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Fertility and Sterility, ISSN 0015-0282, 2011, Volume 95, Issue 7, pp. 2324 - 2329.e3
Journal Article
Endocrinology and Metabolism Clinics of North America, ISSN 0889-8529, 03/2015, Volume 44, Issue 1, pp. 199 - 209
Pituitary apoplexy (PA) is a rare clinical syndrome caused by sudden hemorrhaging and/or infarction of the pituitary gland, generally within a pituitary... 
Pituitary apoplexy | Corticotropic deficiency | Magnetic resonance imaging | Pituitary adenoma | Emergency | Neurosurgery | Hemorrhage | Necrosis | SURGERY | MRI | CLINICAL-FEATURES | TUMOR APOPLEXY | ENDOCRINOLOGY & METABOLISM | PRECIPITATING FACTORS | CONSERVATIVE MANAGEMENT | OUTCOMES | ADENOMAS | Pituitary Apoplexy - therapy | Pituitary Apoplexy - diagnosis | Humans
Journal Article
Bulletin du Cancer, ISSN 0007-4551, 07/2015, Volume 102, Issue 7-8, pp. 612 - 621
Endocrine sequelae are among the most frequently reported complications in childhood cancer survivors, affecting 40 to 60% of these patients during adult life.... 
Endocrine sequelae | Long-term follow-up | Growth hormone therapy | Growth hormone deficiency | Radiotherapy | Childhood cancer
Journal Article
Annales d'endocrinologie, 06/2016, Volume 77, Issue 2, p. 135
Journal Article
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 09/2019
BACKGROUNDNon-classic 21-hydroxylase deficiency is usually diagnosed in post-pubertal women because of androgen excess. Indication of systematic steroid... 
Journal Article
Journal Article
Journal Article