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

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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