Inherited adrenal hypoplasia: not just for kids!
- 16 March 2004
- journal article
- review article
- Published by Wiley in Clinical Endocrinology
- Vol. 60 (5) , 529-537
- https://doi.org/10.1111/j.1365-2265.2004.01988.x
Abstract
No abstract availableKeywords
This publication has 65 references indexed in Scilit:
- Pituitary Development: Regulatory Codes in Mammalian OrganogenesisScience, 2002
- Dehydroepiandrosterone replacement for patients with adrenal insufficiencyThe Lancet, 2001
- Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasiaHuman Molecular Genetics, 2001
- Congenital Adrenal Hyperplasia due to 21-Hydroxylase DeficiencyEndocrine Reviews, 2000
- Functional Characterization of Naturally Occurring Mutations of the Human Adrenocorticotropin Receptor: Poor Correlation of Phenotype and GenotypeJournal of Clinical Endocrinology & Metabolism, 1999
- "Hot Spot" in the PROP1 Gene Responsible for Combined Pituitary Hormone DeficiencyJournal of Clinical Endocrinology & Metabolism, 1999
- Longitudinal Hormonal and Pituitary Imaging Changes in Two Females with Combined Pituitary Hormone Deficiency due to Deletion of A301,G302 in the PROP1 GeneJournal of Clinical Endocrinology & Metabolism, 1999
- Adrenocorticotropin Insensitivity SyndromesEndocrine Reviews, 1998
- Mutations in PROP1 cause familial combined pituitary hormone deficiencyNature Genetics, 1998
- Obesity and impaired prohormone processing associated with mutations in the human prohormone convertase 1 geneNature Genetics, 1997