about
Diagnosis of GH deficiency in the transition period: accuracy of insulin tolerance test and insulin-like growth factor-I measurementPosterior pituitary (PP) evaluation in patients with anterior pituitary defect associated with ectopic PP and septo-optic dysplasia.Heterozygous mutations of growth hormone receptor gene in children with idiopathic short stature.Four new cases of PHACES syndrome: variable phenotypic expression and endocrine features.The Italian screening program for primary congenital hypothyroidism: actions to improve screening, diagnosis, follow-up, and surveillance.Classical and non-classical causes of GH deficiency in the paediatric age.Diagnostic potential of hepcidin testing in pediatrics.JAG1 Loss-Of-Function Variations as a Novel Predisposing Event in the Pathogenesis of Congenital Thyroid Defects.Postnatal evaluation of intrauterine growth retarded infants.Thyroid function in children and adolescents with Hashimoto's thyroiditis after l-thyroxine discontinuation.Phenotypic and functional characterization of switch memory B cells from patients with oligoarticular juvenile idiopathic arthritisPeculiarities of Graves' disease in children and adolescents with Down's syndrome.Serum thyrotropin concentration in children with isolated thyroid nodules.Diagnostic features of thyroid nodules in pediatrics.Levothyroxine treatment in pediatric benign thyroid nodules.Iodine deficiency and its consequences for cognitive and psychomotor development of children.Thyroid nodules and cancer in children and adolescents affected by autoimmune thyroiditis.Outcome after depot gonadotrophin-releasing hormone agonist treatment for central precocious puberty: effects on body mass index and final height.Collectrin gene screening in Turner syndrome patients with kidney malformation.The advantage of measuring spontaneous growth hormone (GH) secretion compared with the insulin tolerance test in the diagnosis of GH deficiency in young adults.Hypogonadotropic hypogonadism in a trisomy X carrier: phenotype description and genotype correlation.Graves disease in children: thyroid-stimulating hormone receptor antibodies as remission markers.Auxological and metabolic study in small for gestational age children during 2 years follow-up.Controlled ovarian stimulation and IVF pregnancy in a trisomy X carrier with associated hypogonadotropic hypogonadism.Impaired GH Secretion in Patients with SHOX Deficiency and Efficacy of Recombinant Human GH TherapyUse of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Bartter and Gitelman syndromesFluconazole therapy in an underweight infantA proposal for a pediatric version of the Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index based on the analysis of 1,015 patients with juvenile-onset systemic lupus erythematosusAbsence of sonic hedgehog (Shh) germline mutations in patients with thyroid dysgenesisThe natural history of the normal/mild elevated TSH serum levels in children and adolescents with Hashimoto's thyroiditis and isolated hyperthyrotropinaemia: a 3-year follow-upRole of MRI T2-DRIVE in the assessment of pituitary stalk abnormalities without gadolinium in pituitary diseases
P50
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P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Roberto Gastaldi
@ast
Roberto Gastaldi
@en
Roberto Gastaldi
@es
Roberto Gastaldi
@nl
type
label
Roberto Gastaldi
@ast
Roberto Gastaldi
@en
Roberto Gastaldi
@es
Roberto Gastaldi
@nl
prefLabel
Roberto Gastaldi
@ast
Roberto Gastaldi
@en
Roberto Gastaldi
@es
Roberto Gastaldi
@nl
P106
P1153
7004029463
P21
P31
P496
0000-0002-2157-1158