Katsuno M - Search Results

1

Clinicopathological features of adult-onset neuronal intranuclear inclusion disease.

Sone J, Mori K, Inagaki T, Katsumata R, Takagi S, Yokoi S, Araki K, Kato T, Nakamura T, Koike H, Takashima H, Hashiguchi A, Kohno Y, Kurashige T, Kuriyama M, Takiyama Y, Tsuchiya M, Kitagawa N, Kawamoto M, Yoshimura H, Suto Y, Nakayasu H, Uehara N, Sugiyama H, Takahashi M, Kokubun N, Konno T, Katsuno M, Tanaka F, Iwasaki Y, Yoshida M, Sobue G. Sone J, et al. Among authors: katsuno m. Brain. 2016 Dec;139(Pt 12):3170-3186. doi: 10.1093/brain/aww249. Epub 2016 Oct 25. Brain. 2016. PMID: 27797808 Free PMC article.

2

[A case of familial hypokalemic periodic paralysis with hyperuricemia during paralytic attack and genetic analysis of the pedigree].

Katsuno M, Ando T, Hakusui S, Yanagi T, Adachi Y, Sobue G. Katsuno M, et al. Rinsho Shinkeigaku. 2001 Jul;41(7):397-401. Rinsho Shinkeigaku. 2001. PMID: 11808349 Japanese.

3

Motor conduction studies in Miller Fisher syndrome with severe tetraparesis.

Katsuno M, Ando T, Hakusui S, Yanagi T, Sobue G. Katsuno M, et al. Muscle Nerve. 2002 Mar;25(3):378-82. doi: 10.1002/mus.10055. Muscle Nerve. 2002. PMID: 11870714

4

Testosterone reduction prevents phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy.

Katsuno M, Adachi H, Kume A, Li M, Nakagomi Y, Niwa H, Sang C, Kobayashi Y, Doyu M, Sobue G. Katsuno M, et al. Neuron. 2002 Aug 29;35(5):843-54. doi: 10.1016/s0896-6273(02)00834-6. Neuron. 2002. PMID: 12372280 Free article.

5

Leuprorelin rescues polyglutamine-dependent phenotypes in a transgenic mouse model of spinal and bulbar muscular atrophy.

Katsuno M, Adachi H, Doyu M, Minamiyama M, Sang C, Kobayashi Y, Inukai A, Sobue G. Katsuno M, et al. Nat Med. 2003 Jun;9(6):768-73. doi: 10.1038/nm878. Epub 2003 May 18. Nat Med. 2003. PMID: 12754502

6

Transgenic mouse models of spinal and bulbar muscular atrophy (SBMA).

Katsuno M, Adachi H, Inukai A, Sobue G. Katsuno M, et al. Cytogenet Genome Res. 2003;100(1-4):243-51. doi: 10.1159/000072860. Cytogenet Genome Res. 2003. PMID: 14526186 Review.

7

Multiple regional 1H-MR spectroscopy in multiple system atrophy: NAA/Cr reduction in pontine base as a valuable diagnostic marker.

Watanabe H, Fukatsu H, Katsuno M, Sugiura M, Hamada K, Okada Y, Hirayama M, Ishigaki T, Sobue G. Watanabe H, et al. Among authors: katsuno m. J Neurol Neurosurg Psychiatry. 2004 Jan;75(1):103-9. J Neurol Neurosurg Psychiatry. 2004. PMID: 14707317 Free PMC article. Clinical Trial.

8

Sweet relief for Huntington disease.

Katsuno M, Adachi H, Sobue G. Katsuno M, et al. Nat Med. 2004 Feb;10(2):123-4. doi: 10.1038/nm0204-123. Nat Med. 2004. PMID: 14760414 No abstract available.

9

Polyglutamine diminishes VEGF; passage to motor neuron death?

Katsuno M, Sobue G. Katsuno M, et al. Neuron. 2004 Mar 4;41(5):677-9. doi: 10.1016/s0896-6273(04)00110-2. Neuron. 2004. PMID: 15003165 Free article. Review.

10

Sodium butyrate ameliorates phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy.

Minamiyama M, Katsuno M, Adachi H, Waza M, Sang C, Kobayashi Y, Tanaka F, Doyu M, Inukai A, Sobue G. Minamiyama M, et al. Among authors: katsuno m. Hum Mol Genet. 2004 Jun 1;13(11):1183-92. doi: 10.1093/hmg/ddh131. Epub 2004 Apr 21. Hum Mol Genet. 2004. PMID: 15102712

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