Takahashi Y - Search Results

1

Identification and in silico characterization of a novel compound heterozygosity associated with hereditary aceruloplasminemia.

Hofmann WP, Welsch C, Takahashi Y, Miyajima H, Mihm U, Krick C, Zeuzem S, Sarrazin C. Hofmann WP, et al. Among authors: takahashi y. Scand J Gastroenterol. 2007 Sep;42(9):1088-94. doi: 10.1080/00365520701278810. Scand J Gastroenterol. 2007. PMID: 17710675

2

Aceruloplasminemia, an inherited disorder of iron metabolism.

Miyajima H, Takahashi Y, Kono S. Miyajima H, et al. Among authors: takahashi y. Biometals. 2003 Mar;16(1):205-13. doi: 10.1023/a:1020775101654. Biometals. 2003. PMID: 12572680

3

Hepatic iron overload associated with a decreased serum ceruloplasmin level in a novel clinical type of aceruloplasminemia.

Kono S, Suzuki H, Takahashi K, Takahashi Y, Shirakawa K, Murakawa Y, Yamaguchi S, Miyajima H. Kono S, et al. Among authors: takahashi y, takahashi k. Gastroenterology. 2006 Jul;131(1):240-5. doi: 10.1053/j.gastro.2006.04.017. Gastroenterology. 2006. PMID: 16831606

4

Increased lipid peroxidation and mitochondrial dysfunction in aceruloplasminemia brains.

Miyajima H, Kono S, Takahashi Y, Sugimoto M. Miyajima H, et al. Among authors: takahashi y. Blood Cells Mol Dis. 2002 Nov-Dec;29(3):433-8. doi: 10.1006/bcmd.2002.0561. Blood Cells Mol Dis. 2002. PMID: 12547232

5

Glucose and oxygen hypometabolism in aceruloplasminemia brains.

Miyajima H, Takahashi Y, Kono S, Sugimoto M, Suzuki Y, Hishida A, Sakamoto M, Ouchi Y. Miyajima H, et al. Among authors: takahashi y. Intern Med. 2002 Mar;41(3):186-90. doi: 10.2169/internalmedicine.41.186. Intern Med. 2002. PMID: 11929178 Free article.

6

Cys-881 is essential for the trafficking and secretion of truncated mutant ceruloplasmin in aceruloplasminemia.

Kono S, Suzuki H, Oda T, Shirakawa K, Takahashi Y, Kitagawa M, Miyajima H. Kono S, et al. Among authors: takahashi y. J Hepatol. 2007 Dec;47(6):844-50. doi: 10.1016/j.jhep.2007.05.013. Epub 2007 Jun 18. J Hepatol. 2007. PMID: 17637479

7

Frontal lobe dysfunction associated with glucose hypometabolism in aceruloplasminemia.

Miyajima H, Takahashi Y, Kono S, Hishida A, Ishikawa K, Sakamoto M. Miyajima H, et al. Among authors: takahashi y. J Neurol. 2005 Aug;252(8):996-7. doi: 10.1007/s00415-005-0796-x. Epub 2005 Mar 16. J Neurol. 2005. PMID: 15765266 No abstract available.

8

Biochemical features of ceruloplasmin gene mutations linked to aceruloplasminemia.

Kono S, Suzuki H, Oda T, Miyajima H, Takahashi Y, Shirakawa K, Ishikawa K, Kitagawa M. Kono S, et al. Among authors: takahashi y. Neuromolecular Med. 2006;8(3):361-74. doi: 10.1385/NMM:8:3:361. Neuromolecular Med. 2006. PMID: 16775387

9

Multiple motor system dysfunction associated with a heterozygous ceruloplasmin gene mutation.

Jiménez-Huete A, Bernar J, Miyajima H, Takahashi Y, Alvarez-Linera J, Franch O, van der Knaap MS. Jiménez-Huete A, et al. Among authors: takahashi y. J Neurol. 2008 Jul;255(7):1083-4. doi: 10.1007/s00415-008-0823-9. Epub 2008 Feb 25. J Neurol. 2008. PMID: 18293024 No abstract available.

10

Extrapyramidal and cerebellar movement disorder in association with heterozygous ceruloplasmin gene mutation.

Kuhn J, Miyajima H, Takahashi Y, Kunath B, Hartmann-Klosterkoetter U, Cooper-Mahkorn D, Schaefer M, Bewermeyer H. Kuhn J, et al. Among authors: takahashi y. J Neurol. 2005 Jan;252(1):111-3. doi: 10.1007/s00415-005-0608-3. J Neurol. 2005. PMID: 15654567 No abstract available.

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