AACX - Aguzzi,A.; Brandner,S.; Fischer,M.B.; Furukawa,H.; Glatzel,M.; Hawkins,C.; Heppner,F.L.; Montrasio,F.; Navarro,B.; Parizek,P.; Pekarik,V.; Prinz,M.; Raeber,A.J.; Rockl,C.; Klein,M.A. - Spongiform encephalopathies: insights from transgenic models. - Advances in Virus Research 2001; 56: 313-52
AADB - Aguzzi,A.; Klein,M.A.; Montrasio,F.; Pekarik,V.; Brandner,S.; Furukawa,H.; Kaser,P.; Rockl,C.; Glatzel,M. - Prions: pathogenesis and reverse genetics. - Annals of the New York Academy of Sciences 2000; 920: 140-57
AQJN - Furukawa,H.; Doh-ura,K.; Sasaki,K.; Iwaki,T. - Accumulation of prion protein in muscle fibers of experimental chloroquine myopathy: in vivo model for deposition of prion protein in non-neuronal tissues. - Laboratory Investigation 2004 Jul; 84(7): 828-35
AQJM - Furukawa,H.; Doh-ura,K.; Okuwaki,R.; Shirabe,S.; Yamamoto,K.; Udono,H.; Ito,T.; Katamine,S.; Niwa,M. - A pitfall in diagnosis of human prion diseases using detection of protease-resistant prion protein in urine. Contamination with bacterial outer membrane proteins. - The Journal of Biological Chemistry 2004 May 28; 279(22): 23661-7
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
AEGP - Furukawa,H. - [Current topics in prion diseases] - No to Shinkei. Brain and Nerve 2002 Apr; 54(4): 283-8
AEGQ - Furukawa,H.; Doh-ura,K. - [Current topics of prion disease] - Uirusu 2001 Dec; 51(2): 151-8
AEGR - Furukawa,H.; Doh-ura,K.; Kikuchi,H.; Tateishi,J.; Iwaki,T. - A comparative study of abnormal prion protein isoforms between Gerstmann-Sträussler-Scheinker syndrome and Creutzfeldt-Jakob disease - Journal of the Neurological Sciences 1998 Jun 11; 158(1): 71-5
AEGS - Furukawa,H.; Kitamoto,T.; Hashiguchi,H.; Tateishi,J. - A Japanese case of Creutzfeldt-Jakob disease with a point mutation in the prion protein gene at codon 210 - Journal of the Neurological Sciences 1996 Sep 15; 141(1-2): 120-2
AEGT - Furukawa,H.; Kitamoto,T.; Tanaka,Y.; Tateishi,J. - New variant prion protein in a Japanese family with Gerstmann-Sträussler syndrome - Brain Research. Molecular Brain Research 1995 Jun; 30(2): 385-8
AFNN - Hoque,M.Z.; Kitamoto,T.; Furukawa,H.; Muramoto,T.; Tateishi,J. - Mutation in the prion protein gene at codon 232 in Japanese patients with Creutzfeldt-Jakob disease: a clinicopathological, immunohistochemical and transmission study. - Acta Neuropathologica 1996 Nov; 92(5): 441-6
AGGP - Kawashima,T.; Furukawa,H.; Doh-ura,K.; Iwaki,T. - Diagnosis of new variant Creutzfeldt-Jakob disease by tonsil biopsy - Lancet 1997 Jul 5; 350(9070): 68-9
AGQI - Koide,T.; Ohtake,H.; Nakajima,T.; Furukawa,H.; Sakai,K.; Kamei,H.; Makifuchi,T.; Fukuhara,N. - A patient with dementia with Lewy bodies and codon 232 mutation of PRNP - Neurology 2002 Nov 26; 59(10): 1619-21
AHDL - Lee,H.S.; Sambuughin,N.; Cervenakova,L.; Chapman,J.C.; Pocchiari,M.; Litvak,S.; Qi,H.Y.; Budka,H.; del Ser,T.; Furukawa,H.; Brown,P.; Gajdusek,D.C.; Long,J.C.; Korczyn,A.D.; Goldfarb,L.G. - Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease - American Journal of Human Genetics 1999 Apr; 64(4): 1063-70
AISA - Nagayama,M.; Shinohara,Y.; Furukawa,H.; Kitamoto,T. - Fatal familial insomnia with a mutation at codon 178 of the prion protein gene: first report from Japan. - Neurology 1996 Nov; 47(5): 1313-6
