AESI - Gomi,H.; Yokoyama,T.; Fujimoto,K.; Ikeda,T.; Katoh,A.; Itoh,T.; Itohara,S. - Mice devoid of the glial fibrillary acidic protein develop normally and are susceptible to scrapie prions - Neuron 1995 Jan; 14(1): 29-41
ATBH - Ono,K.; Kamihira,M.; Kuga,Y.; Matsumoto,H.; Hotta,A.; Itoh,T.; Nishijima,K.; Nakamura,N.; Matsuda,H.; Iijima,S. - Production of anti-prion scFv-Fc fusion proteins by recombinant animal cells - Journal of Bioscience and Bioengineering 2003; 95(3): 231-8
AAGN - Amano,N.; Yagishita,S.; Yokoi,S.; Itoh,Y.; Kinoshita,J.; Mizutani,T.; Matsuishi,T. - Gerstmann-Sträussler syndrome - a variant type: amyloid plaques and Alzheimer's neurofibrillary tangles in cerebral cortex. - Acta Neuropathologica 1992; 84(1): 15-23
AFUK - Inoue,M.; Yagishita,S.; Itoh,Y.; Koyano,S.; Amano,N.; Matsushita,M. - Eosinophilic bodies in the cerebral cortex of Alzheimer's disease cases - Acta Neuropathologica 1996 Dec; 92(6): 555-61
AFWQ - Itoh,Y.; Amano,T.; Shimizu,T.; Hashimoto,J.; Kubo,A.; Fukuuchi,Y. - Single-photon emission computed tomography image of benzodiazepine receptors in a patient with Creutzfeldt-Jakob disease - Internal Medicine 1998 Oct; 37(10): 896-900
AFWR - Itoh,Y.; Yamada,M.; Hayakawa,M.; Shozawa,T.; Tanaka,J.; Matsushita,M.; Kitamoto,T.; Tateishi,J.; Otomo,E. - A variant of Gerstmann-Sträussler-Scheinker disease carrying codon 105 mutation with codon 129 polymorphism of the prion protein gene: a clinicopathological study. - Journal of the Neurological Sciences 1994 Dec 1; 127(1): 77-86
AMUB - Yamada,M.; Itoh,Y.; Inaba,A.; Wada,Y.; Takashima,M.; Satoh,S.; Kamata,T.; Okeda,R.; Kayano,T.; Suematsu,N.; Kitamoto,T.; Otomo,E.; Matsushita,M.; Mizusawa,H. - An inherited prion disease with a PrP P105L mutation: clinicopathologic and PrP heterogeneity. - Neurology 1999 Jul 13; 53(1): 181-8
AMUC - Yamada,M.; Tomimitsu,H.; Yokota,T.; Tomi,H.; Sunohara,N.; Mukoyama,M.; Itoh,Y.; Suematsu,N.; Otomo,E.; Okeda,R.; Matsushita,M.; Mizusawa,H. - Involvement of the spinal posterior horn in Gerstmann-Sträussler-Scheinker disease (PrP P102L) - Neurology 1999 Jan 15; 52(2): 260-5
AMUD - Yamada,M.; Itoh,Y.; Suematsu,N.; Matsushita,M.; Otomo,E. - Panencephalopathic type of Creutzfeldt-Jakob disease associated with cadaveric dura mater graft - Journal of Neurology, Neurosurgery and Psychiatry 1997 Oct; 63(4): 524-7
ASFW - Yamada,M.; Itoh,Y.; Satoh,S.; Wada,Y.; Matsushita,M. - An inherited prion disease linked with a missense mutation at codon-105 in the prion protein gene - Annals of Neurology 1996; 40(N3): M 44-44
AMUE - Yamada,M.; Satoh,S.; Sodeyama,N.; Fujigasaki,H.; Kaneko,K.; Wada,Y.; Itoh,Y.; Matsushita,M. - Spastic paraparesis and mutations in the prion protein gene - Journal of the Neurological Sciences 1995 Dec; 134(1-2): 215-6
ASFX - Yamada,M.; Itoh,Y.; Fujigasaki,H.; Naruse,S.; Kaneko,K.; Otomo,E.; Miyatake,T. - A Deletion in the Prion Protein Gene in a Japanese Family - Biomedical Research 1994 Apr; 15(2): 131-133
AMUG - Yamada,M.; Itoh,Y.; Fujigasaki,H.; Naruse,S.; Kaneko,K.; Kitamoto,T.; Tateishi,J.; Otomo,E.; Hayakawa,M.; Tanaka,J.; et al. - A missense mutation at codon 105 with codon 129 polymorphism of the prion protein gene in a new variant of Gerstmann-Sträussler-Scheinker disease - Neurology 1993 Dec; 43(12): 2723-4