STAGI, STEFANO
 Distribuzione geografica
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Continente #
NA - Nord America 8.327
EU - Europa 7.550
AS - Asia 1.306
AF - Africa 53
SA - Sud America 5
Continente sconosciuto - Info sul continente non disponibili 2
OC - Oceania 1
Totale 17.244
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Nazione #
US - Stati Uniti d'America 8.307
PL - Polonia 3.039
RU - Federazione Russa 2.173
IT - Italia 710
IE - Irlanda 593
SE - Svezia 473
SG - Singapore 366
HK - Hong Kong 313
CN - Cina 311
FI - Finlandia 139
IN - India 103
DE - Germania 100
UA - Ucraina 94
GB - Regno Unito 84
JO - Giordania 78
VN - Vietnam 65
CI - Costa d'Avorio 46
CH - Svizzera 40
FR - Francia 35
ES - Italia 33
TR - Turchia 33
KR - Corea 29
CA - Canada 20
BE - Belgio 13
SC - Seychelles 6
NL - Olanda 5
AT - Austria 4
GR - Grecia 4
BR - Brasile 3
IR - Iran 3
RO - Romania 3
EU - Europa 2
HU - Ungheria 2
SA - Arabia Saudita 2
AR - Argentina 1
AU - Australia 1
CO - Colombia 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
DZ - Algeria 1
EE - Estonia 1
IL - Israele 1
LU - Lussemburgo 1
PK - Pakistan 1
PT - Portogallo 1
QA - Qatar 1
SI - Slovenia 1
Totale 17.244
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Città #
Warsaw 3.034
Santa Clara 1.526
Fairfield 1.084
Chandler 643
Dublin 593
Ashburn 540
Woodbridge 473
Cambridge 407
Houston 397
Seattle 374
Wilmington 357
Singapore 285
Princeton 221
Lawrence 186
Altamura 183
Hong Kong 183
Ann Arbor 178
Boston 128
Beijing 116
Florence 116
Jacksonville 113
Kent 77
Mumbai 73
Shanghai 73
Boardman 63
Moscow 57
Dong Ket 56
Buffalo 52
San Diego 50
Abidjan 46
Medford 46
New York 44
Falls Church 39
Barcelona 30
Bern 30
Milan 27
Izmir 26
Los Angeles 26
Norwalk 24
Pune 24
Rome 24
Phoenix 19
Toronto 19
Andover 15
Hillsboro 15
Munich 15
Brussels 13
Guangzhou 13
London 13
Castelliri 12
Bremen 11
Padova 11
Bologna 10
West Jordan 10
Yubileyny 10
Detroit 9
Helsinki 9
Seoul 9
Modena 6
Naples 6
Verona 6
Washington 6
Catania 5
Düsseldorf 5
Frankfurt Am Main 5
Rui'an 5
Bari 4
Cagliari 4
Chennai 4
Chicago 4
Dearborn 4
Fano 4
Jiaxing 4
Laurel 4
Messina 4
Pederobba 4
Pozzallo 4
Rapallo 4
Redmond 4
Salerno 4
Sesto San Giovanni 4
Shenzhen 4
Vienna 4
Cassola 3
Castelli Calepio 3
Codevigo 3
Hofheim am Taunus 3
Istanbul 3
Kilburn 3
Lappeenranta 3
Pescara 3
Pistoia 3
Polska 3
Prato 3
São Paulo 3
Trasacco 3
Trieste 3
Aachen 2
Arezzo 2
Arnhem 2
Totale 12.397
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Nome #
Long-term safety and efficacy of Omnitrope®, a somatropin biosimilar, in children requiring growth hormone treatment: Italian interim analysis of the PATRO Children study. 325
Agenesis of internal carotid artery associated with isolated growth hormone deficiency: A case report and literature review 261
Peripheral quantitative computed tomography (pQCT) for the assessment of bone strength in most of bone affecting conditions in developmental age: a review. 258
The ever-expanding conundrum of primary osteoporosis: aetiopathogenesis, diagnosis, and treatment. 257
Bone mass and quality in patients with juvenile idiopathic arthritis: longitudinal evaluation of bone mass determinants using dual energy X-ray absorptiometry, peripheral quantitative computed tomography, and quantitative ultrasonography. 256
Hydrocortisone malabsorption due to polyethylene glycols (Macrogol 3350) in a girl with congenital adrenal insufficiency. 254
Determinants of Vitamin D Levels in Italian Children and Adolescents: A Longitudinal Evaluation of Cholecalciferol Supplementation versus the Improvement of Factors Influencing 25(OH)D Status 249
Increased incidence of thyroid dysfunction and autoimmunity in patients with vernal keratoconjunctivitis 247
Undetectable serum IgA and low IgM concentration in children with congenitalhypothyroidism. 246
A new case of de novo 6q24.2-q25.2 deletion on paternal chromosome 6 with growth hormone deficiency: A twelve-year follow-up and literature review 239
Diabetes mellitus in a girl with thyroid hormone resistance syndrome: A little recognized interaction between the two diseases 235
Kawasaki disease in a girl with turner syndrome: A remarkable association 234
Growth Hormone Axis in Skeletal Dysplasias 232
Orange-colored diapers as first sign of Lesch-Nyhan disease in an asymptomatic infant. 229
Comparison of bone mass and quality determinants in adolescents and young adults with juvenile systemic lupus erythematosus (JSLE) and juvenile idiopathic arthritis (JIA) 227
Type II diabetes and impaired glucose tolerance due to severe hyperinsulinism in patients with 1p36 deletion syndrome and a Prader-Willi-like phenotype 225
Managing pediatric osteoporosis 220
