Congenital hypopituitarism: how to select the patients for genetic analyses
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
http://link.springer.com/content/pdf/10.1186/s13052-018-0484-y.pdf
Reference17 articles.
1. Murray PG, Dattani MT, Clayton PE. Controversies in the diagnosis and management of growth hormone deficiency in childhood and adolescence. Arch Dis Child. 2016;101:96–100.
2. Giordano M. Genetic causes of isolated and combined pituitary hormone deficiency. Best Pract Res Clin Endocrinol Metab. 2016;30:679–91.
3. De Rienzo F, Mellone S, Bellone S, Babu D, Fusco I, Prodam F, et al. Frequency of genetic defects in combined pituitary hormone deficiency: a systematic review and analysis of a multicenter Italian cohort. Clin Endocrinol. 2015;83:849–60.
4. Scommegna S, Galeazzi D, Picone S, Farinelli E, Agostino R, Bozzao A, et al. Neonatal identification of pituitary aplasia: a life-saving diagnosis. Review of five cases. Horm Res. 2004;62:10–6.
5. Arrigo T, Wasniewska M, De Luca F, Valenzise M, Lombardo F, Vivenza D, et al. Congenital adenohypophysis aplasia: clinical features and analysis of the transcriptional factors for embryonic pituitary development. J Endocrinol Investig. 2006;29:208–13.
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1. Management of Neonatal Isolated and Combined Growth Hormone Deficiency: Current Status;International Journal of Molecular Sciences;2023-06-14
2. Delayed Diagnosis of Congenital Combined Pituitary Hormone Deficiency including Severe Growth Hormone Deficiency in Children with Persistent Neonatal Hypoglycemia—Case Reports and Review;International Journal of Molecular Sciences;2022-09-21
3. The Genetic Backdrop of Hypogonadotropic Hypogonadism;International Journal of Molecular Sciences;2021-12-08
4. Congenital Hypopituitarism During the Neonatal Period: Epidemiology, Pathogenesis, Therapeutic Options, and Outcome;Frontiers in Pediatrics;2021-02-02
5. Homozygous HESX1 and COL1A1 Gene Variants in a Boy with Growth Hormone Deficiency and Early Onset Osteoporosis;International Journal of Molecular Sciences;2021-01-13
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