IRIS
VALENZISE, Mariella
 Distribuzione geografica
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Continente #
NA - Nord America 8.175
EU - Europa 5.858
AS - Asia 4.477
SA - Sud America 1.876
AF - Africa 133
OC - Oceania 14
Continente sconosciuto - Info sul continente non disponibili 5
AN - Antartide 1
Totale 20.539
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Nazione #
US - Stati Uniti d'America 8.013
SG - Singapore 1.979
BR - Brasile 1.653
IT - Italia 1.291
CN - Cina 1.263
IE - Irlanda 1.210
SE - Svezia 1.152
HK - Hong Kong 603
DE - Germania 461
UA - Ucraina 414
FI - Finlandia 267
PL - Polonia 224
RU - Federazione Russa 205
VN - Vietnam 196
GB - Regno Unito 179
FR - Francia 173
AT - Austria 90
AR - Argentina 78
IN - India 77
CA - Canada 72
MX - Messico 59
TR - Turchia 49
ZA - Sudafrica 41
IQ - Iraq 40
BE - Belgio 39
BD - Bangladesh 38
EC - Ecuador 36
ES - Italia 35
NL - Olanda 35
JP - Giappone 34
UZ - Uzbekistan 34
ID - Indonesia 33
CI - Costa d'Avorio 25
VE - Venezuela 25
CO - Colombia 22
MA - Marocco 22
PK - Pakistan 22
CZ - Repubblica Ceca 18
PY - Paraguay 16
TN - Tunisia 15
CL - Cile 14
PE - Perù 14
KE - Kenya 11
LT - Lituania 11
AE - Emirati Arabi Uniti 10
AZ - Azerbaigian 10
EG - Egitto 10
KZ - Kazakistan 10
UY - Uruguay 10
AU - Australia 9
JO - Giordania 9
EE - Estonia 8
DO - Repubblica Dominicana 7
IL - Israele 7
BO - Bolivia 6
DK - Danimarca 6
HN - Honduras 6
OM - Oman 6
IR - Iran 5
KG - Kirghizistan 5
LB - Libano 5
NO - Norvegia 5
QA - Qatar 5
SA - Arabia Saudita 5
BG - Bulgaria 4
GR - Grecia 4
NP - Nepal 4
RS - Serbia 4
BB - Barbados 3
BH - Bahrain 3
BY - Bielorussia 3
CH - Svizzera 3
DZ - Algeria 3
JM - Giamaica 3
KR - Corea 3
LU - Lussemburgo 3
NZ - Nuova Zelanda 3
PA - Panama 3
PS - Palestinian Territory 3
SV - El Salvador 3
SY - Repubblica araba siriana 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AL - Albania 2
BA - Bosnia-Erzegovina 2
BN - Brunei Darussalam 2
CR - Costa Rica 2
HU - Ungheria 2
KH - Cambogia 2
LA - Repubblica Popolare Democratica del Laos 2
LV - Lettonia 2
MN - Mongolia 2
MY - Malesia 2
NG - Nigeria 2
PW - Palau 2
SK - Slovacchia (Repubblica Slovacca) 2
XK - ???statistics.table.value.countryCode.XK??? 2
AM - Armenia 1
AO - Angola 1
AQ - Antartide 1
CG - Congo 1
Totale 20.521
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Città #
Dallas 1.383
Dublin 1.209
Ashburn 1.059
Singapore 925
Chandler 861
Jacksonville 833
Hong Kong 599
Nyköping 576
Beijing 505
Dearborn 226
Princeton 218
Messina 213
Warsaw 213
Los Angeles 208
Medford 203
Cambridge 192
The Dalles 168
Des Moines 162
São Paulo 160
Ann Arbor 142
Boardman 123
Buffalo 106
Munich 99
Jinan 88
Vienna 76
New York 72
Ho Chi Minh City 67
Rome 66
Wilmington 65
Washington 61
Shenyang 58
Moscow 55
Rio de Janeiro 53
Milan 49
Redondo Beach 49
Tianjin 47
Nanjing 46
Turku 45
Catania 43
Woodbridge 42
Belo Horizonte 37
San Mateo 36
Houston 34
Bremen 33
Hanoi 32
Brussels 31
Johannesburg 31
Hebei 30
Helsinki 30
Tokyo 30
Haikou 29
Brooklyn 28
London 28
Brasília 27
Tashkent 26
Zhengzhou 26
Abidjan 25
Campinas 25
Ningbo 25
Frankfurt am Main 24
Hyderabad 24
Nuremberg 24
Atlanta 23
Santa Clara 23
Seattle 22
Lancaster 21
Palermo 21
Curitiba 20
Fuzhou 20
Jiaxing 20
Stockholm 20
Dong Ket 19
Jakarta 19
Phoenix 19
Chicago 18
Montreal 18
Porto Alegre 18
Boston 17
Falls Church 17
Hangzhou 17
Ankara 16
Changsha 16
Denver 16
Guangzhou 16
Nanchang 16
Ottawa 16
Baghdad 15
Council Bluffs 15
Naples 15
Ribeirão Preto 15
São José dos Campos 15
Chennai 14
Düsseldorf 14
Fortaleza 14
Frederick 14
Guarulhos 14
Quito 14
