IRIS
WEBER, GIOVANNA
 Distribuzione geografica
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Continente #
AS - Asia 4.602
EU - Europa 3.943
NA - Nord America 3.495
SA - Sud America 1.260
AF - Africa 88
Continente sconosciuto - Info sul continente non disponibili 41
OC - Oceania 4
Totale 13.433
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Nazione #
US - Stati Uniti d'America 3.309
RU - Federazione Russa 2.491
SG - Singapore 1.672
CN - Cina 1.551
BR - Brasile 1.021
HK - Hong Kong 552
SE - Svezia 546
VN - Vietnam 417
IT - Italia 287
FR - Francia 208
DE - Germania 109
AR - Argentina 104
BD - Bangladesh 100
IN - India 78
GB - Regno Unito 73
CA - Canada 66
MX - Messico 54
FI - Finlandia 49
EC - Ecuador 43
ID - Indonesia 43
AT - Austria 35
ZA - Sudafrica 34
IE - Irlanda 33
CO - Colombia 26
PL - Polonia 25
TR - Turchia 25
IQ - Iraq 24
JP - Giappone 23
JM - Giamaica 19
NL - Olanda 19
MA - Marocco 18
PY - Paraguay 17
PK - Pakistan 16
SA - Arabia Saudita 16
ES - Italia 14
VE - Venezuela 14
CL - Cile 11
PE - Perù 11
UA - Ucraina 11
UY - Uruguay 11
UZ - Uzbekistan 11
TT - Trinidad e Tobago 10
TN - Tunisia 8
CR - Costa Rica 7
IR - Iran 7
JO - Giordania 7
KE - Kenya 7
KZ - Kazakistan 6
LT - Lituania 6
MD - Moldavia 6
PH - Filippine 6
AE - Emirati Arabi Uniti 5
EG - Egitto 5
HN - Honduras 5
MY - Malesia 5
PS - Palestinian Territory 5
RS - Serbia 5
TW - Taiwan 5
AL - Albania 4
AU - Australia 4
AZ - Azerbaigian 4
DO - Repubblica Dominicana 4
IL - Israele 4
NI - Nicaragua 4
OM - Oman 4
PR - Porto Rico 4
SV - El Salvador 4
BE - Belgio 3
CH - Svizzera 3
DK - Danimarca 3
DZ - Algeria 3
NP - Nepal 3
PT - Portogallo 3
AM - Armenia 2
AO - Angola 2
BA - Bosnia-Erzegovina 2
BB - Barbados 2
HR - Croazia 2
RO - Romania 2
SN - Senegal 2
TH - Thailandia 2
XK - ???statistics.table.value.countryCode.XK??? 2
AW - Aruba 1
BH - Bahrain 1
BO - Bolivia 1
BS - Bahamas 1
BW - Botswana 1
BY - Bielorussia 1
CI - Costa d'Avorio 1
CY - Cipro 1
CZ - Repubblica Ceca 1
ET - Etiopia 1
GA - Gabon 1
GE - Georgia 1
GH - Ghana 1
GM - Gambi 1
GP - Guadalupe 1
GR - Grecia 1
GT - Guatemala 1
GY - Guiana 1
Totale 13.381
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Città #
Singapore 628
Hong Kong 548
Moscow 544
Ashburn 433
San Jose 432
Dallas 348
Shanghai 280
Council Bluffs 227
Hefei 225
Princeton 223
Lawrence 222
Lauterbourg 190
Beijing 177
Ho Chi Minh City 160
New York 95
Hanoi 90
São Paulo 78
Santa Clara 72
Milan 58
Los Angeles 52
Phoenix 45
Nuremberg 37
Rio de Janeiro 36
Helsinki 34
Dublin 31
Rome 29
Orem 27
Atlanta 23
Chicago 23
Curitiba 23
Washington 22
Tokyo 20
Warsaw 20
Brooklyn 19
Da Nang 19
Haiphong 19
Houston 19
Brasília 18
Guangzhou 18
Pune 18
Johannesburg 17
Vienna 17
Boston 16
Chennai 16
Mexico City 16
Quito 16
The Dalles 16
Baghdad 14
Guarulhos 14
Guayaquil 14
Hangzhou 14
Campinas 13
Frankfurt am Main 13
Montreal 13
Turku 13
Denver 12
Kingston 12
Stockholm 12
Belo Horizonte 11
Biên Hòa 11
Manchester 11
Parma 11
Seattle 11
Southwark 11
Bologna 10
Buffalo 10
Caxias do Sul 10
Columbus 10
Hải Dương 10
London 10
Montevideo 10
Naples 10
Philadelphia 10
Poplar 10
Porto Alegre 10
Santo André 10
Shenzhen 10
Tashkent 10
Thái Bình 10
Tianjin 10
Munich 9
Salvador 9
Toronto 9
Bogotá 8
Goiânia 8
La Plata 8
Wuxi 8
Ankara 7
Buenos Aires 7
Bắc Ninh 7
Changsha 7
Cincinnati 7
Dhaka 7
Florence 7
Fortaleza 7
Giessen 7
Istanbul 7
Lahore 7
Las Vegas 7
Lima 7
Totale 6.216
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Nome #
