IRIS
WEBER, GIOVANNA
 Distribuzione geografica
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Continente #
AS - Asia 3.674
NA - Nord America 1.773
EU - Europa 1.297
SA - Sud America 1.201
AF - Africa 70
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 2
Totale 8.020
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Nazione #
US - Stati Uniti d'America 1.677
SG - Singapore 1.587
CN - Cina 1.010
BR - Brasile 992
SE - Svezia 543
HK - Hong Kong 514
VN - Vietnam 306
RU - Federazione Russa 209
IT - Italia 191
AR - Argentina 99
DE - Germania 95
IN - India 60
GB - Regno Unito 49
FI - Finlandia 48
MX - Messico 42
ID - Indonesia 38
EC - Ecuador 37
BD - Bangladesh 36
AT - Austria 35
IE - Irlanda 32
ZA - Sudafrica 31
CA - Canada 29
TR - Turchia 20
CO - Colombia 19
IQ - Iraq 18
PL - Polonia 18
JP - Giappone 17
NL - Olanda 17
FR - Francia 14
MA - Marocco 13
PY - Paraguay 13
VE - Venezuela 12
CL - Cile 10
ES - Italia 10
UZ - Uzbekistan 10
UA - Ucraina 9
UY - Uruguay 9
PE - Perù 8
SA - Arabia Saudita 8
IR - Iran 7
JM - Giamaica 7
PK - Pakistan 7
KZ - Kazakistan 6
PS - Palestinian Territory 5
TN - Tunisia 5
AZ - Azerbaigian 4
EG - Egitto 4
IL - Israele 4
KE - Kenya 4
LT - Lituania 4
RS - Serbia 4
TT - Trinidad e Tobago 4
AE - Emirati Arabi Uniti 3
AL - Albania 3
AU - Australia 3
DK - Danimarca 3
DO - Repubblica Dominicana 3
HN - Honduras 3
JO - Giordania 3
AO - Angola 2
BA - Bosnia-Erzegovina 2
BB - Barbados 2
CR - Costa Rica 2
DZ - Algeria 2
NP - Nepal 2
OM - Oman 2
PT - Portogallo 2
RO - Romania 2
SN - Senegal 2
SV - El Salvador 2
XK - ???statistics.table.value.countryCode.XK??? 2
AM - Armenia 1
BO - Bolivia 1
BW - Botswana 1
BY - Bielorussia 1
CH - Svizzera 1
CI - Costa d'Avorio 1
CY - Cipro 1
CZ - Repubblica Ceca 1
ET - Etiopia 1
GA - Gabon 1
GE - Georgia 1
GR - Grecia 1
GT - Guatemala 1
GY - Guiana 1
HR - Croazia 1
LK - Sri Lanka 1
LY - Libia 1
MD - Moldavia 1
MK - Macedonia 1
MN - Mongolia 1
MU - Mauritius 1
MY - Malesia 1
NG - Nigeria 1
PA - Panama 1
SY - Repubblica araba siriana 1
Totale 8.020
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Città #
Singapore 577
Hong Kong 513
Dallas 340
Ashburn 281
Shanghai 274
Hefei 225
Lawrence 222
Princeton 222
Beijing 146
Ho Chi Minh City 123
São Paulo 74
Moscow 66
Hanoi 57
New York 54
Milan 43
Los Angeles 42
Nuremberg 36
Rio de Janeiro 35
Helsinki 34
Dublin 30
Curitiba 23
Washington 19
Pune 18
Brasília 17
Brooklyn 17
Haiphong 17
Santa Clara 17
Guangzhou 16
The Dalles 16
Tokyo 16
Vienna 16
Johannesburg 15
Quito 15
Rome 15
Warsaw 15
Guarulhos 14
Campinas 13
Turku 13
Chennai 12
Chicago 12
Orem 12
Atlanta 11
Baghdad 11
Belo Horizonte 11
Biên Hòa 11
Boston 11
Da Nang 11
Parma 11
Southwark 11
Stockholm 11
Caxias do Sul 10
Denver 10
Guayaquil 10
Hangzhou 10
Montreal 10
Santo André 10
Seattle 10
Thái Bình 10
Munich 9
Porto Alegre 9
Salvador 9
Shenzhen 9
Tashkent 9
Tianjin 9
Bologna 8
Hải Dương 8
La Plata 8
London 8
Montevideo 8
Poplar 8
Wuxi 8
Ankara 7
Columbus 7
Giessen 7
Goiânia 7
Manaus 7
Querétaro 7
Québec 7
Recife 7
Ribeirão Preto 7
Sumaré 7
São Bernardo do Campo 7
São José do Rio Preto 7
Bogotá 6
Buenos Aires 6
Changsha 6
Florence 6
Fortaleza 6
Houston 6
Istanbul 6
Juiz de Fora 6
Mauá 6
Mexico City 6
New Delhi 6
Santa Luzia 6
Shijiazhuang 6
Sorocaba 6
Xi'an 6
Aracaju 5
Barra Mansa 5
Totale 4.195
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Nome #
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 88
Asymptomatic Thyrotropin-secreting Pituitary Macroadenoma in a Thirteen Year-old Girl: Successful First-line Treatment with Somatostatin Analogues 83
"Block-and-replace" method in pediatric Graves' disease 78
Autosomal dominant hypocalcemia in monozygotic twins caused by a de novo germline mutation near the amino-terminus of the human calcium receptor 74
Thyroid function and puberty 73
Anterior pituitary gland aplasia: neuroradiological, phenotypical and hormonal evaluation 71
Autosomal dominant hypocalcemia with mild type 5 Bartter syndrome 69
A frequent oligogenic involvement in congenital hypothyroidism 68
A 7-year experience with low blood TSH cutoff levels for neonatal screening reveals an unsuspected frequency of congenital hypothyroidism (CH) 66
Alternative diagnostic approach to the etiology definition of Congenital Hypothyroidism" 65
Persistent mild hypothyroidism associated with novel sequenze variants of the DUOX2 gene in two siblings 64