Long-term auxological and endocrinological evaluation of patients with 9p trisomy: a focus on the growth hormone-insulin-like growth factor-I axis 217
Update sulla pubertà precoce 207
Bone metabolism in children and adolescents: main characteristics of the determinants of peak bone mass. 204
Bone health in children and adolescents: the available imaging techniques. 194
L'IGF-I e l'IGFBP-3 sono utili nella diagnosi di deficit di GH nel bambino? 192
Bone mineral status and metabolism in patients with Williams-Beuren syndrome. 170
New Thoughts on Pediatric Genetic Obesity: Pathogenesis, Clinical Characteristics and Treatment Approach 169
Bone mineral status in children and adolescents with klinefelter syndrome 169
An early diagnosis of trichorhinophalangeal syndrome type 1: A case report and a review of literature 160
Cross-sectional and longitudinal evaluation of bone mass and quality in children and young adults with juvenile onset systemic lupus erythematosus (JSLE): role of bone mass determinants analyzed by DXA, PQCT and QUS. 159
Thyroid Function in Rett Syndrome 157
Transient Hypothyroidism and Autoimmune Thyroiditis in Children with Chronic Hepatitis C Treated with Pegylated-interferon-α-2b and Ribavirin 148
Changed bone status in human immunodeficiency virus type 1 (HIV-1) perinatally infected children is related to low serum free IGF-I 143
Comportamenti sessuali e contraccezione 140
Bone status in genetic syndromes: A review. 138
The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosis 138
Bone density and metabolism in subjects with microdeletion of chromosome 22q11 (del22q11) 137
Reverse phenotyping after whole-Exome sequencing in steroid-resistant nephrotic syndrome 137
AB0976 Association of Vitamin D Receptor Polymorphisms with Juvenile Idiopathic Arthritis (JIA) 135
Central precocious puberty due to hypothalamic hamartoma in neurofibromatosis type 1 135
Reversible weight gain and prolactin levels--long-term follow-up in childhood. 133
Oral clonidine provocative test in the diagnosis of growth hormone deficiency in childhood: should we make the timing uniform? 131
Vitamin D levels in children, adolescents, and young adults with juvenile-onset systemic lupus erythematosus: a cross-sectional study. 131
Thyroid function and morphology in subjects with microdeletion of chromosome 22q11 (del(22)(q11)). 131
Comparison of bone mass and quality determinants in adolescents and young adults with juvenile systemic lupus erythematosus (JSLE) and juvenile idiopathic arthritis (JIA). 128
Thyroid hypoplasia as a cause of congenital hypothyroidism in Williams syndrome 127
Changes of thyroid function during long-term hGH therapy in GHD children. A possible relationship with catch-up growth? 125
Determinants of Vitamin D Levels in Children, Adolescents, and Young Adults with Juvenile Idiopathic Arthritis. 124
Precocious, early and fast puberty in males with Chiari I malformation. 122
Diagnosis of growth hormone deficiency by using the arginine provocative test: is it possible to shorten testing time without altering validity? 121
Acute motor axonal neuropathy in a Turner's syndrome patient with a "potential" celiac disease 121
Cross-sectional study shows that impaired bone mineral status and metabolism are found in non mosaic triple X syndrome 121
Vitamin D levels and effects of vitamin D replacement in children with periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome 118
Thyroid function and morphology in patients affected by Williams syndrome 117
Final height in patients perinatally infected with the Human Immunodeficiency Virus. 115
Autoimmune thyroiditis, pernicious anaemia, vitiligo and scleroatrophic lichen in a boy with short-chain acylcoa dehydrogenase deficiency 115
Amenorrhea after Endoscopic Third Ventriculostomy for a Failed Shunt in Spina Bifida: Case Report and Review of the Literature 114
Retrospective evaluation of metformin and/or metformin plus a new polysaccharide complex in treating severe hyperinsulinism and insulin resistance in obese children and adolescents with metabolic syndrome 113
Thyroid function and anti-thyroid autoantibodies in untreated children with vertically acquired chronic hepatitis C virus infection 112
Precocious puberty in a girl with floating-harbor syndrome 111
Bone mass predictors in a large cohort of children with juvenile idiopathic arthritis (JIA) 109
Osteoprotegerin serum levels in children with type 1 diabetes: a potential modulating role in bone status. 108
X-linked ichthyosis in a patient with congenital hypothyroidism 108
Partial growth hormone deficiency and changed bone quality and mass in type I trichorhinophalangeal syndrome 107
