IRIS
WEBER, GIOVANNA
 Distribuzione geografica
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Continente #
AS - Asia 4.484
EU - Europa 3.904
NA - Nord America 2.483
SA - Sud America 1.248
AF - Africa 86
OC - Oceania 4
Continente sconosciuto - Info sul continente non disponibili 2
Totale 12.211
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Nazione #
RU - Federazione Russa 2.490
US - Stati Uniti d'America 2.349
SG - Singapore 1.657
CN - Cina 1.498
BR - Brasile 1.019
HK - Hong Kong 548
SE - Svezia 546
VN - Vietnam 408
IT - Italia 263
FR - Francia 207
DE - Germania 107
AR - Argentina 103
BD - Bangladesh 86
IN - India 74
GB - Regno Unito 67
MX - Messico 52
FI - Finlandia 49
CA - Canada 47
ID - Indonesia 42
EC - Ecuador 38
AT - Austria 35
ZA - Sudafrica 34
IE - Irlanda 33
TR - Turchia 25
CO - Colombia 24
IQ - Iraq 24
PL - Polonia 23
JP - Giappone 21
MA - Marocco 18
NL - Olanda 17
PY - Paraguay 17
PK - Pakistan 16
SA - Arabia Saudita 16
ES - Italia 13
VE - Venezuela 13
CL - Cile 11
PE - Perù 11
UA - Ucraina 11
UZ - Uzbekistan 11
JM - Giamaica 10
UY - Uruguay 10
TN - Tunisia 8
IR - Iran 7
JO - Giordania 6
KZ - Kazakistan 6
LT - Lituania 6
MD - Moldavia 6
PH - Filippine 6
EG - Egitto 5
KE - Kenya 5
PS - Palestinian Territory 5
RS - Serbia 5
TT - Trinidad e Tobago 5
AL - Albania 4
AU - Australia 4
AZ - Azerbaigian 4
DO - Repubblica Dominicana 4
HN - Honduras 4
IL - Israele 4
OM - Oman 4
AE - Emirati Arabi Uniti 3
BE - Belgio 3
CH - Svizzera 3
DK - Danimarca 3
DZ - Algeria 3
MY - Malesia 3
NP - Nepal 3
PT - Portogallo 3
AO - Angola 2
BA - Bosnia-Erzegovina 2
BB - Barbados 2
CR - Costa Rica 2
HR - Croazia 2
NI - Nicaragua 2
RO - Romania 2
SN - Senegal 2
SV - El Salvador 2
XK - ???statistics.table.value.countryCode.XK??? 2
AM - Armenia 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
MU - Mauritius 1
NG - Nigeria 1
Totale 12.207
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Città #
Singapore 619
Hong Kong 544
Moscow 543
Ashburn 405
San Jose 359
Dallas 345
Shanghai 280
Hefei 225
Lawrence 222
Princeton 222
Lauterbourg 190
Beijing 166
Ho Chi Minh City 156
Hanoi 89
New York 87
São Paulo 78
Milan 54
Los Angeles 47
Nuremberg 37
Rio de Janeiro 36
Helsinki 34
Santa Clara 33
Dublin 31
Orem 26
Rome 25
Curitiba 23
Tokyo 20
Warsaw 20
Da Nang 19
Haiphong 19
Washington 19
Brooklyn 18
Guangzhou 18
Pune 18
Atlanta 17
Brasília 17
Johannesburg 17
Chennai 16
Chicago 16
The Dalles 16
Vienna 16
Mexico City 15
Quito 15
Baghdad 14
Guarulhos 14
Campinas 13
Hangzhou 13
Montreal 13
Turku 13
Frankfurt am Main 12
Stockholm 12
Belo Horizonte 11
Biên Hòa 11
Boston 11
Denver 11
Guayaquil 11
Parma 11
Seattle 11
Southwark 11
Caxias do Sul 10
Hải Dương 10
London 10
Poplar 10
Porto Alegre 10
Santo André 10
Shenzhen 10
Tashkent 10
Thái Bình 10
Bologna 9
Buffalo 9
Houston 9
Manchester 9
Montevideo 9
Munich 9
Naples 9
Salvador 9
Tianjin 9
Columbus 8
Goiânia 8
La Plata 8
Phoenix 8
Wuxi 8
Ankara 7
Bogotá 7
Buenos Aires 7
Bắc Ninh 7
Changsha 7
Florence 7
Fortaleza 7
Giessen 7
Istanbul 7
Kingston 7
Lahore 7
Lima 7
Manaus 7
Querétaro 7
Québec 7
Recife 7
Ribeirão Preto 7
Sumaré 7
Totale 5.701
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Nome #
Asymptomatic Thyrotropin-secreting Pituitary Macroadenoma in a Thirteen Year-old Girl: Successful First-line Treatment with Somatostatin Analogues 129
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 125
Autosomal dominant hypocalcemia in monozygotic twins caused by a de novo germline mutation near the amino-terminus of the human calcium receptor 113
"Block-and-replace" method in pediatric Graves' disease 106
Thyroid function and puberty 104
Autosomal dominant hypocalcemia with mild type 5 Bartter syndrome 103
A 7-year experience with low blood TSH cutoff levels for neonatal screening reveals an unsuspected frequency of congenital hypothyroidism (CH) 102
Anterior pituitary gland aplasia: neuroradiological, phenotypical and hormonal evaluation 101
Alternative diagnostic approach to the etiology definition of Congenital Hypothyroidism" 98
