IRIS
SALZANO, Giuseppina
 Distribuzione geografica
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Continente #
EU - Europa 4.282
NA - Nord America 3.907
AS - Asia 1.239
SA - Sud America 17
Continente sconosciuto - Info sul continente non disponibili 5
OC - Oceania 5
AF - Africa 4
Totale 9.459
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Nazione #
US - Stati Uniti d'America 3.887
IE - Irlanda 1.054
SE - Svezia 967
IT - Italia 895
CN - Cina 591
SG - Singapore 503
UA - Ucraina 334
DE - Germania 258
PL - Polonia 258
FI - Finlandia 159
AT - Austria 94
GB - Regno Unito 93
FR - Francia 71
VN - Vietnam 52
IN - India 44
BE - Belgio 35
ID - Indonesia 29
RU - Federazione Russa 16
NL - Olanda 14
BR - Brasile 11
CA - Canada 11
CH - Svizzera 10
MX - Messico 6
SI - Slovenia 5
EU - Europa 4
IR - Iran 4
AE - Emirati Arabi Uniti 3
AU - Australia 3
CU - Cuba 3
NO - Norvegia 3
TR - Turchia 3
BD - Bangladesh 2
CL - Cile 2
EC - Ecuador 2
ES - Italia 2
HK - Hong Kong 2
HR - Croazia 2
IQ - Iraq 2
LT - Lituania 2
NZ - Nuova Zelanda 2
A2 - ???statistics.table.value.countryCode.A2??? 1
BG - Bulgaria 1
CO - Colombia 1
CZ - Repubblica Ceca 1
EG - Egitto 1
GR - Grecia 1
JP - Giappone 1
LU - Lussemburgo 1
LV - Lettonia 1
ME - Montenegro 1
MK - Macedonia 1
MU - Mauritius 1
NG - Nigeria 1
PE - Perù 1
PH - Filippine 1
PK - Pakistan 1
PT - Portogallo 1
RO - Romania 1
RS - Serbia 1
SC - Seychelles 1
TM - Turkmenistan 1
Totale 9.459
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Città #
Dublin 1.054
Chandler 755
Jacksonville 689
Nyköping 531
Singapore 413
Ashburn 258
Warsaw 255
Messina 205
Dearborn 197
Beijing 178
Princeton 177
Medford 168
Cambridge 146
Des Moines 127
Boardman 101
Ann Arbor 96
Vienna 93
Rome 73
Milan 57
Catania 53
Dong Ket 52
Woodbridge 50
Jinan 49
Shenyang 49
Wilmington 40
Nanjing 32
Brussels 29
Bremen 27
Los Angeles 27
San Mateo 26
Jakarta 25
Tianjin 25
Zhengzhou 25
Bologna 22
Ningbo 22
Hebei 20
Pune 20
Washington 20
Haikou 19
Helsinki 18
New York 18
Florence 17
Munich 16
Seattle 16
Hangzhou 15
Taizhou 15
Nanchang 14
Guangzhou 13
London 13
Fuzhou 11
Hyderabad 11
Jiaxing 11
Lancaster 11
Changsha 10
Frankfurt am Main 10
Norwalk 10
Palermo 10
Naples 9
Shenzhen 9
Bari 8
Houston 8
Lanzhou 8
Verona 7
Amsterdam 6
Parma 6
Saint Petersburg 6
São Paulo 6
Auburn Hills 5
Maldon 5
Pisa 5
Taiyuan 5
Tappahannock 5
Waanrode 5
Ardabil 4
Cagliari 4
Castrofilippo 4
Edinburgh 4
Lewisham 4
Livorno 4
Maribor 4
Montesilvano Marina 4
Ottawa 4
Palazzolo 4
Rende 4
Sovizzo 4
Tehuacán 4
Toronto 4
Turin 4
Acireale 3
Augusta 3
Aversa 3
Brugnera 3
Casal di Principe 3
Dallas 3
Düsseldorf 3
Fagnano Castello 3
Giaveno 3
Havana 3
Hefei 3
Kemerovo 3
Totale 6.643
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Nome #
ESPRESSIONE CLINICA DELLA SINDROME DI WOLFRAM IN UN’AMPIA CASISTICA SICILIANA 366
LA PREVALENZA DELLA SINDROME DI WOLFRAM IN UN’AREA GEOGRAFICA RISTRETTA DELL’ENTROTERRA SICILIANO 183
11-Hydroxylase deficiency as a cause of pre-pubertal gynecomastia 104
Allergic contact dermatitis in pediatric patients with type 1 diabetes: An emerging issue 101
Hearing loss in congenital hypothalamic hypothyroidism: a wide therapeutic window 92
Allergic contact dermatitis and diabetes medical devices: 2 clinical cases 92
Analysis of the factors affecting the evolution over time of subclinical hypothyroidism in children 88
Early Discrimination between Transient and Permanent Congenital Hypothyroidism in Children with Eutopic Gland 87
Ginecomastia puberale e sindrome adreno-genitale non classica: un'associazione poco conosciuta. 85
La sindrome adreno-genitale non classica da deficit di 21-idrossilasi quale causa di ginecomastia prepuberale e puberale. 84
Maturity Onset Diabetes of the Young is Not Necessarily Associated with Autosomal Inheritance: Case Description of a De Novo HFN1A Mutation 84
Omalizumab in children with severe allergic disease: A case series 83
Birth length and weight in congenital adrenal hyperplasia according to the different phenotype 81
Peculiarities of autoimmune thyroid diseases in children with Turner or Down syndrome: an overview 78
Birth length and weight in congenital adrenal hyperplasia according to the different phenotype. 76
4A syndrome: ocular surface investigation in an Italian young patient 76
A novel PAR 1 deletion associated with Leri-Weill dyschondrosteosis 72
Menarcheal age in celiac disease may not be delayed and may be irrespective of age at diagnosis and dietary management 71
