IRIS
VALENZISE, Mariella
 Distribuzione geografica
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Continente #
EU - Europa 11.476
NA - Nord America 9.462
AS - Asia 5.624
SA - Sud America 2.010
AF - Africa 167
OC - Oceania 18
Continente sconosciuto - Info sul continente non disponibili 5
AN - Antartide 1
Totale 28.763
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Nazione #
US - Stati Uniti d'America 9.272
RU - Federazione Russa 5.448
SG - Singapore 2.473
BR - Brasile 1.721
CN - Cina 1.574
IT - Italia 1.342
IE - Irlanda 1.212
SE - Svezia 1.153
HK - Hong Kong 639
DE - Germania 498
UA - Ucraina 418
FR - Francia 374
FI - Finlandia 268
VN - Vietnam 255
PL - Polonia 228
GB - Regno Unito 211
IN - India 137
AR - Argentina 96
AT - Austria 94
CA - Canada 81
MX - Messico 70
TR - Turchia 66
BD - Bangladesh 64
IQ - Iraq 56
ZA - Sudafrica 48
JP - Giappone 47
EC - Ecuador 45
NL - Olanda 45
ES - Italia 44
ID - Indonesia 43
BE - Belgio 41
UZ - Uzbekistan 38
PK - Pakistan 36
VE - Venezuela 36
CO - Colombia 34
MA - Marocco 29
TH - Thailandia 26
CI - Costa d'Avorio 25
SA - Arabia Saudita 24
CL - Cile 22
CZ - Repubblica Ceca 19
PE - Perù 18
PY - Paraguay 17
TN - Tunisia 17
AE - Emirati Arabi Uniti 14
KE - Kenya 14
AU - Australia 13
AZ - Azerbaigian 12
JO - Giordania 12
LT - Lituania 12
UY - Uruguay 12
EG - Egitto 11
KZ - Kazakistan 10
LB - Libano 10
NP - Nepal 9
PH - Filippine 9
DO - Repubblica Dominicana 8
EE - Estonia 8
IL - Israele 8
OM - Oman 8
BO - Bolivia 7
DZ - Algeria 7
MY - Malesia 7
DK - Danimarca 6
HN - Honduras 6
KG - Kirghizistan 6
PA - Panama 6
PS - Palestinian Territory 6
QA - Qatar 6
RS - Serbia 6
AL - Albania 5
ET - Etiopia 5
GR - Grecia 5
IR - Iran 5
JM - Giamaica 5
NO - Norvegia 5
BG - Bulgaria 4
CH - Svizzera 4
HU - Ungheria 4
BA - Bosnia-Erzegovina 3
BB - Barbados 3
BH - Bahrain 3
BY - Bielorussia 3
KR - Corea 3
LU - Lussemburgo 3
LV - Lettonia 3
NG - Nigeria 3
NZ - Nuova Zelanda 3
SK - Slovacchia (Repubblica Slovacca) 3
SV - El Salvador 3
SY - Repubblica araba siriana 3
TT - Trinidad e Tobago 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AO - Angola 2
BN - Brunei Darussalam 2
CR - Costa Rica 2
GE - Georgia 2
KH - Cambogia 2
LA - Repubblica Popolare Democratica del Laos 2
MN - Mongolia 2
Totale 28.734
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Città #
Moscow 1.623
Ashburn 1.550
Dallas 1.393
Singapore 1.328
Dublin 1.210
Chandler 861
Jacksonville 835
Hong Kong 635
Nyköping 576
Beijing 529
San Jose 394
The Dalles 287
Dearborn 226
Messina 223
Princeton 218
Los Angeles 217
Warsaw 215
Medford 203
Cambridge 192
Lauterbourg 189
Des Moines 166
São Paulo 166
Ann Arbor 142
Boardman 123
Buffalo 108
Munich 99
Jinan 88
New York 82
Ho Chi Minh City 80
Vienna 78
Rome 73
Tianjin 73
Wilmington 65
Washington 61
Rio de Janeiro 58
Shenyang 58
Milan 54
Frankfurt am Main 52
Redondo Beach 49
Orem 48
Council Bluffs 47
Nanjing 47
Catania 46
Guangzhou 46
Turku 45
Santa Clara 44
Tokyo 43
Hanoi 42
Woodbridge 42
Belo Horizonte 39
Houston 38
San Mateo 36
Johannesburg 34
Bremen 33
Brussels 33
London 32
Helsinki 31
Hebei 30
Atlanta 29
Brooklyn 29
Haikou 29
Tashkent 29
Brasília 28
Chennai 27
Nuremberg 27
Campinas 26
Zhengzhou 26
Abidjan 25
Chicago 25
Hyderabad 25
Ningbo 25
Bangkok 23
Mumbai 23
Palermo 23
Lancaster 22
Seattle 22
Shanghai 22
Curitiba 21
Jakarta 21
Stockholm 21
Baghdad 20
Denver 20
Fuzhou 20
Jiaxing 20
Ottawa 20
Phoenix 20
Porto Alegre 20
Boston 19
Dong Ket 19
Hangzhou 19
Montreal 19
Ankara 18
Manchester 18
Mexico City 18
Falls Church 17
Istanbul 17
Nanchang 17
Amsterdam 16
Changsha 16
Quito 16
Totale 16.252
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Nome #
APECED: PECULIARITÀ FENOTIPICHE E GENOTIPICHE IN UNA CASISTICA PEDIATRICA 925
Growth impairment in children with severe autoimmune primary hypothyroidism and pituitary hyperplasia without goiter 260
