IRIS
VALENZISE, Mariella
 Distribuzione geografica
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Continente #
EU - Europa 8.301
NA - Nord America 8.263
AS - Asia 4.571
SA - Sud America 1.882
AF - Africa 135
OC - Oceania 14
Continente sconosciuto - Info sul continente non disponibili 5
AN - Antartide 1
Totale 23.172
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Nazione #
US - Stati Uniti d'America 8.098
RU - Federazione Russa 2.634
SG - Singapore 2.055
BR - Brasile 1.657
IT - Italia 1.292
CN - Cina 1.272
IE - Irlanda 1.210
SE - Svezia 1.153
HK - Hong Kong 603
DE - Germania 461
UA - Ucraina 414
FI - Finlandia 267
PL - Polonia 224
VN - Vietnam 197
GB - Regno Unito 183
FR - Francia 173
AT - Austria 93
IN - India 79
AR - Argentina 78
CA - Canada 73
MX - Messico 60
TR - Turchia 50
ZA - Sudafrica 43
BD - Bangladesh 41
IQ - Iraq 40
BE - Belgio 39
EC - Ecuador 36
ES - Italia 36
NL - Olanda 36
JP - Giappone 34
UZ - Uzbekistan 34
ID - Indonesia 33
VE - Venezuela 26
CI - Costa d'Avorio 25
PK - Pakistan 23
CO - Colombia 22
MA - Marocco 22
CZ - Repubblica Ceca 18
PY - Paraguay 16
CL - Cile 15
TN - Tunisia 15
PE - Perù 14
LT - Lituania 12
KE - Kenya 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
LB - Libano 6
OM - Oman 6
IR - Iran 5
KG - Kirghizistan 5
NO - Norvegia 5
QA - Qatar 5
SA - Arabia Saudita 5
BG - Bulgaria 4
GR - Grecia 4
NP - Nepal 4
PA - Panama 4
RS - Serbia 4
AL - Albania 3
BB - Barbados 3
BH - Bahrain 3
BY - Bielorussia 3
CH - Svizzera 3
DZ - Algeria 3
HU - Ungheria 3
JM - Giamaica 3
KR - Corea 3
LU - Lussemburgo 3
NZ - Nuova Zelanda 3
PS - Palestinian Territory 3
SV - El Salvador 3
SY - Repubblica araba siriana 3
A2 - ???statistics.table.value.countryCode.A2??? 2
BA - Bosnia-Erzegovina 2
BN - Brunei Darussalam 2
CR - Costa Rica 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 23.154
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Città #
Dallas 1.383
Moscow 1.354
Dublin 1.209
Ashburn 1.104
Singapore 1.000
Chandler 861
Jacksonville 833
Hong Kong 599
Nyköping 576
Beijing 505
Dearborn 226
Princeton 218
Messina 213
Warsaw 213
Los Angeles 210
Medford 203
Cambridge 192
The Dalles 168
Des Moines 162
São Paulo 160
Ann Arbor 142
Boardman 123
Buffalo 106
Munich 99
Jinan 88
New York 78
Vienna 77
Ho Chi Minh City 68
Rome 66
Wilmington 65
Washington 61
Shenyang 58
Rio de Janeiro 54
Milan 49
Redondo Beach 49
Tianjin 49
Nanjing 46
Turku 45
Catania 43
Woodbridge 42
Belo Horizonte 38
San Mateo 36
Houston 35
Bremen 33
Johannesburg 33
Hanoi 32
Brussels 31
Hebei 30
Helsinki 30
London 30
Tokyo 30
Brooklyn 29
Haikou 29
Brasília 27
Tashkent 26
Zhengzhou 26
Abidjan 25
Atlanta 25
Campinas 25
Ningbo 25
Santa Clara 25
Frankfurt am Main 24
Hyderabad 24
Nuremberg 24
Seattle 22
Lancaster 21
Palermo 21
Stockholm 21
Curitiba 20
Fuzhou 20
Jiaxing 20
Chicago 19
Dong Ket 19
Jakarta 19
Phoenix 19
Boston 18
Denver 18
Montreal 18
Porto Alegre 18
Falls Church 17
Hangzhou 17
Ankara 16
Changsha 16
Guangzhou 16
Nanchang 16
Ottawa 16
Baghdad 15
Chennai 15
Council Bluffs 15
Naples 15
Ribeirão Preto 15
São José dos Campos 15
Düsseldorf 14
Fortaleza 14
Frederick 14
Guarulhos 14
Orem 14
Quito 14
Salvador 14
Taizhou 14
Totale 14.098
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Nome #
APECED: PECULIARITÀ FENOTIPICHE E GENOTIPICHE IN UNA CASISTICA PEDIATRICA 885
Growth impairment in children with severe autoimmune primary hypothyroidism and pituitary hyperplasia without goiter 222
Adenoipofisite in un adolescente con pansinusite e meningite 181
Analysis of the factors affecting the evolution over time of subclinical hypothyroidism in children 181
A novel PAR 1 deletion associated with Leri-Weill dyschondrosteosis 178
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 178
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. 172
A case of adenohypophysitis in a boy affected by sinusitis and acute meningitis: outcome 171
A peculiar cognitive and behavioural phenotype as the first clue to suspect Klinefelter syndrome in prepubertal males 170
Adult height of girls with Turner syndrome treated from before six years of age with a fixed per kg growth hormone dose. 169
A 7-Years Active Pharmacovigilance Study of Adverse Drug Reactions Causing Children Admission to a Pediatric Emergency Department in Sicily 160
48, XXYY syndrome in a newborn with ambiguous genitalia 157
Adult height following a combined treatment of ketoconazole - cyproterone acetate - leuprolide depot in a boy with atypical McCune-Albright syndrome 157
Adult height of girls with Turner syndrome treated from before six years of age with a fixed per kilo GH dose 152
