Hayakawa M - Search Results

1

A missense mutation at codon 105 with codon 129 polymorphism of the prion protein gene in a new variant of Gerstmann-Sträussler-Scheinker disease.

Yamada M, Itoh Y, Fujigasaki H, Naruse S, Kaneko K, Kitamoto T, Tateishi J, Otomo E, Hayakawa M, Tanaka J, et al. Yamada M, et al. Among authors: hayakawa m. Neurology. 1993 Dec;43(12):2723-4. doi: 10.1212/wnl.43.12.2723-a. Neurology. 1993. PMID: 7902972 No abstract available.

2

High frequency of mitochondrial ND4 gene mutation in Japanese pedigrees with Leber hereditary optic neuropathy.

Nakamura M, Ara F, Yamada M, Hotta Y, Hayakawa M, Fujiki K, Kanai A, Sakai J, Inoue M, Yamamoto M, et al. Nakamura M, et al. Among authors: hayakawa m. Jpn J Ophthalmol. 1992;36(1):56-61. Jpn J Ophthalmol. 1992. PMID: 1635296

3

Absence of the cystatin C amyloid in the cerebral amyloid angiopathy, senile plaque, and extra-CNS amyloid deposits of aged Japanese.

Yamada M, Tsukagoshi H, Wada Y, Otomo E, Hayakawa M, Thorsteinsson L, Jensson O. Yamada M, et al. Among authors: hayakawa m. Acta Neurol Scand. 1989 Jun;79(6):504-9. doi: 10.1111/j.1600-0404.1989.tb03822.x. Acta Neurol Scand. 1989. PMID: 2782031

4

Systemic amyloid deposition in old age and dementia of Alzheimer type: the relationship of brain amyloid to other amyloid.

Yamada M, Tsukagoshi H, Otomo E, Hayakawa M. Yamada M, et al. Among authors: hayakawa m. Acta Neuropathol. 1988;77(2):136-41. doi: 10.1007/BF00687423. Acta Neuropathol. 1988. PMID: 3067504

5

A quantitative Golgi study of basal dendrites of hippocampal CA1 pyramidal cells in senile dementia of Alzheimer type.

Yamada M, Wada Y, Tsukagoshi H, Otomo E, Hayakawa M. Yamada M, et al. Among authors: hayakawa m. J Neurol Neurosurg Psychiatry. 1988 Aug;51(8):1088-90. doi: 10.1136/jnnp.51.8.1088. J Neurol Neurosurg Psychiatry. 1988. PMID: 3216211 Free PMC article.

6

Cerebral amyloid angiopathy in the aged.

Yamada M, Tsukagoshi H, Otomo E, Hayakawa M. Yamada M, et al. Among authors: hayakawa m. J Neurol. 1987 Aug;234(6):371-6. doi: 10.1007/BF00314080. J Neurol. 1987. PMID: 3655840

7

A variant of Gerstmann-Sträussler-Scheinker disease carrying codon 105 mutation with codon 129 polymorphism of the prion protein gene: a clinicopathological study.

Itoh Y, Yamada M, Hayakawa M, Shozawa T, Tanaka J, Matsushita M, Kitamoto T, Tateishi J, Otomo E. Itoh Y, et al. Among authors: hayakawa m. J Neurol Sci. 1994 Dec 1;127(1):77-86. doi: 10.1016/0022-510x(94)90138-4. J Neurol Sci. 1994. PMID: 7699395 Review.

8

Computer-assisted three-dimensional image analysis of cerebral amyloid angiopathy.

Maeda A, Yamada M, Itoh Y, Otomo E, Hayakawa M, Miyatake T. Maeda A, et al. Among authors: hayakawa m. Stroke. 1993 Dec;24(12):1857-64. doi: 10.1161/01.str.24.12.1857. Stroke. 1993. PMID: 8248968

9

Cerebral amyloid angiopathy: a significant cause of cerebellar as well as lobar cerebral hemorrhage in the elderly.

Itoh Y, Yamada M, Hayakawa M, Otomo E, Miyatake T. Itoh Y, et al. Among authors: hayakawa m. J Neurol Sci. 1993 Jun;116(2):135-41. doi: 10.1016/0022-510x(93)90317-r. J Neurol Sci. 1993. PMID: 8336159

10

Subpial beta/A4 peptide deposits are closely associated with amyloid angiopathy in the elderly.

Itoh Y, Yamada M, Hayakawa M, Otomo E, Miyatake T. Itoh Y, et al. Among authors: hayakawa m. Neurosci Lett. 1993 Jun 11;155(2):144-7. doi: 10.1016/0304-3940(93)90693-f. Neurosci Lett. 1993. PMID: 8377943

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