Asymptomatic Thyrotropin-secreting Pituitary Macroadenoma in a Thirteen Year-old Girl: Successful First-line Treatment with Somatostatin Analogues 140
Different Efficacy of Burosumab on Physical Performance and Serum Phosphate in Adult Patients with X-Linked Hyphophosphatemic Rickets during the First Six-Month of Treatment 134
Autosomal dominant hypocalcemia with mild type 5 Bartter syndrome 134
Autosomal dominant hypocalcemia in monozygotic twins caused by a de novo germline mutation near the amino-terminus of the human calcium receptor 122
Thyroid function and puberty 122
"Block-and-replace" method in pediatric Graves' disease 115
A 7-year experience with low blood TSH cutoff levels for neonatal screening reveals an unsuspected frequency of congenital hypothyroidism (CH) 113
A frequent oligogenic involvement in congenital hypothyroidism 111
Frequent TSH Receptor Genetic Alterations with Variable Signaling Impairment in a Large Series of Children with Nonautoimmune Isolated Hyperthyrotropinemia 107
Anterior pituitary gland aplasia: neuroradiological, phenotypical and hormonal evaluation 104
Biallelic inactivation of the dual oxidase maturation factor 2 (DUOXA2) gene as a novel cause of congenital hypothyroidism 103
Alternative diagnostic approach to the etiology definition of Congenital Hypothyroidism" 101
Diagnosis of hypochondroplasia: the role of radiological interpretation. Italian Study Group for Hypochondroplasia 98
Clinical presentation of McCune-Albright syndrome in males 96
"Effect of long-term glucocorticoid therapy on bone density and bone remodeling indexes in patients with congenital adrenal hyperplasia" 95
A case of metabolic syndrome in an adolescent: diagnosis and management 94
Attention abilities in preadolescents and adolescents with congenital hypothyroidism 93
Analysis of 21-deoxycortisol, a marker of congenital adrenal hyperplasia, in blood by atmospheric pressure chemical ionization and electrospray ionization using multiple reaction monitoring 92
Persistent mild hypothyroidism associated with novel sequenze variants of the DUOX2 gene in two siblings 92
Conoscenze fondamentali dello sviluppo fisiologico e principi di igiene scolastica 92
X-linked hypophosphatemic rickets: An Italian experts' opinion survey 92
Accuracy of fine needle aspiration biopsy of thyroid nodules in detecting malignancy in childhood: comparison with conventional clinical, laboratory, and imaging approaches 91
Absence of sonic hedgehog (Shh) germline mutations in patients with thyroid dysgenesis 90
A novel germline mutation in the TSH receptor gene causes non-autoimmune autosomal dominant hyperthyroidism 88
Neurophysiological studies and cognitive function in congenital hypopthyroid children 87
Allungamento chirurgico degli arti: in quali casi intervenire? A che età iniziare? 86
Total iodide organification defect: clinical and molecular characterization of an Italian family 86
Follow Up dell'ipoparatiroidismo e dello pseudoipoparatiroidismo in pediatria durante terapia con metaboliti attivi della Vitamina D 85
A new mutation in AVPR2 gene discovered in an infant with nephrogenic diabetes insipidus 82
Analysis of TSH Receptor gene in four cases with the clinical features of partial TSH resistance" 80
Hypocalciuric effect of chlorthalidone in two hypoparathyroid children 79
Neurosurgical treatment of craniopharyngioma in adults and children: early and long-term results in a large case series 79
Cognitive function and neurophysiological evaluation in early-treated hypothyroid children 78
