Mori H - Search Results

1

Myoclonic tremulous movements in multiple system atrophy are a form of cortical myoclonus.

Okuma Y, Fujishima K, Miwa H, Mori H, Mizuno Y. Okuma Y, et al. Among authors: mori h. Mov Disord. 2005 Apr;20(4):451-456. doi: 10.1002/mds.20346. Mov Disord. 2005. PMID: 15593313

2

Mixed multiple system atrophy and progressive supranuclear palsy: a clinical and pathological report of one case.

Takanashi M, Ohta S, Matsuoka S, Mori H, Mizuno Y. Takanashi M, et al. Among authors: mori h. Acta Neuropathol. 2002 Jan;103(1):82-7. doi: 10.1007/s004010100433. Acta Neuropathol. 2002. PMID: 11837750

3

Prognosis of Parkinson's disease: time to stage III, IV, V, and to motor fluctuations.

Sato K, Hatano T, Yamashiro K, Kagohashi M, Nishioka K, Izawa N, Mochizuki H, Hattori N, Mori H, Mizuno Y; Juntendo Parkinson Study Group. Sato K, et al. Among authors: mori h. Mov Disord. 2006 Sep;21(9):1384-95. doi: 10.1002/mds.20993. Mov Disord. 2006. PMID: 16763980

4

Genotype-phenotype correlation: familial Parkinson disease.

Mori H, Hattori N, Mizuno Y. Mori H, et al. Neuropathology. 2003 Mar;23(1):90-4. doi: 10.1046/j.1440-1789.2003.00476.x. Neuropathology. 2003. PMID: 12722931 Review.

5

Nuclear localization of the 20S proteasome subunit in Parkinson's disease.

Nakamura A, Kitami T, Mori H, Mizuno Y, Hattori N. Nakamura A, et al. Among authors: mori h. Neurosci Lett. 2006 Oct 2;406(1-2):43-8. doi: 10.1016/j.neulet.2006.07.050. Neurosci Lett. 2006. PMID: 16911859

6

Lewy body pathology in a patient with a homozygous parkin deletion.

Miyakawa S, Ogino M, Funabe S, Uchino A, Shimo Y, Hattori N, Ichinoe M, Mikami T, Saegusa M, Nishiyama K, Mori H, Mizuno Y, Murayama S, Mochizuki H. Miyakawa S, et al. Among authors: mori h. Mov Disord. 2013 Mar;28(3):388-91. doi: 10.1002/mds.25346. Epub 2013 Feb 11. Mov Disord. 2013. PMID: 23401296

7

[A 65-year-old woman with progressive loss of vision and visual field defects].

Furuya T, Namihira T, Yamazaki S, Mori H, Hattori N, Mizuno Y. Furuya T, et al. Among authors: mori h. No To Shinkei. 2003 Jan;55(1):87-96. No To Shinkei. 2003. PMID: 12649905 Japanese.

8

Pathological and biochemical studies on a case of Pick disease with severe white matter atrophy.

Yamakawa K, Takanashi M, Watanabe M, Nakamura N, Kobayashi T, Hasegawa M, Mizuno Y, Tanaka S, Mori H. Yamakawa K, et al. Among authors: mori h. Neuropathology. 2006 Dec;26(6):586-91. doi: 10.1111/j.1440-1789.2006.00738.x. Neuropathology. 2006. PMID: 17203597

9

[A 68-year-old woman with dementia and parkinsonism].

Yokoyama K, Ikebe S, Komatsuzaki Y, Takanashi M, Mori H, Mochizuki H, Mizuno Y. Yokoyama K, et al. Among authors: mori h. No To Shinkei. 2002 Feb;54(2):175-84. No To Shinkei. 2002. PMID: 11889767 Japanese.

10

Contrasting genotypes of the tau gene in two phenotypically distinct patients with P301L mutation of frontotemporal dementia and parkinsonism linked to chromosome 17.

Kobayashi T, Mori H, Okuma Y, Dickson DW, Cookson N, Tsuboi Y, Motoi Y, Tanaka R, Miyashita N, Anno M, Narabayashi H, Mizuno Y. Kobayashi T, et al. Among authors: mori h. J Neurol. 2002 Jun;249(6):669-75. doi: 10.1007/s00415-002-0687-3. J Neurol. 2002. PMID: 12111297

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