A frequent oligogenic involvement in congenital hypothyroidism 95
Diagnosis of hypochondroplasia: the role of radiological interpretation. Italian Study Group for Hypochondroplasia 93
A case of metabolic syndrome in an adolescent: diagnosis and management 91
"Effect of long-term glucocorticoid therapy on bone density and bone remodeling indexes in patients with congenital adrenal hyperplasia" 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
Conoscenze fondamentali dello sviluppo fisiologico e principi di igiene scolastica 89
Attention abilities in preadolescents and adolescents with congenital hypothyroidism 89
Biallelic inactivation of the dual oxidase maturation factor 2 (DUOXA2) gene as a novel cause of congenital hypothyroidism 88
Persistent mild hypothyroidism associated with novel sequenze variants of the DUOX2 gene in two siblings 87
Accuracy of fine needle aspiration biopsy of thyroid nodules in detecting malignancy in childhood: comparison with conventional clinical, laboratory, and imaging approaches 87
Absence of sonic hedgehog (Shh) germline mutations in patients with thyroid dysgenesis 86
Allungamento chirurgico degli arti: in quali casi intervenire? A che età iniziare? 82
Total iodide organification defect: clinical and molecular characterization of an Italian family 80
A novel germline mutation in the TSH receptor gene causes non-autoimmune autosomal dominant hyperthyroidism 80
Clinical presentation of McCune-Albright syndrome in males 79
Neurophysiological studies and cognitive function in congenital hypopthyroid children 78
A new mutation in AVPR2 gene discovered in an infant with nephrogenic diabetes insipidus 78
Follow Up dell'ipoparatiroidismo e dello pseudoipoparatiroidismo in pediatria durante terapia con metaboliti attivi della Vitamina D 76
X-linked hypophosphatemic rickets: An Italian experts' opinion survey 76
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 74
Saturazione dell’emoglobina nell’Ipotiroidismo congenito alla diagnosi 72
Hypocalciuric effect of chlorthalidone in two hypoparathyroid children 72
Cognitive function and neurophysiological evaluation in early-treated hypothyroid children 71
Frequent TSH Receptor Genetic Alterations with Variable Signaling Impairment in a Large Series of Children with Nonautoimmune Isolated Hyperthyrotropinemia 71
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 68
Nephrocalcinosis in children and adolescents: sonographic evaluation during long-term treatment with 1,25-dihydroxycholecalciferol. 67
Clinical and molecular heterogeneity in a large series of patients with hypophosphatemic rickets 66
Validation of food frequency questionnaire for assessing dietary macronutrients and calcium intake in Italian children and adolescents 66
Neurosurgical treatment of craniopharyngioma in adults and children: early and long-term results in a large case series 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
Endocrinopatie 65
Endocrinopatie 65
Ipotiroidismo subclinico nella prima infanzia 65
Physical and sport activity in thge prevention and treatment of obesity and diabetes in children 64
Growth hormone therapy in children: predictive factors and short-term and long-term response criteria 64
INTERACTIONS AMONG PRO-INFLAMMATORY CYTOKINES, IGF SYSTEM AND THYROID FUNCTION IN PRE-PUBERTAL OBESE SUBJECTS 63
JAG1 Loss-Of-Function Variations as a Novel Predisposing Event in the Pathogenesis of Congenital Thyroid Defects. 63
The Italian screening programfor primary congenital hypothyroidism: Actions to improve screening, diagnosis, follow-up, and surveillance 63
Bone mineral density (DEXA) in celiac children and adolescents before and during gluten-free diet 62
Growth hormone-releasing hormone resistance in pseudohypoparathyroidism type ia: new evidence for imprinting of the Gs alpha gene 61
Genetic defects of hydrogen peroxide generation in the thyroid gland 61
Coherence EEG modifications in children with congenital hypothyroidism 61
Thyroid autoimmunity and congenital hypothyroidism 61
