Therapy-Induced Growth and Sexual Maturation in a Developmentally Infantile Adult Patient with a PROP1 Mutation
Author:
Publisher
Frontiers Media SA
Subject
Endocrinology, Diabetes and Metabolism
Reference27 articles.
1. Mutations in PROP1 cause familial combined pituitary hormone deficiency;Wu;Nat Genet,1998
2. Frequency of genetic defects in combined pituitary hormone deficiency: a systematic review and analysis of a multicentre Italian cohort;De Rienzo;Clin Endocrinol (Oxf),2015
3. Molecular analysis of Brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations;Madeira;Clin Endocrinol (Oxf),2017
4. Regulation of pituitary stem cells by epithelial to mesenchymal transition events and signaling pathways;Cheung;Mol Cell Endocrinol,2017
5. Auxological and endocrine phenotype in a population-based cohort of patients with PROP1 gene defects;Lebl;Eur J Endocrinol,2005
Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. A Large PROP1 Gene Deletion in a Turkish Pedigree;Case Reports in Endocrinology;2018
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