IRIS
CAVALLO, Luciano
 Distribuzione geografica
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Continente #
NA - Nord America 14.025
AS - Asia 5.427
EU - Europa 4.644
SA - Sud America 1.506
AF - Africa 216
OC - Oceania 18
Continente sconosciuto - Info sul continente non disponibili 7
Totale 25.843
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Nazione #
US - Stati Uniti d'America 13.853
SG - Singapore 2.410
CN - Cina 1.254
BR - Brasile 1.232
IT - Italia 879
DE - Germania 754
HK - Hong Kong 686
SE - Svezia 672
UA - Ucraina 548
RU - Federazione Russa 455
FR - Francia 443
FI - Finlandia 381
VN - Vietnam 282
GB - Regno Unito 252
IN - India 189
BD - Bangladesh 109
IQ - Iraq 79
AR - Argentina 77
CA - Canada 64
MX - Messico 57
TR - Turchia 57
CI - Costa d'Avorio 48
CO - Colombia 48
ZA - Sudafrica 48
EC - Ecuador 44
PK - Pakistan 44
NL - Olanda 39
SA - Arabia Saudita 37
ID - Indonesia 35
IE - Irlanda 35
PL - Polonia 34
MA - Marocco 33
UZ - Uzbekistan 32
BE - Belgio 31
VE - Venezuela 31
JP - Giappone 29
AE - Emirati Arabi Uniti 27
ES - Italia 27
MY - Malesia 23
BO - Bolivia 21
PY - Paraguay 21
TN - Tunisia 19
CL - Cile 18
PH - Filippine 18
AT - Austria 17
KE - Kenya 16
JO - Giordania 14
RO - Romania 14
GT - Guatemala 13
AU - Australia 11
CZ - Repubblica Ceca 11
EG - Egitto 11
LT - Lituania 11
NP - Nepal 10
IR - Iran 9
OM - Oman 9
AZ - Azerbaigian 8
DZ - Algeria 8
IL - Israele 8
JM - Giamaica 8
KR - Corea 8
PS - Palestinian Territory 8
AL - Albania 7
AO - Angola 7
LB - Libano 7
DO - Repubblica Dominicana 6
EU - Europa 6
KZ - Kazakistan 6
PE - Perù 6
UY - Uruguay 6
BB - Barbados 5
NZ - Nuova Zelanda 5
RS - Serbia 5
ET - Etiopia 4
HR - Croazia 4
HU - Ungheria 4
KW - Kuwait 4
PA - Panama 4
SY - Repubblica araba siriana 4
TH - Thailandia 4
BY - Bielorussia 3
CH - Svizzera 3
CR - Costa Rica 3
NI - Nicaragua 3
QA - Qatar 3
TT - Trinidad e Tobago 3
AM - Armenia 2
BH - Bahrain 2
GE - Georgia 2
GH - Ghana 2
GR - Grecia 2
KH - Cambogia 2
KI - Kiribati 2
LY - Libia 2
MD - Moldavia 2
MK - Macedonia 2
MN - Mongolia 2
NG - Nigeria 2
PT - Portogallo 2
SN - Senegal 2
Totale 25.809
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Città #
Fairfield 1.404
Jacksonville 1.271
Singapore 1.254
Woodbridge 1.251
Chandler 1.124
Ashburn 1.105
Houston 846
Hong Kong 682
San Jose 660
Ann Arbor 572
Seattle 541
Cambridge 528
Nyköping 500
Wilmington 478
Nanjing 294
Lawrence 282
Roxbury 280
Beijing 274
Lauterbourg 245
Bari 196
Des Moines 178
Boardman 175
Dallas 161
New York 159
Princeton 141
Los Angeles 131
Inglewood 124
São Paulo 112
Helsinki 97
Ho Chi Minh City 85
Santa Clara 83
Brooklyn 75
Buffalo 72
Shenyang 72
San Diego 69
Milan 68
Munich 67
Hanoi 62
Hebei 59
Nanchang 56
Jiaxing 55
Rome 51
London 49
Abidjan 48
Rio de Janeiro 48
Changsha 39
Dearborn 37
Dublin 34
Baghdad 33
Belo Horizonte 31
Frankfurt am Main 31
Moscow 31
Tianjin 29
Tashkent 28
Brasília 27
Pune 27
Tokyo 27
Orem 26
Brussels 25
Redwood City 25
Paris 24
Guangzhou 23
Chicago 22
Dhaka 22
Johannesburg 22
Porto Alegre 22
Chennai 20
Medellín 20
Toronto 20
Bologna 19
Falkenstein 19
Mexico City 19
San Francisco 19
Warsaw 19
Auburn Hills 18
Council Bluffs 18
Lahore 18
Manchester 17
Montreal 17
Mumbai 17
Curitiba 16
Washington 16
Marseille 15
Norwalk 15
Amman 14
Campinas 14
Nairobi 14
San Mateo 14
Stockholm 14
Zhengzhou 14
Fortaleza 13
Istanbul 13
Jeddah 13
Kuala Lumpur 13
Leawood 13
Nuremberg 13
Palermo 13
Trani 13
Vienna 13
Abu Dhabi 12
Totale 17.204
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Nome #
Secrezione di prolattina alla diagnosi di celiachia e dopo 6 mesi di dieta priva di glutine: studio longitudinale 419
The p53 family member p73 modulates the proproliferative role of IGFBP3 in short children born small for gestational age 209