Hearing loss in congenital hypothalamic hypothyroidism: a wide therapeutic window 151
AGE OF ONSET OF ANOREXIA NERVOSA (AN) CAN AFFECT FINAL HEIGHT 150
Aldosterone synthase deficiency type I with no documented homozygous mutations in the CYP11B2 gene 149
Atypical phenotypic aspects of autoimmune thyroid disorders in young patients with Turner syndrome 149
Acute suppurative thyroiditis disclosing diagnosis of thyroid cancer in a boy 148
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 147
Adenohypophysitis in a boy with pan-sinusitis and meningitis 147
A not very essential obesity: the Rohhad syndrome. Description of two cases and review of the literature 147
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease 146
Birth length and weight in congenital adrenal hyperplasia according to the different phenotype 146
Even in the era of congenital hypothyroidism screening mild and subclinical sensorineural hearing loss remains a relatively common complication of severe congenital hypothyroidism 145
Ascite tubercolare: descrizione di un caso in età pediatrica 142
Adherence to sublingual immunotherapy in preschool children 138
Fibroscan: a new non-invasive method for evaluation of liver dysfunction in Turner syndrome 137
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 137
Does family history of obesity, cardiovascular, and metabolic diseases influence onset and severity of childhood obesity? 137
DIFFERENCES IN LEVOTHYROXINE DOSAGES FOR REPLACEMENT OF CHILDREN WITH PRIMARY AND CENTRAL PERMANENT HYPOTHYROIDISM 136
Adult Height Outcome of Girls with Idiopathic Central Precocious Puberty Treated with GnRH Analogs is Irrespective of BMI 135
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. 133
Trattamento di tumori ipofisari mediante Cyber-Knife: Dati preliminari a medio termine su efficacia e sicurezza 131
Underlying Hashimoto's thyroiditis negatively affects the evolution of subclinical hypothyroidism in children irrespective of other concomitant risk factors. 129
STUDIO TRASVERSALE E PROSPETTICO DEGLI EFFETTI DELLA TERAPIA CON GH SUL QUADRO METABOLICO E SULLA COMPOSIZIONE CORPOREA IN BAMBINI CON DEFICIT DI GH 128
Evaluation of the AIRE gene mutations in a cohort of Italian patients with autoimmune-polyendocrinopathy-candidiasis-ectodermal-dystrophy (APECED) and intheir relatives. 127
Valutazione elastografica (fibroscan) del fegato nelle pazienti con sindrome di Turner 126
Association of five autoimmune diseases in a young woman with Down's syndrome 126
A rare cause of pediatric hypoglycemia in a boy: a malignat insulinoma 126
Even in the Era of Congenital Hypothyroidism Screening Mild and Subclinical Sensorineural Hearing Loss Remains a Relatively Common Complication of Severe Congenital Hypothyroidism 125
Birth length and weight in congenital adrenal hyperplasia according to the different phenotype. 124
Amenorrea primaria in una adolescente con iperprolattinemia:mancato riconoscimento di una sindrome di Turner 124
Acute interstitial nephritis.A cause of inflammatory renal glycosuria 122
Autoimmune polyendocrinopathy-candidiasis-ectodermal-distrophy: peculiar evidences from the first report of a Sicilian family 122
Nefrite interstiziale acuta 121
A characteristic cognitive and behavioural pattern as a clue to suspect Klinefelter syndrome in prepubertal age. 121
Key-role of thyrotropin deficiency in disclosing craniopharyngioma diagnosis in a short girl with Hashimoto's thyroiditis. 120
Flecainide-responsive myotonia permanens with SNEL onset: A new case and literature review 120
Direct comparison between continuous and coseasonal regimen for sublingual immunotherapy in children with grass allergy: a randomized controlled study 119
Aldosterone syndrome deficiency type I with non documentations in the CYP 11 B2 gene 118
APECED in Sicilia: peculiarità cliniche e genotipiche 118
Increased intima media thickness at many arterial sites in obese adolescents with abdominal adiposity, insulin resistance, and high LDL-cholesterol. 118
Peculiarities of autoimmune thyroid diseases in children with Turner or Down syndrome: an overview 118
Clinical features in a patient with Turner syndrome and pericentric inversion of chromosome 9 118
Evaluation of liver stiffness using transient elastography (fibroscan) in young adults with Turner syndrome. 115
Late hormonal function after testicular torsion 115
APECED syndrome in childhood: Clinical spectrum is enlarging 115
Increased large artery intima media thickness in adolescents with classical and non-classical congenital adrenal hyperplasia is unrelated to metabolic syndrome 114
