IRIS
VALENZISE, Mariella
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
EU - Europa 11.529
NA - Nord America 9.915
AS - Asia 5.723
SA - Sud America 2.012
AF - Africa 167
OC - Oceania 18
Continente sconosciuto - Info sul continente non disponibili 5
AN - Antartide 1
Totale 29.370
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 9.707
RU - Federazione Russa 5.449
SG - Singapore 2.488
BR - Brasile 1.721
CN - Cina 1.601
IT - Italia 1.388
IE - Irlanda 1.212
SE - Svezia 1.153
HK - Hong Kong 643
DE - Germania 498
UA - Ucraina 418
FR - Francia 374
FI - Finlandia 268
VN - Vietnam 258
PL - Polonia 228
GB - Regno Unito 211
IN - India 139
BD - Bangladesh 103
AR - Argentina 96
CA - Canada 95
AT - Austria 94
MX - Messico 70
TR - Turchia 67
IQ - Iraq 56
JP - Giappone 49
NL - Olanda 48
ZA - Sudafrica 48
EC - Ecuador 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 27
CI - Costa d'Avorio 25
SA - Arabia Saudita 24
CL - Cile 22
PE - Perù 20
CZ - Repubblica Ceca 19
PY - Paraguay 17
TN - Tunisia 17
AE - Emirati Arabi Uniti 16
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 10
MY - Malesia 9
PH - Filippine 9
DO - Repubblica Dominicana 8
EE - Estonia 8
IL - Israele 8
OM - Oman 8
BO - Bolivia 7
DZ - Algeria 7
HN - Honduras 7
BG - Bulgaria 6
DK - Danimarca 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
BB - Barbados 4
CH - Svizzera 4
HU - Ungheria 4
BA - Bosnia-Erzegovina 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
MD - Moldavia 2
Totale 29.338
Salva come PNG Salva come JPEG
Città #
Ashburn 1.649
Moscow 1.623
Dallas 1.399
Singapore 1.333
Dublin 1.210
Chandler 862
Jacksonville 835
Hong Kong 639
Nyköping 576
Beijing 534
San Jose 527
The Dalles 288
Dearborn 226
Messina 224
Los Angeles 222
Princeton 218
Warsaw 215
Medford 203
Cambridge 192
Lauterbourg 189
Des Moines 166
São Paulo 166
Ann Arbor 142
Boardman 124
Buffalo 112
Council Bluffs 101
Munich 99
New York 89
Jinan 88
Ho Chi Minh City 81
Vienna 78
Rome 75
Tianjin 73
Wilmington 65
Washington 61
Milan 60
Rio de Janeiro 58
Shenyang 58
Santa Clara 53
Frankfurt am Main 52
Orem 51
Redondo Beach 49
Catania 47
Nanjing 47
Guangzhou 46
Turku 45
Tokyo 43
Hanoi 42
Houston 42
Woodbridge 42
Belo Horizonte 39
San Mateo 36
Atlanta 35
Johannesburg 34
Bremen 33
Brussels 33
London 32
Helsinki 31
Brooklyn 30
Hebei 30
Haikou 29
Tashkent 29
Brasília 28
Chennai 27
Chicago 27
Nuremberg 27
Campinas 26
Montreal 26
Zhengzhou 26
Abidjan 25
Hyderabad 25
Ningbo 25
Bangkok 24
Shanghai 24
Mumbai 23
Palermo 23
Seattle 23
Lancaster 22
Phoenix 22
Curitiba 21
Jakarta 21
Stockholm 21
Baghdad 20
Denver 20
Fuzhou 20
Hangzhou 20
Jiaxing 20
Ottawa 20
Porto Alegre 20
Boston 19
Dong Ket 19
Ankara 18
Manchester 18
Mexico City 18
Falls Church 17
Istanbul 17
Nanchang 17
Amsterdam 16
Changsha 16
Naples 16
Totale 16.627
Salva come PNG Salva come JPEG
Nome #
APECED: PECULIARITÀ FENOTIPICHE E GENOTIPICHE IN UNA CASISTICA PEDIATRICA 938
Growth impairment in children with severe autoimmune primary hypothyroidism and pituitary hyperplasia without goiter 263
Analysis of the factors affecting the evolution over time of subclinical hypothyroidism in children 225
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
A novel PAR 1 deletion associated with Leri-Weill dyschondrosteosis 223
Adenoipofisite in un adolescente con pansinusite e meningite 221
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 214
A 7-Years Active Pharmacovigilance Study of Adverse Drug Reactions Causing Children Admission to a Pediatric Emergency Department in Sicily 214
A peculiar cognitive and behavioural phenotype as the first clue to suspect Klinefelter syndrome in prepubertal males 207
Adult height of girls with Turner syndrome treated from before six years of age with a fixed per kg growth hormone dose. 206
Adult height following a combined treatment of ketoconazole - cyproterone acetate - leuprolide depot in a boy with atypical McCune-Albright syndrome 205
A case of adenohypophysitis in a boy affected by sinusitis and acute meningitis: outcome 204
48, XXYY syndrome in a newborn with ambiguous genitalia 195
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease 192
Aldosterone synthase deficiency type I with no documented homozygous mutations in the CYP11B2 gene 192
AGE OF ONSET OF ANOREXIA NERVOSA (AN) CAN AFFECT FINAL HEIGHT 191
