VALENZISE, Mariella
 Distribuzione geografica
Continente #
EU - Europa 4839
NA - Nord America 3885
AS - Asia 830
SA - Sud America 6
Continente sconosciuto - Info sul continente non disponibili 3
OC - Oceania 3
AF - Africa 1
Totale 9567
Nazione #
US - Stati Uniti d'America 3860
IE - Irlanda 1353
SE - Svezia 1129
IT - Italia 885
CN - Cina 786
UA - Ucraina 391
DE - Germania 293
PL - Polonia 201
FI - Finlandia 191
FR - Francia 121
GB - Regno Unito 98
AT - Austria 88
BE - Belgio 43
RU - Federazione Russa 24
VN - Vietnam 19
CA - Canada 17
NL - Olanda 12
MX - Messico 8
IN - India 6
JP - Giappone 5
IR - Iran 4
AU - Australia 3
BR - Brasile 3
CL - Cile 3
IL - Israele 3
KR - Corea 3
NO - Norvegia 3
A2 - ???statistics.table.value.countryCode.A2??? 2
CH - Svizzera 1
CY - Cipro 1
DK - Danimarca 1
ES - Italia 1
EU - Europa 1
HK - Hong Kong 1
HU - Ungheria 1
KH - Cambogia 1
LT - Lituania 1
LU - Lussemburgo 1
LV - Lettonia 1
NG - Nigeria 1
SG - Singapore 1
Totale 9567
Città #
Dublin 1353
Chandler 859
Jacksonville 832
Nyköping 574
Beijing 317
Dearborn 226
Princeton 218
Medford 203
Cambridge 192
Warsaw 192
Des Moines 162
Messina 158
Ann Arbor 142
Boardman 103
Vienna 83
Jinan 74
Wilmington 65
Shenyang 58
Nanjing 46
Woodbridge 42
San Mateo 36
Brussels 35
Bremen 33
Hebei 30
Haikou 29
Ashburn 28
Rome 26
Ningbo 25
Catania 24
Houston 24
Milan 24
Zhengzhou 23
Lancaster 21
Tianjin 21
Dong Ket 19
Jiaxing 19
Fuzhou 18
Falls Church 17
Nanchang 16
Hangzhou 15
Frederick 14
Guangzhou 14
Auburn Hills 13
Changsha 13
Napoli 13
Norwalk 13
Seattle 13
Redwood City 12
Taizhou 12
Brescia 11
Lanzhou 10
Helsinki 9
Verona 9
Ottawa 8
Palermo 8
Taiyuan 8
Waanrode 8
Genova 7
Cesena 6
Crotone 6
Fairfield 6
Genoa 6
Torino 6
Florence 5
Sassari 5
Scilla 5
Bari 4
Bologna 4
London 4
Mumbai 4
Philadelphia 4
Rimini 4
Saint Petersburg 4
Turin 4
Cagliari 3
Caserta 3
Castelnuovo Rangone 3
Dalmine 3
Los Angeles 3
Montréal 3
Naples 3
Poggio a Caiano 3
Ravenna 3
Reggio Calabria 3
Salerno 3
Serra San Bruno 3
São Paulo 3
Trondheim 3
Altavilla Vicentina 2
Apice 2
Arezzo 2
Atella 2
Belpasso 2
Bergamo 2
Bolzano Vicentino 2
Brisbane 2
Carlentini 2
Casoria 2
Chicago 2
Fagnano Castello 2
Totale 6720
Nome #
APECED: PECULIARITÀ FENOTIPICHE E GENOTIPICHE IN UNA CASISTICA PEDIATRICA 604
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 89
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. 89
Valutazione elastografica (fibroscan) del fegato nelle pazienti con sindrome di Turner 87
Adenoipofisite in un adolescente con pansinusite e meningite 81
Analysis of the factors affecting the evolution over time of subclinical hypothyroidism in children 78
Does family history of obesity, cardiovascular, and metabolic diseases influence onset and severity of childhood obesity? 78
Metamorphic thyroid autoimmunity in Down Syndrome: from Hashimoto's thyroiditis to Graves' disease and beyond. 77
Outbreak of Brucella melitensis infection in Eastern Sicily: risk factors, clinical characteristics and complication rate 76
Key-role of thyrotropin deficiency in disclosing craniopharyngioma diagnosis in a short girl with Hashimoto's thyroiditis. 73
Underlying Hashimoto's thyroiditis negatively affects the evolution of subclinical hypothyroidism in children irrespective of other concomitant risk factors. 73
Trattamento di tumori ipofisari mediante Cyber-Knife: Dati preliminari a medio termine su efficacia e sicurezza 71
Birth length and weight in congenital adrenal hyperplasia according to the different phenotype. 70
Aldosterone synthase deficiency type I with no documented homozygous mutations in the CYP11B2 gene 69
Nefrite interstiziale acuta 68
Terapia estroprogestinica nella sindrome di Turner 67
Even in the era of congenital hypothyroidism screening mild and subclinical sensorineural hearing loss remains a relatively common complication of severe congenital hypothyroidism 67
Birth length and weight in congenital adrenal hyperplasia according to the different phenotype 65
Peculiarities of autoimmune thyroid diseases in children with Turner or Down syndrome: an overview 65
A novel PAR 1 deletion associated with Leri-Weill dyschondrosteosis 64
Late hormonal function after testicular torsion 63
Five-year prospective evaluation of thyroid function in girls with subclinical mild hypothyroidism of different etiology 63
