Works matching IS 16632818 AND DT 2011 AND VI 76 AND IP 3
Results: 13
Primary Generalized Glucocorticoid Resistance and Hypersensitivity.
- Published in:
- Hormone Research in Paediatrics, 2011, v. 76, n. 3, p. 145, doi. 10.1159/000330759
- By:
- Publication type:
- Article
The Predictive Value of the Individual Components of the Metabolic Syndrome for Insulin Resistance in Obese Children.
- Published in:
- Hormone Research in Paediatrics, 2011, v. 76, n. 3, p. 156, doi. 10.1159/000327371
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- Publication type:
- Article
Auxological Evaluation in Patients with a 22q11.2 Microdeletion Syndrome: Normal Prevalence of Obesity and Neonatal Length and Gender Influence on Body Mass Index Evolution.
- Published in:
- Hormone Research in Paediatrics, 2011, v. 76, n. 3, p. 172, doi. 10.1159/000328454
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- Publication type:
- Article
Familial Glucocorticoid Deficiency in Five Arab Kindreds with Homozygous Point Mutations of the ACTH Receptor (MC2R): Genotype and Phenotype Correlations.
- Published in:
- Hormone Research in Paediatrics, 2011, v. 76, n. 3, p. 165, doi. 10.1159/000328035
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- Publication type:
- Article
Clinical and Radiological Characteristics of 22 Children with SHOX Anomalies and Familial Short Stature Suggestive of Léri-Weill Dyschondrosteosis.
- Published in:
- Hormone Research in Paediatrics, 2011, v. 76, n. 3, p. 178, doi. 10.1159/000329359
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- Publication type:
- Article
Intra-Abdominal Fat in Children.
- Published in:
- 2011
- By:
- Publication type:
- Letter
Sonographically Assessed Intra-Abdominal Fat.
- Published in:
- 2011
- By:
- Publication type:
- Letter
Increased Risk of Coeliac Disease in Patients with Congenital Hypothyroidism.
- Published in:
- Hormone Research in Paediatrics, 2011, v. 76, n. 3, p. 186, doi. 10.1159/000328723
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- Publication type:
- Article
Molecular Karyotyping: From Microscope to SNP Arrays.
- Published in:
- Hormone Research in Paediatrics, 2011, v. 76, n. 3, p. 208, doi. 10.1159/000330406
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- Publication type:
- Article
Association of p.His38Leu, a Rare CYP21A2 Mutation, with the Classical Simple Virilizing Phenotype of 21-Hydroxylase Deficiency in a 6-Year-Old Boy.
- Published in:
- Hormone Research in Paediatrics, 2011, v. 76, n. 3, p. 214, doi. 10.1159/000327366
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- Publication type:
- Article
Erratum.
- Published in:
- 2011
- Publication type:
- Correction Notice
Normal Tempo of Bone Formation in Turner Syndrome despite Signs of Accelerated Bone Resorption.
- Published in:
- Hormone Research in Paediatrics, 2011, v. 76, n. 3, p. 193, doi. 10.1159/000329046
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- Publication type:
- Article
Resting Energy Expenditure and Metabolic Parameters in Small for Gestational Age Moderately Preterm Infants.
- Published in:
- Hormone Research in Paediatrics, 2011, v. 76, n. 3, p. 202, doi. 10.1159/000329049
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- Publication type:
- Article