Orii T - Search Results

1

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

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

Short latency somatosensory evoked potentials and 99mTc-HMPAO SPECT in a case of flunarizine-effective alternating hemiplegia in infancy.

Imamura A, Komori Y, Fukutomi O, Shimozawa N, Suzuki Y, Kondo N, Orii T. Imamura A, et al. Among authors: orii t. Brain Dev. 1994 Jul-Aug;16(4):325-8. doi: 10.1016/0387-7604(94)90032-9. Brain Dev. 1994. PMID: 7818030

4

Prenatal diagnosis of peroxisomal disorders. Biochemical and immunocytochemical studies on peroxisomes in human amniocytes.

Suzuki Y, Shimozawa N, Kawabata I, Yajima S, Inoue K, Uchida Y, Izai K, Tomatsu S, Kondo N, Orii T. Suzuki Y, et al. Among authors: orii t. Brain Dev. 1994 Jan-Feb;16(1):27-31. doi: 10.1016/0387-7604(94)90109-0. Brain Dev. 1994. PMID: 8059925

5

Correction by gene expression of biochemical abnormalities in fibroblasts from Zellweger patients.

Shimozawa N, Suzuki Y, Tomatsu S, Tsukamoto T, Osumi T, Fujiki Y, Kamijo K, Hashimoto T, Kondo N, Orii T. Shimozawa N, et al. Among authors: orii t. Pediatr Res. 1996 May;39(5):812-5. doi: 10.1203/00006450-199605000-00011. Pediatr Res. 1996. PMID: 8726233

6

Human peroxisome assembly factor-2 (PAF-2): a gene responsible for group C peroxisome biogenesis disorder in humans.

Fukuda S, Shimozawa N, Suzuki Y, Zhang Z, Tomatsu S, Tsukamoto T, Hashiguchi N, Osumi T, Masuno M, Imaizumi K, Kuroki Y, Fujiki Y, Orii T, Kondo N. Fukuda S, et al. Among authors: orii t. Am J Hum Genet. 1996 Dec;59(6):1210-20. Am J Hum Genet. 1996. PMID: 8940266 Free PMC article.

7

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.

8

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

9

Peroxisome biogenesis disorders: identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13.

Shimozawa N, Suzuki Y, Zhang Z, Imamura A, Tsukamoto T, Osumi T, Tateishi K, Okumoto K, Fujiki Y, Orii T, Barth PG, Wanders RJ, Kondo N. Shimozawa N, et al. Among authors: orii t. Biochem Biophys Res Commun. 1998 Feb 13;243(2):368-71. doi: 10.1006/bbrc.1997.8067. Biochem Biophys Res Commun. 1998. PMID: 9480815

10

Temperature-sensitive mutation in PEX1 moderates the phenotypes of peroxisome deficiency disorders.

Imamura A, Tamura S, Shimozawa N, Suzuki Y, Zhang Z, Tsukamoto T, Orii T, Kondo N, Osumi T, Fujiki Y. Imamura A, et al. Among authors: orii t. Hum Mol Genet. 1998 Dec;7(13):2089-94. doi: 10.1093/hmg/7.13.2089. Hum Mol Genet. 1998. PMID: 9817926

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