IRIS
WEBER, GIOVANNA
 Distribuzione geografica
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Continente #
AS - Asia 4.568
EU - Europa 3.923
NA - Nord America 2.683
SA - Sud America 1.252
AF - Africa 86
Continente sconosciuto - Info sul continente non disponibili 41
OC - Oceania 4
Totale 12.557
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Nazione #
US - Stati Uniti d'America 2.533
RU - Federazione Russa 2.491
SG - Singapore 1.664
CN - Cina 1.542
BR - Brasile 1.020
HK - Hong Kong 549
SE - Svezia 546
VN - Vietnam 417
IT - Italia 275
FR - Francia 208
DE - Germania 109
AR - Argentina 104
BD - Bangladesh 96
IN - India 76
GB - Regno Unito 67
CA - Canada 53
MX - Messico 52
FI - Finlandia 49
ID - Indonesia 43
EC - Ecuador 39
AT - Austria 35
ZA - Sudafrica 34
IE - Irlanda 33
TR - Turchia 25
CO - Colombia 24
IQ - Iraq 24
PL - Polonia 24
JP - Giappone 23
NL - Olanda 19
MA - Marocco 18
PY - Paraguay 17
PK - Pakistan 16
SA - Arabia Saudita 16
ES - Italia 13
VE - Venezuela 13
JM - Giamaica 12
CL - Cile 11
PE - Perù 11
UA - Ucraina 11
UY - Uruguay 11
UZ - Uzbekistan 11
TN - Tunisia 8
IR - Iran 7
TT - Trinidad e Tobago 7
CR - Costa Rica 6
JO - Giordania 6
KZ - Kazakistan 6
LT - Lituania 6
MD - Moldavia 6
PH - Filippine 6
AE - Emirati Arabi Uniti 5
EG - Egitto 5
KE - Kenya 5
PS - Palestinian Territory 5
RS - Serbia 5
AL - Albania 4
AU - Australia 4
AZ - Azerbaigian 4
DO - Repubblica Dominicana 4
HN - Honduras 4
IL - Israele 4
MY - Malesia 4
OM - Oman 4
BE - Belgio 3
CH - Svizzera 3
DK - Danimarca 3
DZ - Algeria 3
NI - Nicaragua 3
NP - Nepal 3
PT - Portogallo 3
SV - El Salvador 3
TW - Taiwan 3
AO - Angola 2
BA - Bosnia-Erzegovina 2
BB - Barbados 2
HR - Croazia 2
RO - Romania 2
SN - Senegal 2
XK - ???statistics.table.value.countryCode.XK??? 2
AM - Armenia 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
GR - Grecia 1
GT - Guatemala 1
GY - Guiana 1
LK - Sri Lanka 1
LY - Libia 1
MK - Macedonia 1
MN - Mongolia 1
Totale 12.511
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Città #
Singapore 623
Hong Kong 545
Moscow 544
Ashburn 419
San Jose 372
Dallas 346
Shanghai 280
Hefei 225
Princeton 223
Lawrence 222
Lauterbourg 190
Beijing 173
Ho Chi Minh City 160
New York 93
Hanoi 90
São Paulo 78
Santa Clara 60
Milan 57
Los Angeles 47
Nuremberg 37
Rio de Janeiro 36
Helsinki 34
Dublin 31
Orem 27
Rome 26
Curitiba 23
Tokyo 20
Warsaw 20
Washington 20
Da Nang 19
Haiphong 19
Atlanta 18
Brooklyn 18
Chicago 18
Guangzhou 18
Pune 18
Brasília 17
Johannesburg 17
Vienna 17
Boston 16
Chennai 16
The Dalles 16
Mexico City 15
Quito 15
Baghdad 14
Guarulhos 14
Hangzhou 14
Campinas 13
Frankfurt am Main 13
Montreal 13
Turku 13
Denver 12
Guayaquil 12
Houston 12
Stockholm 12
Belo Horizonte 11
Biên Hòa 11
Parma 11
Seattle 11
Southwark 11
Buffalo 10
Caxias do Sul 10
Hải Dương 10
London 10
Montevideo 10
Poplar 10
Porto Alegre 10
Santo André 10
Shenzhen 10
Tashkent 10
Thái Bình 10
Tianjin 10
Bologna 9
Columbus 9
Kingston 9
Manchester 9
Munich 9
Naples 9
Salvador 9
Goiânia 8
La Plata 8
Phoenix 8
Wuxi 8
Ankara 7
Bogotá 7
Buenos Aires 7
Bắc Ninh 7
Changsha 7
Dhaka 7
Florence 7
Fortaleza 7
Giessen 7
Istanbul 7
Lahore 7
Lima 7
Manaus 7
Mumbai 7
Querétaro 7
Québec 7
Recife 7
Totale 5.809
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Nome #
Asymptomatic Thyrotropin-secreting Pituitary Macroadenoma in a Thirteen Year-old Girl: Successful First-line Treatment with Somatostatin Analogues 132
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 129
Autosomal dominant hypocalcemia in monozygotic twins caused by a de novo germline mutation near the amino-terminus of the human calcium receptor 117
Autosomal dominant hypocalcemia with mild type 5 Bartter syndrome 116
Thyroid function and puberty 112
"Block-and-replace" method in pediatric Graves' disease 109
A 7-year experience with low blood TSH cutoff levels for neonatal screening reveals an unsuspected frequency of congenital hypothyroidism (CH) 106
A frequent oligogenic involvement in congenital hypothyroidism 102
Anterior pituitary gland aplasia: neuroradiological, phenotypical and hormonal evaluation 101
Alternative diagnostic approach to the etiology definition of Congenital Hypothyroidism" 99
Biallelic inactivation of the dual oxidase maturation factor 2 (DUOXA2) gene as a novel cause of congenital hypothyroidism 96
Diagnosis of hypochondroplasia: the role of radiological interpretation. Italian Study Group for Hypochondroplasia 95
