AKKW - Satoh,A.; Goto,H.; Satoh,H.; Tomita,I.; Seto,M.; Furukawa,H.; Tsujihata,M. - A case of Creutzfeldt-Jakob disease with a point mutation at codon 232: correlation of MRI and neurologic findings. - Neurology 1997 Nov; 49(5): 1469-70
AYIF - Satoh,K.; Shirabe,S.; Tsujino,A.; Eguchi,H.; Motomura,M.; Honda,H.; Tomita,I.; Satoh,A.; Tsujihata,M.; Matsuo,H.; Nakagawa,M.; Eguchi,K. - Total tau protein in cerebrospinal fluid and diffusion-weighted MRI as an early diagnostic marker for Creutzfeldt-Jakob disease - Dementia and Geriatric Cognitive Disorders 2007; 24(3): 207-12
AXDH - Satoh,K.; Shirabe,S.; Eguchi,H.; Tsujino,A.; Motomura,M.; Satoh,A.; Tsujihata,M.; Eguchi,K. - Chronological changes in MRI and CSF biochemical markers in Creutzfeldt-Jakob disease patients - Dementia and Geriatric Cognitive Disorders 2007; 23(6): 272-81
AUWG - Satoh,K.; Shirabe,S.; Eguchi,H.; Tsujino,A.; Eguchi,K.; Satoh,A.; Tsujihata,M.; Niwa,M.; Katamine,S.; Kurihara,S.; Matsuo,H. - 14-3-3 protein, total tau and phosphorylated tau in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease and neurodegenerative disease in Japan - Cellular and Molecular Neurobiology 2006 Feb; 26(1): 45-52
AOYT - Satoh,K.; Shirabe,S.; Tsujino,A.; Nishiura,Y.; Eguchi,K.; Satoh,A.; Tsujihata,M.; Matsuo,H. - Role of phospholylated tau/total tau ratio, 14-3-3 protein in CSF and diffusion weighted MRI in diagnosis of Creutzfeldt-Jakob disease - International Conference - Prion diseases: from basic research to intervention concepts - TSE-Forum, 08.10.-10.10.2003, Gasteig, München - Poster session - DG-07
AQWP - Tomita,I.; Sato,K.; Shirabe,S.; Nagasato,K.; Satoh,A.; Tsujihata,M. - [Serial diffusion-weighted MRI (DWI) in a patient with sporadic Creuztfeldt-Jakob disease] - Rinsho Shinkeigaku. Clinical Neurology 2004 Mar; 44(3): 182-6
AKKW - Satoh,A.; Goto,H.; Satoh,H.; Tomita,I.; Seto,M.; Furukawa,H.; Tsujihata,M. - A case of Creutzfeldt-Jakob disease with a point mutation at codon 232: correlation of MRI and neurologic findings. - Neurology 1997 Nov; 49(5): 1469-70
ASHB - Kuroda,Y.; Tokumoto,H.; Kishikawa,H.; Yukitake,M.; Kurohara,K.; Satoh,J.; Matsui,M. - Codon-102 (p-l) mutation of prion protein (PrP) gene results in CJD-like syndrome - Neurology 1997; 48(3): 6092
ATEC - Satoh,J.; Onoue,H.; Arima,K.; Yamamura,T. - The 14-3-3 protein forms a molecular complex with heat shock protein Hsp60 and cellular prion protein - Journal of Neuropathology and Experimental Neurology 2005 Oct; 64(10): 858-68
ARSY - Satoh,J.; Yamamura,T. - Gene expression profile following stable expression of the cellular prion protein - Cellular and Molecular Neurobiology 2004 Dec; 24(6): 793-814
ANZG - Satoh,J.; Yukitake,M.; Kurohara,K.; Takashima,H.; Kuroda,Y. - Detection of the 14-3-3 protein in the cerebrospinal fluid of Japanese multiple sclerosis patients presenting with severe myelitis - Journal of the Neurological Sciences 2003 Aug 15; 212(1-2): 11-20
AKKX - Satoh,J.; Kuroda,Y. - Differing effects of IFN beta vs IFN gamma in MS: gene expression in cultured astrocytes. - Neurology 2001 Aug 28; 57(4): 681-5
AKKY - Satoh,J.; Kuroda,Y.; Katamine,S. - Gene expression profile in prion protein-deficient fibroblasts in culture - American Journal of Pathology 2000 Jul; 157(1): 59-68
AKKZ - Satoh,J.; Kurohara,K.; Yukitake,M.; Kuroda,Y. - The 14-3-3 protein detectable in the cerebrospinal fluid of patients with prion-unrelated neurological diseases is expressed constitutively in neurons and glial cells in culture - European Neurology 1999; 41(4): 216-25
AKLA - Satoh,J.; Yukitake,M.; Kurohara,K.; Nishida,N.; Katamine,S.; Miyamoto,T.; Kuroda,Y. - Cultured skin fibroblasts isolated from mice devoid of the prion protein gene express major heat shock proteins in response to heat stress - Experimental Neurology 1998 May; 151(1): 105-15
