IRIS
CAVALLO, Luciano
 Distribuzione geografica
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Continente #
NA - Nord America 13.023
AS - Asia 4.588
EU - Europa 4.157
SA - Sud America 1.255
AF - Africa 126
OC - Oceania 16
Continente sconosciuto - Info sul continente non disponibili 7
Totale 23.172
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Nazione #
US - Stati Uniti d'America 12.883
SG - Singapore 2.159
CN - Cina 1.175
BR - Brasile 1.109
IT - Italia 821
DE - Germania 718
HK - Hong Kong 676
SE - Svezia 672
UA - Ucraina 541
RU - Federazione Russa 444
FI - Finlandia 318
GB - Regno Unito 228
VN - Vietnam 208
FR - Francia 192
IN - India 103
CA - Canada 56
BD - Bangladesh 47
CI - Costa d'Avorio 47
MX - Messico 47
AR - Argentina 46
IE - Irlanda 34
NL - Olanda 32
ZA - Sudafrica 32
BE - Belgio 31
PL - Polonia 30
EC - Ecuador 27
IQ - Iraq 26
TR - Turchia 25
ES - Italia 20
ID - Indonesia 20
AE - Emirati Arabi Uniti 19
JP - Giappone 18
PY - Paraguay 17
AT - Austria 15
MA - Marocco 15
SA - Arabia Saudita 15
UZ - Uzbekistan 15
VE - Venezuela 15
CO - Colombia 13
RO - Romania 13
GT - Guatemala 12
CZ - Repubblica Ceca 11
LT - Lituania 11
CL - Cile 10
PK - Pakistan 10
AU - Australia 9
IR - Iran 9
KE - Kenya 9
BO - Bolivia 8
IL - Israele 8
KR - Corea 8
EG - Egitto 6
EU - Europa 6
JO - Giordania 6
TN - Tunisia 6
AL - Albania 5
AZ - Azerbaigian 5
BB - Barbados 5
KZ - Kazakistan 5
NZ - Nuova Zelanda 5
PE - Perù 5
UY - Uruguay 5
DO - Repubblica Dominicana 4
JM - Giamaica 4
MY - Malesia 4
NP - Nepal 4
RS - Serbia 4
AO - Angola 3
CH - Svizzera 3
KW - Kuwait 3
LB - Libano 3
PA - Panama 3
SY - Repubblica araba siriana 3
TT - Trinidad e Tobago 3
BY - Bielorussia 2
HR - Croazia 2
KH - Cambogia 2
KI - Kiribati 2
MD - Moldavia 2
OM - Oman 2
PH - Filippine 2
PS - Palestinian Territory 2
PT - Portogallo 2
QA - Qatar 2
SN - Senegal 2
SV - El Salvador 2
AM - Armenia 1
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
CR - Costa Rica 1
DJ - Gibuti 1
DK - Danimarca 1
DZ - Algeria 1
ET - Etiopia 1
GA - Gabon 1
GE - Georgia 1
GR - Grecia 1
HN - Honduras 1
HU - Ungheria 1
MG - Madagascar 1
Totale 23.165
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Città #
Fairfield 1.404
Jacksonville 1.269
Woodbridge 1.251
Chandler 1.124
Singapore 1.077
Ashburn 960
Houston 845
Hong Kong 672
Ann Arbor 572
Seattle 541
Cambridge 528
Nyköping 500
Wilmington 478
Nanjing 294
Lawrence 282
Roxbury 280
Beijing 271
Bari 196
Des Moines 176
Boardman 175
Dallas 156
New York 151
Princeton 141
Los Angeles 126
Inglewood 124
São Paulo 97
Buffalo 72
Santa Clara 72
Shenyang 72
Brooklyn 71
San Diego 69
Munich 67
Ho Chi Minh City 60
Hebei 59
Nanchang 56
Jiaxing 55
Milan 53
Rome 49
Abidjan 47
Hanoi 46
London 46
Rio de Janeiro 43
Changsha 39
Dearborn 37
Dublin 34
Helsinki 34
Moscow 30
Tianjin 29
Belo Horizonte 28
Pune 26
Brussels 25
Redwood City 25
Paris 23
Brasília 22
Guangzhou 22
Chicago 20
Porto Alegre 20
Toronto 20
Johannesburg 19
Auburn Hills 18
Bologna 18
Frankfurt am Main 18
Chennai 17
San Francisco 16
Tokyo 16
Warsaw 16
Washington 16
Marseille 15
Mexico City 15
Norwalk 15
Curitiba 14
San Mateo 14
Stockholm 14
Tashkent 14
Zhengzhou 14
Campinas 13
Dhaka 13
Leawood 13
Montreal 13
Trani 13
Manchester 12
Mumbai 12
Palermo 12
Columbus 11
Denver 11
Guatemala City 11
Haiphong 11
Hefei 11
Vienna 11
Amsterdam 10
Asunción 10
Council Bluffs 10
Fortaleza 10
Joinville 10
Poplar 10
Taizhou 10
Turin 10
Baghdad 9
Boston 9
Goiânia 9
Totale 15.604
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Nome #
Secrezione di prolattina alla diagnosi di celiachia e dopo 6 mesi di dieta priva di glutine: studio longitudinale 392
