Doyu M - Search Results

1

[DNA diagnosis of X-linked recessive bulbospinal muscular atrophy by androgen receptor gene mutations].

Doyu M, Sobue G, Mukai E, Takahashi A, Mitsuma T. Doyu M, et al. Rinsho Shinkeigaku. 1992 Mar;32(3):336-9. Rinsho Shinkeigaku. 1992. PMID: 1628462 Japanese.

2

Comparison between valsartan and amlodipine regarding cardiovascular morbidity and mortality in hypertensive patients with glucose intolerance: NAGOYA HEART Study.

Muramatsu T, Matsushita K, Yamashita K, Kondo T, Maeda K, Shintani S, Ichimiya S, Ohno M, Sone T, Ikeda N, Watarai M, Murohara T; NAGOYA HEART Study Investigators. Muramatsu T, et al. Hypertension. 2012 Mar;59(3):580-6. doi: 10.1161/HYPERTENSIONAHA.111.184226. Epub 2012 Jan 9. Hypertension. 2012. Retraction in: Hypertension. 2018 Sep;72(3):e37-e38. doi: 10.1161/HYP.0000000000000079. PMID: 22232134 Retracted. Clinical Trial.

3

The Influence of Age on the Outcomes of Traumatic Brain Injury: Findings from a Japanese Nationwide Survey (J-ASPECT Study-Traumatic Brain Injury).

Yamagami K, Kurogi R, Kurogi A, Nishimura K, Onozuka D, Ren N, Kada A, Nishimura A, Arimura K, Ido K, Mizoguchi M, Sakamoto T, Kayama T, Suzuki M, Arai H, Hagihara A, Iihara K; J-ASPECT Study Collaborators. Yamagami K, et al. World Neurosurg. 2019 Oct;130:e26-e46. doi: 10.1016/j.wneu.2019.05.140. Epub 2019 May 24. World Neurosurg. 2019. PMID: 31132488

4

Impact of low levels of vascular endothelial growth factor after myocardial infarction on 6-month clinical outcome. Results from the Nagoya Acute Myocardial Infarction Study.

Matsudaira K, Maeda K, Okumura N, Yoshikawa D, Morita Y, Mitsuhashi H, Ishii H, Kondo T, Murohara T; Nagoya Acute Myocardial Infarction Study (NAMIS) Group. Matsudaira K, et al. Circ J. 2012;76(6):1509-16. doi: 10.1253/circj.cj-11-1127. Epub 2012 Mar 27. Circ J. 2012. PMID: 22452999 Free article.

5

Severity of X-linked recessive bulbospinal neuronopathy correlates with size of the tandem CAG repeat in androgen receptor gene.

Doyu M, Sobue G, Mukai E, Kachi T, Yasuda T, Mitsuma T, Takahashi A. Doyu M, et al. Ann Neurol. 1992 Nov;32(5):707-10. doi: 10.1002/ana.410320517. Ann Neurol. 1992. PMID: 1449253

6

Extensive demyelinating changes in the peripheral nerves of Crow-Fukase syndrome: a pathological study of one autopsied case.

Sobue G, Doyu M, Watanabe M, Hayashi F, Mitsuma T. Sobue G, et al. Among authors: doyu m. Acta Neuropathol. 1992;84(2):171-7. doi: 10.1007/BF00311391. Acta Neuropathol. 1992. PMID: 1523972

7

Human peripheral nerve sheath neoplasm: expression of Schwann cell-related markers and their relation to malignant transformation.

Yasuda T, Sobue G, Ito T, Doyu M, Sugiura I, Hashizume Y, Kato K. Yasuda T, et al. Among authors: doyu m. Muscle Nerve. 1991 Sep;14(9):812-9. doi: 10.1002/mus.880140903. Muscle Nerve. 1991. PMID: 1656253

8

X-linked recessive bulbospinal neuronopathy: clinical phenotypes and CAG repeat size in androgen receptor gene.

Shimada N, Sobue G, Doyu M, Yamamoto K, Yasuda T, Mukai E, Kachi T, Mitsuma T. Shimada N, et al. Among authors: doyu m. Muscle Nerve. 1995 Dec;18(12):1378-84. doi: 10.1002/mus.880181206. Muscle Nerve. 1995. PMID: 7477059

9

[Abnormality of PMP-22 gene in Japanese patients with Charcot-Marie-Tooth disease--comparison between Southern blot and polymerase chain reaction analysis in the detection of PMP-22 gene duplication].

Yamamoto M, Sobue G, Kumazawa K, Doyu M, Mitsuma T, Hayasaka K. Yamamoto M, et al. Among authors: doyu m. No To Shinkei. 1995 Jul;47(7):687-91. No To Shinkei. 1995. PMID: 7612387 Japanese.

10

Molecular features of the CAG repeats and clinical manifestation of Machado-Joseph disease.

Maruyama H, Nakamura S, Matsuyama Z, Sakai T, Doyu M, Sobue G, Seto M, Tsujihata M, Oh-i T, Nishio T, et al. Maruyama H, et al. Among authors: doyu m. Hum Mol Genet. 1995 May;4(5):807-12. doi: 10.1093/hmg/4.5.807. Hum Mol Genet. 1995. PMID: 7633439

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