@article{3088137,
    title = "Familial pituitary apoplexy as the only presentation of a novel AIP mutation",
    author = "Xekouki, P. and Mastroyiannis, S.A. and Avgeropoulos, D. and De La Luz Sierra, M. and Trivellin, G. and Gourgari, E.A. and Lyssikatos, C. and Quezado, M. and Patronas, N. and Kanaka-Gantenbein, C. and Chrousos, G.P. and Stratakis, C.A.",
    journal = "Endocrine-Related Cancer",
    year = "2013",
    volume = "20",
    number = "5",
    pages = "L11-L14",
    issn = "1351-0088, 1479-6821",
    doi = "10.1530/ERC-13-0218",
    keywords = "aryl hydrocarbon receptor interacting protein;  carrier proteins and binding proteins;  growth hormone;  hydrocortisone;  keratin;  levothyroxine;  reticulin;  unclassified drug, adult;  case report;  child;  DNA flanking region;  empty sella syndrome;  gene mutation;  genetic analysis;  gigantism;  growth hormone secreting adenoma;  hormone substitution;  human;  hypophysis adenoma;  hypophysis apoplexy;  hypopituitarism;  letter;  libido disorder;  male;  nuclear magnetic resonance imaging;  oral glucose tolerance test;  physical disease by body function;  preschool child;  school child;  stop codon;  tall stature"
}