Salvador 14
Taizhou 14
Auburn Hills 13
Totale 12.648
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Nome #
APECED: PECULIARITÀ FENOTIPICHE E GENOTIPICHE IN UNA CASISTICA PEDIATRICA 872
Growth impairment in children with severe autoimmune primary hypothyroidism and pituitary hyperplasia without goiter 201
Adenoipofisite in un adolescente con pansinusite e meningite 164
Analysis of the factors affecting the evolution over time of subclinical hypothyroidism in children 164
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 159
A novel PAR 1 deletion associated with Leri-Weill dyschondrosteosis 158
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. 157
A peculiar cognitive and behavioural phenotype as the first clue to suspect Klinefelter syndrome in prepubertal males 154
Adult height of girls with Turner syndrome treated from before six years of age with a fixed per kg growth hormone dose. 153
A case of adenohypophysitis in a boy affected by sinusitis and acute meningitis: outcome 152
48, XXYY syndrome in a newborn with ambiguous genitalia 139
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 137
Adult height of girls with Turner syndrome treated from before six years of age with a fixed per kilo GH dose 137
Adult height following a combined treatment of ketoconazole - cyproterone acetate - leuprolide depot in a boy with atypical McCune-Albright syndrome 137
A 7-Years Active Pharmacovigilance Study of Adverse Drug Reactions Causing Children Admission to a Pediatric Emergency Department in Sicily 137
Aldosterone synthase deficiency type I with no documented homozygous mutations in the CYP11B2 gene 135
Hearing loss in congenital hypothalamic hypothyroidism: a wide therapeutic window 133
AGE OF ONSET OF ANOREXIA NERVOSA (AN) CAN AFFECT FINAL HEIGHT 133
Atypical phenotypic aspects of autoimmune thyroid disorders in young patients with Turner syndrome 133
Does family history of obesity, cardiovascular, and metabolic diseases influence onset and severity of childhood obesity? 132
Adenohypophysitis in a boy with pan-sinusitis and meningitis 130
Birth length and weight in congenital adrenal hyperplasia according to the different phenotype 129
A not very essential obesity: the Rohhad syndrome. Description of two cases and review of the literature 129
Acute suppurative thyroiditis disclosing diagnosis of thyroid cancer in a boy 128
Even in the era of congenital hypothyroidism screening mild and subclinical sensorineural hearing loss remains a relatively common complication of severe congenital hypothyroidism 128
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease 124
Ascite tubercolare: descrizione di un caso in età pediatrica 123
Adherence to sublingual immunotherapy in preschool children 123
Adult Height Outcome of Girls with Idiopathic Central Precocious Puberty Treated with GnRH Analogs is Irrespective of BMI 122
Underlying Hashimoto's thyroiditis negatively affects the evolution of subclinical hypothyroidism in children irrespective of other concomitant risk factors. 121
Trattamento di tumori ipofisari mediante Cyber-Knife: Dati preliminari a medio termine su efficacia e sicurezza 121
Fibroscan: a new non-invasive method for evaluation of liver dysfunction in Turner syndrome 119
DIFFERENCES IN LEVOTHYROXINE DOSAGES FOR REPLACEMENT OF CHILDREN WITH PRIMARY AND CENTRAL PERMANENT HYPOTHYROIDISM 119
Evaluation of the AIRE gene mutations in a cohort of Italian patients with autoimmune-polyendocrinopathy-candidiasis-ectodermal-dystrophy (APECED) and intheir relatives. 118
