496 results on '"De Sanctis, Luisa"'
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2. International consensus statement on the diagnosis and management of phaeochromocytoma and paraganglioma in children and adolescents
3. Impaired salivary gland function in children with osteogenesis imperfecta: a case-control study
4. Cardiometabolic risk in children and adolescents with obesity: a position paper of the Italian Society for Pediatric Endocrinology and Diabetology
5. Author Correction: International consensus statement on the diagnosis and management of phaeochromocytoma and paraganglioma in children and adolescents
6. The diagnostic role of arginine-stimulated copeptin in the differential diagnosis of polyuria-polydipsia syndrome (PPS) in pediatric age
7. Recommendations for recognizing, risk stratifying, treating, and managing children and adolescents with hypoglycemia
8. Clinical features of thyroid cancer in paediatric age. Experience of a tertiary centre in the 2000–2020 period
9. Adrenal insufficiency management in the pediatric emergency setting and risk factors for adrenal crisis development
10. The Italian registry for patients with Prader–Willi syndrome
11. Diabetes care practices and outcomes in 40.000 children and adolescents with type 1 diabetes from the SWEET registry during the COVID-19 pandemic
12. “Lymphocyte population in peripheral blood in children and adolescents with graves disease. Potential predictive tool for severity of the disease”
13. Unusual Mild Phenotype Presentation in an Elderly Patient with Homozygous Tangier Disease.
14. Menorrhagia as main presentation sign of severe hypothyroidism in a pediatric patient: a case report
15. Paediatric type 1 diabetes mellitus: A comparison between multi‐injection therapy and advanced hybrid closed‐loop pump in the first year after diabetes onset
16. “Thyroid nodular disease and PTEN mutation in a multicentre series of children with PTEN hamartoma tumor syndrome (PHTS)”
17. Predictive factors of malignancy in pediatric patients with thyroid nodules and performance of the Italian classification (SIAPEC 2014) in the outcome of the cytological FNA categories
18. Approccio diagnostico-terapeutico della Sindrome di McCune-Albright
19. Prevention and management of hypertensive crises in children with pheochromocytoma and paraganglioma.
20. Neurological dysfunction screening in a cohort of adolescents with type 1 diabetes: a six-year follow-up
21. Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation
22. Simplified Criteria for Identification of Familial Hypercholesterolemia in Children: Application in Real Life
23. High Fat Diet and Polycystic Ovary Syndrome (PCOS) in Adolescence: An Overview of Nutritional Strategies
24. Variants in the 5′UTR reduce SHOX expression and contribute to SHOX haploinsufficiency
25. Incidence of primary congenital hypothyroidism and relationship between diagnostic categories and associated malformations
26. Distribution of plasma copeptin levels and influence of obesity in children and adolescents
27. Impact of lockdown during COVID-19 emergency on glucose metrics of children and adolescents with type 1 diabetes in Piedmont, Italy
28. Pseudohypoparathyroidism: application of the Italian common healthcare-pathway for a homogeneous clinical approach and a shared follow up
29. The diagnostic role of arginine-stimulated copeptin in the differential diagnosis of polyuria-polydipsia syndrome (PPS) in pediatric age
30. Evaluation of the performance of Dutch Lipid Clinic Network score in an Italian FH population: The LIPIGEN study
31. Teriparatide (rhPTH 1–34) treatment in the pediatric age: long-term efficacy and safety data in a cohort with genetic hypoparathyroidism
32. Plasma cortisol and ACTH levels in 416 VLBW preterm infants during the first month of life: distribution in the AGA/SGA population
33. Perinatal asphyxia and hypothermic treatment from the endocrine perspective
34. Editorial: Thyroid nodules and tumors in childhood
35. SHOX deficiency in children with growth impairment: evaluation of known and new auxological and radiological indicators
36. Jaffe-Campanacci syndrome or neurofibromatosis type 1: a case report of phenotypic overlap with detection of NF1 gene mutation in non-ossifying fibroma
37. Diagnosis, treatment, and management of rickets: a position statement from the Bone and Mineral Metabolism Group of the Italian Society of Pediatric Endocrinology and Diabetology.
38. Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement
39. Apolipoprotein B and Lipid Profile in Italian Children and Adolescents.
40. Lipoprotein(a) Genotype Influences the Clinical Diagnosis of Familial Hypercholesterolemia
41. 24 - Is obesity a risk factor for children enuresis?
42. Skeptical Look at the Clinical Implication of Metabolic Syndrome in Childhood Obesity
43. Has air pollution any role in the incidence of congenital hypothyroidism?
44. Adrenal insufficiency management in the pediatric emergency setting and risk factors for adrenal crisis development
45. Neonatal Screening for Congenital Hypothyroidism in Preterm Infants: Is a Targeted Strategy Required?
46. Trends and cyclic variation in the incidence of childhood type 1 diabetes in two Italian regions over 33 years and during the COVID ‐19 pandemic
47. Pediatric thyroid surgery: Retrospective analysis on the first 25 pediatric thyroidectomies performed in a reference center for adult thyroid diseases
48. Clinical features of thyroid cancer in paediatric age. Experience of a tertiary centre in the 2000-2020 period
49. Additional file 1 of Adrenal insufficiency management in the pediatric emergency setting and risk factors for adrenal crisis development
50. COVID-19 forced restrictions did not affect metabolic control in youth with T2D in Italy
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