IRIS
DELVECCHIO, MAURIZIO
 Distribuzione geografica
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Continente #
NA - Nord America 1.366
EU - Europa 297
AS - Asia 119
Totale 1.782
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Nazione #
US - Stati Uniti d'America 1.363
SE - Svezia 108
CN - Cina 95
IT - Italia 76
DE - Germania 37
GB - Regno Unito 19
FI - Finlandia 16
FR - Francia 16
SG - Singapore 13
IN - India 8
BE - Belgio 7
CZ - Repubblica Ceca 6
IE - Irlanda 4
UA - Ucraina 4
AE - Emirati Arabi Uniti 3
NL - Olanda 3
CA - Canada 2
PA - Panama 1
PL - Polonia 1
Totale 1.782
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Città #
Fairfield 185
Chandler 161
Woodbridge 134
Ashburn 114
Houston 114
Nyköping 93
Cambridge 78
Seattle 74
Ann Arbor 62
Wilmington 61
Jacksonville 32
New York 32
Beijing 31
Lawrence 29
Roxbury 28
Bari 23
Nanjing 21
Inglewood 19
Des Moines 12
San Diego 10
Princeton 9
Nanchang 7
Singapore 7
Brno 6
Brooklyn 6
Grumo Appula 6
Munich 6
Redwood City 6
Renton 6
Brussels 5
Chandigarh 5
Los Angeles 5
Paris 5
Shenyang 5
Trani 5
Washington 5
Dublin 4
Milan 4
Modugno 4
Nürnberg 4
Abu Dhabi 3
Boardman 3
Chicago 3
Dearborn 3
Hebei 3
Salerno 3
Cerignola 2
Changsha 2
Hounslow 2
Kilburn 2
Marseille 2
Montreal 2
New Bedfont 2
Ningbo 2
Novi Ligure 2
Ostuni 2
Pune 2
San Giovanni Rotondo 2
Simi Valley 2
St Louis 2
Waanrode 2
Wuhan 2
Zhengzhou 2
Agoura Hills 1
Bologna 1
Boydton 1
Chiswick 1
Indiana 1
Jinhua 1
Kunming 1
London 1
Manchester 1
Mumbai 1
Nagold 1
Novara 1
Padova 1
Pescara 1
Piazza Armerina 1
Scorzè 1
Seelze 1
Shanghai 1
Stockholm 1
Treviso 1
Warsaw 1
Wuxi 1
Xian 1
Totale 1.498
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Nome #
Impaired bone remodeling in children with osteogenesis imperfecta treated and untreated with bisphosphonates: the role of DKK1, RANKL, and TNF-α 128
High Sclerostin and Dickkopf-1 (DKK-1) serum levels in children and adolescents with type 1 diabetes mellitus 127
A novel OTX2 gene frameshift mutation in a child with microphthalmia, ectopic pituitary and growth hormone deficiency 119
Final height in Italian patients with congenital hypothyroidism detected by neonatal screening: A 20-year observational study 119
Non-alcoholic fatty liver disease is associated with early left ventricular dysfunction in childhood acute lymphoblastic leukaemia survivors. 100
Growth hormone treatment improves final height and nutritional status of children with chronic kidney disease and growth deceleration 94
Can Anti-Thyroid Antibodies Influence the Outcome of Primary Chronic Immune Thrombocytopenia in Children? 93
Cardiovascular dysfunction and vitamin D status in childhood acute lymphoblastic leukemia survivors 89
Analysis of Circulating Mediators of Bone Remodeling in Prader-Willi Syndrome 88
Metabolic Outcomes, Bone Health, and Risk of Polycystic Ovary Syndrome in Girls with Idiopathic Central Precocious Puberty Treated with Gonadotropin-Releasing Hormone Analogues 85
Levothyroxine requirement in congenital hypothyroidism: a 12-year longitudinal study 81
Alagille syndrome: A novel mutation in JAG1 gene 74
A Novel OTX2 Gene Mutation in a Child with Growth Hormone Deficiency 56
Metabolic Syndrome in Childhood Acute Lymphoblastic Leukaemia Survivors 52
Low prevalence of HNF1A mutations after molecular screening of multiple MODY genes in 58 Italian families recruited in the pediatric or adult diabetes clinic from a single Italian hospital 51
Mechanism of Bone Disease in Prader-Willi Syndrome 51
The Effect of Gaseous Ozone Therapy in Conjunction with Periodontal Treatment on Glycated Hemoglobin Level in Subjects with Type 2 Diabetes Mellitus: An Unmasked Randomized Controlled Trial 51
Dietary cholesterol supplementation and inhibitory factor 1 serum levels in two dizygotic Smith-Lemli-Opitz syndrome twins: a case report 50
Caring and living with Prader-Willi syndrome in Italy: integrating children, adults and parents' experiences through a multicentre narrative medicine research. 47
Permanent Neonatal Diabetes Mellitus (PNDM) in a patient with R201H/KCNJ11 gene mutation: Unusual clinical course 46
Polimorfismi del promotore del gene della IGFBP3 in un ampia coorte di bambini nati piccoli per l'età gestazionale 40
The Hyperphagia Questionnaire: Insights From a Multicentric Validation Study in Individuals With Prader Willi Syndrome 37
Final Height in Italian Patients with Congenital Hypothyroidism Detected by Neonatal Screening: An Observational Study Over 20 Years 34
PTPN11/SH2 gene analysis and linear growth in Noonan syndrome 34
Iodine absorption in celiac children: A longitudinal pilot study 34
Linear growth and puberty in childhood obesity: what is new? 32
Circulating Inhibitory Factor 1 levels in adult patients with Prader-Willi syndrome 22
Isolated childhood growth hormone deficiency: a 30-year experience on final height and a new prediction model 17
Unexpected high prevalence of primary subclinical hypothyroidism (PSH) in children with celiac disease at diagnosis (CC) 12
null 12
Inflammation as Prognostic Hallmark of Clinical Outcome in Patients with SARS-CoV-2 Infection 11
Vascular and Myocardial Function in Young People with Type 1 Diabetes Mellitus: Insulin Pump Therapy Versus Multiple Daily Injections Insulin Regimen 10
Clinical Spectrum Associated with Wolfram Syndrome Type 1 and Type 2: A Review on Genotype–Phenotype Correlations 2
Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation 1
Totale 1.899
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Categoria #
all - tutte 9.239
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 9.239
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020326 0 15 19 39 31 28 29 37 43 39 32 14
2020/2021309 24 16 13 31 50 26 14 42 31 37 13 12
2021/2022223 19 17 8 5 6 17 15 13 15 13 40 55
2022/2023407 51 68 22 31 38 55 5 49 68 1 9 10
2023/2024166 10 32 12 11 26 48 9 4 1 2 2 9
2024/202545 41 4 0 0 0 0 0 0 0 0 0 0
Totale 1.899