Últimos Artículos de Hormone Research in Paediatrics
- Isolated 17, 20 Lyase Deficiency Secondary to a Novel CYB5A Variant: Comparison of Steroid Metabolomic Findings with Published Cases Provides Diagnostic Guidelines and Greater Insight into Its Biological Role
- Diagnosis of Growth Hormone Deficiency in Children: The Efficacy of Glucagon versus Clonidine Stimulation Test
- Birthweight Differences in Adolescent Monozygotic Twins Influence Androgens, Psychological Morbidity, and Health-Related Quality of Life
- Cortisol and Cortisone in Early Childhood in Very-Low-Birthweight Infants and Term-Born Infants
- The Unique Role of 11-Oxygenated C19 Steroids in Both Premature Adrenarche and Premature Pubarche
- Outcomes of Zoledronic Acid Use in Paediatric Conditions
- Immunological Profile and Autoimmunity in Turner Syndrome
- Clinical Characteristics, Molecular Features, and Long-Term Follow-Up of 15 Patients with Neonatal Diabetes: A Single-Centre Experience
- Preliminary Pages
- 29th Annual Meeting, Mexico, December 2020: Abstracts
- Pediatric Endocrinology in the Time of COVID-19: Considerations for the Rapid Implementation of Telemedicine and Management of Pediatric Endocrine Conditions
- Long-Term Effectiveness and Safety of Childhood Growth Hormone Treatment in Noonan Syndrome
- For Premature Thelarche and Premature Adrenarche, the Case for Waiting before Testing
- Diagnostic Value of Serum Acid-Labile Subunit Alone and in combination with IGF-I and IGFBP-3 in the Diagnosis of Growth Hormone Deficiency
- Age-Related Association of Calcitonin with Parameters of Anthropometry, Bone and Calcium Metabolism during Childhood
- Severe Fibrous Dysplasia in McCune-Albright Syndrome: A Need for Continuous Surveillance
- Role of Body Weight in the Onset and the Progression of Idiopathic Premature Pubarche
- Acromesomelic Dysplasia, Type Maroteaux: Impact of Long-Term (8 Years) High-Dose Growth Hormone Treatment on Growth Velocity and Final Height in 2 Siblings
- Clinical Predictors of Transient versus Persistent Neonatal Hyperinsulinism
- Cinacalcet as a First-Line Treatment in Neonatal Severe Hyperparathyroidism Secondary to Calcium Sensing Receptor (CaSR) Mutation