Yamada M - Search Results

1

Neuronal atrophy and synaptic alteration in a mouse model of dentatorubral-pallidoluysian atrophy.

Sakai K, Yamada M, Sato T, Yamada M, Tsuji S, Takahashi H. Sakai K, et al. Among authors: yamada m. Brain. 2006 Sep;129(Pt 9):2353-62. doi: 10.1093/brain/awl182. Epub 2006 Aug 3. Brain. 2006. PMID: 16891319

2

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. 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.

3

[Sisters with early onset hereditary dentatorubral-pallidoluysian atrophy of childhood--DNA analysis and clinicopathological findings].

Yamashita S, Iwamoto H, Hara M, Kondo I, Shimasaki Y, Higashi K, Miyake S, Yamada M. Yamashita S, et al. Among authors: yamada m. No To Hattatsu. 1995 Nov;27(6):473-9. No To Hattatsu. 1995. PMID: 8534513 Japanese.

4

Regional and cellular expression of the dentatorubral-pallidoluysian atrophy gene in brains of normal and affected individuals.

Nishiyama K, Nakamura K, Murayama S, Yamada M, Kanazawa I. Nishiyama K, et al. Among authors: yamada m. Ann Neurol. 1997 May;41(5):599-605. doi: 10.1002/ana.410410508. Ann Neurol. 1997. PMID: 9153521

5

Hereditary dentatorubral-pallidoluysian atrophy: detection of widespread ubiquitinated neuronal and glial intranuclear inclusions in the brain.

Hayashi Y, Kakita A, Yamada M, Koide R, Igarashi S, Takano H, Ikeuchi T, Wakabayashi K, Egawa S, Tsuji S, Takahashi H. Hayashi Y, et al. Among authors: yamada m. Acta Neuropathol. 1998 Dec;96(6):547-52. doi: 10.1007/s004010050933. Acta Neuropathol. 1998. PMID: 9845282

6

Formation of granular cytoplasmic aggregates in COS7 cells expressing mutant Cu/Zn superoxide dismutase associated with familial amyotrophic lateral sclerosis.

Koide T, Igarashi S, Kikugawa K, Nakano R, Inuzuka T, Yamada M, Takahashi H, Tsuji S. Koide T, et al. Among authors: yamada m. Neurosci Lett. 1998 Nov 20;257(1):29-32. doi: 10.1016/s0304-3940(98)00800-3. Neurosci Lett. 1998. PMID: 9857958

7

Immunohistochemical distribution of the two isoforms of synaphin/complexin involved in neurotransmitter release: localization at the distinct central nervous system regions and synaptic types.

Yamada M, Saisu H, Ishizuka T, Takahashi H, Abe T. Yamada M, et al. Neuroscience. 1999;93(1):7-18. doi: 10.1016/s0306-4522(99)00104-9. Neuroscience. 1999. PMID: 10430466

8

Nuclear accumulation of truncated atrophin-1 fragments in a transgenic mouse model of DRPLA.

Schilling G, Wood JD, Duan K, Slunt HH, Gonzales V, Yamada M, Cooper JK, Margolis RL, Jenkins NA, Copeland NG, Takahashi H, Tsuji S, Price DL, Borchelt DR, Ross CA. Schilling G, et al. Among authors: yamada m. Neuron. 1999 Sep;24(1):275-86. doi: 10.1016/s0896-6273(00)80839-9. Neuron. 1999. PMID: 10677044 Free article.

9

[Familial amyotrophic lateral sclerosis associated with mutant Cu/Zn superoxide dismutase as a conformational disease].

Koide T, Igarashi S, Kikugawa K, Nakano R, Inuzuka T, Tsuji S, Yamada M, Takahashi H. Koide T, et al. Among authors: yamada m. Rinsho Shinkeigaku. 1999 Dec;39(12):1283-4. Rinsho Shinkeigaku. 1999. PMID: 10791098 Japanese.

10

Atrophy of the basal ganglia as the initial diagnostic sign of germinoma in the basal ganglia.

Okamoto K, Ito J, Ishikawa K, Morii K, Yamada M, Takahashi N, Tokiguchi S, Furusawa T, Sakai K. Okamoto K, et al. Among authors: yamada m. Neuroradiology. 2002 May;44(5):389-94. doi: 10.1007/s00234-001-0735-1. Epub 2002 Feb 16. Neuroradiology. 2002. PMID: 12012122

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