ANZS - Yamazaki,K.; Yamada,E.; Kanaji,Y.; Yanagisawa,T.; Kato,Y.; Sato,K.; Takano,K.; Sakasegawa,Y.; Kaneko,K. - Stimulation of cellular prion protein expression by TSH in human thyrocytes - Biochemical and Biophysical Research Communications 2003 Jun 13; 305(4): 1034-9
ARQO - Kamatari,Y.O.; Kitahara,R.; Yamada,H.; Yokoyama,S.; Akasaka,K. - High-pressure NMR spectroscopy for characterizing folding intermediates and denatured states of proteins - Methods (San Diego, Calif.) 2004 Sep; 34(1): 133-43
AGXW - Kuwata,K.; Li,H.; Yamada,H.; Legname,G.; Prusiner,S.B.; Akasaka,K.; James,T.L. - Locally disordered conformer of the hamster prion protein: a crucial intermediate to PrPsc? - Biochemistry 2002 Oct 15; 41(41): 12277-83
AGXA - Kuramoto,T.; Mori,M.; Yamada,J.; Serikawa,T. - Tremor and zitter, causative mutant genes for epilepsy with spongiform encephalopathy in spontaneously epileptic rat (SER), are tightly linked to synaptobrevin-2 and prion protein genes, respectively - Biochemical and Biophysical Research Communications 1994 Apr 29; 200(2): 1161-8
ARPU - Hachiya,N.S.; Yamada,M.; Watanabe,K.; Jozuka,A.; Ohkubo,T.; Sano,K.; Takeuchi,Y.; Kozuka,Y.; Sakasegawa,Y.; Kaneko,K. - Mitochondrial localization of cellular prion protein (PrPc) invokes neuronal apoptosis in aged transgenic mice overexpressing PrPc - Neuroscience Letters 2005 Feb 10; 374(2): 98-103
AQKC - Hachiya,N.S.; Watanabe,K.; Yamada,M.; Sakasegawa,Y.; Kaneko,K. - Anterograde and retrograde intracellular trafficking of fluorescent cellular prion protein - Biochemical and Biophysical Research Communications 2004 Mar 19; 315(4): 802-7
AXNW - Hamaguchi,T.; Noguchi-Shinohara,M.; Nakamura,Y.; Sato,T.; Kitamoto,T.; Mizusawa,H.; Yamada,M. - Ophthalmic Surgery in Prion Diseases - International Conference - Prion 2007 (26.-28.9.2007) Edinburgh International Conference Centre, Edinburgh, Scotland, UK - Book of Abstracts: Epidemiology, Risk Assessment and Transmission P04.15
AWTQ - Hamaguchi,T.; Noguchi-Shinohara,M.; Nakamura,Y.; Sato,T.; Kitamoto,T.; Mizusawa,H.; Yamada,M. - Ophthalmic surgery in prion diseases - Emerging Infectious Diseases 2007 Jan; 13(1): 162-4
ASZT - Hamaguchi,T.; Kitamoto,T.; Sato,T.; Mizusawa,H.; Nakamura,Y.; Noguchi,M.; Furukawa,Y.; Ishida,C.; Kuji,I.; Mitani,K.; Murayama,S.; Kohriyama,T.; Katayama,S.; Yamashita,M.; Yamamoto,T.; Udaka,F.; Kawakami,A.; Ihara,Y.; Nishinaka,T.; Kuroda,S.; Suzuki,N.; Shiga,Y.; Arai,H.; Maruyama,M.; Yamada,M. - Clinical diagnosis of MM2-type sporadic Creutzfeldt-Jakob disease - Neurology 2005 Feb 22; 64(4): 643-8
ARQI - Ishida,C.; Okino,S.; Kitamoto,T.; Yamada,M. - Involvement of the peripheral nervous system in human prion diseases including dural graft associated Creutzfeldt-Jakob disease - Journal of Neurology, Neurosurgery and Psychiatry 2005 Mar; 76(3): 325-9
ANMK - Ishida,C.; Kakishima,A.; Okino,S.; Furukawa,Y.; Kano,M.; Oda,Y.; Nakanishi,I.; Makifuchi,T.; Kitamoto,T.; Yamada,M. - Sporadic Creutzfeldt-Jakob disease with MM1-type prion protein and plaques - Neurology 2003 Feb 11; 60(3): 514-7
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
AVWS - Iwasaki,Y.; Iijima,M.; Kimura,S.; Yoshida,M.; Hashizume,Y.; Yamada,M.; Kitamoto,T.; Sobue,G. - Autopsy case of sporadic Creutzfeldt-Jakob disease presenting with signs suggestive of brainstem and spinal cord involvement - Neuropathology 2006 Dec; 26(6): 550-6