Analysis of the factors affecting the evolution over time of subclinical hypothyroidism in children 223
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
Adenoipofisite in un adolescente con pansinusite e meningite 219
A novel PAR 1 deletion associated with Leri-Weill dyschondrosteosis 218
A novel frameshift mutation of the DAX-1 gene in a boy with Xlinked adrenal hypoplasia congenita and no early impairement of the hypothalamus-pituitary-gonadal axis 212
A 7-Years Active Pharmacovigilance Study of Adverse Drug Reactions Causing Children Admission to a Pediatric Emergency Department in Sicily 208
A peculiar cognitive and behavioural phenotype as the first clue to suspect Klinefelter syndrome in prepubertal males 206
Adult height of girls with Turner syndrome treated from before six years of age with a fixed per kg growth hormone dose. 205
A case of adenohypophysitis in a boy affected by sinusitis and acute meningitis: outcome 203
Adult height following a combined treatment of ketoconazole - cyproterone acetate - leuprolide depot in a boy with atypical McCune-Albright syndrome 200
48, XXYY syndrome in a newborn with ambiguous genitalia 195
Aldosterone synthase deficiency type I with no documented homozygous mutations in the CYP11B2 gene 192
Adult height of girls with Turner syndrome treated from before six years of age with a fixed per kilo GH dose 190
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease 189
Hearing loss in congenital hypothalamic hypothyroidism: a wide therapeutic window 186
AGE OF ONSET OF ANOREXIA NERVOSA (AN) CAN AFFECT FINAL HEIGHT 186
Atypical phenotypic aspects of autoimmune thyroid disorders in young patients with Turner syndrome 186
A not very essential obesity: the Rohhad syndrome. Description of two cases and review of the literature 186
Even in the era of congenital hypothyroidism screening mild and subclinical sensorineural hearing loss remains a relatively common complication of severe congenital hypothyroidism 185
Acute suppurative thyroiditis disclosing diagnosis of thyroid cancer in a boy 183
Adenohypophysitis in a boy with pan-sinusitis and meningitis 182
Fibroscan: a new non-invasive method for evaluation of liver dysfunction in Turner syndrome 180
Bone Maturation as a Predictive Factor of Catch-Up Growth During the First Year of Life in Born Small for Gestational Age Infants: A Prospective Study 180
DIFFERENCES IN LEVOTHYROXINE DOSAGES FOR REPLACEMENT OF CHILDREN WITH PRIMARY AND CENTRAL PERMANENT HYPOTHYROIDISM 179
Birth length and weight in congenital adrenal hyperplasia according to the different phenotype 177
Ascite tubercolare: descrizione di un caso in età pediatrica 176
Adherence to sublingual immunotherapy in preschool children 172
A rare cause of pediatric hypoglycemia in a boy: a malignat insulinoma 171
Two-year prospective evaluation of the factors affecting honeymoon frequency and duration in children with insulin dependent diabetes mellitus: The key-role of age at diagnosis 169
Does family history of obesity, cardiovascular, and metabolic diseases influence onset and severity of childhood obesity? 169
Amenorrea primaria in una adolescente con iperprolattinemia:mancato riconoscimento di una sindrome di Turner 168
Adult Height Outcome of Girls with Idiopathic Central Precocious Puberty Treated with GnRH Analogs is Irrespective of BMI 165
A characteristic cognitive and behavioural pattern as a clue to suspect Klinefelter syndrome in prepubertal age. 162
Association of five autoimmune diseases in a young woman with Down's syndrome 161
Clinical features in a patient with Turner syndrome and pericentric inversion of chromosome 9 160
Acute interstitial nephritis.A cause of inflammatory renal glycosuria 159
