21-Hydroxylase Deficiency Transiently Mimicking Combined 21- and 11β-Hydroxylase Deficiency

Articles in the same Issue

1. TABLE OF CONTENTS
2. Anti-epileptic Drugs and Thyroid Function
3. Complete Vaginal Agenesis in a Girl with Mayer-Rokitansky-Küster-Hauser Syndrome Type II
4. Predictors of First-Year Growth Response to a Fixed-dose Growth Hormone Treatment in Children Born Small for Gestational Age: Results of an Open-Label, Multicenter Trial in the United States
5. Efficacy and Safety of Growth Hormone Treatment in Children Born Small for Gestational Age in Japan
6. A Comparison of Published Criteria for Assuming Attainment of Adult Height in Girls who have Received Growth Hormone Treatment
7. Differences in Endocrine Parameters and Psychopathology in Girls with Premature Adrenarche versus On-time Adrenarche
8. Long-term Follow-up of Tamoxifen Treatment in Adolescents with Gynecomastia
9. The Actual Incidence of Congenital Adrenal Hyperplasia in Brazil May Not be as High as Inferred - An Estimate Based on a Public Neonatal Screening Program in the State of Goiás
10. Treatment of Childhood Obesity in Obese Families
11. Prevalence of Early Microalbuminuria in Children with Type 1 Diabetes Mellitus
12. Juvenile Multiple Sclerosis Similar to Type I Diabetes Mellitus has a Seasonality of Month of Birth which Differs from that in the General Population
13. Congenital Neonatal Hyperthyroidism Caused by Germline Mutations in the TSH Receptor Gene
14. 21-Hydroxylase Deficiency Transiently Mimicking Combined 21- and 11β-Hydroxylase Deficiency
15. Treatment of Precocious Puberty in a Female with Prader-Willi Syndrome
16. CALENDAR