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Items: 10

1.

Neurosyphilis presenting as frontal and mesial temporal encephalitis.

Aizawa H, Yomono H, Kurisaki H.

Intern Med. 2013;52(20):2381-2. No abstract available.

2.

A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants.

Sharma M, Ioannidis JP, Aasly JO, Annesi G, Brice A, Bertram L, Bozi M, Barcikowska M, Crosiers D, Clarke CE, Facheris MF, Farrer M, Garraux G, Gispert S, Auburger G, Vilariño-Güell C, Hadjigeorgiou GM, Hicks AA, Hattori N, Jeon BS, Jamrozik Z, Krygowska-Wajs A, Lesage S, Lill CM, Lin JJ, Lynch T, Lichtner P, Lang AE, Libioulle C, Murata M, Mok V, Jasinska-Myga B, Mellick GD, Morrison KE, Meitnger T, Zimprich A, Opala G, Pramstaller PP, Pichler I, Park SS, Quattrone A, Rogaeva E, Ross OA, Stefanis L, Stockton JD, Satake W, Silburn PA, Strom TM, Theuns J, Tan EK, Toda T, Tomiyama H, Uitti RJ, Van Broeckhoven C, Wirdefeldt K, Wszolek Z, Xiromerisiou G, Yomono HS, Yueh KC, Zhao Y, Gasser T, Maraganore D, Krüger R; GEOPD consortium.

J Med Genet. 2012 Nov;49(11):721-6. doi: 10.1136/jmedgenet-2012-101155. Erratum in: J Med Genet. 2013 Mar;50(3):202.

3.

Spinocerebellar ataxia type 2 is associated with Parkinsonism and Lewy body pathology.

Takao M, Aoyama M, Ishikawa K, Sakiyama Y, Yomono H, Saito Y, Kurisaki H, Mihara B, Murayama S.

BMJ Case Rep. 2011 Apr 1;2011. pii: bcr0120113685. doi: 10.1136/bcr.01.2011.3685.

4.

[Autopsy case of SCA2 with Parkinsonian phenotype].

Yomono HS, Kurisaki H, Hebisawa A, Sakiyama Y, Saito Y, Murayama S.

Rinsho Shinkeigaku. 2010 Mar;50(3):156-62. Japanese.

PMID:
20235484
5.

Total deletion and a missense mutation of ITPR1 in Japanese SCA15 families.

Hara K, Shiga A, Nozaki H, Mitsui J, Takahashi Y, Ishiguro H, Yomono H, Kurisaki H, Goto J, Ikeuchi T, Tsuji S, Nishizawa M, Onodera O.

Neurology. 2008 Aug 19;71(8):547-51. doi: 10.1212/01.wnl.0000311277.71046.a0. Epub 2008 Jun 25.

PMID:
18579805
6.

[Case of opticospinal multiple sclerosis showing phenotype change to conventional type induced by interferon beta-1b].

Kanzaki M, Yomono H, Ogawa G, Motoyoshi K, Kurisaki H, Kamakura K.

Rinsho Shinkeigaku. 2007 Feb-Mar;47(2-3):100-4. Japanese.

PMID:
17511277
7.

Japanese SCA families with an unusual phenotype linked to a locus overlapping with SCA15 locus.

Hara K, Fukushima T, Suzuki T, Shimohata T, Oyake M, Ishiguro H, Hirota K, Miyashita A, Kuwano R, Kurisaki H, Yomono H, Goto J, Kanazawa I, Tsuji S.

Neurology. 2004 Feb 24;62(4):648-51.

PMID:
14981189
8.

[An autopsy case of multiple system atrophy with a heteroallelic ceruloplasmin gene mutation].

Yomono H, Kurisaki H, Murayama S, Hebisawa A, Miyajima H, Takahashi Y.

Rinsho Shinkeigaku. 2003 Jul;43(7):398-402. Japanese.

PMID:
14582365
9.

[Multiple system atrophy with a-/hypo-ceruloplasminemia: distribution of iron in brains of 2 autopsy cases].

Kurisaki H, Yomono H, Murayama S, Hebisawa A.

Rinsho Shinkeigaku. 2002 Apr;42(4):293-8. Japanese.

PMID:
12561083
10.

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