STUDIO TRASVERSALE E PROSPETTICO DEGLI EFFETTI DELLA TERAPIA CON GH SUL QUADRO METABOLICO E SULLA COMPOSIZIONE CORPOREA IN BAMBINI CON DEFICIT DI GH 159
Underlying Hashimoto's thyroiditis negatively affects the evolution of subclinical hypothyroidism in children irrespective of other concomitant risk factors. 157
Even in the Era of Congenital Hypothyroidism Screening Mild and Subclinical Sensorineural Hearing Loss Remains a Relatively Common Complication of Severe Congenital Hypothyroidism 157
APECED syndrome in childhood: Clinical spectrum is enlarging 157
Nefrite interstiziale acuta 156
Late hormonal function after testicular torsion 156
A heritable cause of cleft lip and palate--Van der Woude syndrome caused by a novel IRF6 mutation. Review of the literature and of the differential diagnosis. 156
Flecainide-responsive myotonia permanens with SNEL onset: A new case and literature review 156
Key-role of thyrotropin deficiency in disclosing craniopharyngioma diagnosis in a short girl with Hashimoto's thyroiditis. 154
Aumento dello spessore medio-intimale in diversi siti arteriosi in adolescenti obesi con adiposità addominale, insulino-resistenza e alti livelli di colesterolo-LDL. 154
Aldosterone syndrome deficiency type I with non documentations in the CYP 11 B2 gene 153
A possible relationship between Beckwith-Wiedemann syndrome and prune belly syndrome. Clin Dysmorph 153
Birth length and weight in congenital adrenal hyperplasia according to the different phenotype. 153
Trattamento di tumori ipofisari mediante Cyber-Knife: Dati preliminari a medio termine su efficacia e sicurezza 153
Direct comparison between continuous and coseasonal regimen for sublingual immunotherapy in children with grass allergy: a randomized controlled study 153
Bone Maturation as a Predictive Factor of Catch-up Growth During the First Year of Life in Born Small for Gestational Age Infants: A Prospective Study 153
APECED in Sicilia: peculiarità cliniche e genotipiche 152
Evans syndrome: A case report 150
Adrenal Cushing Syndrome: Diagnosis and Management in a 10-Year-Old Boy with Carney Complex 149
Increased large artery intima media thickness in adolescents with classical and non-classical congenital adrenal hyperplasia is unrelated to metabolic syndrome 147
Autoimmune polyendocrinopathy-candidiasis-ectodermal-distrophy: peculiar evidences from the first report of a Sicilian family 146
Evaluation of the AIRE gene mutations in a cohort of Italian patients with autoimmune-polyendocrinopathy-candidiasis-ectodermal-dystrophy (APECED) and intheir relatives. 146
Hypoceruloplasminemia as a Marker of Severe Hypothyroidism 145
Increased intima media thickness at many arterial sites in obese adolescents with abdominal adiposity, insulin resistance, and high LDL-cholesterol. 144
A Rare Case of Precocious Puberty in a Child with a Novel GATA-4 Gene Mutation: Implications for Disorders of Sex Development (DSD) and Review of the Literature 143
Graves' disease prevalence in a young population with Turner syndrome 143
Valutazione elastografica (fibroscan) del fegato nelle pazienti con sindrome di Turner 142
Clinical Peculiarities in a Cohort of Patients with Wolfram Syndrome 1 142
Evaluation of liver stiffness using transient elastography (fibroscan) in young adults with Turner syndrome. 141
Outbreak of Brucella melitensis infection in Eastern Sicily: risk factors, clinical characteristics and complication rate 141
Metamorphic thyroid autoimmunity in Down Syndrome: from Hashimoto's thyroiditis to Graves' disease and beyond. 141
Malignant insulinoma, a very rare cause of pediatric hypoglycemia 141
Peculiarities of autoimmune thyroid diseases in children with Turner or Down syndrome: an overview 140
Growth Hormone Treatment to Final Height in Turner Syndrome: Systematic Review 138