AISD - Nakagawa,Y.; Kitamoto,T.; Furukawa,H.; Ogomori,K.; Tateishi,J. - Allelic variation of apolipoprotein E in Japanese sporadic Creutzfeldt-Jakob disease patients - Neuroscience Letters 1995 Mar 10; 187(3): 209-11
AISE - Nakagawa,Y.; Kitamoto,T.; Furukawa,H.; Ogomori,K.; Tateishi,J. - Apolipoprotein E in Creutzfeldt-Jakob disease - Lancet 1995 Jan 7; 345(8941): 68
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
ARJL - Prinz,M.; Montrasio,F.; Furukawa,H.; van der Haar,M.E.; Schwarz,P.; Rülicke,T.; Giger,O.T.; Hausler,K.G.; Perez,D.; Glatzel,M.; Aguzzi,A. - Intrinsic resistance of oligodendrocytes to prion infection - Journal of Neuroscience 2004 Jun 30; 24(26): 5974-81
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
ALJE - Takashima,S.; Tateishi,J.; Taguchi,Y.; Hirade,S.; Inoue,H.; Matsui,Y.; Furukawa,H. - [Creutzfeldt-Jakob disease with a widespread presence of kuru-type plaques after cadaveric dural graft replacement. An autopsy case] - Rinsho Shinkeigaku. Clinical Neurology 1997 Sep; 37(9): 824-8
ALKC - Tanaka,Y.; Minematsu,K.; Moriyasu,H.; Yamaguchi,T.; Yutani,C.; Kitamoto,T.; Furukawa,H. - A Japanese family with a variant of Gerstmann-Sträussler-Scheinker disease - Journal of Neurology, Neurosurgery and Psychiatry 1997 May; 62(5): 454-7
ALLD - Tateishi,J.; Kitamoto,T.; Hoque,M.Z.; Furukawa,H. - Experimental transmission of Creutzfeldt-Jakob disease and related diseases to rodents - Neurology 1996 Feb; 46(2): 532-7
ANNJ - Yamamoto,S.; Furukawa,H.; Kitamoto,T.; Takamaru,Y.; Morita,N.; Yasuda,M.; Okada,Y.; Sawa,H.; Nagashima,K. - An atypical form of sporadic panencephalopathic Creutzfeldt-Jakob disease in Japan - Neuropathology and Applied Neurobiology 2003 Feb; 29(1): 77-80
AVED - Mitsuiki,S.; Hui,Z.; Matsumoto,D.; Sakai,M.; Moriyama,Y.; Furukawa,K.; Kanouchi,H.; Oka,T. - Degradation of PrPsc by keratinolytic protease from Nocardiopsis sp. TOA-1. - Bioscience, Biotechnology, and Biochemistry 2006 May; 70(5): 1246-8
AWXP - Yamamoto,S.; Kinoshita,M.; Furukawa,S.; Kajiyama,K. - Early abnormality of diffusion-weighted magnetic resonance imaging followed by brain atrophy in a case of Gerstmann-Sträussler-Scheinker disease - Archives of Neurology 2007 Mar; 64(3): 450-1
AGIR - Kikyo,H.; Furukawa,T. - Creutzfeldt-Jakob-like syndrome induced by lithium, levomepromazine, and phenobarbitone - Journal of Neurology, Neurosurgery and Psychiatry 1999 Jun; 66(6): 802-3
AJAE - Okiyama,R.; Tsuchiya,K.; Furukawa,T.; Tsukagoshi,H.; Kosaka,K. - [An autopsy case of panencephalopathic type of Creutzfeldt-Jakob disease: an early clinical sign documented by magnetic resonance imaging] - Rinsho Shinkeigaku. Clinical Neurology 1989 Aug; 29(8): 1048-51
AJAS - Ono,S.; Fukunaga,M.; Otsuka,N.; Nagai,K.; Morita,K.; Muranaka,A.; Furukawa,T.; Yanagimoto,S.; Tomomitsu,T.; Kawai,K.; et al. - [A case of Creutzfeldt-Jakob disease followed up by N-isopropyl-[123I]-p-iodoamphetamine and 99mTc-hexamethylpropyleneamine oxime SPECT] - Kaku Igaku. Japanese Journal of Nuclear Medicine 1989 Jan; 26(1): 77-88
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
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