Sobue G - Search Results

1

Visuoperceptual disturbances in Parkinson's disease.

Kawabata K, Ohdake R, Watanabe H, Bagarinao E, Hara K, Ogura A, Masuda M, Kato T, Yokoi T, Katsuno M, Sobue G. Kawabata K, et al. Among authors: sobue g. Clin Park Relat Disord. 2020 Jan 16;3:100036. doi: 10.1016/j.prdoa.2020.100036. eCollection 2020. Clin Park Relat Disord. 2020. PMID: 34316622 Free PMC article.

2

[18F-fluorodeoxyglucose positron emission tomography in Parkinson's disease].

Arahata Y, Kato T, Tadokoro M, Sobue G. Arahata Y, et al. Among authors: sobue g. Nihon Rinsho. 1997 Jan;55(1):222-6. Nihon Rinsho. 1997. PMID: 9014454 Review. Japanese.

3

Frequency analysis of autosomal dominant cerebellar ataxias in Japanese patients and clinical characterization of spinocerebellar ataxia type 6.

Watanabe H, Tanaka F, Matsumoto M, Doyu M, Ando T, Mitsuma T, Sobue G. Watanabe H, et al. Among authors: sobue g. Clin Genet. 1998 Jan;53(1):13-9. doi: 10.1034/j.1399-0004.1998.531530104.x. Clin Genet. 1998. PMID: 9550356

4

The protective effect of a persistent trigeminal artery on brain stem infarctions: a follow-up case report.

Ito Y, Watanabe H, Niwa H, Hakusui S, Ando T, Yasuda T, Sobue G, Yanagi T. Ito Y, et al. Among authors: sobue g. Intern Med. 1998 Mar;37(3):334-7. doi: 10.2169/internalmedicine.37.334. Intern Med. 1998. PMID: 9617875 Free article.

5

Parieto-occipital glucose hypometabolism in Parkinson's disease with autonomic failure.

Arahata Y, Hirayama M, Ieda T, Koike Y, Kato T, Tadokoro M, Ikeda M, Ito K, Sobue G. Arahata Y, et al. Among authors: sobue g. J Neurol Sci. 1999 Mar 1;163(2):119-26. doi: 10.1016/s0022-510x(99)00011-8. J Neurol Sci. 1999. PMID: 10371072

6

[CNS cryptococcosis with idiopathic CD4+ T lymphocytopenia].

Watanabe H, Inukai A, Doyu M, Sobue G. Watanabe H, et al. Among authors: sobue g. Rinsho Shinkeigaku. 2000 Mar;40(3):249-53. Rinsho Shinkeigaku. 2000. PMID: 10885336 Review. Japanese.

7

Sisters homozygous for the spinocerebellar ataxia type 6 (SCA6)/CACNA1A gene associated with different clinical phenotypes.

Kato T, Tanaka F, Yamamoto M, Yosida E, Indo T, Watanabe H, Yoshiwara T, Doyu M, Sobue G. Kato T, et al. Among authors: sobue g. Clin Genet. 2000 Jul;58(1):69-73. doi: 10.1034/j.1399-0004.2000.580112.x. Clin Genet. 2000. PMID: 10945665

8

Reduced expression of DMAHP/SIX5 gene in myotonic dystrophy muscle.

Inukai A, Doyu M, Kato T, Liang Y, Kuru S, Yamamoto M, Kobayashi Y, Sobue G. Inukai A, et al. Among authors: sobue g. Muscle Nerve. 2000 Sep;23(9):1421-6. doi: 10.1002/1097-4598(200009)23:9<1421::aid-mus14>3.0.co;2-y. Muscle Nerve. 2000. PMID: 10951446

9

The role of lymphotoxin in pathogenesis of polymyositis.

Liang Y, Inukai A, Kuru S, Kato T, Doyu M, Sobue G. Liang Y, et al. Among authors: sobue g. Acta Neuropathol. 2000 Nov;100(5):521-7. doi: 10.1007/s004010000207. Acta Neuropathol. 2000. PMID: 11045674

10

Differential somatic CAG repeat instability in variable brain cell lineage in dentatorubral pallidoluysian atrophy (DRPLA): a laser-captured microdissection (LCM)-based analysis.

Watanabe H, Tanaka F, Doyu M, Riku S, Yoshida M, Hashizume Y, Sobue G. Watanabe H, et al. Among authors: sobue g. Hum Genet. 2000 Nov;107(5):452-7. doi: 10.1007/s004390000400. Hum Genet. 2000. PMID: 11140942

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