IRIS
VALENZISE, Mariella
 Distribuzione geografica
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Continente #
EU - Europa 5.048
NA - Nord America 4.918
AS - Asia 1.526
OC - Oceania 11
SA - Sud America 8
AF - Africa 4
Continente sconosciuto - Info sul continente non disponibili 3
Totale 11.518
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Nazione #
US - Stati Uniti d'America 4.885
IE - Irlanda 1.206
IT - Italia 1.170
SE - Svezia 1.131
CN - Cina 824
SG - Singapore 585
UA - Ucraina 391
DE - Germania 312
FI - Finlandia 214
PL - Polonia 201
FR - Francia 122
GB - Regno Unito 115
AT - Austria 69
IN - India 44
BE - Belgio 38
RU - Federazione Russa 24
CA - Canada 23
VN - Vietnam 19
ID - Indonesia 17
CZ - Repubblica Ceca 15
NL - Olanda 13
MX - Messico 9
AU - Australia 8
JP - Giappone 7
ES - Italia 5
NO - Norvegia 5
HK - Hong Kong 4
IR - Iran 4
BR - Brasile 3
CH - Svizzera 3
CL - Cile 3
IL - Israele 3
KR - Corea 3
LT - Lituania 3
NZ - Nuova Zelanda 3
QA - Qatar 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AE - Emirati Arabi Uniti 2
AZ - Azerbaigian 2
DZ - Algeria 2
GR - Grecia 2
LU - Lussemburgo 2
SY - Repubblica araba siriana 2
BD - Bangladesh 1
BG - Bulgaria 1
CO - Colombia 1
CY - Cipro 1
DK - Danimarca 1
EC - Ecuador 1
EG - Egitto 1
EU - Europa 1
HU - Ungheria 1
KH - Cambogia 1
LV - Lettonia 1
MD - Moldavia 1
NG - Nigeria 1
PA - Panama 1
PK - Pakistan 1
RS - Serbia 1
SI - Slovenia 1
TH - Thailandia 1
TR - Turchia 1
TW - Taiwan 1
Totale 11.518
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Città #
Dublin 1.206
Chandler 861
Jacksonville 832
Nyköping 576
Singapore 480
Ashburn 449
Beijing 319
Dearborn 226
Princeton 218
Medford 203
Messina 196
Cambridge 192
Warsaw 192
Des Moines 162
Ann Arbor 142
Boardman 121
Jinan 88
Vienna 67
Wilmington 65
Washington 59
Shenyang 58
Rome 48
Nanjing 46
Los Angeles 44
Woodbridge 42
Milan 38
Catania 36
San Mateo 36
Bremen 33
Brussels 30
Hebei 30
Haikou 29
Houston 25
Ningbo 25
Helsinki 24
Zhengzhou 24
Hyderabad 23
New York 23
Lancaster 21
Tianjin 21
Fuzhou 20
Palermo 20
Dong Ket 19
Jiaxing 19
Falls Church 17
Jakarta 17
Seattle 17
Nanchang 16
Guangzhou 15
Hangzhou 15
Changsha 14
Frederick 14
Munich 14
Auburn Hills 13
Brno 13
Napoli 13
Norwalk 13
Taizhou 13
Redwood City 12
Brescia 11
Naples 11
Ottawa 11
Palmi 11
Florence 10
Lanzhou 10
Pune 10
Verona 10
Trento 9
Cosenza 8
London 8
Rovereto 8
Taiyuan 8
Tappahannock 8
Waanrode 8
Bari 7
Genova 7
San Benedetto del Tronto 7
Cesena 6
Crotone 6
Fairfield 6
Genoa 6
Torino 6
Acireale 5
Bologna 5
Caserta 5
Modica 5
Padova 5
Ravenna 5
Santa Clara 5
Sassari 5
Scilla 5
Shanghai 5
Soriano Calabro 5
Turin 5
Bacchereto 4
Lappeenranta 4
Mumbai 4
Philadelphia 4
Rimini 4
Saint Petersburg 4
Totale 7.880
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Nome #
APECED: PECULIARITÀ FENOTIPICHE E GENOTIPICHE IN UNA CASISTICA PEDIATRICA 782
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. 101
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 98
Valutazione elastografica (fibroscan) del fegato nelle pazienti con sindrome di Turner 96
Hearing loss in congenital hypothalamic hypothyroidism: a wide therapeutic window 92
Adenoipofisite in un adolescente con pansinusite e meningite 91
Does family history of obesity, cardiovascular, and metabolic diseases influence onset and severity of childhood obesity? 90
Analysis of the factors affecting the evolution over time of subclinical hypothyroidism in children 88
Outbreak of Brucella melitensis infection in Eastern Sicily: risk factors, clinical characteristics and complication rate 82
Key-role of thyrotropin deficiency in disclosing craniopharyngioma diagnosis in a short girl with Hashimoto's thyroiditis. 81
Birth length and weight in congenital adrenal hyperplasia according to the different phenotype 81
Aldosterone synthase deficiency type I with no documented homozygous mutations in the CYP11B2 gene 81
Metamorphic thyroid autoimmunity in Down Syndrome: from Hashimoto's thyroiditis to Graves' disease and beyond. 81
Underlying Hashimoto's thyroiditis negatively affects the evolution of subclinical hypothyroidism in children irrespective of other concomitant risk factors. 79
Trattamento di tumori ipofisari mediante Cyber-Knife: Dati preliminari a medio termine su efficacia e sicurezza 78
Peculiarities of autoimmune thyroid diseases in children with Turner or Down syndrome: an overview 78
