Orii T - Search Results

1

Trial of docosahexaenoic acid supplementation on a Japanese patient with a peroxisome biogenesis defect.

Suzuki Y, Shimozawa N, Imamura A, Fukuda Y, Ichihashi H, Orii T, Kondo N. Suzuki Y, et al. Among authors: orii t. Acta Paediatr Jpn. 1996 Oct;38(5):520-3. doi: 10.1111/j.1442-200x.1996.tb03537.x. Acta Paediatr Jpn. 1996. PMID: 8942014 Clinical Trial.

2

Effects of erucic acid therapy on Japanese patients with X-linked adrenoleukodystrophy.

Asano J, Suzuki Y, Yajima S, Inoue K, Shimozawa N, Kondo N, Murase M, Orii T. Asano J, et al. Among authors: orii t. Brain Dev. 1994 Nov-Dec;16(6):454-8. doi: 10.1016/0387-7604(94)90007-8. Brain Dev. 1994. PMID: 7694994

3

Incidence of peroxisomal disorders in Japan.

Suzuki Y, Shimozawa N, Yajima S, Inoue K, Orii T, Kondo N. Suzuki Y, et al. Among authors: orii t. Jpn J Hum Genet. 1996 Mar;41(1):167-75. doi: 10.1007/BF01892624. Jpn J Hum Genet. 1996. PMID: 8914632

4

Peroxisomal disorders: clinical aspects.

Suzuki Y, Shimozawa N, Takahashi Y, Imamura A, Kondo N, Orii T. Suzuki Y, et al. Among authors: orii t. Ann N Y Acad Sci. 1996 Dec 27;804:442-9. doi: 10.1111/j.1749-6632.1996.tb18635.x. Ann N Y Acad Sci. 1996. PMID: 8993563

5

Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders.

Shimozawa N, Suzuki Y, Zhang Z, Imamura A, Toyama R, Mukai S, Fujiki Y, Tsukamoto T, Osumi T, Orii T, Wanders RJ, Kondo N. Shimozawa N, et al. Among authors: orii t. Hum Mol Genet. 1999 Jun;8(6):1077-83. doi: 10.1093/hmg/8.6.1077. Hum Mol Genet. 1999. PMID: 10332040

6

Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disorders.

Zhang Z, Suzuki Y, Shimozawa N, Fukuda S, Imamura A, Tsukamoto T, Osumi T, Fujiki Y, Orii T, Wanders RJ, Barth PG, Moser HW, Paton BC, Besley GT, Kondo N. Zhang Z, et al. Among authors: orii t. Hum Mutat. 1999;13(6):487-96. doi: 10.1002/(SICI)1098-1004(1999)13:6<487::AID-HUMU9>3.0.CO;2-T. Hum Mutat. 1999. PMID: 10408779

7

Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders.

Shimozawa N, Imamura A, Zhang Z, Suzuki Y, Orii T, Tsukamoto T, Osumi T, Fujiki Y, Wanders RJ, Besley G, Kondo N. Shimozawa N, et al. Among authors: orii t. J Med Genet. 1999 Oct;36(10):779-81. doi: 10.1136/jmg.36.10.779. J Med Genet. 1999. PMID: 10528859 Free PMC article.

8

Restoration of biochemical function of the peroxisome in the temperature-sensitive mild forms of peroxisome biogenesis disorder in humans.

Imamura A, Shimozawa N, Suzuki Y, Zhang Z, Tsukamoto T, Fujiki Y, Orii T, Osumi T, Kondo N. Imamura A, et al. Among authors: orii t. Brain Dev. 2000 Jan;22(1):8-12. doi: 10.1016/s0387-7604(99)00072-8. Brain Dev. 2000. PMID: 10761827

9

Temperature-sensitive mutation of PEX6 in peroxisome biogenesis disorders in complementation group C (CG-C): comparative study of PEX6 and PEX1.

Imamura A, Shimozawa N, Suzuki Y, Zhang Z, Tsukamoto T, Fujiki Y, Orii T, Osumi T, Wanders RJ, Kondo N. Imamura A, et al. Among authors: orii t. Pediatr Res. 2000 Oct;48(4):541-5. doi: 10.1203/00006450-200010000-00020. Pediatr Res. 2000. PMID: 11004248

10

Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders.

Suzuki Y, Shimozawa N, Imamura A, Fukuda S, Zhang Z, Orii T, Kondo N. Suzuki Y, et al. Among authors: orii t. J Inherit Metab Dis. 2001 Apr;24(2):151-65. doi: 10.1023/a:1010310816743. J Inherit Metab Dis. 2001. PMID: 11405337 Review.

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