TY - JOUR
TI - Familial pituitary apoplexy as the only presentation of a novel AIP mutation
AU - Xekouki, P.
AU - Mastroyiannis, S.A.
AU - Avgeropoulos, D.
AU - De La Luz Sierra, M.
AU - Trivellin, G.
AU - Gourgari, E.A.
AU - Lyssikatos, C.
AU - Quezado, M.
AU - Patronas, N.
AU - Kanaka-Gantenbein, C.
AU - Chrousos, G.P.
AU - Stratakis, C.A.
JO - Endocrine-Related Cancer
PY - 2013
VL - 20
TODO - 5
SP - L11-L14
PB - 
SN - 1351-0088, 1479-6821
TODO - 10.1530/ERC-13-0218
TODO - 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
TODO - null
ER -