Fukada K - Search Results

1

Stabilization of mutant Cu/Zn superoxide dismutase (SOD1) protein by coexpressed wild SOD1 protein accelerates the disease progression in familial amyotrophic lateral sclerosis mice.

Fukada K, Nagano S, Satoh M, Tohyama C, Nakanishi T, Shimizu A, Yanagihara T, Sakoda S. Fukada K, et al. Eur J Neurosci. 2001 Dec;14(12):2032-6. doi: 10.1046/j.0953-816x.2001.01828.x. Eur J Neurosci. 2001. PMID: 11860498

2

The efficacy of trientine or ascorbate alone compared to that of the combined treatment with these two agents in familial amyotrophic lateral sclerosis model mice.

Nagano S, Fujii Y, Yamamoto T, Taniyama M, Fukada K, Yanagihara T, Sakoda S. Nagano S, et al. Among authors: fukada k. Exp Neurol. 2003 Feb;179(2):176-80. doi: 10.1016/s0014-4886(02)00014-6. Exp Neurol. 2003. PMID: 12618124

3

Identification of two novel mutations in the Cu/Zn superoxide dismutase gene with familial amyotrophic lateral sclerosis: mass spectrometric and genomic analyses.

Sato T, Yamamoto Y, Nakanishi T, Fukada K, Sugai F, Zhou Z, Okuno T, Nagano S, Hirata S, Shimizu A, Sakoda S. Sato T, et al. Among authors: fukada k. J Neurol Sci. 2004 Mar 15;218(1-2):79-83. doi: 10.1016/j.jns.2003.11.003. J Neurol Sci. 2004. PMID: 14759637

4

Rapid disease progression correlates with instability of mutant SOD1 in familial ALS.

Sato T, Nakanishi T, Yamamoto Y, Andersen PM, Ogawa Y, Fukada K, Zhou Z, Aoike F, Sugai F, Nagano S, Hirata S, Ogawa M, Nakano R, Ohi T, Kato T, Nakagawa M, Hamasaki T, Shimizu A, Sakoda S. Sato T, et al. Among authors: fukada k. Neurology. 2005 Dec 27;65(12):1954-7. doi: 10.1212/01.wnl.0000188760.53922.05. Epub 2005 Nov 16. Neurology. 2005. PMID: 16291929

5

Clinical and pathological studies of familial amyotrophic lateral sclerosis (FALS) with SOD1 H46R mutation in large Japanese families.

Arisato T, Okubo R, Arata H, Abe K, Fukada K, Sakoda S, Shimizu A, Qin XH, Izumo S, Osame M, Nakagawa M. Arisato T, et al. Among authors: fukada k. Acta Neuropathol. 2003 Dec;106(6):561-8. doi: 10.1007/s00401-003-0763-5. Epub 2003 Sep 27. Acta Neuropathol. 2003. PMID: 14517684

6

[A patient presented with atypical paroxysmal kinesigenic choreoathetosis and Becker muscular dystrophy].

Fukada K, Moriya M, Kaido M, Abe K, Umi M, Yanagihara T. Fukada K, et al. Rinsho Shinkeigaku. 2000 Feb;40(2):174-7. Rinsho Shinkeigaku. 2000. PMID: 10835941 Japanese.

7

[Risk factors for fractures in Parkinson's disease: a questionnaire survey].

Fukada K, Yokoe M, Hazama T, Yamamoto Y, Mochizuki H, Sakoda S. Fukada K, et al. Brain Nerve. 2013 Jun;65(6):687-92. Brain Nerve. 2013. PMID: 23735531 Japanese.

8

A quantitative characterization of postural sway during human quiet standing using a thin pressure distribution measurement system.

Nomura K, Fukada K, Azuma T, Hamasaki T, Sakoda S, Nomura T. Nomura K, et al. Among authors: fukada k. Gait Posture. 2009 Jun;29(4):654-7. doi: 10.1016/j.gaitpost.2009.02.001. Epub 2009 Mar 10. Gait Posture. 2009. PMID: 19278852

9

L-threo-3,4-dihydroxyphenylserine (L-DOPS) co-administered with entacapone improves freezing of gait in Parkinson's disease.

Fukada K, Endo T, Yokoe M, Hamasaki T, Hazama T, Sakoda S. Fukada K, et al. Med Hypotheses. 2013 Feb;80(2):209-12. doi: 10.1016/j.mehy.2012.11.031. Epub 2012 Dec 21. Med Hypotheses. 2013. PMID: 23265352 Clinical Trial.

10

Porphyria with double errors in the heme biosynthetic pathway.

Kaido M, Fukada K, Moriya M, Abe K, Sakoda S, Kondo M, Yanagihara T. Kaido M, et al. Among authors: fukada k. J Neurol. 2001 Apr;248(4):328-9. doi: 10.1007/s004150170209. J Neurol. 2001. PMID: 11374099 No abstract available.

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