Kitamoto T - Search Results

1

Japanese family with Creutzfeldt-Jakob disease with codon 200 point mutation of the prion protein gene.

Inoue I, Kitamoto T, Doh-ura K, Shii H, Goto I, Tateishi J. Inoue I, et al. Among authors: kitamoto t. Neurology. 1994 Feb;44(2):299-301. doi: 10.1212/wnl.44.2.299. Neurology. 1994. PMID: 7906019

2

Successful transmission of Creutzfeldt-Jakob disease from human to mouse verified by prion protein accumulation in mouse brains.

Muramoto T, Kitamoto T, Tateishi J, Goto I. Muramoto T, et al. Among authors: kitamoto t. Brain Res. 1992 Dec 25;599(2):309-16. doi: 10.1016/0006-8993(92)90406-y. Brain Res. 1992. PMID: 1291035

3

Gerstmann-Sträussler-Scheinker disease in an Alsatian family: clinical and genetic studies.

Tranchant C, Doh-ura K, Warter JM, Steinmetz G, Chevalier Y, Hanauer A, Kitamoto T, Tateishi J. Tranchant C, et al. Among authors: kitamoto t. J Neurol Neurosurg Psychiatry. 1992 Mar;55(3):185-7. doi: 10.1136/jnnp.55.3.185. J Neurol Neurosurg Psychiatry. 1992. PMID: 1348783 Free PMC article.

4

Colocalization of prion protein and beta protein in the same amyloid plaques in patients with Gerstmann-Sträussler syndrome.

Miyazono M, Kitamoto T, Iwaki T, Tateishi J. Miyazono M, et al. Among authors: kitamoto t. Acta Neuropathol. 1992;83(4):333-9. doi: 10.1007/BF00713522. Acta Neuropathol. 1992. PMID: 1349451

5

Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease.

Kitamoto T, Shin RW, Doh-ura K, Tomokane N, Miyazono M, Muramoto T, Tateishi J. Kitamoto T, et al. Am J Pathol. 1992 Jun;140(6):1285-94. Am J Pathol. 1992. PMID: 1351366 Free PMC article.

6

The primary structure of the prion protein influences the distribution of abnormal prion protein in the central nervous system.

Kitamoto T, Doh-ura K, Muramoto T, Miyazono M, Tateishi J. Kitamoto T, et al. Am J Pathol. 1992 Aug;141(2):271-7. Am J Pathol. 1992. PMID: 1353945 Free PMC article.

7

Creutzfeldt-Jakob disease with codon 129 polymorphism (valine): a comparative study of patients with codon 102 point mutation or without mutations.

Miyazono M, Kitamoto T, Doh-ura K, Iwaki T, Tateishi J. Miyazono M, et al. Among authors: kitamoto t. Acta Neuropathol. 1992;84(4):349-54. doi: 10.1007/BF00227660. Acta Neuropathol. 1992. PMID: 1359725

8

Massive accumulation of modified tau and severe depletion of normal tau characterize the cerebral cortex and white matter of Alzheimer's disease. Demonstration using the hydrated autoclaving method.

Shin RW, Iwaki T, Kitamoto T, Sato Y, Tateishi J. Shin RW, et al. Among authors: kitamoto t. Am J Pathol. 1992 Apr;140(4):937-45. Am J Pathol. 1992. PMID: 1373272 Free PMC article.

9

The sequential development of abnormal prion protein accumulation in mice with Creutzfeldt-Jakob disease.

Muramoto T, Kitamoto T, Tateishi J, Goto I. Muramoto T, et al. Among authors: kitamoto t. Am J Pathol. 1992 Jun;140(6):1411-20. Am J Pathol. 1992. PMID: 1376559 Free PMC article.

10

The coexistence of Alzheimer's disease and Creutzfeldt-Jakob disease in a patient with dementia of long duration.

Muramoto T, Kitamoto T, Koga H, Tateishi J. Muramoto T, et al. Among authors: kitamoto t. Acta Neuropathol. 1992;84(6):686-9. doi: 10.1007/BF00227747. Acta Neuropathol. 1992. PMID: 1471476

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