Orii T - Search Results

1

Mutational and structural analysis of Japanese patients with mucopolysaccharidosis type II.

Kato T, Kato Z, Kuratsubo I, Tanaka N, Ishigami T, Kajihara JI, Sukegawa-Hayasaka K, Orii K, Isogai K, Fukao T, Shimozawa N, Orii T, Kondo N, Suzuki Y. Kato T, et al. Among authors: orii t, orii k. J Hum Genet. 2005;50(8):395-402. doi: 10.1007/s10038-005-0266-4. Epub 2005 Aug 30. J Hum Genet. 2005. PMID: 16133661

2

Mucopolysaccharidosis IVA: characterization of a common mutation found in Finnish patients with attenuated phenotype.

Montaño AM, Kaitila I, Sukegawa K, Tomatsu S, Kato Z, Nakamura H, Fukuda S, Orii T, Kondo N. Montaño AM, et al. Among authors: orii t. Hum Genet. 2003 Jul;113(2):162-9. doi: 10.1007/s00439-003-0959-8. Epub 2003 Apr 30. Hum Genet. 2003. PMID: 12721840

3

Portal hypertension in a patient with Hunter disease.

Kato T, Isogai K, Orii K, Kuratsubo I, Kondo N, Orii T, Suzuki Y. Kato T, et al. Among authors: orii t, orii k. J Inherit Metab Dis. 2006 Oct;29(5):686. doi: 10.1007/s10545-006-0308-x. Epub 2006 Aug 5. J Inherit Metab Dis. 2006. PMID: 16972178

4

Psychological status of patients with mucopolysaccharidosis type II and their parents.

Kuratsubo I, Suzuki Y, Orii KO, Kato T, Orii T, Kondo N. Kuratsubo I, et al. Among authors: orii ko, orii t. Pediatr Int. 2009 Feb;51(1):41-7. doi: 10.1111/j.1442-200X.2008.02652.x. Pediatr Int. 2009. PMID: 19371276

5

Evaluation of ADL in patients with Hunter disease using FIM score.

Kato T, Kato Z, Kuratsubo I, Ota T, Orii T, Kondo N, Suzuki Y. Kato T, et al. Among authors: orii t. Brain Dev. 2007 Jun;29(5):298-305. doi: 10.1016/j.braindev.2006.08.015. Epub 2007 Feb 20. Brain Dev. 2007. PMID: 17307320

6

Epidemiology of X-linked adrenoleukodystrophy in Japan.

Takemoto Y, Suzuki Y, Tamakoshi A, Onodera O, Tsuji S, Hashimoto T, Shimozawa N, Orii T, Kondo N. Takemoto Y, et al. Among authors: orii t. J Hum Genet. 2002;47(11):590-3. doi: 10.1007/s100380200090. J Hum Genet. 2002. PMID: 12436195

7

Production of MPS VII mouse (Gus(tm(hE540A x mE536A)Sly)) doubly tolerant to human and mouse beta-glucuronidase.

Tomatsu S, Orii KO, Vogler C, Grubb JH, Snella EM, Gutierrez M, Dieter T, Holden CC, Sukegawa K, Orii T, Kondo N, Sly WS. Tomatsu S, et al. Among authors: orii ko, orii t. Hum Mol Genet. 2003 May 1;12(9):961-73. doi: 10.1093/hmg/ddg119. Hum Mol Genet. 2003. PMID: 12700165 Free PMC article.

8

General implications for CpG hot spot mutations: methylation patterns of the human iduronate-2-sulfatase gene locus.

Tomatsu S, Orii KO, Bi Y, Gutierrez MA, Nishioka T, Yamaguchi S, Kondo N, Orii T, Noguchi A, Sly WS. Tomatsu S, et al. Among authors: orii ko, orii t. Hum Mutat. 2004 Jun;23(6):590-8. doi: 10.1002/humu.20046. Hum Mutat. 2004. PMID: 15146464

9

Mucopolysaccharidosis IVA (Morquio A): identification of novel common mutations in the N-acetylgalactosamine-6-sulfate sulfatase (GALNS) gene in Italian patients.

Tomatsu S, Filocamo M, Orii KO, Sly WS, Gutierrez MA, Nishioka T, Serrato OP, Di Natale P, Montaño AM, Yamaguchi S, Kondo N, Orii T, Noguchi A. Tomatsu S, et al. Among authors: orii ko, orii t. Hum Mutat. 2004 Aug;24(2):187-8. doi: 10.1002/humu.9265. Hum Mutat. 2004. PMID: 15241807

10

Activities of daily living in patients with Hunter syndrome: impact of enzyme replacement therapy and hematopoietic stem cell transplantation.

Tanjuakio J, Suzuki Y, Patel P, Yasuda E, Kubaski F, Tanaka A, Yabe H, Mason RW, Montaño AM, Orii KE, Orii KO, Fukao T, Orii T, Tomatsu S. Tanjuakio J, et al. Among authors: orii ke, orii ko, orii t. Mol Genet Metab. 2015 Feb;114(2):161-9. doi: 10.1016/j.ymgme.2014.11.002. Epub 2014 Nov 8. Mol Genet Metab. 2015. PMID: 25468646 Free PMC article.

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