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Metaphyseal Condrodysplasia, Schmid-type, a Differential Diagnosis with Rickets

  • Cresio Alves , Marina M. Sobral und Fabrizio Ney-Oliveira
Veröffentlicht/Copyright: 17. September 2010
Journal of Pediatric Endocrinology and Metabolism
Aus der Zeitschrift Band 23 Heft 4

Published Online: 2010-09-17
Published in Print: 2010-April

© Freund Publishing House Ltd.

Artikel in diesem Heft

  1. Growth hormone (GH) testing nutrition and metabolic balance, do we have the full picture?
  2. Primary Aldosteronism and its Impact on the Generation of Arterial Hypertension, Endothelial Injury and Oxidative Stress
  3. Metaphyseal Condrodysplasia, Schmid-type, a Differential Diagnosis with Rickets
  4. Adiposity, Physical Activity and Blood Lipid Profile in 13-year-old Adolescents
  5. Relationship between Metabolic Parameters and Thyroid Hormones and the Level of Gastric Peptides in Children with Autoimmune Thyroid Diseases
  6. Stimulated Growth Hormone Concentrations in Obese Pediatric Patients with Mild and Severe Insulin Resistance: A Pilot Study
  7. Amiodarone-induced Thyrotoxicosis in Children and Adolescents is a Possible Outcome in Patients with Low Iodine Intake
  8. Analysis of Serum Adiponectin, Resistin and Leptin Levels in Children and Adolescents with Autoimmune Thyroid Disorders
  9. Molecular Diagnosis of 46,XY DSD and Identification of a Novel 8 Nucleotide Deletion in Exon 1 of the SRD5A2 Gene
  10. Can Auxology, IGF-I and IGFBP-3 Measurements Followed by MRI and Genetic Tests Replace GH Stimulation Tests in the Diagnosis of GH Deficiency in Children?
  11. Body Fat Measurements in Elite Adolescent Volleyball Players: Correlation between Skinfold Thickness, Bioelectrical Impedance Analysis, Air-displacement Plethysmography, and Body Mass Index Percentiles
  12. Autonomic Bladder Dysfunction in an Adolescent with Type 1 Diabetes
  13. Autoimune Thyroiditis and Diabetes Mellitus Type 1 after Long-term Gonadotropin-releasing Hormone Agonist Treatment for Central Precocious Puberty: Evolution or Coincidence?
  14. Novel Growth Hormone Receptor Gene Mutation in a Patient with Laron Syndrome
  15. A Novel Missense Mutation in the AVPR2 Gene of a Japanese Infant with Nephrogenic Diabetes Insipidus
  16. Early Presentation of Familial Paraganglioma with SDHB Mutation in a 13 year old Child and its Mother
Heruntergeladen am 3.10.2025 von https://www.degruyterbrill.com/document/doi/10.1515/jpem.2010.053/html
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