Congenital Hypothyroidism Caused by a Novel Homozygous Mutation in the Thyroid Peroxidase Gene

Articles in the same Issue

1. TABLE OF CONTENTS
2. EDITORIAL
3. Presidential Address for the 4th Annual Meeting of the European Society of Paediatric Endocrinology
4. Severe Acanthosis Nigricans in a 17 Year-old Female with Partial Lipodystrophie Syndrome
5. Aortic Elasticity Alterations in Obesity - Even in Children!
6. Correlation of Abdominal Fat Accumulation and Stiffness of the Abdominal Aorta in Obese Children
7. Everyday Physical Activity and Adiposity in Prader-Willi Syndrome
8. Reassessment of the Optimal Growth Hormone Cut-off Level in Insulin Tolerance Testing for Growth Hormone Secretion in Patients with Childhood-Onset Growth Hormone Deficiency During Transition to Adulthood
9. Short Stature in Partially Corrected X-linked Severe Combined Immunodeficiency - Suboptimal Response to Growth Hormone
10. Bone Speed of Sound Curves of Twin and Singleton Neonates
11. Torsion of Malignant Ovarian Tumors in Childhood and Adolescence
12. Impaired Sertoli Cell Function in Males Diagnosed with Noonan Syndrome
13. Thyroid Stimulating Immunoglobulin is Often Negative in Children with Graves' Disease
14. Congenital Hypothyroidism in Young-Simpson Syndrome
15. Congenital Hypothyroidism Caused by a Novel Homozygous Mutation in the Thyroid Peroxidase Gene
16. Reversible Benign Intracranial Hypertension in a Child with Hyperthyroidism
17. Possible Relationship Between Ring X Chromosome and Neonatal Hypoglycemia
18. CALENDAR