AFXB - Iwasaki,Y.; Sone,M.; Kato,T.; Yoshida,E.; Indo,T.; Yoshida,M.; Hashizume,Y.; Yamada,M. - [Clinicopathological characteristics of Creutzfeldt-Jakob disease with a PrP V180I mutation and M129V polymorphism on different alleles] - Rinsho Shinkeigaku. Clinical Neurology 1999 Aug; 39(8): 800-6
AGLR - Kimura,K.; Nonaka,A.; Tashiro,H.; Yaginuma,M.; Shimokawa,R.; Okeda,R.; Yamada,M. - Atypical form of dural graft associated Creutzfeldt-Jakob disease: report of a postmortem case with review of the literature. - Journal of Neurology, Neurosurgery and Psychiatry 2001 May; 70(5): 696-9
AVUY - Nakamura,Y.; Watanabe,M.; Nagoshi,K.; Yamada,M.; Mizusawa,H. - Geographic difference of mortality of Creutzfeldt-Jakob disease in Japan - Journal of Epidemiology / Japan Epidemiological Association 2007 Jan; 17(1): 19-24
AIWZ - Nishida,Y.; Yamada,M.; Hara,K.; Tsunemi,T.; Yamawaki,M.; Shimokawa,R.; Okeda,R.; Tsutsumi,T.; Mizusawa,H. - Creutzfeldt-Jakob disease after Jannetta's operation with cadaveric dura mater graft: initial manifestations related to the grafted site. - Journal of Neurology. Zeitschrift für Neurologie 2002 Apr; 249(4): 480-3
AYCY - Noguchi-Shinohara,M.; Hamaguchi,T.; Yamada,M. - [Epidemiology and surveillance system of prion disease in Japan] - Nippon Rinsho. Japanese Journal of Clinical Medicine 2007 Aug; 65(8): 1379-83
AXFR - Noguchi-Shinohara,M.; Hamaguchi,T.; Kitamoto,T.; Sato,T.; Nakamura,Y.; Mizusawa,H.; Yamada,M. - Clinical features and diagnosis of dura mater graft associated Creutzfeldt Jakob disease - Neurology 2007 Jul 24; 69(4): 360-7
AVBR - Nozaki,I.; Hamaguchi,T.; Noguchi-Shinohara,M.; Ono,K.; Shirasaki,H.; Komai,K.; Kitamoto,T.; Yamada,M. - The MM2-cortical form of sporadic Creutzfeldt-Jakob disease presenting with visual disturbance - Neurology 2006 Aug 8; 67(3): 531-3
AJBI - Orimo,S.; Ozawa,E.; Uematsu,M.; Yoshida,E.; Hino,H.; Yamada,M.; Okeda,R.; Mizusawa,H. - A case of Creutzfeldt-Jakob disease presenting with auditory agnosia as an initial manifestation - European Neurology 2000; 44(4): 256-8
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
ANFZ - Shiraishi,A.; Mizusawa,H.; Yamada,M. - Early and persistent sensory-psychiatric symptoms in an inherited prion disease with a PrP P105L mutation - Journal of Neurology. Zeitschrift für Neurologie 2002 Dec; 249(12): 1740-1
ALFY - Suetsugu,M.; Moriyama,N.; Mitsuyama,Y.; Yamada,M.; Takamatsu,I. - [Temporal profile of mental symptoms in Creutzfeldt-Jakob syndrome (author's transl)] - No to Shinkei. Brain and Nerve 1982 Feb; 34(2): 159-64
AXZD - Yamada,M.; Noguchi-Shinohara,M.; Hamaguchi,T.; Kitamoto,T.; Sato,T.; Nakamura,Y.; Mizusawa,H.; CJD Surveillance Committee, Japan - Plaque and Non-plaque Types of Dura Mater Graft-associated Creutzfeldt-Jakob Disease: Clinicopathological and Molecular Analysis - International Conference - Prion 2007 (26.-28.9.2007) Edinburgh International Conference Centre, Edinburgh, Scotland, UK - Book of Abstracts: Epidemiology, Risk Assessment and Transmission P04.11
AUEO - Yamada,M. - Variant CJD Working Group, Creutzfeldt-Jakob Disease Surveillance Committee, Japan. - The first Japanese case of variant Creutzfeldt-Jakob disease showing periodic electroencephalogram - Lancet 2006 Mar 11; 367(9513): 874
ARLF - Yamada,M. - Cerebral amyloid angiopathy and gene polymorphisms - Journal of the Neurological Sciences 2004 Nov 15; 226(1-2): 41-4
AQQN - Yamada,M. - [Surveillance of prion diseases in Japan: analysis of 409 patients] - Rinsho Shinkeigaku. Clinical Neurology 2003 Nov; 43(11): 806-9
AMUA - Yamada,M. - Cerebral amyloid angiopathy: an overview. - Neuropathology 2000 Mar; 20(1): 8-22