A case of metabolic syndrome in an adolescent: diagnosis and management 91
Clinical presentation of McCune-Albright syndrome in males 90
"Effect of long-term glucocorticoid therapy on bone density and bone remodeling indexes in patients with congenital adrenal hyperplasia" 90
Conoscenze fondamentali dello sviluppo fisiologico e principi di igiene scolastica 90
Analysis of 21-deoxycortisol, a marker of congenital adrenal hyperplasia, in blood by atmospheric pressure chemical ionization and electrospray ionization using multiple reaction monitoring 89
Attention abilities in preadolescents and adolescents with congenital hypothyroidism 89
Persistent mild hypothyroidism associated with novel sequenze variants of the DUOX2 gene in two siblings 88
Accuracy of fine needle aspiration biopsy of thyroid nodules in detecting malignancy in childhood: comparison with conventional clinical, laboratory, and imaging approaches 88
Absence of sonic hedgehog (Shh) germline mutations in patients with thyroid dysgenesis 87
Total iodide organification defect: clinical and molecular characterization of an Italian family 84
Allungamento chirurgico degli arti: in quali casi intervenire? A che età iniziare? 83
Follow Up dell'ipoparatiroidismo e dello pseudoipoparatiroidismo in pediatria durante terapia con metaboliti attivi della Vitamina D 82
Neurophysiological studies and cognitive function in congenital hypopthyroid children 82
A novel germline mutation in the TSH receptor gene causes non-autoimmune autosomal dominant hyperthyroidism 80
A new mutation in AVPR2 gene discovered in an infant with nephrogenic diabetes insipidus 79
Frequent TSH Receptor Genetic Alterations with Variable Signaling Impairment in a Large Series of Children with Nonautoimmune Isolated Hyperthyrotropinemia 78
X-linked hypophosphatemic rickets: An Italian experts' opinion survey 76
Saturazione dell’emoglobina nell’Ipotiroidismo congenito alla diagnosi 75
Hypocalciuric effect of chlorthalidone in two hypoparathyroid children 75
Analysis of TSH Receptor gene in four cases with the clinical features of partial TSH resistance" 75
Accidental exposure to polychlorinated biphenyls in a farm 75
Cognitive function and neurophysiological evaluation in early-treated hypothyroid children 73
Neurosurgical treatment of craniopharyngioma in adults and children: early and long-term results in a large case series 72
Clinical and molecular heterogeneity in a large series of patients with hypophosphatemic rickets 70
Validation of food frequency questionnaire for assessing dietary macronutrients and calcium intake in Italian children and adolescents 70
JAG1 Loss-Of-Function Variations as a Novel Predisposing Event in the Pathogenesis of Congenital Thyroid Defects. 70
Study of hydro-saline metabolism during phosphate therapy in a subject with vitamin-D resistant rickets 69
Bone density in adolescents and young adults with congenital adrenal hyperplasia 69
Nephrocalcinosis in children and adolescents: sonographic evaluation during long-term treatment with 1,25-dihydroxycholecalciferol. 68
Endocrinopatie 68
Growth hormone-releasing hormone resistance in pseudohypoparathyroidism type ia: new evidence for imprinting of the Gs alpha gene 66
Heterogeneous phenotype in children affected by non-autoimmune hypothyroidism: an update. 66
Endocrinopatie 66
The Italian screening programfor primary congenital hypothyroidism: Actions to improve screening, diagnosis, follow-up, and surveillance 66
Reversal of low bone density with gluten-free diet in children and adolescents with celiac disease 65
Graves Disease in Children: Thyroid-Stimulating Hormone Receptor Antibodies as Remission Markers 65
Ipotiroidismo subclinico nella prima infanzia 65
Growth hormone therapy in children: predictive factors and short-term and long-term response criteria 65
INTERACTIONS AMONG PRO-INFLAMMATORY CYTOKINES, IGF SYSTEM AND THYROID FUNCTION IN PRE-PUBERTAL OBESE SUBJECTS 64
Physical and sport activity in thge prevention and treatment of obesity and diabetes in children 64
COVID-19 pandemic: implications on the surgical treatment of gastrointestinal and hepatopancreatobiliary tumours in Europe 64
Genetic defects of hydrogen peroxide generation in the thyroid gland 63
Bone mineral density (DEXA) in celiac children and adolescents before and during gluten-free diet 63
Coherence EEG modifications in children with congenital hypothyroidism 63
Thyroid scintigraphy and perchlorate test after recombinant human TSH: a new tool for the differential diagnosis of congenital hypothyroidism during infancy 61