Hypoceruloplasminemia as a Marker of Severe Hypothyroidism 114
Adrenal Cushing Syndrome: Diagnosis and Management in a 10-Year-Old Boy with Carney Complex 113
Aumento dello spessore medio-intimale in diversi siti arteriosi in adolescenti obesi con adiposità addominale, insulino-resistenza e alti livelli di colesterolo-LDL. 113
Three-year prospective evaluation of glucose tolerance, beta- cell function and peripheral insulin sensitivity in non- diabetic patients with thalassemia major 112
Outbreak of Brucella melitensis infection in Eastern Sicily: risk factors, clinical characteristics and complication rate 112
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 111
A possible relationship between Beckwith-Wiedemann syndrome and prune belly syndrome. Clin Dysmorph 111
Metamorphic thyroid autoimmunity in Down Syndrome: from Hashimoto's thyroiditis to Graves' disease and beyond. 111
Natural history of glucose tolerance, beta-cell function and peripheral insulin sensitivity in cystic fibrosis patients with fasting euglycemia 110
Evans syndrome: A case report 110
Novel SHOX Gene Mutation in a Short Boy with Becker Muscular Dystrophy: Double Trouble in Two Adjacent Genes. 109
Malignant insulinoma, a very rare cause of pediatric hypoglycemia 109
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 109
Clinical Peculiarities in a Cohort of Patients with Wolfram Syndrome 1 109
Terapia estroprogestinica nella sindrome di Turner 108
Novel insight into Chronic Inflammatory Demyelinating Polineuropathy in APECED syndrome: molecular mechanisms and clinical implications in children 108
Mental retardation, peculiar facial dysmorphism and HbH inclusions in a 4 year-old boy. ) 106
Epidemiological and clinical peculiarities of polyglandular syndrome type 3 in pediatric age 106
Erythrocytosis as the first manifestation of adrenal carcinoma 106
Dyscondrosteosis in a child with Becker muscular dystrophy: an unreported association between Xp21 gene (DMD/BMD) deletion and a novel homozygous SHOX gene mutation 105
Valutazione comparativa di due differenti schemi di terapia frenante la pubertà in bambine con pubertà precoce vera. 103
Congenital Hypopituitarism Associated with Complex Cranio-vertebral Junction Anomalies 103
Infezioni respiratorie in età pediatrica : ruoli del mycoplasma e della chlamydia nella nostra esperienza 102
Autoimmune polyglandular disease (APECED) and mutineuropathy: a case report 102
AIRE gene mutations and autoantibodies to interferon omega in patients with chronic hypoparathyroidism without APECED 102
Hurthle cell carcinoma in childhood: Retrospective analysis of a large series 102
Graves' disease prevalence in a young population with Turner syndrome 101
Pseudotumor cerebri e Papilledema Idiopatico: un'analisi retrospettiva di tre centri pediatrici italiani. 101
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 100
R298Q mutation of p63 gene in autosomal dominant ectodermal dysplasia associated with arrhythmogenic right ventricular cardiomyopathy 100
Congenital adenohypophysis aplasia: clinical features and analysis of thetranscriptional factors for embryonic pituitary development. 100
Thyroid Function Patterns at Hashimoto's Thyroiditis Presentation in Childhood and Adolescence Are Mainly Conditioned by Patients' Age. 100
Subclinical hypothyroidism in children: is it always subclinical? 99
INCREASED LARGE ARTERY INTIMA MEDIA THICKNESS IN ADOLESCENTS WITH EITHER CLASSICAL OR NON-CLASSICAL CONGENITAL ADRENAL HYPERPLASIA. 99
Final height in isolated GH deficiency type 1A: effects of 5- year treatment with IGF-I 98
Five-year prospective evaluation of thyroid function in girls with subclinical mild hypothyroidism of different etiology 98
The CX3C-chemokine fractalkine (CX3CL1) is detectable in serum of patients affected by active pityriasis rosea 97
Mayer-Rokitansky-Küster-Hauser syndrome: rare cause of amenorrhea 96
Novel mutation of CYP21A2 gene (N387K) affecting a nonconserved amino acid residue in Exon 9. 96
Prevalenza della malattia di Graves in una popolazione giovanile con la sindrome di Turner 96
Thyroid function test evolution in children with Hashimoto's thyroiditis is closely conditioned by the biochemical picture at diagnosis 96
Totale 13.296
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Categoria #
all - tutte 82.016
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 82.016
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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
2025/20267.772 647 1.023 1.413 924 1.007 2.758 0 0 0 0 0 0
Totale 23.547