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Growth hormone deficiency and antipituitary antibodies in a patient with common variable immunodeficiency.A novel CISD2 intragenic deletion, optic neuropathy and platelet aggregation defect in Wolfram syndrome type 2.The prevalence of growth hormone deficiency and celiac disease in short children.Prevalence of positive atopy patch test in an unselected pediatric population.Final height in Italian patients with congenital hypothyroidism detected by neonatal screening: a 20-year observational study.Incidence of Type 1 Diabetes among Children and Adolescents in Italy between 2009 and 2013: The Role of a Regional Childhood Diabetes Registry.Clinical, endocrine, and molecular findings in 17beta-hydroxysteroid dehydrogenase type 3 deficiency.Identification of candidate children for maturity-onset diabetes of the young type 2 (MODY2) gene testing: a seven-item clinical flowchart (7-iF).Endothelial dysfunction and cardiovascular risk factors in childhood acute lymphoblastic leukemia survivors.Disorders of glucose metabolism in Prader-Willi syndrome: Results of a multicenter Italian cohort study.Monogenic Diabetes Accounts for 6.3% of Cases Referred to 15 Italian Pediatric Diabetes Centers During 2007 to 2012.Non-alcoholic fatty liver disease is associated with early left ventricular dysfunction in childhood acute lymphoblastic leukaemia survivors.Levothyroxine requirement in congenital hypothyroidism: a 12-year longitudinal study.Survey on etiological diagnosis of diabetes in 1244 Italian diabetic children and adolescents: impact of access to genetic testing.Clinical heterogeneity of abnormal glucose homeostasis associated with the HNF4A R311H mutation.IGF2 gene variants and risk of hypertension in obese children and adolescents.17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence.[Constitutional delay of growth and puberty]In congenital hypothyroidism bone maturation at birth may be a predictive factor of psychomotor development during the first Year of life irrespective of other variables related to treatment.Sodium fraction excretion rate in nocturnal enuresis correlates with nocturnal polyuria and osmolality.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.Prolactin may be increased in newly diagnosed celiac children and adolescents and decreases after 6 months of gluten-free diet.Metabolic syndrome in childhood leukemia survivors: a meta-analysis.Thyroid function and thyroid autoimmunity in childhood acute lymphoblastic leukemia off-therapy patients treated only with chemotherapy.Effects of moderate-severe exercise on blood glucose in Type 1 diabetic adolescents treated with insulin pump or glargine insulin.Sulfonylurea treatment in a girl with neonatal diabetes (KCNJ11 R201H) and celiac disease: impact of low compliance to the gluten free diet.Transient neonatal diabetes mellitus is associated with a recurrent (R201H) KCNJ11 (KIR6.2) mutation.Growth hormone treatment improves final height and nutritional status of children with chronic kidney disease and growth deceleration.Factors predicting final height in early treated congenital hypothyroid patients.Final height in short polytransfused thalassemia major patients treated with recombinant growth hormone.Coeliac children treated for growth hormone deficiency reach normal final height.Sleep-disordered breathing in obese children: the southern Italy experience.Anti-pituitary antibodies in children with newly diagnosed celiac disease: a novel finding contributing to linear-growth impairment.Acute pancreatitis in a girl with panhypopituitarism due to craniopharyngioma on growth hormone treatment. A combination of risk factors.A novel OTX2 gene frameshift mutation in a child with microphthalmia, ectopic pituitary and growth hormone deficiency.Analysis of Circulating Mediators of Bone Remodeling in Prader-Willi Syndrome.[Neonatal hearing screening during the first and second day of life]High Sclerostin and Dickkopf-1 (DKK-1) Serum Levels in Children and Adolescents With Type 1 Diabetes Mellitus.Graves disease in children: thyroid-stimulating hormone receptor antibodies as remission markers.Metabolic, inflammatory, endothelial and haemostatic markers in a group of Italian obese children and adolescents.
P50
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P50
description
hulumtues
@sq
onderzoeker
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researcher
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հետազոտող
@hy
name
Maurizio Delvecchio
@ast
Maurizio Delvecchio
@en
Maurizio Delvecchio
@es
Maurizio Delvecchio
@nl
Maurizio Delvecchio
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type
label
Maurizio Delvecchio
@ast
Maurizio Delvecchio
@en
Maurizio Delvecchio
@es
Maurizio Delvecchio
@nl
Maurizio Delvecchio
@sl
prefLabel
Maurizio Delvecchio
@ast
Maurizio Delvecchio
@en
Maurizio Delvecchio
@es
Maurizio Delvecchio
@nl
Maurizio Delvecchio
@sl
P1053
K-8762-2012
P106
P1153
15063916700
9242083400
P21
P2798
P31
P3829
P496
0000-0002-1528-0012