Fujita K - Search Results

1

Long-Term Follow-Up of 12 Patients Treated with Bilateral Pallidal Stimulation for Tardive Dystonia.

Koyama H, Mure H, Morigaki R, Miyamoto R, Miyake K, Matsuda T, Fujita K, Izumi Y, Kaji R, Goto S, Takagi Y. Koyama H, et al. Among authors: fujita k. Life (Basel). 2021 May 24;11(6):477. doi: 10.3390/life11060477. Life (Basel). 2021. PMID: 34074009 Free PMC article.

2

Diffusion tensor imaging in patients with Creutzfeldt-Jakob disease.

Fujita K, Nakane S, Harada M, Izumi Y, Kaji R. Fujita K, et al. J Neurol Neurosurg Psychiatry. 2008 Nov;79(11):1304-6. doi: 10.1136/jnnp.2008.148528. J Neurol Neurosurg Psychiatry. 2008. PMID: 18940995 No abstract available.

3

Temporal evolution of sporadic Creutzfeldt-Jakob disease monitored by 3-Tesla MR spectroscopy.

Fujita K, Harada M, Yuasa T, Sasaki M, Izumi Y, Kaji R. Fujita K, et al. J Neurol. 2011 Jul;258(7):1368-70. doi: 10.1007/s00415-011-5939-7. Epub 2011 Feb 17. J Neurol. 2011. PMID: 21327850 No abstract available.

4

Effects of a brain-engraftable microglial cell line expressing anti-prion scFv antibodies on survival times of mice infected with scrapie prions.

Fujita K, Yamaguchi Y, Mori T, Muramatsu N, Miyamoto T, Yano M, Miyata H, Ootsuyama A, Sawada M, Matsuda H, Kaji R, Sakaguchi S. Fujita K, et al. Cell Mol Neurobiol. 2011 Oct;31(7):999-1008. doi: 10.1007/s10571-011-9696-z. Epub 2011 Apr 23. Cell Mol Neurobiol. 2011. PMID: 21516351

5

Brainstem and spinal cord motor neuron involvement with optineurin inclusions in proximal-dominant hereditary motor and sensory neuropathy.

Fujita K, Yoshida M, Sako W, Maeda K, Hashizume Y, Goto S, Sobue G, Izumi Y, Kaji R. Fujita K, et al. J Neurol Neurosurg Psychiatry. 2011 Dec;82(12):1402-3. doi: 10.1136/jnnp-2011-300783. Epub 2011 Aug 11. J Neurol Neurosurg Psychiatry. 2011. PMID: 21836032 No abstract available.

6

Multicentre multiobserver study of diffusion-weighted and fluid-attenuated inversion recovery MRI for the diagnosis of sporadic Creutzfeldt-Jakob disease: a reliability and agreement study.

Fujita K, Harada M, Sasaki M, Yuasa T, Sakai K, Hamaguchi T, Sanjo N, Shiga Y, Satoh K, Atarashi R, Shirabe S, Nagata K, Maeda T, Murayama S, Izumi Y, Kaji R, Yamada M, Mizusawa H. Fujita K, et al. BMJ Open. 2012 Jan 30;2(1):e000649. doi: 10.1136/bmjopen-2011-000649. Print 2012. BMJ Open. 2012. PMID: 22290397 Free PMC article.

7

[Inflammatory mechanisms in amyotrophic lateral sclerosis].

Fujita K, Izumi Y, Kaji R. Fujita K, et al. Brain Nerve. 2012 Mar;64(3):273-8. Brain Nerve. 2012. PMID: 22402721 Review. Japanese.

8

Early detection of familial Creutzfeldt-Jakob disease on diffusion-weighted imaging before symptom onset.

Terasawa Y, Fujita K, Izumi Y, Kaji R. Terasawa Y, et al. Among authors: fujita k. J Neurol Sci. 2012 Aug 15;319(1-2):130-2. doi: 10.1016/j.jns.2012.04.004. Epub 2012 May 27. J Neurol Sci. 2012. PMID: 22640903

9

Analysis of C9orf72 repeat expansion in 563 Japanese patients with amyotrophic lateral sclerosis.

Ogaki K, Li Y, Atsuta N, Tomiyama H, Funayama M, Watanabe H, Nakamura R, Yoshino H, Yato S, Tamura A, Naito Y, Taniguchi A, Fujita K, Izumi Y, Kaji R, Hattori N, Sobue G; Japanese Consortium for Amyotrophic Lateral Sclerosis research (JaCALS). Ogaki K, et al. Among authors: fujita k. Neurobiol Aging. 2012 Oct;33(10):2527.e11-6. doi: 10.1016/j.neurobiolaging.2012.05.011. Epub 2012 Jun 21. Neurobiol Aging. 2012. PMID: 22727276

10

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: fujita k. Clin Neuropathol. 2012 Nov-Dec;31(6):418-23. doi: 10.5414/NP300493. Clin Neuropathol. 2012. PMID: 22762947

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