Works matching IS 16632818 AND DT 2015 AND VI 84 AND IP 3
Results: 11
Front & Back Matter.
- Published in:
- Hormone Research in Paediatrics, 2015, v. 84, n. 3, p. X, doi. 10.1159/000441209
- Publication type:
- Article
Von Hippel-Lindau Syndrome.
- Published in:
- Hormone Research in Paediatrics, 2015, v. 84, n. 3, p. 145, doi. 10.1159/000431323
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- Publication type:
- Article
Novel Mutations in HESX1 and PROP1 Genes in Combined Pituitary Hormone Deficiency.
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- Hormone Research in Paediatrics, 2015, v. 84, n. 3, p. 153, doi. 10.1159/000433468
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- Publication type:
- Article
Early Discrimination between Transient and Permanent Congenital Hypothyroidism in Children with Eutopic Gland.
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- Hormone Research in Paediatrics, 2015, v. 84, n. 3, p. 159, doi. 10.1159/000435811
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- Publication type:
- Article
Health-Related Quality of Life in Children with Congenital Adrenal Hyperplasia.
- Published in:
- Hormone Research in Paediatrics, 2015, v. 84, n. 3, p. 165, doi. 10.1159/000435855
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- Publication type:
- Article
Description of the SAGhE Cohort: A Large European Study of Mortality and Cancer Incidence Risks after Childhood Treatment with Recombinant Growth Hormone.
- Published in:
- Hormone Research in Paediatrics, 2015, v. 84, n. 3, p. 172, doi. 10.1159/000435856
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- Publication type:
- Article
Tamoxifen Improves Final Height Prediction in Girls with McCune-Albright Syndrome: A Long Follow-Up.
- Published in:
- Hormone Research in Paediatrics, 2015, v. 84, n. 3, p. 184, doi. 10.1159/000435881
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- Publication type:
- Article
Hyperthyroidism in 276 Children and Adolescents with Type 1 Diabetes from Germany and Austria.
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- Hormone Research in Paediatrics, 2015, v. 84, n. 3, p. 190, doi. 10.1159/000436964
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- Publication type:
- Article
Risk for Nonalcoholic Fatty Liver Disease in Young Adults Born Preterm.
- Published in:
- Hormone Research in Paediatrics, 2015, v. 84, n. 3, p. 199, doi. 10.1159/000437054
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- Publication type:
- Article
Variable Phenotype of Diabetes Mellitus in Siblings with a Homozygous PTF1A Enhancer Mutation.
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- Hormone Research in Paediatrics, 2015, v. 84, n. 3, p. 206, doi. 10.1159/000435782
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- Publication type:
- Article
Loss-of-Function SOX10 Mutation in a Patient with Kallmann Syndrome, Hearing Loss, and Iris Hypopigmentation.
- Published in:
- Hormone Research in Paediatrics, 2015, v. 84, n. 3, p. 212, doi. 10.1159/000436965
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- Publication type:
- Article