Effect of estrogen replacement therapy on bone mineral content in girls with Turner syndrome. 61
Thyroid autoimmunity and congenital hypothyroidism 61
Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH) 61
Comparison between liquid L-thyroxine (L-T4) solution and tablet in congenital hypothyroidism (CH) 61
Sonographic evaluation of distal femoral epiphysis in newborns 60
The DNA methylation as a predisposition factor in the pathogenesis of congenital hypothyroidism in prematur infants 60
Congenital Hypothyroidism Treatment in Infants: A Comparative Study between Liquid and Tablet Formulations of Levothyroxine 60
Conferma diagnostica di Ipotiroidismo congenito: studio comparativo tra ecografia e scintigrafia tiroidea 59
Bone demineralization in Turner's Syndrome 59
“Block-and-replace” treatment in Graves’ disease: experience in a cohort of pediatric patients 59
Effect of gluten-free diet on bone mineral content in growing patients with celiac disease 58
Neurophysiological abnormalities of CNS in congenital hypothyroid school age children 58
Problems in the long term therapeutical management of hypoparathyroidism in childhood 58
I rachitismi; la diagnosi differenziale dei dolori osteoarticolari; tetanie ipocalcemiche 58
Final height in Italian patients with congenital hypothyroidism detected by neonatal screening: a 20-year observational study 58
Brain M.R.I. in congenital hypothyroidism in infants at diagnosis " 58
Possible defect of calcium cell-permeability in pseudohypoparathyroidism: Case report 57
Genetics and phenomics of hypothyroidism due to TSH resistance 57
Non-endocrine growth retardation. Diagnostic and therapeutic indications 57
Maturation of preterm newborn brains: a longitudinal fMRI and DTI study of auditory system 57
Bone density and bone metabolism are normal after long-term gluten free diet in young celiac, patients 56
The clinical and molecular characterization of patients with dyshormonogenic congenital hypothyroidism reveals specific diagnostic clues for DUOX2 defects 56
Study of calcium homeostasis in children with type 1 diabetes mellitus at onset 56
Vitamin D in childhood and adolescence: an expert position statement 56
Neonatal Screening for Congenital Hypothyroidism: What can we learn from Discordant twins? 56
Comparison of clinical-radiological and molecular findings in hypochondroplasia 55
Levothyroxine Treatment in Pediatric Benign Thyroid Nodules 55
Crying abnormalities in congenital hypothyroidism: preliminary spectrographic study 55
Osteopenia in premature children: an emerging problem 55
Studio delle vie acustiche mediante analisi dei potenziali evocati uditivi e dell’elettroencelografia in bambini affetti da ipotiroidismo congenito in terapia sostitutiva 55
Neonatal screening program for congenital hypothyroidism: A 7-year experience with low TSH cut-off levels 55
Type 5 Bartter Syndrome: a crossroad among alterations of calcium and sodium metabolism 55
Decreased Parietal Cortex Activity during Mental Rotation in Children with Congenital Hypothyroidism 54
Molecular characterization of three italian families affected with dishormogenetic goiter and sensorineural hearing loss: description of a new mutation in the PDS gene 54
“Transiet hypothyroidism secondary to Wolff-Chaikoff effect: the importance of urinary iodine excretion in precocious differential diagnosis 54
Ipotalamo ipofisi 54
Epidemiology of congenital hypothyroidism: what can be deduced from the Italian registry of infants with congenital hypothyroidism 54
Snyder-Robinson syndrome: A novel nonsense mutation in spermine synthase and expansion of the phenotype 54
Mild TSH resistance: Clinical and hormonal features in childhood and adulthood 54
Sleep and upper airway obstruction in children with achondroplasia 53
Severe hypocalcemia due to a de novo mutation in the fifth transmembrane domain of the calcium-sensing receptor 53
Surgical lengthening of limbs in achondroplastic children: a medical and psycho-social program to select and treat patients. 53
Ipotiroidismo transitorio, esperienze a confronto 53
Totale 7.087
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Categoria #
all - tutte 91.800
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 91.800
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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
2026/2027171 161 10 0 0 0 0 0 0 0 0 0 0
Totale 12.557