A case of metabolic syndrome in an adolescent: diagnosis and management 62
Diagnosis of hypochondroplasia: the role of radiological interpretation. Italian Study Group for Hypochondroplasia 61
Analysis of 21-deoxycortisol, a marker of congenital adrenal hyperplasia, in blood by atmospheric pressure chemical ionization and electrospray ionization using multiple reaction monitoring 60
Total iodide organification defect: clinical and molecular characterization of an Italian family 59
Biallelic inactivation of the dual oxidase maturation factor 2 (DUOXA2) gene as a novel cause of congenital hypothyroidism 59
Accuracy of fine needle aspiration biopsy of thyroid nodules in detecting malignancy in childhood: comparison with conventional clinical, laboratory, and imaging approaches 59
"Effect of long-term glucocorticoid therapy on bone density and bone remodeling indexes in patients with congenital adrenal hyperplasia" 58
Absence of sonic hedgehog (Shh) germline mutations in patients with thyroid dysgenesis 57
Attention abilities in preadolescents and adolescents with congenital hypothyroidism 56
Follow Up dell'ipoparatiroidismo e dello pseudoipoparatiroidismo in pediatria durante terapia con metaboliti attivi della Vitamina D 55
Saturazione dell’emoglobina nell’Ipotiroidismo congenito alla diagnosi 54
Allungamento chirurgico degli arti: in quali casi intervenire? A che età iniziare? 52
Analysis of TSH Receptor gene in four cases with the clinical features of partial TSH resistance" 51
Bone density in adolescents and young adults with congenital adrenal hyperplasia 51
Ipotiroidismo subclinico nella prima infanzia 51
A novel germline mutation in the TSH receptor gene causes non-autoimmune autosomal dominant hyperthyroidism 51
Conoscenze fondamentali dello sviluppo fisiologico e principi di igiene scolastica 50
X-linked hypophosphatemic rickets: An Italian experts' opinion survey 49
A new mutation in AVPR2 gene discovered in an infant with nephrogenic diabetes insipidus 48
The Italian screening programfor primary congenital hypothyroidism: Actions to improve screening, diagnosis, follow-up, and surveillance 48
Hypocalciuric effect of chlorthalidone in two hypoparathyroid children 47
Neurophysiological studies and cognitive function in congenital hypopthyroid children 47
Endocrinopatie 46
Genetic defects of hydrogen peroxide generation in the thyroid gland 45
COVID-19 pandemic: implications on the surgical treatment of gastrointestinal and hepatopancreatobiliary tumours in Europe 45
Study of hydro-saline metabolism during phosphate therapy in a subject with vitamin-D resistant rickets 44
JAG1 Loss-Of-Function Variations as a Novel Predisposing Event in the Pathogenesis of Congenital Thyroid Defects. 44
Accidental exposure to polychlorinated biphenyls in a farm 44
Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH) 44
Clinical and molecular heterogeneity in a large series of patients with hypophosphatemic rickets 43
Cognitive function and neurophysiological evaluation in early-treated hypothyroid children 43
Congenital Hypothyroidism Treatment in Infants: A Comparative Study between Liquid and Tablet Formulations of Levothyroxine 43
Growth hormone-releasing hormone resistance in pseudohypoparathyroidism type ia: new evidence for imprinting of the Gs alpha gene 42
Validation of food frequency questionnaire for assessing dietary macronutrients and calcium intake in Italian children and adolescents 42
Study of calcium homeostasis in children with type 1 diabetes mellitus at onset 42
Growth hormone therapy in children: predictive factors and short-term and long-term response criteria 42
Heterogeneous phenotype in children affected by non-autoimmune hypothyroidism: an update. 41
Reversal of low bone density with gluten-free diet in children and adolescents with celiac disease 41
Congenital hypothyroidism with gland in situ: diagnostic re-evaluation 40
Problems in the long term therapeutical management of hypoparathyroidism in childhood 40
Bone mineral density (DEXA) in celiac children and adolescents before and during gluten-free diet 40
I rachitismi; la diagnosi differenziale dei dolori osteoarticolari; tetanie ipocalcemiche 40
INTERACTIONS AMONG PRO-INFLAMMATORY CYTOKINES, IGF SYSTEM AND THYROID FUNCTION IN PRE-PUBERTAL OBESE SUBJECTS 39
Physical and sport activity in thge prevention and treatment of obesity and diabetes in children 39
