about
Agenesis of internal carotid artery associated with isolated growth hormone deficiency: a case report and literature reviewA new case of de novo 6q24.2-q25.2 deletion on paternal chromosome 6 with growth hormone deficiency: a twelve-year follow-up and literature reviewA SOX3 (Xq26.3-27.3) duplication in a boy with growth hormone deficiency, ocular dyspraxia, and intellectual disability: a long-term follow-up and literature reviewBone metabolism in children and adolescents: main characteristics of the determinants of peak bone massBone status in genetic syndromes: a reviewEpigenetic control of the immune system: a lesson from Kabuki syndrome.Coeliac disease and risk for other autoimmune diseases in patients with Williams-Beuren syndrome.Retrospective Evaluation of Metformin and/or Metformin Plus a New Polysaccharide Complex in Treating Severe Hyperinsulinism and Insulin Resistance in Obese Children and Adolescents with Metabolic Syndrome.Bone mass and quality in patients with juvenile idiopathic arthritis: longitudinal evaluation of bone-mass determinants by using dual-energy x-ray absorptiometry, peripheral quantitative computed tomography, and quantitative ultrasonography.The ever-expanding conundrum of primary osteoporosis: aetiopathogenesis, diagnosis, and treatment.Increased incidence of thyroid dysfunction and autoimmunity in patients with vernal keratoconjunctivitis.Determinants of Vitamin D Levels in Italian Children and Adolescents: A Longitudinal Evaluation of Cholecalciferol Supplementation versus the Improvement of Factors Influencing 25(OH)D Status.Determinants of vitamin d levels in children and adolescents with down syndromeLong-term auxological and endocrinological evaluation of patients with 9p trisomy: a focus on the growth hormone-insulin-like growth factor-I axis.Policaptil Gel Retard significantly reduces body mass index and hyperinsulinism and may decrease the risk of type 2 diabetes mellitus (T2DM) in obese children and adolescents with family history of obesity and T2DM.Hydrocortisone malabsorption due to polyethylene glycols (Macrogol 3350) in a girl with congenital adrenal insufficiency.Bone Mineral Status in Children and Adolescents with Klinefelter Syndrome.Long-term safety and efficacy of Omnitrope®, a somatropin biosimilar, in children requiring growth hormone treatment: Italian interim analysis of the PATRO Children study.Type II diabetes and impaired glucose tolerance due to severe hyperinsulinism in patients with 1p36 deletion syndrome and a Prader-Willi-like phenotype.Bone health in children and adolescents: the available imaging techniques.Kawasaki disease in a girl with Turner syndrome: a remarkable associationGlucocorticoid-associated osteoporosis in chronic inflammatory diseases: epidemiology, mechanisms, diagnosis, and treatment.Amenorrhea after Endoscopic Third Ventriculostomy for a Failed Shunt in Spina Bifida: Case Report and Review of the Literature.Pharmacological considerations in the use of stiripentol for the treatment of epilepsy.Cessation of epilepsy therapy in children.The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosis.Bone modeling, remodeling, and skeletal health in children and adolescents: mineral accrual, assessment and treatment.Vitamin D levels and effects of vitamin D replacement in children with periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome.Parathyroid Hormone Levels in Healthy Children and Adolescents.Diabetes mellitus in a girl with thyroid hormone resistance syndrome: a little recognized interaction between the two diseases.Possible effects of an early diagnosis and treatment in patients with growth hormone deficiency: the state of artReversible weight gain and prolactin levels--long-term follow-up in childhood.Triple X syndrome and puberty: focus on the hypothalamus-hypophysis-gonad axis.Cross-sectional and longitudinal evaluation of bone mass in children and young adults with juvenile idiopathic arthritis: the role of bone mass determinants in a large cohort of patients.Autoimmune Thyroiditis, Pernicious Anaemia, Vitiligo and Scleroatrophic Lichen in a boy with short-chain acylCoA dehydrogenase deficiency.Diagnosis of growth hormone deficiency by using the arginine provocative test: is it possible to shorten testing time without altering validity?Thyroid function, autoimmune thyroiditis and coeliac disease in juvenile connective tissue diseases.Bone density and metabolism in subjects with microdeletion of chromosome 22q11 (del22q11).Cross-sectional and longitudinal evaluation of bone mass and quality in children and young adults with juvenile onset systemic lupus erythematosus (JSLE): role of bone mass determinants analyzed by DXA, PQCT and QUS.Association of low bone mass with vitamin d receptor gene and calcitonin receptor gene polymorphisms in juvenile idiopathic arthritis.
P50
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P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Stefano Stagi
@ast
Stefano Stagi
@en
Stefano Stagi
@es
Stefano Stagi
@nl
Stefano Stagi
@sl
type
label
Stefano Stagi
@ast
Stefano Stagi
@en
Stefano Stagi
@es
Stefano Stagi
@nl
Stefano Stagi
@sl
prefLabel
Stefano Stagi
@ast
Stefano Stagi
@en
Stefano Stagi
@es
Stefano Stagi
@nl
Stefano Stagi
@sl
P1053
R-1453-2016
P106
P1153
6506305399
P21
P2798
P31
P3829
P496
0000-0002-2259-4685