VALENZISE, Mariella
 Distribuzione geografica
Continente #
EU - Europa 5.153
NA - Nord America 5.005
AS - Asia 1.715
SA - Sud America 588
AF - Africa 26
OC - Oceania 11
Continente sconosciuto - Info sul continente non disponibili 3
Totale 12.501
Nazione #
US - Stati Uniti d'America 4.956
IT - Italia 1.211
IE - Irlanda 1.206
SE - Svezia 1.133
CN - Cina 859
SG - Singapore 644
BR - Brasile 524
UA - Ucraina 400
DE - Germania 325
FI - Finlandia 216
PL - Polonia 202
FR - Francia 122
GB - Regno Unito 116
AT - Austria 74
IN - India 44
RU - Federazione Russa 44
BE - Belgio 38
CA - Canada 24
VN - Vietnam 19
ID - Indonesia 18
AR - Argentina 17
NL - Olanda 17
TR - Turchia 17
CZ - Repubblica Ceca 16
IQ - Iraq 15
MX - Messico 15
BD - Bangladesh 13
UZ - Uzbekistan 13
EC - Ecuador 11
VE - Venezuela 11
PK - Pakistan 9
AU - Australia 8
HK - Hong Kong 8
MA - Marocco 8
JP - Giappone 7
PE - Perù 7
CO - Colombia 6
EG - Egitto 6
AE - Emirati Arabi Uniti 5
AZ - Azerbaigian 5
CL - Cile 5
ES - Italia 5
IL - Israele 5
NO - Norvegia 5
QA - Qatar 5
DO - Repubblica Dominicana 4
IR - Iran 4
PY - Paraguay 4
CH - Svizzera 3
GR - Grecia 3
HN - Honduras 3
JO - Giordania 3
KE - Kenya 3
KR - Corea 3
LT - Lituania 3
NZ - Nuova Zelanda 3
OM - Oman 3
SY - Repubblica araba siriana 3
TN - Tunisia 3
A2 - ???statistics.table.value.countryCode.A2??? 2
DZ - Algeria 2
HU - Ungheria 2
KG - Kirghizistan 2
KH - Cambogia 2
KZ - Kazakistan 2
LB - Libano 2
LU - Lussemburgo 2
NP - Nepal 2
RS - Serbia 2
UY - Uruguay 2
ZA - Sudafrica 2
AL - Albania 1
BG - Bulgaria 1
BO - Bolivia 1
BY - Bielorussia 1
CG - Congo 1
CY - Cipro 1
DK - Danimarca 1
EU - Europa 1
LV - Lettonia 1
MD - Moldavia 1
NG - Nigeria 1
PA - Panama 1
PR - Porto Rico 1
PT - Portogallo 1
SI - Slovenia 1
SV - El Salvador 1
TH - Thailandia 1
TW - Taiwan 1
Totale 12.501
Città #
Dublin 1.206
Chandler 861
Jacksonville 832
Nyköping 576
Singapore 519
Ashburn 451
Beijing 322
Dearborn 226
Princeton 218
Messina 212
Medford 203
Warsaw 193
Cambridge 192
Des Moines 162
Ann Arbor 142
Boardman 121
Jinan 88
Vienna 68
Wilmington 65
Washington 59
Shenyang 58
Rome 51
Los Angeles 46
Nanjing 46
São Paulo 46
Woodbridge 42
Milan 40
Catania 39
San Mateo 36
Bremen 33
Brussels 30
Hebei 30
Haikou 29
The Dalles 27
Helsinki 26
Houston 26
Ningbo 25
Zhengzhou 25
New York 24
Hyderabad 23
Lancaster 21
Tianjin 21
Fuzhou 20
Palermo 20
Rio de Janeiro 20
Dong Ket 19
Jiaxing 19
Seattle 19
Falls Church 17
Jakarta 17
Changsha 16
Guangzhou 16
Nanchang 16
Hangzhou 15
Frederick 14
Munich 14
Auburn Hills 13
Belo Horizonte 13
Brno 13
Napoli 13
Norwalk 13
Taizhou 13
Ottawa 12
Redwood City 12
Brescia 11
Naples 11
Palmi 11
Florence 10
Lanzhou 10
Pune 10
Tashkent 10
Verona 10
Bari 9
Brasília 9
Nuremberg 9
Trento 9
Baghdad 8
Cosenza 8
Curitiba 8
London 8
Rovereto 8
São José dos Campos 8
Taiyuan 8
Tappahannock 8
Waanrode 8
Fortaleza 7
Genova 7
Lima 7
San Benedetto del Tronto 7
Sorocaba 7
Campinas 6
Cesena 6
Crotone 6
Fairfield 6
Genoa 6
Quito 6
Torino 6
Acireale 5
Baku 5
Bologna 5
Totale 8.087
Nome #
APECED: PECULIARITÀ FENOTIPICHE E GENOTIPICHE IN UNA CASISTICA PEDIATRICA 798
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 107
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. 104
Hearing loss in congenital hypothalamic hypothyroidism: a wide therapeutic window 98
Analysis of the factors affecting the evolution over time of subclinical hypothyroidism in children 97
Does family history of obesity, cardiovascular, and metabolic diseases influence onset and severity of childhood obesity? 97
Valutazione elastografica (fibroscan) del fegato nelle pazienti con sindrome di Turner 96
Adenoipofisite in un adolescente con pansinusite e meningite 96
Birth length and weight in congenital adrenal hyperplasia according to the different phenotype 88
Aldosterone synthase deficiency type I with no documented homozygous mutations in the CYP11B2 gene 87
Evaluation of the AIRE gene mutations in a cohort of Italian patients with autoimmune-polyendocrinopathy-candidiasis-ectodermal-dystrophy (APECED) and intheir relatives. 84
Underlying Hashimoto's thyroiditis negatively affects the evolution of subclinical hypothyroidism in children irrespective of other concomitant risk factors. 83
Birth length and weight in congenital adrenal hyperplasia according to the different phenotype. 83