Novel insight into Chronic Inflammatory Demyelinating Polineuropathy in APECED syndrome: molecular mechanisms and clinical implications in children 63
Hearing loss in congenital hypothalamic hypothyroidism: a wide therapeutic window 62
Epidemiological and clinical peculiarities of polyglandular syndrome type 3 in pediatric age 62
Subclinical hypothyroidism in children: is it always subclinical? 62
Association of five autoimmune diseases in a young woman with Down's syndrome 60
Natural history of glucose tolerance, beta-cell function and peripheral insulin sensitivity in cystic fibrosis patients with fasting euglycemia 59
APECED in Sicilia: peculiarità cliniche e genotipiche 59
Adult height of girls with Turner syndrome treated from before six years of age with a fixed per kg growth hormone dose. 59
Cutaneous hemangiomas, hemihypertrophy and macrodactyly at birth 58
Mayer-Rokitansky-Küster-Hauser syndrome: rare cause of amenorrhea 57
Ascite tubercolare: descrizione di un caso in età pediatrica 57
Valutazione comparativa di due differenti schemi di terapia frenante la pubertà in bambine con pubertà precoce vera. 57
Fibroscan: a new non-invasive method for evaluation of liver dysfunction in Turner syndrome 57
Adenohypophysitis in a boy with pan-sinusitis and meningitis 57
Dyscondrosteosis in a child with Becker muscular dystrophy: an unreported association between Xp21 gene (DMD/BMD) deletion and a novel homozygous SHOX gene mutation 56
AGE OF ONSET OF ANOREXIA NERVOSA (AN) CAN AFFECT FINAL HEIGHT 55
Increased large artery intima media thickness in adolescents with classical and non-classical congenital adrenal hyperplasia is unrelated to metabolic syndrome 55
APECED syndrome in childhood: Clinical spectrum is enlarging 55
DIFFERENCES IN LEVOTHYROXINE DOSAGES FOR REPLACEMENT OF CHILDREN WITH PRIMARY AND CENTRAL PERMANENT HYPOTHYROIDISM 54
Clinical picture,evolution and peculiar molecular findings in a very large pedegree with Wolfram syndrome 53
Autoimmune polyendocrinopathy-candidiasis-ectodermal-distrophy: peculiar evidences from the first report of a Sicilian family 53
Flecainide-responsive myotonia permanens with SNEL onset: A new case and literature review 53
Dystrophin gene and SHOX gene mutations in a child with Becker muscular dystrophy and short stature 52
Acute suppurative thyroiditis disclosing diagnosis of thyroid cancer in a boy 52
Hypoceruloplasminemia as a Marker of Severe Hypothyroidism 52
Final height in isolated GH deficiency type 1A: effects of 5- year treatment with IGF-I 51
Aldosterone syndrome deficiency type I with non documentations in the CYP 11 B2 gene 51
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 51
Three-year prospective evaluation of glucose tolerance, beta- cell function and peripheral insulin sensitivity in non- diabetic patients with thalassemia major 51
Neurocognitive profile in Turner's syndrome is not affected by growth impairment. 51
Novel SHOX Gene Mutation in a Short Boy with Becker Muscular Dystrophy: Double Trouble in Two Adjacent Genes. 51
Evaluation of liver stiffness using transient elastography (fibroscan) in young adults with Turner syndrome. 51
A peculiar cognitive and behavioural phenotype as the first clue to suspect Klinefelter syndrome in prepubertal males 51
Increased intima media thickness at many arterial sites in obese adolescents with abdominal adiposity, insulin resistance, and high LDL-cholesterol. 51
Adult height of girls with Turner syndrome treated from before six years of age with a fixed per kilo GH dose 51
Amenorrea primaria in una adolescente con iperprolattinemia:mancato riconoscimento di una sindrome di Turner 50
STUDIO TRASVERSALE E PROSPETTICO DEGLI EFFETTI DELLA TERAPIA CON GH SUL QUADRO METABOLICO E SULLA COMPOSIZIONE CORPOREA IN BAMBINI CON DEFICIT DI GH 50
Atypical phenotypic aspects of autoimmune thyroid disorders in young patients with Turner syndrome 50
Graves' disease prevalence in a young population with Turner syndrome 49
Regulation of spermatogenesis in McCune- Albright syndrome :lessons from fifteen year follow-up 49
Autoimmune polyglandular disease (APECED) and mutineuropathy: a case report 49