Terapia estroprogestinica nella sindrome di Turner 77
Even in the era of congenital hypothyroidism screening mild and subclinical sensorineural hearing loss remains a relatively common complication of severe congenital hypothyroidism 77
Birth length and weight in congenital adrenal hyperplasia according to the different phenotype. 76
Evaluation of the AIRE gene mutations in a cohort of Italian patients with autoimmune-polyendocrinopathy-candidiasis-ectodermal-dystrophy (APECED) and intheir relatives. 74
Mental retardation, peculiar facial dysmorphism and HbH inclusions in a 4 year-old boy. ) 73
Nefrite interstiziale acuta 73
Ascite tubercolare: descrizione di un caso in età pediatrica 72
Increased large artery intima media thickness in adolescents with classical and non-classical congenital adrenal hyperplasia is unrelated to metabolic syndrome 72
A novel PAR 1 deletion associated with Leri-Weill dyschondrosteosis 72
Adult height of girls with Turner syndrome treated from before six years of age with a fixed per kg growth hormone dose. 69
Epidemiological and clinical peculiarities of polyglandular syndrome type 3 in pediatric age 69
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
Cutaneous hemangiomas, hemihypertrophy and macrodactyly at birth 67
Fibroscan: a new non-invasive method for evaluation of liver dysfunction in Turner syndrome 67
APECED in Sicilia: peculiarità cliniche e genotipiche 67
A peculiar cognitive and behavioural phenotype as the first clue to suspect Klinefelter syndrome in prepubertal males 67
Natural history of glucose tolerance, beta-cell function and peripheral insulin sensitivity in cystic fibrosis patients with fasting euglycemia 66
AGE OF ONSET OF ANOREXIA NERVOSA (AN) CAN AFFECT FINAL HEIGHT 66
Valutazione comparativa di due differenti schemi di terapia frenante la pubertà in bambine con pubertà precoce vera. 66
Mayer-Rokitansky-Küster-Hauser syndrome: rare cause of amenorrhea 65
Late hormonal function after testicular torsion 65
Adenohypophysitis in a boy with pan-sinusitis and meningitis 65
Amenorrea primaria in una adolescente con iperprolattinemia:mancato riconoscimento di una sindrome di Turner 65
Adult height of girls with Turner syndrome treated from before six years of age with a fixed per kilo GH dose 65
DIFFERENCES IN LEVOTHYROXINE DOSAGES FOR REPLACEMENT OF CHILDREN WITH PRIMARY AND CENTRAL PERMANENT HYPOTHYROIDISM 65
Three-year prospective evaluation of glucose tolerance, beta- cell function and peripheral insulin sensitivity in non- diabetic patients with thalassemia major 64
Autoimmune polyendocrinopathy-candidiasis-ectodermal-distrophy: peculiar evidences from the first report of a Sicilian family 64
Increased intima media thickness at many arterial sites in obese adolescents with abdominal adiposity, insulin resistance, and high LDL-cholesterol. 64
Five-year prospective evaluation of thyroid function in girls with subclinical mild hypothyroidism of different etiology 64
Dyscondrosteosis in a child with Becker muscular dystrophy: an unreported association between Xp21 gene (DMD/BMD) deletion and a novel homozygous SHOX gene mutation 63
Final height in isolated GH deficiency type 1A: effects of 5- year treatment with IGF-I 63
Even in the Era of Congenital Hypothyroidism Screening Mild and Subclinical Sensorineural Hearing Loss Remains a Relatively Common Complication of Severe Congenital Hypothyroidism 63
Flecainide-responsive myotonia permanens with SNEL onset: A new case and literature review 63
Aumento dello spessore medio-intimale in diversi siti arteriosi in adolescenti obesi con adiposità addominale, insulino-resistenza e alti livelli di colesterolo-LDL. 62
Hypoceruloplasminemia as a Marker of Severe Hypothyroidism 62
Graves' disease prevalence in a young population with Turner syndrome 61
Atypical phenotypic aspects of autoimmune thyroid disorders in young patients with Turner syndrome 61
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 61
APECED syndrome in childhood: Clinical spectrum is enlarging 61
Clinical picture,evolution and peculiar molecular findings in a very large pedegree with Wolfram syndrome 60
Novel SHOX Gene Mutation in a Short Boy with Becker Muscular Dystrophy: Double Trouble in Two Adjacent Genes. 60
Direct comparison between continuous and coseasonal regimen for sublingual immunotherapy in children with grass allergy: a randomized controlled study 60