The p53 family member p73 modulates the proproliferative role of IGFBP3 in short children born small for gestational age 191
Impaired bone remodeling in children with osteogenesis imperfecta treated and untreated with bisphosphonates: the role of DKK1, RANKL, and TNF-α 184
High Sclerostin and Dickkopf-1 (DKK-1) serum levels in children and adolescents with type 1 diabetes mellitus 182
A novel OTX2 gene frameshift mutation in a child with microphthalmia, ectopic pituitary and growth hormone deficiency 162
Acute pancreatitis in a girl with panhypopituitarism due to craniopharyngioma on growth hormone treatment. A combination of risk factors 158
Bone Fragility in Turner Syndrome: Mechanisms and Prevention Strategies 157
Vascular Function and Myocardial Performance Indices in Children Born Small for Gestational Age. 153
Final height in Italian patients with congenital hypothyroidism detected by neonatal screening: A 20-year observational study 153
High rate of spontaneous normalization of celiac serology in a cohort of 446 children with type 1 diabetes: a prospective study 144
Incomplete testicular feminization with partial mullerian regression 140
Metabolic syndrome in childhood leukemia survivors: a meta-analysis 139
A randomized controlled trial of Lactobacillus GG in children with functional abdominal pain. 137
Endocrine function in four anencephalic infants 136
A large deletion causes apparent homozygosity for the D1152H mutation in the cystic fibrosis transmembrane regulator (CFTR) gene. 133
17b-Hydroxysteroid Dehydrogenase Type 3 Deficiency: Diagnosis, Phenotypic Variability and Molecular Findings 131
High dickkopf-1 levels in sera and leukocytes from children with 21-hydroxylase deficiency on chronic glucocorticoid treatment 131
Endothelial dysfunction and cardiovascular risk factors in childhood acute lymphoblastic leukemia survivors Autori 130
Growth hormone treatment improves final height and nutritional status of children with chronic kidney disease and growth deceleration 130
Risk factors for subclinical atherosclerosis in diabetic and obese children 125
46,XY disorders of sexual development (DSD) caused by a rare mutation of the 17-β-hydroxysteroid dehydrogenase type 3 gene (HSD17B3) 124
46,XY disorders of sexual development (DSD) caused by a rare mutation of the 17-beta-hydroxysteroid dehydrogenase type 3 gene (HSD17B3) 123
Transient neonatal diabetes mellitus is associated with a recurrent (R201H) KCNJ11 (KIR6.2) mutation 122
Comparison of esophageal pH and multichannel intraluminal impedance testing in pediatric patients with suspected gastroesophageal reflux. 119
Metabolic Outcomes, Bone Health, and Risk of Polycystic Ovary Syndrome in Girls with Idiopathic Central Precocious Puberty Treated with Gonadotropin-Releasing Hormone Analogues 119
Analysis of endothelial protein c receptor gene and metabolic profile in Prader-Willi syndrome and obese subjects. 118
To test or not to test…this is the problem 118
17beta-Hydroxysteroid Dehydrogenase Type 3 Deficiency: Diagnosis, Phenotipic Variability and Molecular Findings. 118
46 XY DISORDERS OF SEXUAL DEVELOPMENT (DSD) CAUSED BY A RARE MUTATION OF THE 17 beta HYDROXYSTEROID DEHYDROGENASE TYPE 3 GENE (HSD17B3) 117
Anti-pituitary antibodies in children with newly diagnosed celiac disease: a novel finding contributing to linear-growth impairment 117
Improved efficacy of 10-Day sequential treatment for Helicobacter Pylori eradication in children: a randomized trial 115