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. 118
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 118
Valutazione elastografica (fibroscan) del fegato nelle pazienti con sindrome di Turner 117
Birth length and weight in congenital adrenal hyperplasia according to the different phenotype. 113
Key-role of thyrotropin deficiency in disclosing craniopharyngioma diagnosis in a short girl with Hashimoto's thyroiditis. 112
Amenorrea primaria in una adolescente con iperprolattinemia:mancato riconoscimento di una sindrome di Turner 112
Association of five autoimmune diseases in a young woman with Down's syndrome 111
STUDIO TRASVERSALE E PROSPETTICO DEGLI EFFETTI DELLA TERAPIA CON GH SUL QUADRO METABOLICO E SULLA COMPOSIZIONE CORPOREA IN BAMBINI CON DEFICIT DI GH 111
Peculiarities of autoimmune thyroid diseases in children with Turner or Down syndrome: an overview 111
Even in the Era of Congenital Hypothyroidism Screening Mild and Subclinical Sensorineural Hearing Loss Remains a Relatively Common Complication of Severe Congenital Hypothyroidism 110
A rare cause of pediatric hypoglycemia in a boy: a malignat insulinoma 110
Autoimmune polyendocrinopathy-candidiasis-ectodermal-distrophy: peculiar evidences from the first report of a Sicilian family 109
Direct comparison between continuous and coseasonal regimen for sublingual immunotherapy in children with grass allergy: a randomized controlled study 108
Outbreak of Brucella melitensis infection in Eastern Sicily: risk factors, clinical characteristics and complication rate 106
A characteristic cognitive and behavioural pattern as a clue to suspect Klinefelter syndrome in prepubertal age. 105
Three-year prospective evaluation of glucose tolerance, beta- cell function and peripheral insulin sensitivity in non- diabetic patients with thalassemia major 103
Acute interstitial nephritis.A cause of inflammatory renal glycosuria 103
Terapia estroprogestinica nella sindrome di Turner 103
APECED in Sicilia: peculiarità cliniche e genotipiche 103
Increased intima media thickness at many arterial sites in obese adolescents with abdominal adiposity, insulin resistance, and high LDL-cholesterol. 103
Metamorphic thyroid autoimmunity in Down Syndrome: from Hashimoto's thyroiditis to Graves' disease and beyond. 103
Flecainide-responsive myotonia permanens with SNEL onset: A new case and literature review 103
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 102
Natural history of glucose tolerance, beta-cell function and peripheral insulin sensitivity in cystic fibrosis patients with fasting euglycemia 101
Aldosterone syndrome deficiency type I with non documentations in the CYP 11 B2 gene 101
Nefrite interstiziale acuta 101
Novel SHOX Gene Mutation in a Short Boy with Becker Muscular Dystrophy: Double Trouble in Two Adjacent Genes. 101
Increased large artery intima media thickness in adolescents with classical and non-classical congenital adrenal hyperplasia is unrelated to metabolic syndrome 101
Hypoceruloplasminemia as a Marker of Severe Hypothyroidism 101
Clinical features in a patient with Turner syndrome and pericentric inversion of chromosome 9 101
Late hormonal function after testicular torsion 100
Novel insight into Chronic Inflammatory Demyelinating Polineuropathy in APECED syndrome: molecular mechanisms and clinical implications in children 99
APECED syndrome in childhood: Clinical spectrum is enlarging 99
Clinical Peculiarities in a Cohort of Patients with Wolfram Syndrome 1 99