Adult height of girls with Turner syndrome treated from before six years of age with a fixed per kilo GH dose 191
A not very essential obesity: the Rohhad syndrome. Description of two cases and review of the literature 191
Adult Height Outcome of Girls with Idiopathic Central Precocious Puberty Treated with GnRH Analogs is Irrespective of BMI 190
DIFFERENCES IN LEVOTHYROXINE DOSAGES FOR REPLACEMENT OF CHILDREN WITH PRIMARY AND CENTRAL PERMANENT HYPOTHYROIDISM 190
Hearing loss in congenital hypothalamic hypothyroidism: a wide therapeutic window 188
Atypical phenotypic aspects of autoimmune thyroid disorders in young patients with Turner syndrome 186
Adenohypophysitis in a boy with pan-sinusitis and meningitis 185
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
Fibroscan: a new non-invasive method for evaluation of liver dysfunction in Turner syndrome 183
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 182
Birth length and weight in congenital adrenal hyperplasia according to the different phenotype 177
Ascite tubercolare: descrizione di un caso in età pediatrica 177
A rare cause of pediatric hypoglycemia in a boy: a malignat insulinoma 174
Adherence to sublingual immunotherapy in preschool children 173
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 171
Amenorrea primaria in una adolescente con iperprolattinemia:mancato riconoscimento di una sindrome di Turner 170
Does family history of obesity, cardiovascular, and metabolic diseases influence onset and severity of childhood obesity? 170
Hypoceruloplasminemia as a Marker of Severe Hypothyroidism 164
Association of five autoimmune diseases in a young woman with Down's syndrome 163
A characteristic cognitive and behavioural pattern as a clue to suspect Klinefelter syndrome in prepubertal age. 163
Clinical features in a patient with Turner syndrome and pericentric inversion of chromosome 9 163
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. 161
APECED syndrome in childhood: Clinical spectrum is enlarging 161
Underlying Hashimoto's thyroiditis negatively affects the evolution of subclinical hypothyroidism in children irrespective of other concomitant risk factors. 160
Acute interstitial nephritis.A cause of inflammatory renal glycosuria 160
STUDIO TRASVERSALE E PROSPETTICO DEGLI EFFETTI DELLA TERAPIA CON GH SUL QUADRO METABOLICO E SULLA COMPOSIZIONE CORPOREA IN BAMBINI CON DEFICIT DI GH 160
Nefrite interstiziale acuta 159
Even in the Era of Congenital Hypothyroidism Screening Mild and Subclinical Sensorineural Hearing Loss Remains a Relatively Common Complication of Severe Congenital Hypothyroidism 159
Late hormonal function after testicular torsion 158
Key-role of thyrotropin deficiency in disclosing craniopharyngioma diagnosis in a short girl with Hashimoto's thyroiditis. 157
Aldosterone syndrome deficiency type I with non documentations in the CYP 11 B2 gene 157
APECED in Sicilia: peculiarità cliniche e genotipiche 157
Aumento dello spessore medio-intimale in diversi siti arteriosi in adolescenti obesi con adiposità addominale, insulino-resistenza e alti livelli di colesterolo-LDL. 157
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 157
Trattamento di tumori ipofisari mediante Cyber-Knife: Dati preliminari a medio termine su efficacia e sicurezza 156
Flecainide-responsive myotonia permanens with SNEL onset: A new case and literature review 156
Direct comparison between continuous and coseasonal regimen for sublingual immunotherapy in children with grass allergy: a randomized controlled study 155
A possible relationship between Beckwith-Wiedemann syndrome and prune belly syndrome. Clin Dysmorph 154
Birth length and weight in congenital adrenal hyperplasia according to the different phenotype. 154
Adrenal Cushing Syndrome: Diagnosis and Management in a 10-Year-Old Boy with Carney Complex 153
Evans syndrome: A case report 152
Increased intima media thickness at many arterial sites in obese adolescents with abdominal adiposity, insulin resistance, and high LDL-cholesterol. 151
Growth Hormone Treatment to Final Height in Turner Syndrome: Systematic Review 150
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 149
Evaluation of the AIRE gene mutations in a cohort of Italian patients with autoimmune-polyendocrinopathy-candidiasis-ectodermal-dystrophy (APECED) and intheir relatives. 149
