Researcher profile · Semantic Scholar

H. Furukawa

h-index: 16
Works: 31
Citations: 833

Most-cited papers

Experimental transmission of Creutzfeldt-Jakob disease and related diseases to rodents
J. Tateishi, T. Kitamoto, M. Hoque, H. Furukawa
1996Neurology107 citations
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Results of Quinacrine Administration to Patients with Creutzfeldt-Jakob Disease
M. Nakajima, T. Yamada, T. Kusuhara, H. Furukawa +3 more
2004Dementia and Geriatric Cognitive Disorders94 citations
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Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease.
Hee-Suk Lee, N. Sambuughin, L. Cervenakova, J. Chapman +11 more
1999American Journal of Human Genetics94 citations Open access
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New variant prion protein in a Japanese family with Gerstmann-Sträussler syndrome.
H. Furukawa, Tetsuyuki Kitamoto, Yutaka Tanaka, J. Tateishi
1995Brain Research. Molecular Brain Research62 citations
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Intrinsic Resistance of Oligodendrocytes to Prion Infection
M. Prinz, F. Montrasio, H. Furukawa, M. E. van der Haar +7 more
2004Journal of Neuroscience59 citations Open access
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A Pitfall in Diagnosis of Human Prion Diseases Using Detection of Protease-resistant Prion Protein in Urine
H. Furukawa, K. Doh-ura, R. Okuwaki, Susumu Shirabe +5 more
2004Journal of Biological Chemistry49 citations Open access
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Mutation in the prion protein gene at codon 232 in Japanese patients with Creutzfeldt-Jakob disease: a clinicopathological, immunohistochemical and transmission study
M. Hoque, T. Kitamoto, H. Furukawa, Tamaki Muramoto +1 more
1996Acta Neuropathologica49 citations
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Apolipoprotein E in Creutzfeldt-Jakob disease.
Y. Nakagawa, T. Kitamoto, H. Furukawa, K. Ogomori +10 more
199539 citations
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Fatal familial insomnia with a mutation at codon 178 of the prion protein gene
M. Nagayama, Y. Shinohara, H. Furukawa, T. Kitamoto
1996Neurology38 citations
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A Japanese family with a variant of Gerstmann-Sträussler-Scheinker disease.
Yutaka Tanaka, K. Minematsu, H. Moriyasu, Takenori Yamaguchi +3 more
1997Journal of Neurology Neurosurgery & Psychiatry37 citations Open access
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Diagnosis of new variant Creutzfeldt-Jakob disease by tonsil biopsy.
T. Kawashima, H. Furukawa, K. Doh-ura, T. Iwaki
1997The Lancet31 citations Open access
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A Japanese case of Creutzfeldt-Jakob disease with a point mutation in the prion protein gene at codon 210.
H. Furukawa, T. Kitamoto, H. Hashiguchi, J. Tateishi
1996Journal of Neurological Sciences25 citations
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Allelic variation of apolipoprotein E in Japanese sporadic Creutzfeldt-Jakob disease patients.
Y. Nakagawa, T. Kitamoto, H. Furukawa, K. Ogomori +1 more
1995Neuroscience Letters25 citations
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A comparative study of abnormal prion protein isoforms between Gerstmann-Sträussler-Scheinker syndrome and Creutzfeldt-Jakob disease.
H. Furukawa, K. Doh-ura, H. Kikuchi, J. Tateishi +1 more
1998Journal of Neurological Sciences20 citations
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Prions: Pathogenesis and Reverse Genetics
A. Aguzzi, M. Klein, F. Montrasio, V. Pekarik +5 more
2000Annals of the New York Academy of Sciences18 citations
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[Prospects of the therapeutic approaches to Creutzfeldt-Jakob disease: a clinical trial of antimalarial, quinacrine].
H. Furukawa, Mitsuo Takahashi, M. Nakajima, T. Yamada
2002Nihon rinsho. Japanese journal of clinical medicine16 citations
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Spongiform encephalopathies: insights from transgenic models.
A. Aguzzi, S. Brandner, Michael B. Fischer, H. Furukawa +11 more
2001Advances in Virus Research16 citations
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A case of Creutzfeldt-Jakob disease with a point mutation at codon 232: Correlation of MRI and neurologic findings
Akira Satoh, Hirofumi Goto, H. Satoh, Itsuro Tomita +3 more
1997Neurology16 citations
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Molecular pathology of prion diseases.
A. Aguzzi, Fabio Montrasio, S. Brandner, R. Frigg +4 more
200012 citations
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[Creutzfeldt-Jakob disease with a widespread presence of kuru-type plaques after cadaveric dural graft replacement. An autopsy case].
S. Takashima, J. Tateishi, Y. Taguchi, S. Hirade +3 more
1997Rinshō shinkeigaku Clinical neurology10 citations
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Accumulation of prion protein in muscle fibers of experimental chloroquine myopathy: in vivo model for deposition of prion protein in non-neuronal tissues
H. Furukawa, K. Doh-ura, K. Sasaki, T. Iwaki
2004Laboratory Investigation6 citations Open access
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An atypical form of sporadic panencephalopathic Creutzfeldt–Jakob disease in Japan
S. Yamamoto, H. Furukawa, T. Kitamoto, Y. Takamaru +5 more
2003Neuropathology and Applied Neurobiology5 citations
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Apolipoprotein E in Creutzfeldt-Jakob disease.
Y. Nakagawa, T. Kitamoto, H. Furukawa, K. Ogomori +1 more
1995The Lancet3 citations
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High-resolution electrical resistivity tomography to investigate the origin of the Tsugaru-Juniko Lakes : An example near the Ao-ike
Ching-Ying Tsou, Kousei Yamabe, D. Higaki, Takayo Sasagawa +4 more
2021Journal of the Japan Landslide Society1 citations Open access
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Straussler-Scheinker disease
Yutaka Tanaka, K. Minematsu, H. Moriyasu, T. Yamaguchi +3 more
1 citations
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Year : 2004 Intrinsic resistance of oligodendrocytes to prion infection
M. Prinz, F. Montrasio, H. Furukawa, M. E. van der Haar +7 more
20060 citations
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[Current topics in prion diseases].
H. Furukawa
2002No to shinkei = Brain and nerve0 citations
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[Current topics of prion disease].
H. Furukawa, K. Doh-ura
2001Uirusu0 citations
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非定型的致死性家族性不眠症 PRNP D178N-129M突然変異を伴った家族性Creutzfelt-Jakob病の1剖検例(Atypical fatal familial insomnia: an autopsy case of familial Creutzfeldt-Jakob disease with PRNP D178N-129M mutation)
K. Sasaki, K. Doh-ura, H. Furukawa, T. Iwaki
20010 citations
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101 New variant prion protein in a Japanese family with Gerstmann-Sträussler syndrome : Clinicopathological , molecular genetic studies
H. Furukawa, H. Tashiro, Y. Tanaka, C. Yutani +3 more
19960 citations
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163 Variations in phenotype, genotype, and transmission rate of prion diseases in Japan
T. Kitamoto, Satoshi Shibuya, R. Shin, H. Furukawa +1 more
19960 citations
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A. Aguzzi

×4

T. Iwaki×4

Yutaka Tanaka×3

M. Glatzel×3

K. Ogomori×3

Christiane Röckl×3

M. Hoque×2

M. Nakajima×2