Croxson M, Brown P, Synek B, Harrington M G, Frith R, Clover G, Wilson J, Gajdusek D C
Auckland Hospital, New Zealand.
Neurology. 1988 Jul;38(7):1128-30. doi: 10.1212/wnl.38.7.1128.
A clinically atypical, neuropathologically verified case of Creutzfeldt-Jakob disease is described in a 32-year-old New Zealand woman with idiopathic hypopituitarism who had been treated in late adolescence (1970 to 1973) with human growth hormone processed from pooled cadaveric pituitary glands.
