[1]Vijayanand P, Mahadevan S, Shivbalan S, Reddy N, Ramdoss N. Pituitary stalk interruption syndrome (PSIS)[J]. Indian J Pediatr, 2007, 74(9): 874-875.
[2]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]. J Endocrinol Invest, 2006, 29(3): 208-213.
[4]Rottembourg D, Linglart A, Adamsbaum C, Lahlou N, Teinturier C, Bougnères P,et al. Gonadotrophic status in adolescents with pituitary stalk interruption syndrome[J]. Clin Endocrinol (Oxf), 2008, 69(1): 105-111.
[5]Chen S, Léger J, Garel C, Hassan M, Czernichow P. Growth hormone deficiency with ectopic neurohypophysis: anatomical variations and relationship between the visibility of the pituitary stalk asserted by magnetic resonance imaging and anterior pituitary function[J]. J Clin Endocrinol Metab, 1999, 84(7): 2408-2413.
[6]Binder G, Martin DD, Kanther I, Schwarze CP, Ranke MB. The course of neonatal cholestasis in congenital combined pituitary hormone deficiency[J]. J Pediatr Endocrinol Metab, 2007, 20(6): 695-702.
[7]Binder G, Weidenkeller M, Blumenstock G, Langkamp M, Weber K, Franz AR.Rational approach to the diagnosis of severe growth hormone deficiency in the newborn[J]. J Clin Endocrinol Metab, 2010, 95(5): 2219-2226.