Impaired bone remodeling in children with osteogenesis imperfecta treated and untreated with bisphosphonates: the role of DKK1, RANKL, and TNF-α 204
High Sclerostin and Dickkopf-1 (DKK-1) serum levels in children and adolescents with type 1 diabetes mellitus 202
Acute pancreatitis in a girl with panhypopituitarism due to craniopharyngioma on growth hormone treatment. A combination of risk factors 174
A novel OTX2 gene frameshift mutation in a child with microphthalmia, ectopic pituitary and growth hormone deficiency 174
Bone Fragility in Turner Syndrome: Mechanisms and Prevention Strategies 173
Final height in Italian patients with congenital hypothyroidism detected by neonatal screening: A 20-year observational study 166
A randomized controlled trial of Lactobacillus GG in children with functional abdominal pain. 162
Vascular Function and Myocardial Performance Indices in Children Born Small for Gestational Age. 161
Metabolic syndrome in childhood leukemia survivors: a meta-analysis 154
High rate of spontaneous normalization of celiac serology in a cohort of 446 children with type 1 diabetes: a prospective study 153
Incomplete testicular feminization with partial mullerian regression 153
Endocrine function in four anencephalic infants 147
46,XY disorders of sexual development (DSD) caused by a rare mutation of the 17-β-hydroxysteroid dehydrogenase type 3 gene (HSD17B3) 144
17b-Hydroxysteroid Dehydrogenase Type 3 Deficiency: Diagnosis, Phenotypic Variability and Molecular Findings 143
46,XY disorders of sexual development (DSD) caused by a rare mutation of the 17-beta-hydroxysteroid dehydrogenase type 3 gene (HSD17B3) 143
A large deletion causes apparent homozygosity for the D1152H mutation in the cystic fibrosis transmembrane regulator (CFTR) gene. 142
Endothelial dysfunction and cardiovascular risk factors in childhood acute lymphoblastic leukemia survivors Autori 142
Growth hormone treatment improves final height and nutritional status of children with chronic kidney disease and growth deceleration 141
High dickkopf-1 levels in sera and leukocytes from children with 21-hydroxylase deficiency on chronic glucocorticoid treatment 137
Risk factors for subclinical atherosclerosis in diabetic and obese children 135
Comparison of esophageal pH and multichannel intraluminal impedance testing in pediatric patients with suspected gastroesophageal reflux. 132
46,XY DSD caused by a rare mutation of the 17ß-hydroxysteroid dehydrogenase type 3 gene 132
Metabolic, inflammatory, endothelial and haemostatic markers in a group of Italian obese children and adolescents 131
Analisi di Parametri di Coagulazione e Fibrinolisi in Bambini ed Adolescenti Obesi 131
Metabolic Outcomes, Bone Health, and Risk of Polycystic Ovary Syndrome in Girls with Idiopathic Central Precocious Puberty Treated with Gonadotropin-Releasing Hormone Analogues 131
Analysis of endothelial protein c receptor gene and metabolic profile in Prader-Willi syndrome and obese subjects. 129
Gastroesophageal reflux in preterm infants: how acid should it be? 129
To test or not to test…this is the problem 129
17beta-Hydroxysteroid Dehydrogenase Type 3 Deficiency: Diagnosis, Phenotipic Variability and Molecular Findings. 128
46 XY DISORDERS OF SEXUAL DEVELOPMENT (DSD) CAUSED BY A RARE MUTATION OF THE 17 beta HYDROXYSTEROID DEHYDROGENASE TYPE 3 GENE (HSD17B3) 127
Transient neonatal diabetes mellitus is associated with a recurrent (R201H) KCNJ11 (KIR6.2) mutation 127
Anti-pituitary antibodies in children with newly diagnosed celiac disease: a novel finding contributing to linear-growth impairment 126
A novel HESX1 splice mutation causes isolated GH deficiency by interfering with mRNA processing 123
Analysis of coagulation and fibrinolysis parameters in obese children and adolescents 123