Effect of estrogen replacement therapy on bone mineral content in girls with Turner syndrome. 39
The DNA methylation as a predisposition factor in the pathogenesis of congenital hypothyroidism in prematur infants 39
Thyroid autoimmunity and congenital hypothyroidism 39
Maturation of preterm newborn brains: a longitudinal fMRI and DTI study of auditory system 39
“Block-and-replace” treatment in Graves’ disease: experience in a cohort of pediatric patients 39
Osteopenia in premature children: an emerging problem 38
Nephrocalcinosis in children and adolescents: sonographic evaluation during long-term treatment with 1,25-dihydroxycholecalciferol. 38
Effect of gluten-free diet on bone mineral content in growing patients with celiac disease 38
Defective function of Fas in T cells from paediatric patients with autoimmune thyroid diseases 38
Coherence EEG modifications in children with congenital hypothyroidism 38
Final height in Italian patients with congenital hypothyroidism detected by neonatal screening: a 20-year observational study 38
Brain M.R.I. in congenital hypothyroidism in infants at diagnosis " 38
Comparison between liquid L-thyroxine (L-T4) solution and tablet in congenital hypothyroidism (CH) 38
Neonatal Screening for Congenital Hypothyroidism: What can we learn from Discordant twins? 38
Decreased Parietal Cortex Activity during Mental Rotation in Children with Congenital Hypothyroidism 37
Bone mass in young patients with type 1 diabetes 37
Mineralizzazione ossea in neonati gemelli 37
Neurophysiological abnormalities of CNS in congenital hypothyroid school age children 37
Sonographic evaluation of distal femoral epiphysis in newborns 37
Neonatal screening program for congenital hypothyroidism: A 7-year experience with low TSH cut-off levels 37
Snyder-Robinson syndrome: A novel nonsense mutation in spermine synthase and expansion of the phenotype 37
Mild Hypothyroidism in Childhood: Who, When, and How Should Be Treated? 37
Neonatal transient hypothyroidism: aetiological study 36
Thyroid scintigraphy and perchlorate test after recombinant human TSH: a new tool for the differential diagnosis of congenital hypothyroidism during infancy 36
Bone density and bone metabolism are normal after long-term gluten free diet in young celiac, patients 36
Studio delle vie acustiche mediante analisi dei potenziali evocati uditivi e dell’elettroencelografia in bambini affetti da ipotiroidismo congenito in terapia sostitutiva 36
Identification and functional analysis of DUOX2 variants: biallelic mutations are associated with permanent congenital hypothyroidism 36
“Transiet hypothyroidism secondary to Wolff-Chaikoff effect: the importance of urinary iodine excretion in precocious differential diagnosis 36
Ipotalamo ipofisi 36
Bone demineralization in Turner's Syndrome 36
Endocrinopatie 36
Regolazione del metabolismo calcio-fosforo e fabbisogni di vitamina D durante la gravidanza e l'allattamento 36
Vitamin D in childhood and adolescence: an expert position statement 36
Neonatal Hyperthyroidism: report of eight cases 36
Severe hypocalcemia due to a de novo mutation in the fifth transmembrane domain of the calcium-sensing receptor 35
Conferma diagnostica di Ipotiroidismo congenito: studio comparativo tra ecografia e scintigrafia tiroidea 35
Measuring the mineral content of the distal radius in the age of growth 35
EEG modifications in children with congenital Hypothyroidism 35
Pseudotumor cerebri and diabetes inspidus. Association or coincidence? 35
Problematiche auxologiche ed endocrinologiche 35
Surgical lengthening of limbs in achondroplastic children: a medical and psycho-social program to select and treat patients. 35
Newborn of mothers affected by autoimmune thyroiditis: the importance of thyroid function monitoring in the first months of life 35
Iperparatiroidismo primitivo in paziente con rachitismo ipofosforemico 35
“Ophtalmological follow-up in young patients with Graves Disease” 35
Genetic and epigenetic alterations in the GNAS locus and clinical consequences in Pseudohypoparathyroidism: Italian common healthcare pathways adoption 35
Totale 4.563
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Categoria #
all - tutte 75.888
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 75.888
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211 0 0 0 0 0 0 0 0 0 0 1 0
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
2025/20263.753 570 640 574 1.373 534 62 0 0 0 0 0 0
Totale 8.059