Valutazione comparativa di due differenti schemi di terapia frenante la pubertà in bambine con pubertà precoce vera. 98
Aumento dello spessore medio-intimale in diversi siti arteriosi in adolescenti obesi con adiposità addominale, insulino-resistenza e alti livelli di colesterolo-LDL. 98
Epidemiological and clinical peculiarities of polyglandular syndrome type 3 in pediatric age 97
Evaluation of liver stiffness using transient elastography (fibroscan) in young adults with Turner syndrome. 96
Mental retardation, peculiar facial dysmorphism and HbH inclusions in a 4 year-old boy. ) 95
AIRE gene mutations and autoantibodies to interferon omega in patients with chronic hypoparathyroidism without APECED 95
Malignant insulinoma, a very rare cause of pediatric hypoglycemia 94
Adrenal Cushing Syndrome: Diagnosis and Management in a 10-Year-Old Boy with Carney Complex 93
A possible relationship between Beckwith-Wiedemann syndrome and prune belly syndrome. Clin Dysmorph 93
Pseudotumor cerebri e Papilledema Idiopatico: un'analisi retrospettiva di tre centri pediatrici italiani. 93
Dyscondrosteosis in a child with Becker muscular dystrophy: an unreported association between Xp21 gene (DMD/BMD) deletion and a novel homozygous SHOX gene mutation 92
Subclinical hypothyroidism in children: is it always subclinical? 92
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 92
Evans syndrome: A case report 92
Congenital adenohypophysis aplasia: clinical features and analysis of thetranscriptional factors for embryonic pituitary development. 91
Autoimmune polyglandular disease (APECED) and mutineuropathy: a case report 91
Novel mutation of CYP21A2 gene (N387K) affecting a nonconserved amino acid residue in Exon 9. 90
Prevalenza della malattia di Graves in una popolazione giovanile con la sindrome di Turner 90
Erythrocytosis as the first manifestation of adrenal carcinoma 90
R298Q mutation of p63 gene in autosomal dominant ectodermal dysplasia associated with arrhythmogenic right ventricular cardiomyopathy 89
Cutaneous hemangiomas, hemihypertrophy and macrodactyly at birth 88
The CX3C-chemokine fractalkine (CX3CL1) is detectable in serum of patients affected by active pityriasis rosea 88
Thyroid Function Patterns at Hashimoto's Thyroiditis Presentation in Childhood and Adolescence Are Mainly Conditioned by Patients' Age. 88
Congenital Hypopituitarism Associated with Complex Cranio-vertebral Junction Anomalies 88
Mayer-Rokitansky-Küster-Hauser syndrome: rare cause of amenorrhea 87
Final height in isolated GH deficiency type 1A: effects of 5- year treatment with IGF-I 87
Graves' disease prevalence in a young population with Turner syndrome 87
Infezioni respiratorie in età pediatrica : ruoli del mycoplasma e della chlamydia nella nostra esperienza 86
TREATMENT OF PITUITARY TUMOURS BY CYBERKNIFE: PRELIMINARY DATA OF MIDDLE-TERM EFFECTIVENESS AND SAFETY 86
Five-year prospective evaluation of thyroid function in girls with subclinical mild hypothyroidism of different etiology 86
INCREASED LARGE ARTERY INTIMA MEDIA THICKNESS IN ADOLESCENTS WITH EITHER CLASSICAL OR NON-CLASSICAL CONGENITAL ADRENAL HYPERPLASIA. 86
Analisi dei polimorfismi del gene TTF-2/FOXE1 come possibile causa di disgenesia tiroidea 85
Totale 11.922
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Categoria #
all - tutte 78.157
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 78.157
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021801 0 0 0 0 0 169 63 146 90 178 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
2025/20265.139 647 1.023 1.413 924 1.007 125 0 0 0 0 0 0
Totale 20.914