Startseite Quantitative Computed Tomography Measurements of Bone Mineral Density in Prepubertal Children with Congenital Hypothyroidism Treated with L-Thyroxine
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Quantitative Computed Tomography Measurements of Bone Mineral Density in Prepubertal Children with Congenital Hypothyroidism Treated with L-Thyroxine

  • P. Pitukcheewanont, , D. Safani, , V. Gilsanz, , M. Kleiny, , Y. Chongpison, und G. Costin,
Veröffentlicht/Copyright: 1. Juni 2004

Published Online: 2004-06

©2011 by Walter de Gruyter GmbH & Co.

Artikel in diesem Heft

  1. TABLE OF CONTENTS
  2. Male Pseudohermaphroditism: Long-term Quality of Life Outcome in Five 46,XY Individuals Reared Female
  3. Genital Ambiguity with a Y Chromosome: Does Gender Assignment Matter?
  4. Imaging in Intersex Disorders
  5. Gestational Diabetes Mellitus - Implications of Different Treatment Protocols
  6. Postprandial Hyperlipidemia after a Fat Loading Test in Minority Adolescents with Type 2 Diabetes Mellitus and Obesity
  7. Preschoolers Are Not Miniature Adolescents: A Comparison of Insulin Pump Doses in Two Groups of Children with Type 1 Diabetes Mellitus
  8. Type I and Type 2 Diabetes Mellitus in Childhood in the United States: Practice Patterns by Pediatric Endocrinologists
  9. Decreased Serum Inhibin B/FSH Ratio as a Marker of Sertoli Cell Function in Male Survivors After Chemotherapy in Childhood and Adolescence
  10. Quantitative Computed Tomography Measurements of Bone Mineral Density in Prepubertal Children with Congenital Hypothyroidism Treated with L-Thyroxine
  11. Alterations in Serum Growth Hormone (GH)/GH Dependent Ternary Complex Components (IGF-I, IGFBP-3, ALS, IGF-I/IGFBP-3 Molar Ratio) and the Influence of these Alterations on Growth Pattern in Female Rhythmic Gymnasts
  12. An Unusal Case of Hermaphroditism - A 46,XX/69,XXY Chimera
  13. Bilateral Adrenal Cysts and Ectopic Pancreatic Tissue in Beckwith-Wiedemann Syndrome: Is a Conservative Approach Acceptable?
  14. Bardet-Biedl Syndrome with Syndrome X: A Patient Report
  15. Novel Compound Heterozygous AIRE mutations in a Japanese Patient with APECED
  16. CALENDAR
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