AKLB - Satoh,J.; Kurohara,K.; Yukitake,M.; Kuroda,Y. - Constitutive and cytokine-inducible expression of prion protein gene in human neural cell lines - Journal of Neuropathology and Experimental Neurology 1998 Feb; 57(2): 131-9
APNG - Yukitake,M.; Satoh,J.; Katamine,S.; Kuroda,Y. - EAAT4 mRNA expression is preserved in the cerebellum of prion protein-deficient mice - Neuroscience Letters 2003 Dec 11; 352(3): 171-4
AYDQ - Satoh,K.; Shirabe,S.; Eguchi,K. - [Clinical typing and diagnosis of sporadic human prion diseases (classic sproadic CJD, MM2-cortical form CJD, MM2-thalamic form CJD)] - Nippon Rinsho. Japanese Journal of Clinical Medicine 2007 Aug; 65(8): 1423-32
AYIF - Satoh,K.; Shirabe,S.; Tsujino,A.; Eguchi,H.; Motomura,M.; Honda,H.; Tomita,I.; Satoh,A.; Tsujihata,M.; Matsuo,H.; Nakagawa,M.; Eguchi,K. - Total tau protein in cerebrospinal fluid and diffusion-weighted MRI as an early diagnostic marker for Creutzfeldt-Jakob disease - Dementia and Geriatric Cognitive Disorders 2007; 24(3): 207-12
AXDH - Satoh,K.; Shirabe,S.; Eguchi,H.; Tsujino,A.; Motomura,M.; Satoh,A.; Tsujihata,M.; Eguchi,K. - Chronological changes in MRI and CSF biochemical markers in Creutzfeldt-Jakob disease patients - Dementia and Geriatric Cognitive Disorders 2007; 23(6): 272-81
AUWG - Satoh,K.; Shirabe,S.; Eguchi,H.; Tsujino,A.; Eguchi,K.; Satoh,A.; Tsujihata,M.; Niwa,M.; Katamine,S.; Kurihara,S.; Matsuo,H. - 14-3-3 protein, total tau and phosphorylated tau in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease and neurodegenerative disease in Japan - Cellular and Molecular Neurobiology 2006 Feb; 26(1): 45-52
ARSZ - Satoh,K.; Shirabe,S.; Eguchi,K.; Yamauchi,A.; Kataoka,Y.; Niwa,M.; Nishida,N.; Katamine,S. - Toxicity of quinacrine can be reduced by co-administration of P-glycoprotein inhibitor in sporadic Creutzfeldt-Jakob disease - Cellular and Molecular Neurobiology 2004 Dec; 24(6): 873-5
AQON - Satoh,K.; Shirabe,S.; Katamine,S.; Muramoto,T.; Kitamoto,T. - [Iatrogenic Creutzfeldt-Jakob disease] - Nippon Rinsho. Japanese Journal of Clinical Medicine 2004 Jan; 62 Suppl: 248-51
AOPG - Satoh,K.; Muramoto,T.; Tanaka,T.; Kitamoto,N.; Ironside,J.W.; Nagashima,K.; Yamada,M.; Sato,T.; Mohri,S.; Kitamoto,T. - Association of an 11-12 kDa protease-resistant prion protein fragment with subtypes of dura graft-associated Creutzfeldt-Jakob disease and other prion diseases - Journal of General Virology 2003 Oct; 84(10): 2885-93
AOYT - Satoh,K.; Shirabe,S.; Tsujino,A.; Nishiura,Y.; Eguchi,K.; Satoh,A.; Tsujihata,M.; Matsuo,H. - Role of phospholylated tau/total tau ratio, 14-3-3 protein in CSF and diffusion weighted MRI in diagnosis of Creutzfeldt-Jakob disease - International Conference - Prion diseases: from basic research to intervention concepts - TSE-Forum, 08.10.-10.10.2003, Gasteig, München - Poster session - DG-07
ARTR - Tanaka,T.; Kinoshita,I.; Saitoh,Y.; Satoh,K.; Nishiura,Y.; Shirabe,S.; Kitamoto,T. - [A case of Creutzfeldt-Jakob disease with a point mutation of prion protein at codon 180] - No to Shinkei. Brain and Nerve 2004 Dec; 56(12): 1025-8
ARQX - Kobayashi,A.; Satoh,S.; Ironside,J.W.; Mohri,S.; Kitamoto,T. - Type 1 and type 2 human PrPsc have different aggregation sizes in methionine homozygotes with sporadic, iatrogenic and variant Creutzfeldt-Jakob disease - Journal of General Virology 2005 Jan; 86(1): 237-40
ALLA - Tateishi,J.; Kitamoto,T.; Mohri,S.; Satoh,S.; Sato,T.; Shepherd,A.; Macnaughton,M.R. - Scrapie removal using Planova virus removal filters - Biologicals 2001 Mar; 29(1): 17-25
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
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