Hypocalcemia as a Presenting Feature of Celiac Disease in a Patient with DiGeorge Syndrome

Articles in the same Issue

1. TABLE OF CONTENTS
2. EDITORIAL
3. Role of Physical Exercise in Children and Adolescents with Diabetes Mellitus
4. Transient, Isolated Growth Hormone Deficiency After a BB Gunshot Wound
5. Assessment of Insulin Sensitivity from Measurements in Fasting State and During an Oral Glucose Tolerance Test in Obese Children
6. A Community-based Behavior Modification Intervention for Childhood Obesity
7. Serum Sialic Acid, hs-CRP and Oxidative Stress Parameters in Obese Children
8. Short Stature in Children with Sickle Cell Anemia Correlates with Alterations in the IGF-I Axis
9. Inappropriate Use of Potent Topical Glucocorticoids in Infants
10. Bone Mineral Status in Children with Congenital Adrenal Hyperplasia
11. The Incidence and Evolution of Thyroid Dysfunction During Interferon-α Therapy in Children with Chronic Hepatitis Β Infection
12. Primary Pigmented Nodular Adrenocortical Disease (PPNAD) and Pituitary Adenoma in a Boy with Sporadic Carney Complex Due to a Novel, De Novo Paternal PRKARIA Mutation (R96X)
13. Hypocalcemia as a Presenting Feature of Celiac Disease in a Patient with DiGeorge Syndrome
14. Growth, Growth Hormone Testing and Response to Growth Hormone Treatment in Gitelman Syndrome
15. Re: Evaluation of hypothalamic-pituitary-adrenal axis (ΗΡΑ) suppression by low-dose (0.5 μg) and standard-dose (250 μg) adrenocorticotropic hormone (ACTH) tests in asthmatic children treated with inhaled corticosteroid (JPEM 2006; 19: 1015-1023)
16. Reply: Evaluation of hypothalamic-pituitary-adrenal axis (ΗΡΑ) suppression by low-dose (0.5 μg) and standard-dose (250 μg) adrenocorticotropic hormone (ACTH) tests in asthmatic children treated with inhaled corticosteroid (JPEM 2006; 19: 1015-1023)
17. CALENDAR