Trattamento di tumori ipofisari mediante Cyber-Knife: Dati preliminari a medio termine su efficacia e sicurezza 83
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
Metamorphic thyroid autoimmunity in Down Syndrome: from Hashimoto's thyroiditis to Graves' disease and beyond. 81
Terapia estroprogestinica nella sindrome di Turner 80
Peculiarities of autoimmune thyroid diseases in children with Turner or Down syndrome: an overview 80
Adult height of girls with Turner syndrome treated from before six years of age with a fixed per kg growth hormone dose. 79
Even in the era of congenital hypothyroidism screening mild and subclinical sensorineural hearing loss remains a relatively common complication of severe congenital hypothyroidism 79
A novel PAR 1 deletion associated with Leri-Weill dyschondrosteosis 78
AGE OF ONSET OF ANOREXIA NERVOSA (AN) CAN AFFECT FINAL HEIGHT 75
Ascite tubercolare: descrizione di un caso in età pediatrica 75
Increased large artery intima media thickness in adolescents with classical and non-classical congenital adrenal hyperplasia is unrelated to metabolic syndrome 75
Nefrite interstiziale acuta 74
Valutazione comparativa di due differenti schemi di terapia frenante la pubertà in bambine con pubertà precoce vera. 74
Adult height of girls with Turner syndrome treated from before six years of age with a fixed per kilo GH dose 74
Mental retardation, peculiar facial dysmorphism and HbH inclusions in a 4 year-old boy. ) 73
Increased intima media thickness at many arterial sites in obese adolescents with abdominal adiposity, insulin resistance, and high LDL-cholesterol. 73
Amenorrea primaria in una adolescente con iperprolattinemia:mancato riconoscimento di una sindrome di Turner 73
Epidemiological and clinical peculiarities of polyglandular syndrome type 3 in pediatric age 73
A peculiar cognitive and behavioural phenotype as the first clue to suspect Klinefelter syndrome in prepubertal males 72
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 72
Flecainide-responsive myotonia permanens with SNEL onset: A new case and literature review 72
Autoimmune polyendocrinopathy-candidiasis-ectodermal-distrophy: peculiar evidences from the first report of a Sicilian family 71
Adenohypophysitis in a boy with pan-sinusitis and meningitis 71
Association of five autoimmune diseases in a young woman with Down's syndrome 70
Adult height following a combined treatment of ketoconazole - cyproterone acetate - leuprolide depot in a boy with atypical McCune-Albright syndrome 70
Novel insight into Chronic Inflammatory Demyelinating Polineuropathy in APECED syndrome: molecular mechanisms and clinical implications in children 70
Atypical phenotypic aspects of autoimmune thyroid disorders in young patients with Turner syndrome 70
Natural history of glucose tolerance, beta-cell function and peripheral insulin sensitivity in cystic fibrosis patients with fasting euglycemia 69
Three-year prospective evaluation of glucose tolerance, beta- cell function and peripheral insulin sensitivity in non- diabetic patients with thalassemia major 69
Fibroscan: a new non-invasive method for evaluation of liver dysfunction in Turner syndrome 69
APECED in Sicilia: peculiarità cliniche e genotipiche 69
Subclinical hypothyroidism in children: is it always subclinical? 69
Aldosterone syndrome deficiency type I with non documentations in the CYP 11 B2 gene 68
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 68
Direct comparison between continuous and coseasonal regimen for sublingual immunotherapy in children with grass allergy: a randomized controlled study 68
Pseudotumor cerebri e Papilledema Idiopatico: un'analisi retrospettiva di tre centri pediatrici italiani. 68
Cutaneous hemangiomas, hemihypertrophy and macrodactyly at birth 67
Prevalenza della malattia di Graves in una popolazione giovanile con la sindrome di Turner 67
DIFFERENCES IN LEVOTHYROXINE DOSAGES FOR REPLACEMENT OF CHILDREN WITH PRIMARY AND CENTRAL PERMANENT HYPOTHYROIDISM 67
Mayer-Rokitansky-Küster-Hauser syndrome: rare cause of amenorrhea 66
Novel SHOX Gene Mutation in a Short Boy with Becker Muscular Dystrophy: Double Trouble in Two Adjacent Genes. 66
Graves' disease prevalence in a young population with Turner syndrome 66