Pseudotumor cerebri e Papilledema Idiopatico: un'analisi retrospettiva di tre centri pediatrici italiani. 60
STUDIO TRASVERSALE E PROSPETTICO DEGLI EFFETTI DELLA TERAPIA CON GH SUL QUADRO METABOLICO E SULLA COMPOSIZIONE CORPOREA IN BAMBINI CON DEFICIT DI GH 60
Aldosterone syndrome deficiency type I with non documentations in the CYP 11 B2 gene 59
Acute suppurative thyroiditis disclosing diagnosis of thyroid cancer in a boy 59
Evaluation of liver stiffness using transient elastography (fibroscan) in young adults with Turner syndrome. 59
Adult height following a combined treatment of ketoconazole - cyproterone acetate - leuprolide depot in a boy with atypical McCune-Albright syndrome 59
A case of adenohypophysitis in a boy affected by sinusitis and acute meningitis: outcome 59
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 58
Novel mutation of CYP21A2 gene (N387K) affecting a nonconserved amino acid residue in Exon 9. 58
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. 58
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 58
The CX3C-chemokine fractalkine (CX3CL1) is detectable in serum of patients affected by active pityriasis rosea 57
Regulation of spermatogenesis in McCune- Albright syndrome :lessons from fifteen year follow-up 57
48, XXYY syndrome in a newborn with ambiguous genitalia 57
Hair changes in congenital disorders of glycosylation (CDG) 56
Dystrophin gene and SHOX gene mutations in a child with Becker muscular dystrophy and short stature 56
Neurocognitive profile in Turner's syndrome is not affected by growth impairment. 56
Rigidità di parete vascolare e spessore medio-intimale carotideo in soggetti in eta' pediatrica affetti da ipercolesterolemia familiare e da ipercolesterolemia primaria 56
Autoimmune polyglandular disease (APECED) and mutineuropathy: a case report 56
Prevalenza della malattia di Graves in una popolazione giovanile con la sindrome di Turner 56
TREATMENT OF PITUITARY TUMOURS BY CYBERKNIFE: PRELIMINARY DATA OF MIDDLE-TERM EFFECTIVENESS AND SAFETY 56
Adult Height Outcome of Girls with Idiopathic Central Precocious Puberty Treated with GnRH Analogs is Irrespective of BMI 56
TTF-2/FOXE1 gene polymorphisms in Sicilian patients with permanent primary congenital hypothyroidism. 55
Evoluzione puberale e vita mestruale in un'adolescente con deficit di GH tipo 1A trattata per 5 anni con IGF-1 in epoca prepuberale. 54
Infezioni respiratorie in età pediatrica : ruoli del mycoplasma e della chlamydia nella nostra esperienza 54
Sexual dimorphism affects prenatal thyroid migration but not biochemical severity of gland ectopia and prenatal bone maturation 54
Iatrogenic Cushing syndrome caused by ocular glucocorticoid in a child 54
Premature adrenarche: evaluation of hormonal and metabolic parameters 54
Catechol-o-methyltransferase inhibition in the treatment of tetrahydrobiopterin deficiency 53
Acute interstitial nephritis.A cause of inflammatory renal glycosuria 53
The hair as a diagnostic tool in dysmorphology. Clin Genet 53
Testicular microlithiasis heralding mixed germ cell tumor of the testis in a boy. 53
R298Q mutation of p63 gene in autosomal dominant ectodermal dysplasia associated with arrhythmogenic right ventricular cardiomyopathy 53
Adherence to sublingual immunotherapy in preschool children 53
A 7-Years Active Pharmacovigilance Study of Adverse Drug Reactions Causing Children Admission to a Pediatric Emergency Department in Sicily 53
AIRE gene mutations and autoantibodies to interferon omega in patients with chronic hypoparathyroidism without APECED 52
Analisi dei polimorfismi del gene TTF-2/FOXE1 come possibile causa di disgenesia tiroidea 51
A possible relationship between Beckwith-Wiedemann syndrome and prune belly syndrome. Clin Dysmorph 51
Young adults with cystic fibrosis are shorter than healthy peers because their parents are also short 51
Tuberculoma complicating tuberculous meningitis:description of one paediatric case 50
Totale 7.216
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Categoria #
all - tutte 49.123
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 49.123
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.356 0 0 0 0 0 236 233 217 56 240 298 76
2020/20211.548 153 39 342 77 136 169 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
2024/2025825 95 66 85 305 254 20 0 0 0 0 0 0
Totale 11.872