Books, Original Papers & Review Papers- DOH-URA Katsumi -
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[B]:Books [O]:Original Papers [R]:Review Papers
total:252
[1994]
221.[O] Japanese family with Creutzfeldt-Jakob disease with codon 200 point mutation of the prion protein gene..[Neurology,44(2),(1994),299-301]Inoue I, Kitamoto T, Doh-ura K, Shii H, Goto I, Tateishi J
[1993]
222.[O] Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Straussler syndrome..[Biochem Biophys Res Commun,191(2),(1993),709-714]Kitamoto T, Ohta M, Doh-ura K, Hitoshi S, Terao Y, Tateishi J
[1992]
223.[O] The primary structure of the prion protein influences the distribution of abnormal prion protein in the central nervous system..[Am J Pathol,141(2),(1992),271-277]Kitamoto T, Doh-ura K, Muramoto T, Miyazono M, Tateishi J
224.[O] Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease..[Am J Pathol,140(6),(1992),1285-1294]Kitamoto T, Shin R W, Doh-ura K, Tomokane N, Miyazono M, Muramoto T, Tateishi J
225.[O] Creutzfeldt-Jakob disease with codon 129 polymorphism (valine): a comparative study of patients with codon 102 point mutation or without mutations..[Acta Neuropathol (Berl),84(4),(1992),349-354]Miyazono M, Kitamoto T, Doh-ura K, Iwaki T, Tateishi J
226.[O] Creutzfeldt-Jakob disease with amyloid angiopathy: diagnosis by immunological analyses and transmission experiments. (Acta Neuropathol (Berl)).[Acta Neuropathol (Berl),83(5),(1992),559-563]Tateishi J, Kitamoto T, Doh-ura K, Boellaard J W, Peiffer J
227.[R] Creutzfeldt-Jakob disease with amyloid angiopathy: diagnosis by immunological analyses and transmission experiments. (Acta Neuropathol (Berl)).[Acta Neuropathol (Berl),83(5), (1992), 559-563]Tateishi J, Kitamoto T, Doh-ura K, Boellaard J W, Peiffer J
228.[O] Gerstmann-Straussler-Scheinker disease in an Alsatian family: clinical and genetic studies..[J Neurol Neurosurg Psychiatry,55(3),(1992),185-187]Tranchant C, Doh-ura K, Warter J M, Steinmetz G, Chevalier Y, Hanauer A, Kitamoto T, Tateishi J
[1991]
229.[O] Clustering of three cases of Creutzfeldt-Jakob disease near Fukuoka City, Japan..[Acta Neurol Scand,84(5),(1991),445-447]Arakawa K, Nagara H, Itoyama Y, Doh-ura K, Tomokane N, Tateishi J, Goto I
230.[O] Abnormal isoform of prion protein accumulates in follicular dendritic cells in mice with Creutzfeldt-Jakob disease..[J Virol,65(11),(1991),6292-6295]Kitamoto T, Muramoto T, Mohri S, Doh-Ura K, Tateishi J
231.[O] CJD discrepancy..[Nature,353(6347),(1991),801-802]Doh-ura K, Kitamoto T, Sakaki Y, Tateishi J
232.[O] A comparative immunohistochemical study of Kuru and senile plaques with a special reference to glial reactions at various stages of amyloid plaque formation..[Am J Pathol,139(3),(1991),589-598]Miyazono M, Iwaki T, Kitamoto T, Kaneko Y, Doh-ura K, Tateishi J
233.[O] Genomic organization of the human-amyloid beta-protein precursor gene..[Gene,102(2),(1991),291-292]Yoshikai S, Sasaki H, Doh-ura K, Furuya H, Sakaki Y
234.[O] [Mutation of codon 117 of the prion gene in Gerstmann-Straussler-Scheinker disease].[Rev Neurol (Paris),147(4),(1991),274-278]Tranchant C, Doh-Ura K, Steinmetz G, Chevalier Y, Kitamoto T, Tateishi J, Warter J M
235.[O] A prion protein missense variant is integrated in kuru plaque cores in patients with Gerstmann-Straussler syndrome..[Neurology,41(2 ( Pt 1)),(1991),306-310]Kitamoto T, Yamaguchi K, Doh-ura K, Tateishi J
[1990]
236.[O] Immunochemical, molecular genetic, and transmission studies on a case of Gerstmann-Straussler-Scheinker syndrome..[Neurology,40(10),(1990),1578-1581]Tateishi J, Kitamoto T, Doh-ura K, Sakaki Y, Steinmetz G, Tranchant C, Warter J M, Heldt N
237.[R] バイオテクノロジーの内科診療への応用 プリオンタンパクと遅発性ウイルス疾患 (内科).[内科,66(4), (1990), 714-715]堂浦克美, 立石潤
238.[R] 副鼻腔病変を有する再発性動眼神経麻痺症例 (Clinical Neuroscience).[Clinical Neuroscience,8(7), (1990), 790-791]堂浦克美
239.[O] DNA多型によるネパール人の人類学的位置づけ.[健康科学,12,(1990),19-22]古谷博和, 堂浦克美, 三島造道, 他
240.[O] Genomic organization of the human amyloid beta-protein precursor gene..[Gene,87(2),(1990),257-263]Yoshikai S, Sasaki H, Doh-ura K, Furuya H, Sakaki Y
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