Saturazione dell’emoglobina nell’Ipotiroidismo congenito alla diagnosi 77
Heterogeneous phenotype in children affected by non-autoimmune hypothyroidism: an update. 77
Accidental exposure to polychlorinated biphenyls in a farm 77
Growth hormone therapy in children: predictive factors and short-term and long-term response criteria 76
Clinical and molecular heterogeneity in a large series of patients with hypophosphatemic rickets 75
JAG1 Loss-Of-Function Variations as a Novel Predisposing Event in the Pathogenesis of Congenital Thyroid Defects. 75
Graves Disease in Children: Thyroid-Stimulating Hormone Receptor Antibodies as Remission Markers 74
Validation of food frequency questionnaire for assessing dietary macronutrients and calcium intake in Italian children and adolescents 74
Study of hydro-saline metabolism during phosphate therapy in a subject with vitamin-D resistant rickets 72
Bone density in adolescents and young adults with congenital adrenal hyperplasia 72
Genetic defects of hydrogen peroxide generation in the thyroid gland 71
The Italian screening programfor primary congenital hypothyroidism: Actions to improve screening, diagnosis, follow-up, and surveillance 71
Growth hormone-releasing hormone resistance in pseudohypoparathyroidism type ia: new evidence for imprinting of the Gs alpha gene 70
Nephrocalcinosis in children and adolescents: sonographic evaluation during long-term treatment with 1,25-dihydroxycholecalciferol. 70
Endocrinopatie 70
Ipotiroidismo subclinico nella prima infanzia 69
COVID-19 pandemic: implications on the surgical treatment of gastrointestinal and hepatopancreatobiliary tumours in Europe 69
Thyroid scintigraphy and perchlorate test after recombinant human TSH: a new tool for the differential diagnosis of congenital hypothyroidism during infancy 68
Endocrinopatie 68
“Block-and-replace” treatment in Graves’ disease: experience in a cohort of pediatric patients 68
Reversal of low bone density with gluten-free diet in children and adolescents with celiac disease 67
Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH) 67
INTERACTIONS AMONG PRO-INFLAMMATORY CYTOKINES, IGF SYSTEM AND THYROID FUNCTION IN PRE-PUBERTAL OBESE SUBJECTS 66
Physical and sport activity in thge prevention and treatment of obesity and diabetes in children 66
Genetics and phenomics of hypothyroidism due to TSH resistance 65
Coherence EEG modifications in children with congenital hypothyroidism 65
Effect of estrogen replacement therapy on bone mineral content in girls with Turner syndrome. 64
Bone mineral density (DEXA) in celiac children and adolescents before and during gluten-free diet 64
The clinical and molecular characterization of patients with dyshormonogenic congenital hypothyroidism reveals specific diagnostic clues for DUOX2 defects 63
Sonographic evaluation of distal femoral epiphysis in newborns 63
Thyroid autoimmunity and congenital hypothyroidism 63
Congenital Hypothyroidism Treatment in Infants: A Comparative Study between Liquid and Tablet Formulations of Levothyroxine 63
Comparison between liquid L-thyroxine (L-T4) solution and tablet in congenital hypothyroidism (CH) 63
Effect of gluten-free diet on bone mineral content in growing patients with celiac disease 62
Final height in Italian patients with congenital hypothyroidism detected by neonatal screening: a 20-year observational study 62
Conferma diagnostica di Ipotiroidismo congenito: studio comparativo tra ecografia e scintigrafia tiroidea 61
