Home Cord Blood Leptin and IGF-I in Relation to Birth Weight Differences and Head Circumference in Monozygotic Twins
Article
Licensed
Unlicensed Requires Authentication

Cord Blood Leptin and IGF-I in Relation to Birth Weight Differences and Head Circumference in Monozygotic Twins

  • Bettina C. Gohlke, , Agnes Huber, , Peter Bartmann, , Rolf Fimmers, , Kurt Hecher, , Sebastien G. Bouret, and Christian L. Roth,
Published/Copyright: January 1, 2006

Published Online: 2006-01

©2011 by Walter de Gruyter GmbH & Co.

Articles in the same Issue

  1. TABLE OF CONTENTS
  2. EDITORIAL
  3. Cord Blood Leptin and IGF-I in Relation to Birth Weight Differences and Head Circumference in Monozygotic Twins
  4. Quality of Life and Psychological Outcome in Patients Treated for Craniopharyngioma
  5. Health Related Quality of Life and Psychological Outcome in Patients Treated for Craniopharyngioma in Childhood
  6. Use of the Recombinant Human TSH Stimulated Thyroglobulin Level and Diagnostic Whole Body Scan in Children with Differentiated Thyroid Carcinoma
  7. Congenital Hypothyroidism and the Second Newborn Metabolic Screening in Colorado, USA
  8. Incidence of Iodine Deficiency in Patients Presenting with Goitre - Discrepancy Between Clinical and Ultrasonographic Evaluation of the Thyroid: Comparison of Patients With and Without Autoimmune Thyroiditis - Clinical, Hormonal and Urinary Iodine Excretion Studies
  9. Early Diabetic Complications in a Population of Young Patients with Type 1 Diabetes Mellitus Despite Intensive Treatment
  10. A Workshop on Pubertal Hormone Replacement Options in the United States
  11. A Daily Comprehensive Muscle Training Programme Increases Lean Mass and Spontaneous Activity in Children with Prader-Willi Syndrome after 6 Months
  12. Pamidronate Treatment of Polyostotic Fibrous Dysplasia: Failure to Prevent Expansion of Dysplastic Lesions During Childhood
  13. Tamoxifen Improved Final Height Prediction in a Girl with McCune-Albright Syndrome: Patient Report and Literature Review
  14. A Novel Mutation in the GATA3 Gene in a Family with HDR Syndrome (Hypoparathyroidism, Sensorineural Deafness and Renal Anomaly Syndrome)
  15. A Novel Homozygous Deletion in the Calcium-Sensing Receptor Ligand-Binding Domain Associated with Neonatal Severe Hyperparathyroidism
  16. CALENDAR. ERRATUM
Downloaded on 9.9.2025 from https://www.degruyterbrill.com/document/doi/10.1515/JPEM.2006.19.1.3/pdf
Scroll to top button