COVID-19 pandemic: implications on the surgical treatment of gastrointestinal and hepatopancreatobiliary tumours in Europe 61
Effect of estrogen replacement therapy on bone mineral content in girls with Turner syndrome. 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
Comparison between liquid L-thyroxine (L-T4) solution and tablet in congenital hypothyroidism (CH) 60
Heterogeneous phenotype in children affected by non-autoimmune hypothyroidism: an update. 59
Sonographic evaluation of distal femoral epiphysis in newborns 59
Bone demineralization in Turner's Syndrome 59
Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH) 59
Thyroid scintigraphy and perchlorate test after recombinant human TSH: a new tool for the differential diagnosis of congenital hypothyroidism during infancy 58
Effect of gluten-free diet on bone mineral content in growing patients with celiac disease 58
I rachitismi; la diagnosi differenziale dei dolori osteoarticolari; tetanie ipocalcemiche 58
Brain M.R.I. in congenital hypothyroidism in infants at diagnosis " 58
Possible defect of calcium cell-permeability in pseudohypoparathyroidism: Case report 57
Problems in the long term therapeutical management of hypoparathyroidism in childhood 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
“Block-and-replace” treatment in Graves’ disease: experience in a cohort of pediatric patients 57
Conferma diagnostica di Ipotiroidismo congenito: studio comparativo tra ecografia e scintigrafia tiroidea 56
Bone density and bone metabolism are normal after long-term gluten free diet in young celiac, patients 56
Neurophysiological abnormalities of CNS in congenital hypothyroid school age children 56
Study of calcium homeostasis in children with type 1 diabetes mellitus at onset 56
Final height in Italian patients with congenital hypothyroidism detected by neonatal screening: a 20-year observational study 56
Comparison of clinical-radiological and molecular findings in hypochondroplasia 55
Crying abnormalities in congenital hypothyroidism: preliminary spectrographic study 55
Osteopenia in premature children: an emerging problem 55
Genetics and phenomics of hypothyroidism due to TSH resistance 55
Studio delle vie acustiche mediante analisi dei potenziali evocati uditivi e dell’elettroencelografia in bambini affetti da ipotiroidismo congenito in terapia sostitutiva 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
Neonatal screening program for congenital hypothyroidism: A 7-year experience with low TSH cut-off levels 54
Mild TSH resistance: Clinical and hormonal features in childhood and adulthood 54
Neonatal Screening for Congenital Hypothyroidism: What can we learn from Discordant twins? 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
The clinical and molecular characterization of patients with dyshormonogenic congenital hypothyroidism reveals specific diagnostic clues for DUOX2 defects 53
Ipotalamo ipofisi 53
Epidemiology of congenital hypothyroidism: what can be deduced from the Italian registry of infants with congenital hypothyroidism 53
Snyder-Robinson syndrome: A novel nonsense mutation in spermine synthase and expansion of the phenotype 53
Vitamin D in childhood and adolescence: an expert position statement 53
Surgical lengthening of limbs in achondroplastic children: a medical and psycho-social program to select and treat patients. 52
Mineralizzazione ossea in neonati gemelli 52
Type 1 polyglandular autoimmune syndrome in a girl: Diagnostic and therapeutic problems 52
Identification and functional analysis of DUOX2 variants: biallelic mutations are associated with permanent congenital hypothyroidism 52
Totale 6.891
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Categoria #
all - tutte 87.471
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 87.471
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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
2025/20267.944 570 640 574 1.373 534 201 690 566 2.244 344 189 19
Totale 12.250