Bone density and bone metabolism are normal after long-term gluten free diet in young celiac, patients 61
Problems in the long term therapeutical management of hypoparathyroidism in childhood 61
The DNA methylation as a predisposition factor in the pathogenesis of congenital hypothyroidism in prematur infants 61
Bone demineralization in Turner's Syndrome 61
I rachitismi; la diagnosi differenziale dei dolori osteoarticolari; tetanie ipocalcemiche 61
Brain M.R.I. in congenital hypothyroidism in infants at diagnosis " 61
Possible defect of calcium cell-permeability in pseudohypoparathyroidism: Case report 60
Crying abnormalities in congenital hypothyroidism: preliminary spectrographic study 60
Neurophysiological abnormalities of CNS in congenital hypothyroid school age children 60
Study of calcium homeostasis in children with type 1 diabetes mellitus at onset 60
Snyder-Robinson syndrome: A novel nonsense mutation in spermine synthase and expansion of the phenotype 60
Vitamin D in childhood and adolescence: an expert position statement 60
Non-endocrine growth retardation. Diagnostic and therapeutic indications 60
Maturation of preterm newborn brains: a longitudinal fMRI and DTI study of auditory system 60
Testicular microlithiasis: an unreported feature of McCune-Albright syndrome in males 59
Comparison of clinical-radiological and molecular findings in hypochondroplasia 58
Levothyroxine Treatment in Pediatric Benign Thyroid Nodules 58
Osteopenia in premature children: an emerging problem 58
Mild TSH resistance: Clinical and hormonal features in childhood and adulthood 58
Type 5 Bartter Syndrome: a crossroad among alterations of calcium and sodium metabolism 58
Neonatal Screening for Congenital Hypothyroidism: What can we learn from Discordant twins? 58
Sleep and upper airway obstruction in children with achondroplasia 57
Congenital hypothyroidism with eutopic thyroid gland: Analysis of clinical and biochemical features at diagnosis and after re-evaluation 57
Molecular characterization of three italian families affected with dishormogenetic goiter and sensorineural hearing loss: description of a new mutation in the PDS gene 57
“Transiet hypothyroidism secondary to Wolff-Chaikoff effect: the importance of urinary iodine excretion in precocious differential diagnosis 57
Neonatal screening program for congenital hypothyroidism: A 7-year experience with low TSH cut-off levels 57
Epidemiology of congenital hypothyroidism: what can be deduced from the Italian registry of infants with congenital hypothyroidism 57
La sindrome di Bartter tipo 5: ruolo del cotrasporto Na/Cl/K in due casi clinici 57
Decreased Parietal Cortex Activity during Mental Rotation in Children with Congenital Hypothyroidism 56
Studio delle vie acustiche mediante analisi dei potenziali evocati uditivi e dell’elettroencelografia in bambini affetti da ipotiroidismo congenito in terapia sostitutiva 56
Ipotalamo ipofisi 56
Totale 7.548
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Categoria #
all - tutte 96.413
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 96.413
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022110 0 0 0 47 16 12 11 1 9 5 1 8
2022/20231.048 489 248 75 5 2 123 32 41 14 8 1 10
2023/2024426 11 5 16 124 21 61 7 26 8 11 23 113
2024/20252.680 349 45 37 111 55 208 317 176 541 491 176 174
2025/20268.080 570 640 574 1.373 534 201 690 566 2.244 344 189 155
2026/20271.047 161 493 369 24 0 0 0 0 0 0 0 0
Totale 13.433