Triple-A Syndrome - The First Chinese Patient with Novel Mutations in the AAAS Gene

Articles in the same Issue

1. TABLE OF CONTENTS
2. Fertility in Patients with Congenital Adrenal Hyperplasia
3. Pituitary Dysfunction Following Head Injury - A Common Problem, Rarely Diagnosed
4. Hypothalamo-hypophysial Dysfunction After Traumatic Brain Injury in Children and Adolescents: A Preliminary Retrospective and Prospective Study
5. Blood Pressure in Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
6. Asymptomatic Cardiomyopathy in Children and Adolescents with Type 1 Diabetes Mellitus: Association of Echocardiography Indicators with Duration of Diabetes Mellitus and Metabolic Parameters
7. The Relationship of Maternal Iodine Status and Neonatal Thyrotropin Concentration: A Study in Southern Thailand
8. Genetic Variants in the Promoter Region of the IGF-I Gene as a Reason for Short Stature
9. Plasminogen Activator Inhibitor-1 (PAI-1) Gene Polymorphism (-675 4G/SG) Associated with Obesity and Vascular Risk in Children
10. Childhood Sporadic Pheochromocytoma: Clinical Profile and Outcome in 19 Patients
11. Malignant Insulinoma in Childhood
12. An Unusual Case of Chromosome 22q11 Deletion Syndrome with Psychiatric Disorder, Hypoparathyroidism and Precocious Puberty
13. Triple-A Syndrome - The First Chinese Patient with Novel Mutations in the AAAS Gene
14. Menstruation in a 2 Month-old Infant with Salt-Losing Congenital Adrenal Hyperplasia (CAH)
15. CALENDAR