Utilità della citologia congiuntivale nella diagnosi e nel monitoraggio terapeutico della cheratocongiuntivite Vernal 122
Inhibition of Helicobacter pylori infection in humans by Lactobacillus reuteri ATCC 55730 and effect on eradication therapy: a pilot study 122
Endocrine function in anencephalic newborn infants 122
Prolactin may be increased in newly diagnosed celiac children and adolescents and decreases after 6 months of gluten-free diet 122
Improved efficacy of 10-Day sequential treatment for Helicobacter Pylori eradication in children: a randomized trial 121
Sulfonylurea treatment in a girl with neonatal diabetes (KCNJ11 R201H) and celiac disease; impact of low compliance to the gluten free diet 120
Diagnostic value of growth hormone-releasing hormone test in children and adolescents with idiopathic growth hormone deficiency 120
Levothyroxine requirement in congenital hypothyroidism: a 12-year longitudinal study 120
Analisi di parametri di coagulazione e fibrinolisi in bambini e adolescenti obesi 120
Longitudinal assessment of levo-thyroxine therapy for congenital hypothyroidism: relationship with aetiology, bone maturation and biochemical features 119
Idiopathic short stature 118
Effect of recombinant insulin-like growth factor-1 (rhIGF-1) treatment on short-term linear growth in a child with Majewski Osteodysplastic Primordial Dwarfism type II (MOPD II) and hepatic insufficiency 118
IGF2 gene variants and risk of hypertension in obese children and adolescents. 118
A case of pseudohypoparathyroidism (PHP) with multiple hormone resistance and maternal psoriasis 118
Final height in short polytransfused thalassemia major patients treated with recombinant growth hormone 118
Levothyroxine Requirement in Congenital Hypothyroidism: 12-year Longitudinal Study 117
A case of type 1a pseudohypoparathyroidism (PHP) with multiple hormones resistance and maternal psoriasis 117
Clarithromycin-Resistant Genotypes and Eradication of Helicobacter Pylori 117
17beta-hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence 117
Longitudinal assessment of levo-thyroxine therapy for congenital hypothyroidism: relationship with aetiology, bone maturation and biochemical features. 116
Thyroid function after prolonged treatment for congenital hypothyroidism 116
Effects of moderate-severe exercise on blood glucose in type 1 diabetic adolescents treated with insulin pump or glargine insulin 116
OGTT in thalassemic major children 116
Low Bone Mineral Density is Associated to Poor Glycemic Control and Increased Dickkopf-1 (DKK-1) Serum Levels in Children and Adolescents with Type 1 Diabetes 116
New insights into childhood Vernal keratoconjunctivitis-associated factors. 115
Alterazione del rimodellamento osseo in soggetti in età pediatrica affetti da deficit di 21-idrossilasi (21-OHD): ruolo di DKK1 115
Growth hormone (GH) release during the GH-releasing hormone (GHRH) test in children with idiopathic isolated (IGHD) or multiple (MGHD) GH-deficiency. 115
Transient neonatal diabetes mellitus is associated with a recurrent (R201H) KCNJ11 (KIR6.2) mutation 114
Skeleton and glucose metabolism: a bone-pancreas loop 114
Lactobacillus reuteri therapy to reduce side-effects during anti-Helicobacter pylori treatment in children: a randomized placebo controlled trial 113
Endocrine studies in anencephalic newborns 113
Evidence that fibrynolitic changes in paediatric obesity translate in a hypofibrinolytic state. Relative contribution of TAFI and PAI-1 112
PTPN11 gene mutation and severe neonatal hypertrophic cardiomyopathy: what is the link? 112
A Novel OTX2 Gene Mutation in a Child with Growth Hormone Deficiency 112
Prevention of functional gastrointestinal disorders in neonates: Clinical and socioeconomic impact 112
Gonadotropin release in prepubertal and mid-pubertal patients with testicular feminization syndrome 112
