[
Argyropoulou MI, Kiortsis DN. MRI of the hypothalamic-pituitary axis in children. Pediatr Radiol 35, 1045–1055, 2005.
]Search in Google Scholar
[
Cacciari E, Zucchini S, Carla G, Pirazzoli P, Cicognani A, Mandini M, Busacca M, Trevisan C. Endocrine function and morphological findings in patients with disorders of the hypothalamo-pituitary area: a study with magnetic resonance. Arch Dis Child 65, 1199–1202, 1990.
]Search in Google Scholar
[
Cacciari E, Zucchini S, Ambrosetto P, Tani G, Carla G, Cicognani A, Pirazzoli P, Sganga T, Balsamo A, Cassio A, et al. Empty sella in children and adolescents with possible hypothalamic-pituitary disorders. J Clin Endocrinol Metab 78, 767–771, 1994.
]Search in Google Scholar
[
Dugeroglu H, Karakas A. Multifaceted evaluation of 72 patients with pituitary failure. Acta Endocrinol 14, 539–548, 2018.
]Search in Google Scholar
[
Famini P, Maya MM, Melmed S. Pituitary magnetic resonance imaging for sellar and parasellar masses: ten-year experience in 2598 patients. J Clin Endocrinol Metab 96, 1633–1641, 2011.
]Search in Google Scholar
[
Fraietta R, Zylberstejn DS, Esteves SC. Hypogonadotropic hypogonadism revisited. Clinics 68, 81–88, 2013.
]Search in Google Scholar
[
Freda PU, Beckers AM, Katznelson L, Molitch ME, Montori VM, Post KD, et al. Endocrine society. Pituitary incidentaloma: an endocrine society clinical practice guideline. J Clin Endocrinol Metab 96, 894–904, 2011.
]Search in Google Scholar
[
Hirsch D, Benbassat C, Toledano Y, S’chigol I, Tsvetov G, Shraga-Slutzky I, Ilan YE Shimon. Pituitary imaging findings in male patients with hypogonadotrophic hypogonadism. Pituitary 18, 494–499, 2015.
]Search in Google Scholar
[
Laitinen EM, Vaaralahti K, Tommiska J, Eklund E, Tervaniemi M Valanne L, Raivio T. Incidence, phenotypic features and molecular genetics of Kallmann syndrome in Finland. Orphanet J Rare Dis 6, 41, 2011.
]Search in Google Scholar
[
Molitch ME. Nonfunctioning pituitary tumors and pituitary incidentalomas. Endocrinol Metab Clin North Am 37, 151–171, 2008.
]Search in Google Scholar
[
Nammour GM, Ybarra J, Naheedy MH, Romeo JH, Aron DC. Incidental pituitary macroadenoma: a population-based study. Am J Med Sci 314, 287–291, 1997.
]Search in Google Scholar
[
Shin SJ, Sul Y, Kim JH, Cho JH, Kim GH, Kim JH, Choi JH, Yoo HW. Clinical, endocrinological, and molecular characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: a single center experience. Ann Pediatr Endocrinol Metab 20, 27–33, 2015.
]Search in Google Scholar
[
Takanashi J, Suzuki H, Nagasawa K, Kobayashi K, Saeki N, Kohno Y. Empty sella in children as a key for diagnosis. Brain Dev 23, 422–423, 2001.
]Search in Google Scholar
[
Wang Y, Gong C, Qin M, Liu Y, Tian Y. Clinical and genetic features of 64 young male paediatric patients with congenital hypogonadotropic hypogonadism. Clin Endocrinol 87, 757–766, 2017.
]Search in Google Scholar
[
Young J, Xu C, Papadakis GE, Acierno JS, Maione L, Hietamaki J, Raivio T, Pitteloud N. Clinical management of congenital hypogonadotropic hypogonadism. Endocr Rev 40, 669–710, 2019.
]Search in Google Scholar
