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Metaphyseal Condrodysplasia, Schmid-type, a Differential Diagnosis with Rickets
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Cresio Alves
Veröffentlicht/Copyright:
17. September 2010
Published Online: 2010-09-17
Published in Print: 2010-April
© Freund Publishing House Ltd.
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- Growth hormone (GH) testing nutrition and metabolic balance, do we have the full picture?
- Primary Aldosteronism and its Impact on the Generation of Arterial Hypertension, Endothelial Injury and Oxidative Stress
- Metaphyseal Condrodysplasia, Schmid-type, a Differential Diagnosis with Rickets
- Adiposity, Physical Activity and Blood Lipid Profile in 13-year-old Adolescents
- Relationship between Metabolic Parameters and Thyroid Hormones and the Level of Gastric Peptides in Children with Autoimmune Thyroid Diseases
- Stimulated Growth Hormone Concentrations in Obese Pediatric Patients with Mild and Severe Insulin Resistance: A Pilot Study
- Amiodarone-induced Thyrotoxicosis in Children and Adolescents is a Possible Outcome in Patients with Low Iodine Intake
- Analysis of Serum Adiponectin, Resistin and Leptin Levels in Children and Adolescents with Autoimmune Thyroid Disorders
- Molecular Diagnosis of 46,XY DSD and Identification of a Novel 8 Nucleotide Deletion in Exon 1 of the SRD5A2 Gene
- 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?
- Body Fat Measurements in Elite Adolescent Volleyball Players: Correlation between Skinfold Thickness, Bioelectrical Impedance Analysis, Air-displacement Plethysmography, and Body Mass Index Percentiles
- Autonomic Bladder Dysfunction in an Adolescent with Type 1 Diabetes
- Autoimune Thyroiditis and Diabetes Mellitus Type 1 after Long-term Gonadotropin-releasing Hormone Agonist Treatment for Central Precocious Puberty: Evolution or Coincidence?
- Novel Growth Hormone Receptor Gene Mutation in a Patient with Laron Syndrome
- A Novel Missense Mutation in the AVPR2 Gene of a Japanese Infant with Nephrogenic Diabetes Insipidus
- Early Presentation of Familial Paraganglioma with SDHB Mutation in a 13 year old Child and its Mother
Artikel in diesem Heft
- Growth hormone (GH) testing nutrition and metabolic balance, do we have the full picture?
- Primary Aldosteronism and its Impact on the Generation of Arterial Hypertension, Endothelial Injury and Oxidative Stress
- Metaphyseal Condrodysplasia, Schmid-type, a Differential Diagnosis with Rickets
- Adiposity, Physical Activity and Blood Lipid Profile in 13-year-old Adolescents
- Relationship between Metabolic Parameters and Thyroid Hormones and the Level of Gastric Peptides in Children with Autoimmune Thyroid Diseases
- Stimulated Growth Hormone Concentrations in Obese Pediatric Patients with Mild and Severe Insulin Resistance: A Pilot Study
- Amiodarone-induced Thyrotoxicosis in Children and Adolescents is a Possible Outcome in Patients with Low Iodine Intake
- Analysis of Serum Adiponectin, Resistin and Leptin Levels in Children and Adolescents with Autoimmune Thyroid Disorders
- Molecular Diagnosis of 46,XY DSD and Identification of a Novel 8 Nucleotide Deletion in Exon 1 of the SRD5A2 Gene
- 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?
- Body Fat Measurements in Elite Adolescent Volleyball Players: Correlation between Skinfold Thickness, Bioelectrical Impedance Analysis, Air-displacement Plethysmography, and Body Mass Index Percentiles
- Autonomic Bladder Dysfunction in an Adolescent with Type 1 Diabetes
- Autoimune Thyroiditis and Diabetes Mellitus Type 1 after Long-term Gonadotropin-releasing Hormone Agonist Treatment for Central Precocious Puberty: Evolution or Coincidence?
- Novel Growth Hormone Receptor Gene Mutation in a Patient with Laron Syndrome
- A Novel Missense Mutation in the AVPR2 Gene of a Japanese Infant with Nephrogenic Diabetes Insipidus
- Early Presentation of Familial Paraganglioma with SDHB Mutation in a 13 year old Child and its Mother