Kanda F - Search Results

1

Efficacy and safety of leuprorelin in patients with spinal and bulbar muscular atrophy (JASMITT study): a multicentre, randomised, double-blind, placebo-controlled trial.

Katsuno M, Banno H, Suzuki K, Takeuchi Y, Kawashima M, Yabe I, Sasaki H, Aoki M, Morita M, Nakano I, Kanai K, Ito S, Ishikawa K, Mizusawa H, Yamamoto T, Tsuji S, Hasegawa K, Shimohata T, Nishizawa M, Miyajima H, Kanda F, Watanabe Y, Nakashima K, Tsujino A, Yamashita T, Uchino M, Fujimoto Y, Tanaka F, Sobue G; Japan SBMA Interventional Trial for TAP-144-SR (JASMITT) study group. Katsuno M, et al. Among authors: kanda f. Lancet Neurol. 2010 Sep;9(9):875-84. doi: 10.1016/S1474-4422(10)70182-4. Epub 2010 Aug 4. Lancet Neurol. 2010. PMID: 20691641 Clinical Trial.

2

Clinical features and skewed X-chromosome inactivation in female carriers of X-linked recessive spinal and bulbar muscular atrophy.

Ishihara H, Kanda F, Nishio H, Sumino K, Chihara K. Ishihara H, et al. Among authors: kanda f. J Neurol. 2001 Oct;248(10):856-60. doi: 10.1007/s004150170069. J Neurol. 2001. PMID: 11697521

3

Clinicopathological features of neuropathy associated with lymphoma.

Tomita M, Koike H, Kawagashira Y, Iijima M, Adachi H, Taguchi J, Abe T, Sako K, Tsuji Y, Nakagawa M, Kanda F, Takeda F, Sugawara M, Toyoshima I, Asano N, Sobue G. Tomita M, et al. Among authors: kanda f. Brain. 2013 Aug;136(Pt 8):2563-78. doi: 10.1093/brain/awt193. Brain. 2013. PMID: 23884813

4

Therapeutic regimen of L-arginine for MELAS: 9-year, prospective, multicenter, clinical research.

Koga Y, Povalko N, Inoue E, Nakamura H, Ishii A, Suzuki Y, Yoneda M, Kanda F, Kubota M, Okada H, Fujii K. Koga Y, et al. Among authors: kanda f. J Neurol. 2018 Dec;265(12):2861-2874. doi: 10.1007/s00415-018-9057-7. Epub 2018 Sep 29. J Neurol. 2018. PMID: 30269300 Free PMC article. Clinical Trial.

5

A novel missense mutation in the early growth response 2 gene associated with late-onset Charcot--Marie--Tooth disease type 1.

Yoshihara T, Kanda F, Yamamoto M, Ishihara H, Misu K, Hattori N, Chihara K, Sobue G. Yoshihara T, et al. Among authors: kanda f. J Neurol Sci. 2001 Mar 1;184(2):149-53. doi: 10.1016/s0022-510x(00)00504-9. J Neurol Sci. 2001. PMID: 11239949

6

Decreased expression of full-length mRNA for cBCD541 does not correlate with spinal muscular atrophy phenotype severity.

Nishio H, Ishikawa Y, Lee MJ, Fujii M, Kanda F, Jinnai K, Takahashi K, Takeshima Y, Wada H, Takada S, Nakamura H, Matsuo M, Sumino K. Nishio H, et al. Among authors: kanda f. Neurology. 1997 May;48(5):1266-70. doi: 10.1212/wnl.48.5.1266. Neurology. 1997. PMID: 9153454

7

Low signal intensity in motor cortex on susceptibility-weighted MR imaging is correlated with clinical signs of amyotrophic lateral sclerosis: a pilot study.

Endo H, Sekiguchi K, Shimada H, Ueda T, Kowa H, Kanda F, Toda T. Endo H, et al. Among authors: kanda f. J Neurol. 2018 Mar;265(3):552-561. doi: 10.1007/s00415-017-8728-0. Epub 2018 Jan 22. J Neurol. 2018. PMID: 29356968

8

Loss of serotonin-containing neurons in the raphe of patients with myotonic dystrophy: a quantitative immunohistochemical study and relation to hypersomnia.

Ono S, Takahashi K, Jinnai K, Kanda F, Fukuoka Y, Kurisaki H, Mitake S, Inagaki T, Yamano T, Nagao K. Ono S, et al. Among authors: kanda f. Neurology. 1998 Feb;50(2):535-8. doi: 10.1212/wnl.50.2.535. Neurology. 1998. PMID: 9484393

9

Long-term stabilization of respiratory conditions in patients with spinal muscular atrophy type 2 by continuous positive airway pressure: a report of two cases.

Katayama M, Naritomi H, Nishio H, Watanabe T, Teramoto S, Kanda F, Hazama A. Katayama M, et al. Among authors: kanda f. Kobe J Med Sci. 2011 Dec 28;57(3):E98-105. Kobe J Med Sci. 2011. PMID: 22971944 Free article.

10

Neuronal loss in the medullary reticular formation in myotonic dystrophy: a clinicopathological study.

Ono S, Kanda F, Takahashi K, Fukuoka Y, Jinnai K, Kurisaki H, Mitake S, Inagaki T, Nagao K. Ono S, et al. Among authors: kanda f. Neurology. 1996 Jan;46(1):228-31. doi: 10.1212/wnl.46.1.228. Neurology. 1996. PMID: 8559381

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