Kamada M - Search Results

1

Nuclear factor κ B expression in patients with sporadic amyotrophic lateral sclerosis and hereditary amyotrophic lateral sclerosis with optineurin mutations.

Sako W, Ito H, Yoshida M, Koizumi H, Kamada M, Fujita K, Hashizume Y, Izumi Y, Kaji R. Sako W, et al. Among authors: kamada m. Clin Neuropathol. 2012 Nov-Dec;31(6):418-23. doi: 10.5414/NP300493. Clin Neuropathol. 2012. PMID: 22762947

2

[Copper deficiency with SMON-like neurological symptoms and macrocytic anemia].

Mukai Y, Asanuma K, Mori A, Kamada M, Kawabata Y, Nodera H, Nakane S, Mitsui T, Izumi Y, Kaji R. Mukai Y, et al. Among authors: kamada m. Nihon Naika Gakkai Zasshi. 2008 Aug 10;97(8):1876-8. doi: 10.2169/naika.97.1876. Nihon Naika Gakkai Zasshi. 2008. PMID: 18788419 Japanese. No abstract available.

3

Screening for TARDBP mutations in Japanese familial amyotrophic lateral sclerosis.

Kamada M, Maruyama H, Tanaka E, Morino H, Wate R, Ito H, Kusaka H, Kawano Y, Miki T, Nodera H, Izumi Y, Kaji R, Kawakami H. Kamada M, et al. J Neurol Sci. 2009 Sep 15;284(1-2):69-71. doi: 10.1016/j.jns.2009.04.017. Epub 2009 May 2. J Neurol Sci. 2009. PMID: 19411082 Free article.

4

Mutations of optineurin in amyotrophic lateral sclerosis.

Maruyama H, Morino H, Ito H, Izumi Y, Kato H, Watanabe Y, Kinoshita Y, Kamada M, Nodera H, Suzuki H, Komure O, Matsuura S, Kobatake K, Morimoto N, Abe K, Suzuki N, Aoki M, Kawata A, Hirai T, Kato T, Ogasawara K, Hirano A, Takumi T, Kusaka H, Hagiwara K, Kaji R, Kawakami H. Maruyama H, et al. Among authors: kamada m. Nature. 2010 May 13;465(7295):223-6. doi: 10.1038/nature08971. Epub 2010 Apr 28. Nature. 2010. PMID: 20428114

5

Screening for OPTN mutations in amyotrophic lateral sclerosis in a mainly Caucasian population.

Sugihara K, Maruyama H, Kamada M, Morino H, Kawakami H. Sugihara K, et al. Among authors: kamada m. Neurobiol Aging. 2011 Oct;32(10):1923.e9-10. doi: 10.1016/j.neurobiolaging.2011.03.024. Epub 2011 May 6. Neurobiol Aging. 2011. PMID: 21550138 Free article.

6

Clinicopathologic features of autosomal recessive amyotrophic lateral sclerosis associated with optineurin mutation.

Kamada M, Izumi Y, Ayaki T, Nakamura M, Kagawa S, Kudo E, Sako W, Maruyama H, Nishida Y, Kawakami H, Ito H, Kaji R. Kamada M, et al. Neuropathology. 2014 Feb;34(1):64-70. doi: 10.1111/neup.12051. Epub 2013 Jul 29. Neuropathology. 2014. PMID: 23889540

7

A new CSF1R mutation presenting with an extensive white matter lesion mimicking primary progressive multiple sclerosis.

Inui T, Kawarai T, Fujita K, Kawamura K, Mitsui T, Orlacchio A, Kamada M, Abe T, Izumi Y, Kaji R. Inui T, et al. Among authors: kamada m. J Neurol Sci. 2013 Nov 15;334(1-2):192-5. doi: 10.1016/j.jns.2013.08.020. Epub 2013 Aug 29. J Neurol Sci. 2013. PMID: 24034409

8

Spastic paraplegia type 31: A novel REEP1 splice site donor variant and expansion of the phenotype variability.

Kamada M, Kawarai T, Miyamoto R, Kawakita R, Tojima Y, Montecchiani C, D'Onofrio L, Caltagirone C, Orlacchio A, Kaji R. Kamada M, et al. Parkinsonism Relat Disord. 2018 Jan;46:79-83. doi: 10.1016/j.parkreldis.2017.10.012. Epub 2017 Oct 21. Parkinsonism Relat Disord. 2018. PMID: 29107646

9

Multiple Proteinopathies in Familial ALS Cases With Optineurin Mutations.

Ayaki T, Ito H, Komure O, Kamada M, Nakamura M, Wate R, Kusaka H, Yamaguchi Y, Li F, Kawakami H, Urushitani M, Takahashi R. Ayaki T, et al. Among authors: kamada m. J Neuropathol Exp Neurol. 2018 Feb 1;77(2):128-138. doi: 10.1093/jnen/nlx109. J Neuropathol Exp Neurol. 2018. PMID: 29272468

10

CSF cystatin C and diffusion tensor imaging parameters as biomarkers of upper motor neuron degeneration in amyotrophic lateral sclerosis.

Nakane S, Fujita K, Azuma S, Urushihara R, Kamada M, Harada M, Izumi Y, Kaji R. Nakane S, et al. Among authors: kamada m. Clin Neurol Neurosurg. 2018 Sep;172:162-168. doi: 10.1016/j.clineuro.2018.07.008. Epub 2018 Jul 10. Clin Neurol Neurosurg. 2018. PMID: 30016754

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