Unusual pediatric co-morbility: autoimmune thyroiditis and cortico-resistant nephrotic syndrome in a 6-month-old Italian patient. 112
Basal (bPRL) and peak (PRLp) prolactin levels during the thyrotropin releasing hormone test (TRH test) in children with celiac disease at diagnosis (CD), preliminary results 111
Cardiac function in congenital hypothyroidism: impairment and response to L-T4 therapy 111
The effect of different growth hormone administration frequencies on growth in growth hormone-deficient patients 111
Endocrinological studies in the hypertelorism-hypospadias (BBB) syndrome 111
Elevati livelli sierici di Dkk1, antagonista del segnale di WNT in bambini obesi. 110
Growth and endocrine function in thalassemia major in childhood and adolescence 110
Best determinants of non alcoholic fatty liver disease and intra-abdominal fat in prepubertal children born small for gestational age: ultrasound technique versus anthropometric data. 110
Delayed decrease in serum ferritin in polytransfused children with thalassemia major after continuous subcutaneous infusions of desferrioxamine 109
Genotype-phenotype correlation in juvenile paget disease: Role of molecular alterations of the TNFRSF11B gene 109
Regurgitation in healthy and non healthy infants 108
Clinical, Serologic, and Histologic Features of Gluten Sensitivity in Children 108
Growth hormone deficient children treated from before two years old fail to catch-up completely within five years of therapy 107
Prebiotics improve gastric motility and gastric electrical activity in preterm newborns 107
A novel hesx1 splice mutation causes isolated growth hormone deficiency by interfering with mrna processing 107
Analysis of coagulation and fibrinolysis parameters in obese children and adolescents 105
Evaluation of the growth-hormone-releasing hormone test in short normal and growth hormone-deficient children 105
Identification of new variants of human bmp15 gene in a large cohort of women with premature ovarian failure 103
Basal (bPRL) and peak (PRLp) prolactin levels during the thyrotropin realising hormone test (TRH test) in celiac children at diagnosis (CD). Preliminary results 102
Lactobacillus reuteri strain combination in helicobacter pylori infection: A randomized, double-blind, placebo-controlled study 102
Effect of recombinant insulin-like growth factor-1 treatment on short-term linear growth in a child with Majewski osteodysplastic primordial dwarfism type II and hepatic insufficiency 101
Analisi di parametri di coagulazione e fibrinolisi in bambini adolescenti obesi 101
The effects of probiotics on feeding tolerance, bowel habits, and gastrointestinal motility in preterm newborns 101
The hypertelorism-hypospadias (BBB) syndrome: endocrine evaluation in two prepubertal siblings 101
Analysis of endothelial protein c receptor gene and metabolic profile in Prader-Willi syndrome and obese subjects 101
Valutazione comparativa della determinazione del T4 e della reverse-T3 per lo screening dell’ipotiroidismo congenito 101
Growth hormone deficiency and antipituitary antibodies in a patient with common variable immunodeficiency 101
Bone mineral metabolism in girls with precocious puberty during gonadotrophin-releasing hormone agonist treatment 99
Totale 12.745
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Categoria #
all - tutte 103.983
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 103.983
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021571 0 0 0 0 0 0 0 0 0 314 151 106
2021/20221.803 139 261 16 78 60 90 71 98 100 122 355 413
2022/20233.065 476 251 150 311 425 395 26 275 626 18 62 50
2023/2024924 96 212 51 66 99 175 40 31 20 22 22 90
2024/20253.893 120 61 416 151 75 322 214 299 169 183 570 1.313
2025/20266.298 1.070 372 398 787 711 432 944 286 671 627 0 0
Totale 26.107