180 results on '"Patti, Giuseppa"'
Search Results
2. Correction: Cushing syndrome in paediatric population: who and how to screen
3. Gut-microbiota in children and adolescents with obesity: inferred functional analysis and machine-learning algorithms to classify microorganisms
4. The Italian registry for patients with Prader–Willi syndrome
5. Hypothalamo-pituitary Disorders in Childhood and Adolescence
6. Advances in differential diagnosis and management of growth hormone deficiency in children
7. Sleep disorders in Prader-Willi syndrome, evidence from animal models and humans
8. Central diabetes insipidus in children: Diagnosis and management
9. Wolfram syndrome 1 in the Italian population: genotype–phenotype correlations
10. Uniparental disomy and pretreatment IGF-1 may predict elevated IGF-1 levels in Prader-Willi patients on GH treatment
11. THU172 Accuracy Of The Glucagon Testing In The Diagnosis Of Growth Hormone Deficiency During Transition
12. Update on bone density measurements and their interpretation in children and adolescents
13. Central adrenal insufficiency in children and adolescents
14. Blood Lymphocyte Subsets and Proinflammatory Cytokine Profile in ROHHAD(NET) and non-ROHHAD(NET) Obese Individuals
15. Precocious Puberty Diagnoses Spike, COVID-19 Pandemic, and Body Mass Index: Findings From a 4-year Study
16. Abnormalities of pubertal development and gonadal function in Noonan syndrome
17. A case report of glucose transporter 1 deficiency syndrome with growth hormone deficiency diagnosed before starting ketogenic diet
18. Classical and non-classical causes of GH deficiency in the paediatric age
19. Corrigendum: Pubertal timing in children with Silver Russell syndrome compared to those born small for gestational age
20. Growth Hormone Deficiency in the Transition Age
21. Gut-microbiota in Obese Children and Adolescents: Inferred Functional Analysis and Machine-learning Algorithms to Classify Microorganisms
22. The Italian registry for patients with Prader-Willi syndrome
23. Does the Application of Heat Gel Pack After Eutectic Mixture of Local Anesthetic Cream Improve Venipuncture or Intravenous Cannulation Success Rate in Children? A Randomized Control Trial
24. Infectious diseases associated with pediatric type 1 diabetes mellitus: A narrative review
25. Pubertal timing in children with Silver Russell syndrome compared to those born small for gestational age
26. Clinical, Endocrine and Neuroimaging Findings in Girls With Central Precocious Puberty
27. Approach to the Pediatric Patient: Central Diabetes Insipidus
28. Growth in Children With Noonan Syndrome and Effects of Growth Hormone Treatment on Adult Height
29. The phenotypic spectrum associated with OTX2 mutations in humans
30. Cognitive and White Matter Microstructure Development in Congenital Hypothyroidism and Familial Thyroid Disorders
31. Association of Familial Thyroid disorders with Impaired Cognitive and White Matter Microstructure Development Congenital Hypothyroidism
32. Gut Microbiota Assessment in Obese Children and Adolescents by Machine Learning Algorithms
33. Maternal Uniparental Disomy of Chromosome 20 (UPD(20)mat) as Differential Diagnosis of Silver Russell Syndrome: Identification of Three New Cases
34. Cognitive Impairment and White Matter Microstructure Abnormalities in Children with Congenital Hypothyroidism
35. Primary Adrenal Insufficiency in Childhood: Data From a Large Nationwide Cohort
36. IGF1 for the diagnosis of growth hormone deficiency in children and adolescents: a reappraisal
37. Characterization of Two Novel Variants of the Steroidogenic Acute Regulatory Protein Identified in a Girl with Classic Lipoid Congenital Adrenal Hyperplasia
38. Endocrine Outcomes In Central Diabetes Insipidus: the Predictive Value of Neuroimaging “Mismatch Pattern”
39. Gut Microbiota in T1DM-Onset Pediatric Patients: Machine-Learning Algorithms to Classify Microorganisms as Disease Linked
40. Two-year-old girl with metabolic acidosis and hyperkalaemia
41. Letter to the Editor: “Forty-One Individuals With Mutations in the AVP-NPII Gene Associated With Familial Neurohypophyseal Diabetes Insipidus.”
42. OR16-04 OTX2 Mutations in Congenital Hypopituitarism Patients
43. Antibodies Against Hypothalamus and Pituitary Gland in Childhood-Onset Brain Tumors and Pituitary Dysfunction
44. Changing the diagnostic approach to diabetes insipidus: role of copeptin
45. Sindrome di Silver Russell Correlazione genotipo-fenotipo e SNC
46. Caratteristiche cliniche in pazienti con sindrome ROHHAD e tumore neurale
47. Diabete insipido centrale in età pediatrica: ruolo degli anticorpi anti-GH
48. Cognitive Profiles and Brain Volume Are Affected in Patients with Silver–Russell Syndrome
49. Familial neurohypophyseal diabetes insipidus in 13 kindreds and 2 novel mutations in the vasopressin gene
50. Foramen magnum stenosis (FMS): neuroradiological aspects before and after cervical decompression in paediatric patients with achondroplasia (ACH)
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