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        Congenital Hypothyroidism in Young-Simpson Syndrome
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        S. Stagi,
        
                            Veröffentlicht/Copyright:
                            
                                1. November 2008
                            
                        
                    
                
            
  Published Online: 2008-11
 
©2011 by Walter de Gruyter GmbH & Co.
                                        
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                                    Artikel in diesem Heft
- TABLE OF CONTENTS
- EDITORIAL
- Presidential Address for the 4th Annual Meeting of the European Society of Paediatric Endocrinology
- Severe Acanthosis Nigricans in a 17 Year-old Female with Partial Lipodystrophie Syndrome
- Aortic Elasticity Alterations in Obesity - Even in Children!
- Correlation of Abdominal Fat Accumulation and Stiffness of the Abdominal Aorta in Obese Children
- Everyday Physical Activity and Adiposity in Prader-Willi Syndrome
- 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
- Short Stature in Partially Corrected X-linked Severe Combined Immunodeficiency - Suboptimal Response to Growth Hormone
- Bone Speed of Sound Curves of Twin and Singleton Neonates
- Torsion of Malignant Ovarian Tumors in Childhood and Adolescence
- Impaired Sertoli Cell Function in Males Diagnosed with Noonan Syndrome
- Thyroid Stimulating Immunoglobulin is Often Negative in Children with Graves' Disease
- Congenital Hypothyroidism in Young-Simpson Syndrome
- Congenital Hypothyroidism Caused by a Novel Homozygous Mutation in the Thyroid Peroxidase Gene
- Reversible Benign Intracranial Hypertension in a Child with Hyperthyroidism
- Possible Relationship Between Ring X Chromosome and Neonatal Hypoglycemia
- CALENDAR
Artikel in diesem Heft
- TABLE OF CONTENTS
- EDITORIAL
- Presidential Address for the 4th Annual Meeting of the European Society of Paediatric Endocrinology
- Severe Acanthosis Nigricans in a 17 Year-old Female with Partial Lipodystrophie Syndrome
- Aortic Elasticity Alterations in Obesity - Even in Children!
- Correlation of Abdominal Fat Accumulation and Stiffness of the Abdominal Aorta in Obese Children
- Everyday Physical Activity and Adiposity in Prader-Willi Syndrome
- 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
- Short Stature in Partially Corrected X-linked Severe Combined Immunodeficiency - Suboptimal Response to Growth Hormone
- Bone Speed of Sound Curves of Twin and Singleton Neonates
- Torsion of Malignant Ovarian Tumors in Childhood and Adolescence
- Impaired Sertoli Cell Function in Males Diagnosed with Noonan Syndrome
- Thyroid Stimulating Immunoglobulin is Often Negative in Children with Graves' Disease
- Congenital Hypothyroidism in Young-Simpson Syndrome
- Congenital Hypothyroidism Caused by a Novel Homozygous Mutation in the Thyroid Peroxidase Gene
- Reversible Benign Intracranial Hypertension in a Child with Hyperthyroidism
- Possible Relationship Between Ring X Chromosome and Neonatal Hypoglycemia
- CALENDAR