The Natural History and Genotype-Phenotype Nonconcordance of HLA Identical Siblings with the Same Mutations of the 21-Hydroxylase Gene

Articles in the same Issue

1. TABLE OF CONTENTS
2. The Management of Type 2 Diabetes Mellitus in Children and Adolescents
3. 46,XX Patients with Congenital Adrenal Hyperplasia: Initial Assignment as Male, Reassigned Female
4. Update on the Prenatal Diagnosis and Treatment of Congenital Adrenal Hyperplasia due to 11β-Hydroxylase Deficiency
5. The Natural History and Genotype-Phenotype Nonconcordance of HLA Identical Siblings with the Same Mutations of the 21-Hydroxylase Gene
6. Immunophenotypic Characterisation of Peripheral Blood Lymphocytes in Autoimmune Polyglandular Syndrome Type 1: Clinical Study and Review of the Literature
7. Final Height in Patients with Constitutional Delay of Growth and Development from Tall Statured Families
8. Constitutional Delay of Growth and Puberty: From Presentation to Final Height
9. Longitudinal Investigation of the Relationship between Breast Milk Leptin Levels and Growth in Breast-fed Infants
10. Leptin Profile in Neonatal Gonadotropin Surge and Relationship Between Leptin and Body Mass Index in Early Infancy
11. Three New 46,XX Male Patients: A Clinical, Cytogenetic and Molecular Analysis
12. Growth Hormone Deficiency in a Child with Williams-Beuren Syndrome. The Response to Growth Hormone Therapy
13. Novel Growth Hormone Receptor Mutation in a Chinese Patient with Laron Syndrome
14. Primary Hyperaldosteronism with Normokalaemia Secondary to an Adrenal Adenoma (Conn's Syndrome) in a 12 Year-old Boy
15. Calendar