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
AMUF - Yamada,M. - [Cerebral amyloid angiopathy] - No to Shinkei. Brain and Nerve 1994 May; 46(5): 442-52
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
AHTF - Manaka,H.; Kato,T.; Kurita,K.; Katagiri,T.; Shikama,Y.; Kujirai,K.; Kawanami,T.; Suzuki,Y.; Nihei,K.; Sasaki,H.; Yamada,S.; Hirota,K.; Kusaka,H.; Imai,T. - Marked increase in cerebrospinal fluid ubiquitin in Creutzfeldt-Jakob disease - Neuroscience Letters 1992 May 11; 139(1): 47-9
AMUH - Yamada,S.; Aiba,T.; Endo,Y.; Hara,M.; Kitamoto,T.; Tateishi,J. - Creutzfeldt-Jakob disease transmitted by a cadaveric dura mater graft - Neurosurgery 1994 Apr; 34(4): 740-3; discussion 743-4
AMWD - Yokoyama,T.; Kimura,K.M.; Ushiki,Y.K.; Yamada,S.; Morooka,A.; Nakashiba,T.; Sassa,T.; Itohara,S. - In vivo conversion of cellular prion protein to pathogenic isoforms, as monitored by conformation-specific antibodies - The Journal of Biological Chemistry 2001 Apr 6; 276(14): 11265-71
AEGO - Furukawa,H.; Takahashi,M.; Nakajima,M.; Yamada,T. - [Prospects of the therapeutic approaches to Creutzfeldt-Jakob disease: a clinical trial of antimalarial, quinacrine] - Nippon Rinsho. Japanese Journal of Clinical Medicine 2002 Aug; 60(8): 1649-57
APIU - Kobayashi,Y.; Hirata,K.; Tanaka,H.; Yamada,T. - [Quinacrine administration to a patient with Creutzfeldt-Jakob disease who received a cadaveric dura mater graft - an EEG evaluation] - Rinsho Shinkeigaku. Clinical Neurology 2003 Jul; 43(7): 403-8
AIBO - Matsunaga,Y.; Ierovnik,E.; Yamada,T.; Turk,V. - Conformational changes preceding amyloid-fibril formation of amyloid-beta and stefin B; parallels in pH dependence. - Current Medicinal Chemistry 2002 Oct; 9(19): 1717-24
APVF - Nakajima,M.; Yamada,T.; Kusuhara,T.; Furukawa,H.; Takahashi,M.; Yamauchi,A.; Kataoka,Y. - Results of quinacrine administration to patients with Creutzfeldt-Jakob disease - Dementia and Geriatric Cognitive Disorders 2004; 17(3): 158-163
ALJD - Takase,K.; Furuya,H.; Murai,H.; Yamada,T.; Oh-yagi,Y.; Doh-ura,K.; Iwaki,T.; Tobimatsu,S.; Kira,J. - [A case of Gerstmann-Sträussler-Scheinker syndrome (GSS) with late onset - a haplotype analysis of Glu219Lys polymorphism in PrP gene] - Rinsho Shinkeigaku. Clinical Neurology 2001 Jun; 41(6): 318-21
ALKF - Taniwaki,Y.; Hara,H.; Doh-ura,K.; Murakami,I.; Tashiro,H.; Yamasaki,T.; Shigeto,H.; Arakawa,K.; Araki,E.; Yamada,T.; Iwaki,T.; Kira,J. - Familial Creutzfeldt-Jakob disease with D178N-129M mutation of PRNP presenting as cerebellar ataxia without insomnia - Journal of Neurology, Neurosurgery and Psychiatry 2000 Mar; 68(3): 388
ASRP - Tsuboi,Y.; Baba,Y.; Doh-ura,K.; Imamura,A.; Fujioka,S.; Yamada,T. - Diffusion-weighted MRI in familial Creutzfeldt-Jakob disease with the codon 200 mutation in the prion protein gene - Journal of the Neurological Sciences 2005 May 15; 232(1-2): 45-9
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
AWYF - Kasai,S.; Urushibata,S.; Hozumi,K.; Yokoyama,F.; Ichikawa,N.; Kadoya,Y.; Nishi,N.; Watanabe,N.; Yamada,Y.; Nomizu,M. - Identification of multiple amyloidogenic sequences in laminin-1 - Biochemistry 2007 Apr 3; 46(13): 3966-74
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
AXXQ - Teruya,K.; Yamada,Y.; Nishimura,T.; Suda,Y.; Doh-ura,K. - Characterization of the Interaction between Prion Protein and Heparin - International Conference - Prion 2007 (26.-28.9.2007) Edinburgh International Conference Centre, Edinburgh, Scotland, UK - Book of Abstracts: Protein Misfolding P01.56