AFWV - Iwabuchi,K.; Endoh,S.; Hagimoto,H.; Okamoto,K.; Miyakawa,T.; Yamaguchi,T.; Kajiwara,A.; Inoue,K.; Yamada,Y.; Amano,N.; et al. - [Three patients from two families with familial Creutzfeldt-Jakob disease having a point mutation in the prion protein gene at codon 200 (Glu -> Lys)] - No to Shinkei. Brain and Nerve 1994 Apr; 46(4): 349-54
AILM - Miyakawa,T.; Inoue,K.; Iseki,E.; Kawanishi,C.; Sugiyama,N.; Onishi,H.; Yamada,Y.; Suzuki,K.; Iwabuchi,K.; Kosaka,K. - Japanese Creutzfeldt-Jakob disease patients exhibiting high incidence of the E200K PRNP mutation and located in the basin of a river - Neurological Research 1998 Dec; 20(8): 684-8
AIZL - Oda,T.; Kitamoto,T.; Tateishi,J.; Mitsuhashi,T.; Iwabuchi,K.; Haga,C.; Oguni,E.; Kato,Y.; Tominaga,I.; Yanai,K.; Kashima,H.; Kogure,T.; Hori,K.; Ogino,K. - Prion disease with 144 base pair insertion in a Japanese family line - Acta Neuropathologica 1995; 90(1): 80-6
AMTW - Yagishita,S.; Iwabuchi,K.; Amano,N.; Yokoi,S. - Further observation of Japanese Creutzfeldt-Jakob disease with widespread amyloid plaques - Journal of Neurology. Zeitschrift für Neurologie 1989 Mar; 236(3): 145-8