Diagnostic value of growth hormone-releasing hormone test in children and adolescents with idiopathic growth hormone deficiency 114
A novel HESX1 splice mutation causes isolated GH deficiency by interfering with mRNA processing 114
Utilità della citologia congiuntivale nella diagnosi e nel monitoraggio terapeutico della cheratocongiuntivite Vernal 113
Sulfonylurea treatment in a girl with neonatal diabetes (KCNJ11 R201H) and celiac disease; impact of low compliance to the gluten free diet 113
Gastroesophageal reflux in preterm infants: how acid should it be? 113
Prolactin may be increased in newly diagnosed celiac children and adolescents and decreases after 6 months of gluten-free diet 113
46,XY DSD caused by a rare mutation of the 17ß-hydroxysteroid dehydrogenase type 3 gene 112
Levothyroxine requirement in congenital hypothyroidism: a 12-year longitudinal study 112
Endocrine function in anencephalic newborn infants 112
Effects of moderate-severe exercise on blood glucose in type 1 diabetic adolescents treated with insulin pump or glargine insulin 111
Analisi di Parametri di Coagulazione e Fibrinolisi in Bambini ed Adolescenti Obesi 111
Analysis of coagulation and fibrinolysis parameters in obese children and adolescents 111
Longitudinal assessment of levo-thyroxine therapy for congenital hypothyroidism: relationship with aetiology, bone maturation and biochemical features. 110
Inhibition of Helicobacter pylori infection in humans by Lactobacillus reuteri ATCC 55730 and effect on eradication therapy: a pilot study 110
Metabolic, inflammatory, endothelial and haemostatic markers in a group of Italian obese children and adolescents 110
Analisi di parametri di coagulazione e fibrinolisi in bambini e adolescenti obesi 110
Longitudinal assessment of levo-thyroxine therapy for congenital hypothyroidism: relationship with aetiology, bone maturation and biochemical features 109
A case of type 1a pseudohypoparathyroidism (PHP) with multiple hormones resistance and maternal psoriasis 109
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 108
OGTT in thalassemic major children 108
Thyroid function after prolonged treatment for congenital hypothyroidism 107
Clarithromycin-Resistant Genotypes and Eradication of Helicobacter Pylori 107
Idiopathic short stature 106
PTPN11 gene mutation and severe neonatal hypertrophic cardiomyopathy: what is the link? 106
17beta-hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence 106
Transient neonatal diabetes mellitus is associated with a recurrent (R201H) KCNJ11 (KIR6.2) mutation 105
Evidence that fibrynolitic changes in paediatric obesity translate in a hypofibrinolytic state. Relative contribution of TAFI and PAI-1 105
Endocrine studies in anencephalic newborns 105
Unusual pediatric co-morbility: autoimmune thyroiditis and cortico-resistant nephrotic syndrome in a 6-month-old Italian patient. 105
Cardiac function in congenital hypothyroidism: impairment and response to L-T4 therapy 104
Endocrinological studies in the hypertelorism-hypospadias (BBB) syndrome 104
Prevention of functional gastrointestinal disorders in neonates: Clinical and socioeconomic impact 104
Gonadotropin release in prepubertal and mid-pubertal patients with testicular feminization syndrome 104
Lactobacillus reuteri therapy to reduce side-effects during anti-Helicobacter pylori treatment in children: a randomized placebo controlled trial 103
Growth hormone (GH) release during the GH-releasing hormone (GHRH) test in children with idiopathic isolated (IGHD) or multiple (MGHD) GH-deficiency. 103
Regurgitation in healthy and non healthy infants 103