Aumento dello spessore medio-intimale in diversi siti arteriosi in adolescenti obesi con adiposità addominale, insulino-resistenza e alti livelli di colesterolo-LDL. 49
Acute interstitial nephritis.A cause of inflammatory renal glycosuria 48
Mental retardation, peculiar facial dysmorphism and HbH inclusions in a 4 year-old boy. ) 48
The CX3C-chemokine fractalkine (CX3CL1) is detectable in serum of patients affected by active pityriasis rosea 48
Prevalenza della malattia di Graves in una popolazione giovanile con la sindrome di Turner 48
Direct comparison between continuous and coseasonal regimen for sublingual immunotherapy in children with grass allergy: a randomized controlled study 48
Hair changes in congenital disorders of glycosylation (CDG) 47
Novel mutation of CYP21A2 gene (N387K) affecting a nonconserved amino acid residue in Exon 9. 47
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. 47
48, XXYY syndrome in a newborn with ambiguous genitalia 47
Tuberculoma complicating tuberculous meningitis:description of one paediatric case 46
Infezioni respiratorie in età pediatrica : ruoli del mycoplasma e della chlamydia nella nostra esperienza 46
TTF-2/FOXE1 gene polymorphisms in Sicilian patients with permanent primary congenital hypothyroidism. 46
Young adults with cystic fibrosis are shorter than healthy peers because their parents are also short 46
Sexual dimorphism affects prenatal thyroid migration but not biochemical severity of gland ectopia and prenatal bone maturation 46
Even in the Era of Congenital Hypothyroidism Screening Mild and Subclinical Sensorineural Hearing Loss Remains a Relatively Common Complication of Severe Congenital Hypothyroidism 46
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 46
Catechol-o-methyltransferase inhibition in the treatment of tetrahydrobiopterin deficiency 45
Evaluation of the AIRE gene mutations in a cohort of Italian patients with autoimmune-polyendocrinopathy-candidiasis-ectodermal-dystrophy (APECED) and intheir relatives. 45
Iatrogenic Cushing syndrome caused by ocular glucocorticoid in a child 45
Premature adrenarche: evaluation of hormonal and metabolic parameters 45
Pseudotumor cerebri e Papilledema Idiopatico: un'analisi retrospettiva di tre centri pediatrici italiani. 45
Adult height following a combined treatment of ketoconazole - cyproterone acetate - leuprolide depot in a boy with atypical McCune-Albright syndrome 45
The hair as a diagnostic tool in dysmorphology. Clin Genet 44
A possible relationship between Beckwith-Wiedemann syndrome and prune belly syndrome. Clin Dysmorph 44
Testicular microlithiasis heralding mixed germ cell tumor of the testis in a boy. 44
R298Q mutation of p63 gene in autosomal dominant ectodermal dysplasia associated with arrhythmogenic right ventricular cardiomyopathy 44
Rigidità di parete vascolare e spessore medio-intimale carotideo in soggetti in eta' pediatrica affetti da ipercolesterolemia familiare e da ipercolesterolemia primaria 44
TREATMENT OF PITUITARY TUMOURS BY CYBERKNIFE: PRELIMINARY DATA OF MIDDLE-TERM EFFECTIVENESS AND SAFETY 44
AIRE gene mutations and autoantibodies to interferon omega in patients with chronic hypoparathyroidism without APECED 44
Adherence to sublingual immunotherapy in preschool children 44
Chronic inflammatory demyelinating polyneuropathy as a possible novel component of autoimmune poly-endocrine-candidiasis-ectodermal dystrophy 44
Analisi dei polimorfismi del gene TTF-2/FOXE1 come possibile causa di disgenesia tiroidea 43
Hair anomalies as a sign of mitochondrial disease 43
Congenital adenohypophysis aplasia: clinical features and analysis of thetranscriptional factors for embryonic pituitary development. 43
Adult Height Outcome of Girls with Idiopathic Central Precocious Puberty Treated with GnRH Analogs is Irrespective of BMI 43
Il diabete tipo 1 e la qualità del controllo metabolico condizionano molto l'età del menarca 42
Totale 6042
Categoria #
all - tutte 19072
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 19072


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2017/2018243 0000 00 00 221019714
2018/2019304 161111 15624 3322 121657
2019/20201814 2301031393 19236 233217 5624029876
2020/20211548 1533934277 136169 63146 901786986
2021/20221590 181993063 6439 9461 45288218471
2022/20233690 294262168285 323379 99250 1630000
Totale 9871