Are Children Most of the Submerged Part of SARS-CoV-2 Iceberg? 71
Androgeni e mineralcorticoidi condizionano significativamente la crescita fetale 69
A very rare karyotype in TS syndrome: 45X0, 46X, i(Xq10),X, i(Xq10), i (Xq10) 69
Epidemiological and clinical peculiarities of polyglandular syndrome type 3 in pediatric age 69
Phenotypic expression of Hashimoto's thyroiditis is absolutely atypical in girls with Turner syndrome 69
Inhibin B in adolescents and young adults with Turner syndrome. 68
Association of five autoimmune diseases in a young woman with Down's syndrome 68
Novel insight into Chronic Inflammatory Demyelinating Polineuropathy in APECED syndrome: molecular mechanisms and clinical implications in children 68
Subclinical hypothyroidism in children: is it always subclinical? 68
L'obesità del bambino e dell'adolescente: una nuova malattia sociale 67
Valutazione dei livelli sierici di inibina B e di altri parametri di funzione ipofisi-gonadica in adolescenti con varicocele 66
Emolisi da deficit di G-6-PD in un soggetto diabetico 66
Autoimmune thyroiditis 64
Peculiarities of autoimmune polyglandular syndromes in children and adolescents 64
Clinical and genetic features of maturity-onset diabetes of the young in pediatric patients: a 12-year monocentric experience 64
Autoimmune polyendocrinopathy-candidiasis-ectodermal-distrophy: peculiar evidences from the first report of a Sicilian family 63
Cardiovascular involvement in Wolfram Syndrome 63
CLINICAL PRESENTATION OF MC-CUNE ALBRIGHT SYNDROME IN MALES 62
COMPLIANCE AND ADMINISTRATION METHODS IN MANAGEMENT OF TYPE 1 DIABETES 61
Epidemiologia genetica della sindrome adrenogenitale non classica in una casistica di bambini e adolescenti siciliani. 61
Nella popolazione neonatale italiana la prevalenza di ectopia tiroidea è condizionata da dimorfismo sessuale 61
Graves' disease prevalence in a young population with Turner syndrome 61
Birth lenght and weight in congenital adrenal hyperplasia according to the different phenotypes 61
Atypical phenotypic aspects of autoimmune thyroid disorders in young patients with Turner syndrome 61
Clinical picture,evolution and peculiar molecular findings in a very large pedegree with Wolfram syndrome 60
High-flow priapism in testosterone-treated boys with constitutional delay of growth and puberty may occur even when very low doses are used. 60
Nutritional,glycometabolic and genetic factors affecting menarcheal age in cystic fibrosis 60
STUDIO TRASVERSALE E PROSPETTICO DEL RISCHIO CARDIOVASCOLARE IN ADOLESCENTI CON SINDROME ADRENOGENITALE IN RAPPORTO CON GENOTIPO E FENOTIPO 60
Wolfram Syndrome. Clinical and Genetic Study in an Italian Family 60
Wolfram syndrome in twelve patients from a mountainous area where consanguineous unions are not unusual: phenotypical expression 60
Vulvar contact dermatitis caused by sensitization to colophonium in a patient with type 1 diabetes 60
Uso non convenzionale della metformina in un adolescente non obeso con acanthosis nigricans diffusa e isolata 59
Insulin sensitivity and ultrasound evaluation of intima media thickness at common carotids, carotid bulbs, femoral and abdominal aorta arteries in adolescents with congenital adrenal hyperplasia 59
Novel mutation of CYP21A2 gene (N387K) affecting a nonconserved amino acid residue in Exon 9. 58
Wolfram syndrome. Clinical and genetic study in an Italian family 58
Quarantine Due to the COVID-19 Pandemic From the Perspective of Pediatric Patients With Type 1 Diabetes: A Web-Based Survey 58
Novel nonsense mutation (W22X) in CYP21 causing salt-wasting congenital adrenal hyperplasia in a compound heterozygous girl 57
A randomized cross-over trial to identify the optimal use of insulin glargine in prepubertal children using a three-times daily insulin regimen. 57
Increasing trend of type 1 diabetes incidence in the pediatric population of the Calabria region in 2019-2021 56
Neurocognitive profile in Turner's syndrome is not affected by growth impairment. 56
Novel nonsense mutation (W22X) in CYP21 causing salt-wasting congenital adrenal hyperplasia in a compound heterozygous girl. 56
Prevalenza della malattia di Graves in una popolazione giovanile con la sindrome di Turner 56
Salt-wasting congenital adrenal hyperplasia: Genotypical peculiarities in a Sicilian ethnic group 56
Can HbA1c combined with fasting plasma glucose help to assess priority for GCK-MODY vs HNF1A-MODY genetic testing? 56