Central precocious puberty in a child with metachromatic leukodystrophy 107
A SOX3 (Xq26.3-27.3) duplication in a boy with growth hormone deficiency, ocular dyspraxia, and intellectual disability: A long-term follow-up and literature review. 107
Coeliac disease in patients with Kawasaki disease. Is there a link? 106
Auxological and endocrinological features in internationally adopted children 106
Congenital hypothyroidism in Young-Simpson syndrome 105
Auxologia 105
Alimentazione in età evolutiva 104
Cross-sectional and longitudinal evaluation of bone mass in children and young adults with juvenile idiopathic arthritis: the role of bone mass determinants in a large cohort of patients. 104
Triple X syndrome and puberty: focus on the hypothalamus-hypophysis-gonad axis 103
Thyroid function, autoimmune thyroiditis and coeliac disease in juvenile idiopathic arthritis 101
Bone status over one-year etanercept treatment in juvenile idiopathic arthritis 99
Donkey´s Milk Is Well Accepted and Tolerated by Infants With Cow´s Milk Food Protein-Induced Enterocolitis Syndrome: A Preliminary Study 99
Possible effects of an early diagnosis and treatment in patients with growth hormone deficiency: The state of art 99
Pharmacological considerations in the use of stiripentol for the treatment of epilepsy 98
Bone status in a patient with insulin-like growth factor-1 receptor deletion syndrome: Bone quality and structure evaluation using dual-energy X-ray absorptiometry, peripheral quantitative computed tomography, and quantitative ultrasonography 97
SAT0505 Severe Vitamin D Deficiency in Patients with Kawasaki Disease: its Possible Role in the Risk to Develop Coronary Artery Damage 94
Epigenetic control of the immune system: a lesson from Kabuki syndrome 93
Glucocorticoid-associated osteoporosis in chronic inflammatory diseases: Epidemiology, mechanisms, diagnosis, and treatment 92
Coeliac disease and risk of other autoimmune diseases in patients with Williams-Beuren syndrome 91
PReS-FINAL-2053: Vitamin D receptor polymorphisms in a cohort of Italian patients with juvenile idiopathic arthritis 90
Increased prevalence of growth hormone deficiency in patients with vernal keratoconjuntivitis; an interesting new association. 88
Parathyroid Hormone Levels in Healthy Children and Adolescents. 87
A particular case of pubic pain 87
Turner's syndrome and autoimmunity: Role of FOXP3 and regulatory T-cells. 86
Giant multiple bladder diverticula in Williams-Beuren syndrome 86
Severe vitamin D deficiency in patients with Kawasaki disease: a potential role in the risk to develop heart vascular abnormalities? 86
Association Between Obesity/Overweight and Functional Gastrointestinal Disorders in Children 86
Congenital hypothyroidism due to unexpected iodine sources 85
Longitudinal evaluation of bone mass in adolescents and young adults with juvenile idiopathic arthritis: the role of bone mass determinants in a large cohort of patients 85
Fenotipo Turner associato ad una delezione interstiziale sul braccio lungo del cromosoma 2 84
Association of low bone mass with vitamin d receptor gene and calcitonin receptor gene polymorphisms in juvenile idiopathic arthritis. 84
Increased risk of coeliac disease in patients with congenital hypothyroidism. 83
Cessation of epilepsy therapy in children. 83
Anaphylactic reaction to gonadotropin-releasing hormone analogues: a pediatric case report 83
Age-dependent association of exposure to television screen with children's urinary melatonin excretion? 82
Incidence of diverticular disease and complicated diverticular disease in young patients with Williams syndrome 81
Williams-beuren syndrome is a genetic disorder associated with impaired glucose tolerance and diabetes in childhood and adolescence: new insights from a longitudinal study. 81
Cross-Sectional Evaluation of Plasma Vitamin D Levels in a Large Cohort of Italian Patients with Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal Infections 81
Bone status evaluation with calcaneal ultrasound in children with chronic rheumatic diseases. A one year followup study. 80
Totale 13.903
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Categoria #
all - tutte 48.083
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 48.083
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.944 0 0 0 0 297 334 254 303 249 177 283 47
2020/20211.817 167 195 88 221 100 183 106 144 161 257 67 128
2021/2022948 25 91 81 43 37 40 32 67 45 48 132 307
2022/20232.859 328 542 141 208 185 473 370 154 287 25 85 61
2023/20241.181 44 129 184 85 61 154 54 254 20 49 110 37
2024/20254.785 283 795 573 1.231 1.903 0 0 0 0 0 0 0
Totale 17.495