Found: 10
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Genetic Predictors of Long-Term Response to Growth Hormone (GH) Therapy in Children With GH Deficiency and Turner Syndrome: The Influence of a SOCS2 Polymorphism.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
Novel Heterozygous Nonsense GLI2 Mutations in Patients with Hypopituitarism and Ectopic Posterior Pituitary Lobe without Holoprosencephaly.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2010, v. 95, n. 11, p. E384, doi. 10.1210/jc.2010-1050
- By:
- Publication type:
- Article
Screening of targeted panel genes in Brazilian patients with primary ovarian insufficiency.
- Published in:
- PLoS ONE, 2020, v. 15, n. 10, p. 1, doi. 10.1371/journal.pone.0240795
- By:
- Publication type:
- Article
A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reduced GH1 expression in siblings with isolated GH deficiency (IGHD).
- Published in:
- European Journal of Endocrinology, 2016, v. 175, n. 2, p. K7, doi. 10.1530/EJE-15-0149
- By:
- Publication type:
- Article
Study of the association between 3111T/C polymorphism of the CLOCK gene and the presence of overweight in schoolchildren.
- Published in:
- Jornal de Pediatria, 2014, v. 90, n. 5, p. 500, doi. 10.1016/j.jped.2014.01.011
- By:
- Publication type:
- Article
The Sitting Height/Height Ratio for Age in Healthy and Short Individuals and Its Potential Role in Selecting Short Children for SHOX Analysis.
- Published in:
- Hormone Research in Paediatrics, 2014, v. 80, n. 6, p. 449, doi. 10.1159/000355411
- By:
- Publication type:
- Article
Uremic leontiasis ossea.
- Published in:
- Endocrine (1355008X), 2019, v. 65, n. 3, p. 707, doi. 10.1007/s12020-019-01976-z
- By:
- Publication type:
- Article
Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations.
- Published in:
- Clinical Endocrinology, 2017, v. 87, n. 6, p. 725, doi. 10.1111/cen.13430
- By:
- Publication type:
- Article
Relatively high frequency of non-synonymous GLI2 variants in patients with congenital hypopituitarism without holoprosencephaly.
- Published in:
- Clinical Endocrinology, 2013, v. 78, n. 4, p. 551, doi. 10.1111/cen.12044
- By:
- Publication type:
- Article
Exon 3-deleted genotype of growth hormone receptor ( GHRd3) positively influences IGF-1 increase at generation test in children with idiopathic short stature.
- Published in:
- Clinical Endocrinology, 2007, v. 67, n. 4, p. 500, doi. 10.1111/j.1365-2265.2007.02915.x
- By:
- Publication type:
- Article