AMUU - Yamazaki,M.; Oyanagi,K.; Mori,O.; Kitamura,S.; Ohyama,M.; Terashi,A.; Kitamoto,T.; Katayama,Y. - Variant Gerstmann-Sträussler syndrome with the P105L prion gene mutation: an unusual case with nigral degeneration and widespread neurofibrillary tangles. - Acta Neuropathologica 1999 Nov; 98(5): 506-11
ASFZ - Yamazaki,M.; Oyanagi,K.; Mori,O.; Kitamura,S.; Ohyama,M.; Terashi,A. - An autopsy case of variant Gerstmann-Sträussler-syndrome with codon-105 mutation of the prion protein gene, showing degeneration of the pallidum, thalamus and substantia-nigra, and widely distributed neurofibrillary tangles - Brain Pathology 1997; 7(N4): 1113
AFTW - Ikuta,F.; Kumanishi,T.; Oyanagi,S.; Koizumi,T.; Yamamura,Y. - [Pathological investigation of neuro-Behcet's disease] - Shinkei Kenkyu No Shimpo. Recent Advance in Neurological Sciences 1972 Feb; 16(1): 179-85
AJDE - Oyanagi,S. - [Central nervous system diseases as human slow virus infections] - Nippon Rinsho. Japanese Journal of Clinical Medicine 1977 Sep 10; 35(9): 2799-804