Thyroid Function Patterns at Hashimoto's Thyroiditis Presentation in Childhood and Adolescence Are Mainly Conditioned by Patients' Age. 137
Erythrocytosis as the first manifestation of adrenal carcinoma 137
INCREASED LARGE ARTERY INTIMA MEDIA THICKNESS IN ADOLESCENTS WITH EITHER CLASSICAL OR NON-CLASSICAL CONGENITAL ADRENAL HYPERPLASIA. 137
In congenital hypothyroidism bone maturation at birth may be a predictive factor of psychomotor development during the first year of life irrespective of other variables related to treatment 134
Prevalence and clinical features of severe diabetic ketoacidosis treated in pediatric intensive care unit: a 5-year monocentric experience 133
Bronchiolitis Severity Affects Blood Count and Inflammatory Marker Levels: A Real-Life Experience 133
Congenital Hypopituitarism Associated with Complex Cranio-vertebral Junction Anomalies 133
Hurthle cell carcinoma in childhood: Retrospective analysis of a large series 133
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome 132
Infezioni respiratorie in età pediatrica : ruoli del mycoplasma e della chlamydia nella nostra esperienza 131
Natural history of glucose tolerance, beta-cell function and peripheral insulin sensitivity in cystic fibrosis patients with fasting euglycemia 129
Autoimmune polyglandular disease (APECED) and mutineuropathy: a case report 128
Terapia estroprogestinica nella sindrome di Turner 127
Dyscondrosteosis in a child with Becker muscular dystrophy: an unreported association between Xp21 gene (DMD/BMD) deletion and a novel homozygous SHOX gene mutation 126
Mental retardation, peculiar facial dysmorphism and HbH inclusions in a 4 year-old boy. ) 126
AIRE gene mutations and autoantibodies to interferon omega in patients with chronic hypoparathyroidism without APECED 124
Novel SHOX Gene Mutation in a Short Boy with Becker Muscular Dystrophy: Double Trouble in Two Adjacent Genes. 123
Preventing and treating childhood obesity by sleeping better: a systematic review 122
Three-year prospective evaluation of glucose tolerance, beta- cell function and peripheral insulin sensitivity in non- diabetic patients with thalassemia major 122
I giovani adulti con fibrosi cistica sono più bassi dei controlli, perché anche i loro genitori lo sono 121
Novel insight into Chronic Inflammatory Demyelinating Polineuropathy in APECED syndrome: molecular mechanisms and clinical implications in children 121
Association between osteocalcin and residual β-cell function in children and adolescents newly diagnosed with type 1 diabetes: a pivotal study 121
Thyroid function test evolution in children with Hashimoto's thyroiditis is closely conditioned by the biochemical picture at diagnosis 120
Pseudotumor cerebri e Papilledema Idiopatico: un'analisi retrospettiva di tre centri pediatrici italiani. 118
Epidemiological and clinical peculiarities of polyglandular syndrome type 3 in pediatric age 118
Minipuberty in born small for gestational age infants: A case control prospective pilot study 118
Valutazione comparativa di due differenti schemi di terapia frenante la pubertà in bambine con pubertà precoce vera. 117
Novel mutation of CYP21A2 gene (N387K) affecting a nonconserved amino acid residue in Exon 9. 116
Totale 16.515
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Categoria #
all - tutte 90.753
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 90.753
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021333 0 0 0 0 0 0 0 0 0 178 69 86
2021/20221.590 18 199 30 63 64 39 94 61 45 288 218 471
2022/20233.679 294 262 168 287 323 380 92 236 1.439 20 111 67
2023/20241.187 95 129 80 139 123 264 65 108 10 59 14 101
2024/20254.728 95 66 85 305 254 91 141 918 1.304 265 404 800
2025/202613.375 647 1.023 1.413 924 1.007 2.885 1.759 1.561 1.648 508 0 0
Totale 29.150