Found: 8
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Evolution of gonadotropin deficiency in a patient with type II autosomal dominant GH deficiency.
- Published in:
- European Journal of Endocrinology, 2006, v. 155, n. 6, p. 793, doi. 10.1530/eje.1.02293
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- Publication type:
- Article
Expanding the Spectrum of Mutations in GH1 and GHRHR: Genetic Screening in a Large Cohort of Patients with Congenital Isolated Growth Hormone Deficiency.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2009, v. 94, n. 9, p. 3191, doi. 10.1210/jc.2008-2783
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- Publication type:
- Article
HESX1 mutations are an uncommon cause of septooptic dysplasia and hypopituitarism.
- Published in:
- 2007
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- Publication type:
- journal article
Novel Mutations within the POU1F1 Gene Associated with Variable Combined Pituitary Hormone Deficiency.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 8, p. 4762, doi. 10.1210/jc.2005-0570
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- Publication type:
- Article
Novel Mutations within the POU1F1 Gene Associated with Variable Combined Pituitary Hormone Deficiency.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 6, p. 4762, doi. 10.1210/jc.2005-0570
- By:
- Publication type:
- Article
Congenital hypopituitarism: clinical, molecular and neuroradiological correlates.
- Published in:
- Clinical Endocrinology, 2009, v. 71, n. 3, p. 376, doi. 10.1111/j.1365-2265.2009.03572.x
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- Publication type:
- Article
The role of growth hormone in determining birth size and early postnatal growth, using congenital growth hormone deficiency (GHD) as a model.
- Published in:
- Clinical Endocrinology, 2005, v. 63, n. 2, p. 223, doi. 10.1111/j.1365-2265.2005.02330.x
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- Publication type:
- Article
Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD).
- Published in:
- Clinical Endocrinology, 2005, v. 63, n. 1, p. 10, doi. 10.1111/j.1365-2265.2005.02291.x
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- Publication type:
- Article