Prevalence of overweight and obesity in 2- to 6-year-old Italian children. 55
Ipertensione arteriosa reversibile dopo sospensione di mineralcorticoide in soggetto con SAG SW da 21-OH-D. 55
Safety profile of oral immunotherapy with cow's milk and hen egg: A 10-year experience in controlled trials. 55
An Atypical Case of Late-Onset Wolfram Syndrome 1 without Diabetes Insipidus 54
Premature adrenarche: evaluation of hormonal and metabolic parameters 54
Diabetes and Neurodegeneration in Wolfram Syndrome: A multicenter study of phenotype and genotype 54
Diabetic ketoacidosis as the onset of type 1 diabetes in children 54
GCK-MODY in a child with cystic fibrosis: The doubt of the treatment plan 54
Trattamento precoce nella Sindrome di Turner (Traitement precoce dans le Sindrome de Turner) 53
Abdominal adiposity and cardiovascular risk factors in adolescents with type 1 diabetes. 53
Ruolo degli androgeni e dei mineralcorticoidi sulla crescita fetale 52
Quarantine due to the COVID-19 pandemic from the perspective of adolescents: the crucial role of technology 52
In Sicilian ethnic group non-classical congenital adrenal hyperplasia isfrequently associated with a very mild genotype. 51
Novel nonsense mutation (W22X) in CYP21 causing salt-wasting congenital adrenal hyperplasia in a compound heterozygous girl. 51
L'ipoglicemia factitia: un'eventualità da tenere in considerazione nella gestione di adolescenti con diabete 51
Effect of exercise in diabetic children treated with either an insulin pump or a basal-bolus regimen 51
Mineralcorticoid-related early hypertension in a boy with salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency 51
null 51
Prevalence of Wolfram syndrome is not necessarily so infrequent as generally expected 51
Influence of age on partial clinical remission among children with newly diagnosed type 1 diabetes 51
Subclinical hypothyroidism: the state of the art. 50
Peculiare distribuzione etnico-specifica delle alterazioni molecolari in una casistica siciliana di sindrome adreno-genitale con perdita di sali 50
One-Year Real-World Study on Comparison among Different Continuous Subcutaneous Insulin Infusion Devices for the Management of Pediatric Patients with Type 1 Diabetes: The Supremacy of Hybrid Closed-Loop Systems 49
In South Italy NonClassical Congenital Adrenal Hyperplasia is frequently associated with a very mild genotype 49
Il diabete tipo 1 e la qualità del controllo metabolico condizionano molto l'età del menarca 49
Effects of LHRH analogs for central precocious puberty on IGF1, IGFBP3 and GHBP serum levels 48
Ruolo degli androgeni e dei mineralcorticoidi sulla crescita fetale 48
The association with Down's syndrome can affect phenotypic expression of Hashimoto's thyroiditis in childhood 48
Thyrotropin serum levels and coexistence with Hashimoto's thyroiditis as predictors of malignancy in children with thyroid nodules 48
High Frequency of Dermatological Complications in Children and Adolescents with Type 1 Diabetes: A Web-Based Survey 48
Salt wasting phenotype in a compound heterozygous girl with P482S mutation associated with a novel mutation of CYP21 gene (Q481P) 47
La terapia con microinfusore negli adolescenti diabetici: vantaggi e limiti della nostra esperienza 47
Studio del “drop-out” dalla terapia con microinfusore in due centri pediatrici del Sud Italia 47
Prevalence, presentation and clinical evolution of Graves’ disease in children and adolescents with type 1 diabetes mellitus 47
CONFRONTO TRA DUE TIPI DI TRATTAMENTO INSULINICO INTENSIVO IN UN’AMPIA CASISTICA PEDIATRICA CON DIABETE TIPO 1: ESPERIENZA QUINQUENNALE 47
Clinical Peculiarities in a Cohort of Patients with Wolfram Syndrome 1 47
Quanto più precoce è l'esordio del diabete, tanto più grave è la sua successiva evoluzione 46
Novel nonsense mutation (W22X) in CYP21A2 gene causing salt-wasting congenital adrenal hyperplasia in a compound heterozygous girl 46
Totale 6.543
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Categoria #
all - tutte 40.368
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 40.368
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020874 0 0 0 0 8 183 169 132 29 125 194 34
2020/20211.223 132 41 239 80 110 127 48 104 68 134 57 83
2021/20221.220 8 191 16 63 36 7 50 53 25 226 170 375
2022/20233.301 230 237 158 285 270 315 97 213 1.312 29 98 57
2023/20241.007 68 129 51 109 74 152 36 80 25 63 92 128
2024/2025920 116 131 103 276 294 0 0 0 0 0 0 0
Totale 9.713