Thyrotoxic Periodic Paralysis Associated with a Mutation in the Sodium Channel Gene SCN4A

Articles in the same Issue

1. TABLE OF CONTENTS
2. Hypoparathyroidism-Retardation-Dysmorphism (HRD) Syndrome - A Review
3. Minimal Surgical Intervention in the Management of Intersex Conditions
4. An Open Label 12-Month Pilot Trial on the Effects of the Aromatase Inhibitor Anastrozole in Growth Hormone (GH)-Treated GH Deficient Adolescent Boys
5. The Low Dose Synacthen Test: Experience in Well Preterm Infants
6. Infantile Hyperinsulinism Associated with Enteropathy, Deafness and Renal Tubulopathy: Clinical Manifestations of a Syndrome Caused by a Contiguous Gene Deletion Located on Chromosome 11p
7. Cholecystokinin, Glucose Dependent Insulinotropic Peptide and Glucagon-like Peptide 1 Secretion in Children with Anorexia Nervosa and Simple Obesity
8. Obesity and Type 2 Diabetes Mellitus: A Population-based Study of Adolescents
9. Benefits of an Insulin Dosage Calculation Device for Adolescents with Type 1 Diabetes Mellitus
10. Pubertal Changes in Serum Leptin Levels in Adolescents with Type 1 Diabetes Mellitus: A Controlled Longitudinal Study
11. Urinary Meprin-α: A Potential Marker of Diabetic Nephropathy
12. Acute Pancreatitis and its Association with Diabetes Mellitus in Children
13. Hemolytic Crisis in a Non-Ketotic and Euglycemic Child with Glucose-6-phosphate Dehydrogenase Deficiency and Onset of Type 1 Diabetes Mellitus
14. YqTER Deletion Causes Arrest of Spermatogenesis in Early Puberty
15. Thyrotoxic Periodic Paralysis Associated with a Mutation in the Sodium Channel Gene SCN4A
16. CALENDAR. INDEX