Increased large artery intima media thickness in adolescents with classical and non-classical congenital adrenal hyperplasia is unrelated to metabolic syndrome 149
Autoimmune polyendocrinopathy-candidiasis-ectodermal-distrophy: peculiar evidences from the first report of a Sicilian family 147
Graves' disease prevalence in a young population with Turner syndrome 147
Valutazione elastografica (fibroscan) del fegato nelle pazienti con sindrome di Turner 146
Outbreak of Brucella melitensis infection in Eastern Sicily: risk factors, clinical characteristics and complication rate 146
Erythrocytosis as the first manifestation of adrenal carcinoma 145
Clinical Peculiarities in a Cohort of Patients with Wolfram Syndrome 1 145
Evaluation of liver stiffness using transient elastography (fibroscan) in young adults with Turner syndrome. 144
Metamorphic thyroid autoimmunity in Down Syndrome: from Hashimoto's thyroiditis to Graves' disease and beyond. 143
Peculiarities of autoimmune thyroid diseases in children with Turner or Down syndrome: an overview 142
INCREASED LARGE ARTERY INTIMA MEDIA THICKNESS IN ADOLESCENTS WITH EITHER CLASSICAL OR NON-CLASSICAL CONGENITAL ADRENAL HYPERPLASIA. 142
Malignant insulinoma, a very rare cause of pediatric hypoglycemia 142
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome 140
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 140
Thyroid Function Patterns at Hashimoto's Thyroiditis Presentation in Childhood and Adolescence Are Mainly Conditioned by Patients' Age. 140
Minipuberty in born small for gestational age infants: A case control prospective pilot study 140
Prevalence and clinical features of severe diabetic ketoacidosis treated in pediatric intensive care unit: a 5-year monocentric experience 137
Bronchiolitis Severity Affects Blood Count and Inflammatory Marker Levels: A Real-Life Experience 137
Congenital Hypopituitarism Associated with Complex Cranio-vertebral Junction Anomalies 135
Infezioni respiratorie in età pediatrica : ruoli del mycoplasma e della chlamydia nella nostra esperienza 133
Hurthle cell carcinoma in childhood: Retrospective analysis of a large series 133
Natural history of glucose tolerance, beta-cell function and peripheral insulin sensitivity in cystic fibrosis patients with fasting euglycemia 131
Autoimmune polyglandular disease (APECED) and mutineuropathy: a case report 129
Terapia estroprogestinica nella sindrome di Turner 129
Three-year prospective evaluation of glucose tolerance, beta- cell function and peripheral insulin sensitivity in non- diabetic patients with thalassemia major 128
Preventing and treating childhood obesity by sleeping better: a systematic review 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 127
Mental retardation, peculiar facial dysmorphism and HbH inclusions in a 4 year-old boy. ) 126
Novel SHOX Gene Mutation in a Short Boy with Becker Muscular Dystrophy: Double Trouble in Two Adjacent Genes. 125
AIRE gene mutations and autoantibodies to interferon omega in patients with chronic hypoparathyroidism without APECED 124
Association between osteocalcin and residual β-cell function in children and adolescents newly diagnosed with type 1 diabetes: a pivotal study 123
I giovani adulti con fibrosi cistica sono più bassi dei controlli, perché anche i loro genitori lo sono 122
Novel insight into Chronic Inflammatory Demyelinating Polineuropathy in APECED syndrome: molecular mechanisms and clinical implications in children 122
Thyroid function test evolution in children with Hashimoto's thyroiditis is closely conditioned by the biochemical picture at diagnosis 121
Novel mutation of CYP21A2 gene (N387K) affecting a nonconserved amino acid residue in Exon 9. 119
Pseudotumor cerebri e Papilledema Idiopatico: un'analisi retrospettiva di tre centri pediatrici italiani. 119
Epidemiological and clinical peculiarities of polyglandular syndrome type 3 in pediatric age 119
Five-year prospective evaluation of thyroid function in girls with subclinical mild hypothyroidism of different etiology 118
Totale 16.857
Salva come PNG Salva come JPEG
Categoria #
all - tutte 96.146
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 96.146
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202186 0 0 0 0 0 0 0 0 0 0 0 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
2025/202613.984 647 1.023 1.413 924 1.007 2.885 1.759 1.561 1.648 597 298 222
Totale 29.759