADIOGRAPHIC PROGRESSION IN JUVENILE IDIOPATHIC ARTHRITIS. 114
Sindrome “catastrofica” da anticorpi antifosfolipidi: caso clinico 114
Familial Mediterranean fever: genetic and immunological aspects 114
Neurofibromatosi di tipo 1: aspetti genetici e clinici 113
Mutations in TMEM216 cause Joubert (JBTS2), Meckel (MKS2) and related syndromes 113
sindrome da shock tossico con ARDS: descrizione di un caso 112
Persistent pericarditis and thrombocytosis as presenting manifestations of Crohn disease 109
TINU Syndrome: descrizione di un caso 109
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 108
Pericardite ricorrente in età pediatrica. Descrizione di un caso di difficile inquadramento eziopatogenetico 106
Mevalonico aciduria 105
Celiachia: una malattia da disregolazione immunologica 105
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 103
Juvenile idiopathic arthritis: immunological and genetic factors 102
Un caso di priapismo in paziente affetto da drepanocitosi 102
Descrizione di un raro caso di policistosi renale e displasia renale multicistica sx in un lattante 101
Phenotypic variability and disparities in treatment and outcomes of childhood arthritis throughout the world: an observational cohort study 101
Linfangioma cistico:descrizione di un caso 100
Su un caso di ACG sistemica di difficile diagnosi 100
NGAL as an early biomarker of kidney disease in Joubert syndrome: three brothers compared. 100
Dalla Schönlein-Henoch allo scorbuto: un difficile percorso diagnostico 99
Sindrome di Noonan: un caso di Epatite Autoimmune 99
Clinical impact of MEFV mutations in children with periodic fever in a prevalent western European Caucasian population. 99
Sindrome di munchausen:casistica degli ultimi sei anni 97
Un caso di collagenopatia:dopo 5 anni la diagnosi definitiva 97
Mastocitosi, bassa statura, microtia e ipoacusia conduttiva (OMIM 248910): descrizione del terzo caso 97
Osteoma Osteoide: descrizione di un caso 96
Totale 14.939
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Categoria #
all - tutte 67.423
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 67.423
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021100 0 0 0 0 0 0 0 0 0 0 0 100
2021/20221.284 11 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
2025/20268.603 378 638 592 600 717 1.976 1.089 1.005 974 339 155 140
Totale 21.375