Akagawa H - Search Results

1

Novel SLC20A2 mutation in a Japanese pedigree with primary familial brain calcification.

Kuroi Y, Akagawa H, Yoneyama T, Kikuchi A, Maegawa T, Onda H, Kasuya H. Kuroi Y, et al. Among authors: akagawa h. J Neurol Sci. 2019 Apr 15;399:183-185. doi: 10.1016/j.jns.2019.02.033. Epub 2019 Feb 23. J Neurol Sci. 2019. PMID: 30826713 No abstract available.

2

Association of positional and functional candidate genes FGF1, FBN2, and LOX on 5q31 with intracranial aneurysm.

Yoneyama T, Kasuya H, Onda H, Akagawa H, Jinnai N, Nakajima T, Hori T, Inoue I. Yoneyama T, et al. Among authors: akagawa h. J Hum Genet. 2003;48(6):309-314. doi: 10.1007/s10038-003-0030-6. Epub 2003 May 16. J Hum Genet. 2003. PMID: 12750963

3

Collagen type I alpha2 (COL1A2) is the susceptible gene for intracranial aneurysms.

Yoneyama T, Kasuya H, Onda H, Akagawa H, Hashiguchi K, Nakajima T, Hori T, Inoue I. Yoneyama T, et al. Among authors: akagawa h. Stroke. 2004 Feb;35(2):443-8. doi: 10.1161/01.STR.0000110788.45858.DC. Epub 2004 Jan 22. Stroke. 2004. PMID: 14739420

4

Absence of alpha-1 antitrypsin deficiency alleles (S and Z) in Japanese and Korean patients with aneurysmal subarachnoid hemorrhage.

Yoneyama T, Kasuya H, Akagawa H, Onda H, Nakajima T, Hori T, Inoue I, Lee JC, Yang TK, Kim CJ. Yoneyama T, et al. Among authors: akagawa h. Stroke. 2004 Dec;35(12):e376-8. doi: 10.1161/01.STR.0000147966.81215.be. Epub 2004 Nov 4. Stroke. 2004. PMID: 15528457

5

Influence of endothelial nitric oxide synthase T-786C single nucleotide polymorphism on aneurysm size.

Akagawa H, Kasuya H, Onda H, Yoneyama T, Sasahara A, Kim CJ, Lee JC, Yang TK, Hori T, Inoue I. Akagawa H, et al. J Neurosurg. 2005 Jan;102(1):68-71. doi: 10.3171/jns.2005.102.1.0068. J Neurosurg. 2005. PMID: 15658098

6

Is there any evidence for linkage on chromosome 17cen in affected Japanese sib-pairs with an intracranial aneurysm?

Krischek B, Narita A, Akagawa H, Kasuya H, Tajima A, Onda H, Yoneyama T, Hori T, Inoue I. Krischek B, et al. Among authors: akagawa h. J Hum Genet. 2006;51(5):491-494. doi: 10.1007/s10038-006-0379-4. Epub 2006 Mar 17. J Hum Genet. 2006. PMID: 16544051

7

A haplotype spanning two genes, ELN and LIMK1, decreases their transcripts and confers susceptibility to intracranial aneurysms.

Akagawa H, Tajima A, Sakamoto Y, Krischek B, Yoneyama T, Kasuya H, Onda H, Hori T, Kubota M, Machida T, Saeki N, Hata A, Hashiguchi K, Kimura E, Kim CJ, Yang TK, Lee JY, Kimm K, Inoue I. Akagawa H, et al. Hum Mol Genet. 2006 May 15;15(10):1722-34. doi: 10.1093/hmg/ddl096. Epub 2006 Apr 12. Hum Mol Genet. 2006. PMID: 16611674

8

The alanine/threonine polymorphism of the alpha-1-antichymotrypsin (SERPINA3) gene and ruptured intracranial aneurysms in the Japanese population.

Krischek B, Akagawa H, Tajima A, Narita A, Kasuya H, Hori T, Inoue I. Krischek B, et al. Among authors: akagawa h. Cerebrovasc Dis. 2007;23(1):46-9. doi: 10.1159/000095758. Epub 2006 Sep 12. Cerebrovasc Dis. 2007. PMID: 16968986

9

Using endothelial nitric oxide synthase gene polymorphisms to identify intracranial aneurysms more prone to rupture in Japanese patients.

Krischek B, Kasuya H, Akagawa H, Tajima A, Narita A, Onda H, Hori T, Inoue I. Krischek B, et al. Among authors: akagawa h. J Neurosurg. 2006 Nov;105(5):717-22. doi: 10.3171/jns.2006.105.5.717. J Neurosurg. 2006. PMID: 17121133

10

Systematic screening of lysyl oxidase-like (LOXL) family genes demonstrates that LOXL2 is a susceptibility gene to intracranial aneurysms.

Akagawa H, Narita A, Yamada H, Tajima A, Krischek B, Kasuya H, Hori T, Kubota M, Saeki N, Hata A, Mizutani T, Inoue I. Akagawa H, et al. Hum Genet. 2007 May;121(3-4):377-87. doi: 10.1007/s00439-007-0333-3. Epub 2007 Feb 8. Hum Genet. 2007. PMID: 17287949

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