Kikugawa K - Search Results

1

Corticobasal degeneration with focal, massive tau accumulation in the subcortical white matter astrocytes.

Sakai K, Piao YS, Kikugawa K, Ohara S, Hasegawa M, Takano H, Fukase M, Nishizawa M, Kakita A, Takahashi H. Sakai K, et al. Among authors: kikugawa k. Acta Neuropathol. 2006 Sep;112(3):341-8. doi: 10.1007/s00401-006-0093-5. Epub 2006 Jun 28. Acta Neuropathol. 2006. PMID: 16804710

2

Primary lateral sclerosis: a rare upper-motor-predominant form of amyotrophic lateral sclerosis often accompanied by frontotemporal lobar degeneration with ubiquitinated neuronal inclusions? Report of an autopsy case and a review of the literature.

Tan CF, Kakita A, Piao YS, Kikugawa K, Endo K, Tanaka M, Okamoto K, Takahashi H. Tan CF, et al. Among authors: kikugawa k. Acta Neuropathol. 2003 Jun;105(6):615-20. doi: 10.1007/s00401-003-0687-0. Epub 2003 Mar 1. Acta Neuropathol. 2003. PMID: 12734667

3

Familial amyotrophic lateral sclerosis: a SOD1-unrelated Japanese family of bulbar type with Bunina bodies and ubiquitin-positive skein-like inclusions in lower motor neurons.

Tagawa A, Tan CF, Kikugawa K, Fukase M, Nakano R, Onodera O, Nishizawa M, Takahashi H. Tagawa A, et al. Among authors: kikugawa k. Acta Neuropathol. 2007 Feb;113(2):205-11. doi: 10.1007/s00401-006-0151-z. Epub 2006 Oct 12. Acta Neuropathol. 2007. PMID: 17036243

4

Familial amyotrophic lateral sclerosis with onset in bulbar sign, benign clinical course, and Bunina bodies: a clinical, genetic, and pathological study of a Japanese family.

Tsuchiya K, Shintani S, Nakabayashi H, Kikugawa K, Nakano R, Haga C, Nakano I, Ikeda K, Tsuji S. Tsuchiya K, et al. Among authors: kikugawa k. Acta Neuropathol. 2000 Dec;100(6):603-7. doi: 10.1007/s004010000237. Acta Neuropathol. 2000. PMID: 11078211

5

Instability of mutant Cu/Zn superoxide dismutase (Ala4Thr) associated with familial amyotrophic lateral sclerosis.

Nakano R, Inuzuka T, Kikugawa K, Takahashi H, Sakimura K, Fujii J, Taniguchi N, Tsuji S. Nakano R, et al. Among authors: kikugawa k. Neurosci Lett. 1996 Jun 21;211(2):129-31. doi: 10.1016/0304-3940(96)12701-4. Neurosci Lett. 1996. PMID: 8830861

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: kikugawa k. Neurosci Lett. 1998 Nov 20;257(1):29-32. doi: 10.1016/s0304-3940(98)00800-3. Neurosci Lett. 1998. PMID: 9857958

7

[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: kikugawa k. Rinsho Shinkeigaku. 1999 Dec;39(12):1283-4. Rinsho Shinkeigaku. 1999. PMID: 10791098 Japanese.

8

Transgenic mice harboring a full-length human mutant DRPLA gene exhibit age-dependent intergenerational and somatic instabilities of CAG repeats comparable with those in DRPLA patients.

Sato T, Oyake M, Nakamura K, Nakao K, Fukusima Y, Onodera O, Igarashi S, Takano H, Kikugawa K, Ishida Y, Shimohata T, Koide R, Ikeuchi T, Tanaka H, Futamura N, Matsumura R, Takayanagi T, Tanaka F, Sobue G, Komure O, Takahashi M, Sano A, Ichikawa Y, Goto J, Kanazawa I, et al. Sato T, et al. Among authors: kikugawa k. Hum Mol Genet. 1999 Jan;8(1):99-106. doi: 10.1093/hmg/8.1.99. Hum Mol Genet. 1999. PMID: 9887337

9

Sacsin-related ataxia with neither retinal hypermyelination nor spasticity.

Hara K, Shimbo J, Nozaki H, Kikugawa K, Onodera O, Nishizawa M. Hara K, et al. Among authors: kikugawa k. Mov Disord. 2007 Jul 15;22(9):1362-3. doi: 10.1002/mds.21557. Mov Disord. 2007. PMID: 17516465 No abstract available.

10

Administration of prosaposin ameliorates spatial learning disturbance and reduces cavity formation following stab wounds in rat brain.

Hozumi I, Hiraiwa M, Inuzuka T, Yoneoka Y, Akiyama K, Tanaka R, Kikugawa K, Nakano R, Tsuji S, O'Brien JS. Hozumi I, et al. Among authors: kikugawa k. Neurosci Lett. 1999 May 21;267(1):73-6. doi: 10.1016/s0304-3940(99)00325-0. Neurosci Lett. 1999. PMID: 10400252

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