A Family with Autosomal Dominant Hypocalcaemia with Hypercalciuria (ADHH): Mutational Analysis, Phenotypic Variability and Treatment Challenges

Articles in the same Issue

1. TABLE OF CONTENTS
2. Impact of Environment upon Gender Identity and Sexual Orientation: A Lesson for Parents of Children with Intersex or Gender Confusion
3. Current Perspective on the Pathogenesis of Central Diabetes Insipidus
4. Morbid Obesity is Associated with Short Stature
5. Managing Children with Russell-Silver Syndrome: More than Just Growth Hormone Treatment?
6. Etiologies of Central Diabetes Insipidus in Thai Children
7. Hypoglycaemia and Russell-Silver Syndrome
8. Endocrine Profile of Children with Intrauterine Growth Retardation
9. Evaluation of the Auxological and Metabolic Status in Prepubertal Children Born Small for Gestational Age
10. A Family with Autosomal Dominant Hypocalcaemia with Hypercalciuria (ADHH): Mutational Analysis, Phenotypic Variability and Treatment Challenges
11. Differences in Dental and Bone Maturation in Regions With or Without Hemihypertrophy in Two Patients with Russell-Silver Syndrome
12. Prader-Willi Syndrome and Mosaic Turner's Syndrome
13. Treatment of Malabsorption Vitamin D Deficiency Myopathy with Intramuscular Vitamin D
14. 2nd Annual World Congress on the Insulin Resistance Syndrome
15. CALENDAR