Transitions in Care of the Adolescent with Pituitary Dysfunction
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Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-030-99918-6_5
Reference55 articles.
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3. Castinetti F, Reynaud R, Saveanu A, Quentien M-H, Albarel F, Barlier A, Enjalbert A, Brue T. Clinical and genetic aspects of combined pituitary hormone deficiencies. Ann Endocrinol (Paris). 2008;69:7–17.
4. Kurtoğlu S, Özdemir A, Hatipoğlu N. Neonatal hypopituitarism: approaches to diagnosis and treatment. J Clin Res Pediatr Endocrinol. 2019;11:4–12.
5. Heather NL, Jefferies C, Hofman PL, Derraik JGB, Brennan C, Kelly P, Hamill JKM, Jones RG, Rowe DL, Cutfield WS. Permanent hypopituitarism is rare after structural traumatic brain injury in early childhood. J Clin Endocrinol Metab. 2012;97:599–604.
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