A case of pseudohypoparathyroidism (PHP) with multiple hormone resistance and maternal psoriasis 103
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. 103
New insights into childhood Vernal keratoconjunctivitis-associated factors. 102
Levothyroxine Requirement in Congenital Hypothyroidism: 12-year Longitudinal Study 102
The effect of different growth hormone administration frequencies on growth in growth hormone-deficient patients 102
Evaluation of the growth-hormone-releasing hormone test in short normal and growth hormone-deficient children 102
Final height in short polytransfused thalassemia major patients treated with recombinant growth hormone 101
Alterazione del rimodellamento osseo in soggetti in età pediatrica affetti da deficit di 21-idrossilasi (21-OHD): ruolo di DKK1 100
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 99
Growth and endocrine function in thalassemia major in childhood and adolescence 99
A Novel OTX2 Gene Mutation in a Child with Growth Hormone Deficiency 99
Growth hormone deficient children treated from before two years old fail to catch-up completely within five years of therapy 98
Prebiotics improve gastric motility and gastric electrical activity in preterm newborns 98
Elevati livelli sierici di Dkk1, antagonista del segnale di WNT in bambini obesi. 98
Delayed decrease in serum ferritin in polytransfused children with thalassemia major after continuous subcutaneous infusions of desferrioxamine 98
IGF2 gene variants and risk of hypertension in obese children and adolescents. 98
Genotype-phenotype correlation in juvenile paget disease: Role of molecular alterations of the TNFRSF11B gene 98
Skeleton and glucose metabolism: a bone-pancreas loop 98
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 98
Bone mineral metabolism in girls with precocious puberty during gonadotrophin-releasing hormone agonist treatment 95
Analysis of coagulation and fibrinolysis parameters in obese children and adolescents 95
Identification of new variants of human bmp15 gene in a large cohort of women with premature ovarian failure 93
A novel hesx1 splice mutation causes isolated growth hormone deficiency by interfering with mrna processing 93
Growth hormone deficiency and antipituitary antibodies in a patient with common variable immunodeficiency 93
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 92
The effects of probiotics on feeding tolerance, bowel habits, and gastrointestinal motility in preterm newborns 92
Postmenopausal osteoporosis: the role of Immune system cells 92
Analysis of endothelial protein c receptor gene and metabolic profile in Prader-Willi syndrome and obese subjects 92
Analisi di parametri di coagulazione e fibrinolisi in bambini adolescenti obesi 91
IGF2 gene variants and risk of hypertension in obese children and adolescents 90
Serum levels of thyrotropin, thyroxine, 3,3',5-triiodothyronine, and 3,3',5'-triiodothyronine (reverse T3) in the first six days of life 90
Basal (bPRL) and peak (PRLp) prolactin levels during the thyrotropin realising hormone test (TRH test) in celiac children at diagnosis (CD). Preliminary results 89
Valutazione comparativa della determinazione del T4 e della reverse-T3 per lo screening dell’ipotiroidismo congenito 89
Totale 11.600
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Categoria #
all - tutte 97.954
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 97.954
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.273 0 0 0 0 0 104 211 127 260 314 151 106
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
2025/20263.627 1.070 372 398 787 711 289 0 0 0 0 0 0
Totale 23.436