Yamagata H - Search Results

1

[Effect of elapsed time after standing up on orthostatic blood pressure change in the elderly].

Tabara Y, Kohara K, Ohnishi M, Ueki S, Yano H, Yamamoto Y, Igase M, Yamagata H, Nakura J, Miki T. Tabara Y, et al. Among authors: yamagata h. Nihon Ronen Igakkai Zasshi. 2002 Mar;39(2):193-6. doi: 10.3143/geriatrics.39.193. Nihon Ronen Igakkai Zasshi. 2002. PMID: 11974944 Free article. Japanese.

2

[A very elderly autopsy case of cecal cancer with pulmonary lymphangitis carcinomatosa].

Matsubara M, Kohara K, Uemura K, Taguchi K, Igase M, Yamagata H, Nakura J, Miki T. Matsubara M, et al. Among authors: yamagata h. Nihon Ronen Igakkai Zasshi. 2000 Jul;37(7):561-4. doi: 10.3143/geriatrics.37.561. Nihon Ronen Igakkai Zasshi. 2000. PMID: 11031830 Free article. Japanese.

3

[A case of mild-type myotonic dystrophy with dementia and severe arteriosclerosis obliterans].

Horiki M, Morishima A, Yamagata H, Rakugi H, Ikegami H, Miki T, Ogihara T. Horiki M, et al. Among authors: yamagata h. Nihon Ronen Igakkai Zasshi. 1998 Feb;35(2):136-8. doi: 10.3143/geriatrics.35.136. Nihon Ronen Igakkai Zasshi. 1998. PMID: 9584492 Free article. Japanese.

4

[Genomic instability and neurodegenerative disease].

Miki T, Yamagata H. Miki T, et al. Among authors: yamagata h. Rinsho Byori. 1999 Jan;47(1):37-45. Rinsho Byori. 1999. PMID: 10067364 Japanese.

5

[Molecular genetics of myotonic dystrophy--population genetics of the CTG repeat expansion of the MTPK gene].

Yamagata H, Miki T, Ogihara T. Yamagata H, et al. Nihon Rinsho. 1997 Dec;55(12):3205-9. Nihon Rinsho. 1997. PMID: 9436437 Review. Japanese.

6

The 4,752 C/T polymorphism in the presenilin 1 gene increases the risk of Alzheimer's disease in apolipoprotein E4 carriers.

Matsubara-Tsutsui M, Yamagata H, Morishima A, Nakura J, Mitsuda N, Kamino K, Kondo I, Miki T. Matsubara-Tsutsui M, et al. Among authors: yamagata h. Intern Med. 2002 Oct;41(10):823-8. doi: 10.2169/internalmedicine.41.823. Intern Med. 2002. PMID: 12413003 Free article.

7

Molecular evidence of presenilin 1 mutation in familial early onset dementia.

Matsubara-Tsutsui M, Yasuda M, Yamagata H, Nomura T, Taguchi K, Kohara K, Miyoshi K, Miki T. Matsubara-Tsutsui M, et al. Among authors: yamagata h. Am J Med Genet. 2002 Apr 8;114(3):292-8. doi: 10.1002/ajmg.10250. Am J Med Genet. 2002. PMID: 11920851

8

[Advances in molecular genetics of myotonic dystrophy].

Yamagata H, Yamanaka N, Miki T, Ogihara T. Yamagata H, et al. Nihon Rinsho. 1993 Sep;51(9):2474-80. Nihon Rinsho. 1993. PMID: 8411731 Review. Japanese.

9

Two dinucleotide repeat polymorphisms at the D8S1442 and D8S1443 loci.

Nakura J, Ye L, Kihara K, Yamagata H, Kamino K, Nakamura Y, Miki T, Ogihara T. Nakura J, et al. Among authors: yamagata h. Jpn J Hum Genet. 1995 Sep;40(3):281-2. doi: 10.1007/BF01876188. Jpn J Hum Genet. 1995. PMID: 8527804 No abstract available.

10

[Molecular genetics of myotonic dystrophy].

Miki T, Yamagata H, Ogihara T. Miki T, et al. Among authors: yamagata h. Rinsho Shinkeigaku. 1995 Dec;35(12):1479-81. Rinsho Shinkeigaku. 1995. PMID: 8752436 Review. Japanese.

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