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 66
Novel mutation of CYP21A2 gene (N387K) affecting a nonconserved amino acid residue in Exon 9. 65
Late hormonal function after testicular torsion 65
Aumento dello spessore medio-intimale in diversi siti arteriosi in adolescenti obesi con adiposità addominale, insulino-resistenza e alti livelli di colesterolo-LDL. 65
48, XXYY syndrome in a newborn with ambiguous genitalia 65
Adult Height Outcome of Girls with Idiopathic Central Precocious Puberty Treated with GnRH Analogs is Irrespective of BMI 65
A case of adenohypophysitis in a boy affected by sinusitis and acute meningitis: outcome 65
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
Rigidità di parete vascolare e spessore medio-intimale carotideo in soggetti in eta' pediatrica affetti da ipercolesterolemia familiare e da ipercolesterolemia primaria 63
The CX3C-chemokine fractalkine (CX3CL1) is detectable in serum of patients affected by active pityriasis rosea 63
STUDIO TRASVERSALE E PROSPETTICO DEGLI EFFETTI DELLA TERAPIA CON GH SUL QUADRO METABOLICO E SULLA COMPOSIZIONE CORPOREA IN BAMBINI CON DEFICIT DI GH 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
Hypoceruloplasminemia as a Marker of Severe Hypothyroidism 62
APECED syndrome in childhood: Clinical spectrum is enlarging 62
TREATMENT OF PITUITARY TUMOURS BY CYBERKNIFE: PRELIMINARY DATA OF MIDDLE-TERM EFFECTIVENESS AND SAFETY 61
Clinical picture,evolution and peculiar molecular findings in a very large pedegree with Wolfram syndrome 60
R298Q mutation of p63 gene in autosomal dominant ectodermal dysplasia associated with arrhythmogenic right ventricular cardiomyopathy 60
Acute suppurative thyroiditis disclosing diagnosis of thyroid cancer in a boy 60
Evaluation of liver stiffness using transient elastography (fibroscan) in young adults with Turner syndrome. 60
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. 60
Dystrophin gene and SHOX gene mutations in a child with Becker muscular dystrophy and short stature 59
Congenital adenohypophysis aplasia: clinical features and analysis of thetranscriptional factors for embryonic pituitary development. 59
A 7-Years Active Pharmacovigilance Study of Adverse Drug Reactions Causing Children Admission to a Pediatric Emergency Department in Sicily 59
Clinical Peculiarities in a Cohort of Patients with Wolfram Syndrome 1 59
Testicular microlithiasis heralding mixed germ cell tumor of the testis in a boy. 58
Regulation of spermatogenesis in McCune- Albright syndrome :lessons from fifteen year follow-up 58
Autoimmune polyglandular disease (APECED) and mutineuropathy: a case report 58
Neurocognitive profile in Turner's syndrome is not affected by growth impairment. 57
Hair changes in congenital disorders of glycosylation (CDG) 56
AIRE gene mutations and autoantibodies to interferon omega in patients with chronic hypoparathyroidism without APECED 56
Acute interstitial nephritis.A cause of inflammatory renal glycosuria 55
Infezioni respiratorie in età pediatrica : ruoli del mycoplasma e della chlamydia nella nostra esperienza 55
TTF-2/FOXE1 gene polymorphisms in Sicilian patients with permanent primary congenital hypothyroidism. 55
Young adults with cystic fibrosis are shorter than healthy peers because their parents are also short 55
Sexual dimorphism affects prenatal thyroid migration but not biochemical severity of gland ectopia and prenatal bone maturation 55
Premature adrenarche: evaluation of hormonal and metabolic parameters 55
Catechol-o-methyltransferase inhibition in the treatment of tetrahydrobiopterin deficiency 54
Analisi dei polimorfismi del gene TTF-2/FOXE1 come possibile causa di disgenesia tiroidea 54
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
Iatrogenic Cushing syndrome caused by ocular glucocorticoid in a child 54
Adherence to sublingual immunotherapy in preschool children 54
The hair as a diagnostic tool in dysmorphology. Clin Genet 53
Totale 7.649
Categoria #
all - tutte 53.952
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 53.952


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020887 0 0 0 0 0 0 0 217 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
2024/20251.825 95 66 85 305 254 91 141 788 0 0 0 0
Totale 12.872