Okuyama T - Search Results

1

Automated urinary sediment detection for Fabry disease using deep-learning algorithms.

Uryu H, Migita O, Ozawa M, Kamijo C, Aoto S, Okamura K, Hasegawa F, Okuyama T, Kosuga M, Hata K. Uryu H, et al. Among authors: okuyama t. Mol Genet Metab Rep. 2022 Sep 28;33:100921. doi: 10.1016/j.ymgmr.2022.100921. eCollection 2022 Dec. Mol Genet Metab Rep. 2022. PMID: 36186840 Free PMC article.

2

Prolongation of transgene expression by coexpression of cytokine response modifier a in rodent liver after adenoviral gene transfer.

Li XK, Kosuga M, Tokieda K, Kanaji A, Fukuhara Y, Hashimoto M, Okabe K, Yaginuma H, Yamada M, Suzuki S, Okuyama T. Li XK, et al. Among authors: okuyama t. Mol Ther. 2002 Mar;5(3):262-8. doi: 10.1006/mthe.2002.0543. Mol Ther. 2002. PMID: 11863415 Free article.

3

Improvement of skeletal lesions in mice with mucopolysaccharidosis type VII by neonatal adenoviral gene transfer.

Kanaji A, Kosuga M, Li XK, Fukuhara Y, Tanabe A, Kamata Y, Azuma N, Yamada M, Sakamaki T, Toyama Y, Okuyama T. Kanaji A, et al. Among authors: okuyama t. Mol Ther. 2003 Nov;8(5):718-25. doi: 10.1016/j.ymthe.2003.07.004. Mol Ther. 2003. PMID: 14599804 Free article.

4

Histopathological and behavioral improvement of murine mucopolysaccharidosis type VII by intracerebral transplantation of neural stem cells.

Fukuhara Y, Li XK, Kitazawa Y, Inagaki M, Matsuoka K, Kosuga M, Kosaki R, Shimazaki T, Endo H, Umezawa A, Okano H, Takahashi T, Okuyama T. Fukuhara Y, et al. Among authors: okuyama t. Mol Ther. 2006 Mar;13(3):548-55. doi: 10.1016/j.ymthe.2005.09.020. Epub 2005 Nov 28. Mol Ther. 2006. PMID: 16316785 Free article.

5

Monozygotic twins of Smith-Magenis syndrome.

Kosaki R, Okuyama T, Tanaka T, Migita O, Kosaki K. Kosaki R, et al. Among authors: okuyama t. Am J Med Genet A. 2007 Apr 1;143A(7):768-9. doi: 10.1002/ajmg.a.31647. Am J Med Genet A. 2007. PMID: 17345621 No abstract available.

6

The CASK gene harbored in a deletion detected by array-CGH as a potential candidate for a gene causative of X-linked dominant mental retardation.

Hayashi S, Mizuno S, Migita O, Okuyama T, Makita Y, Hata A, Imoto I, Inazawa J. Hayashi S, et al. Among authors: okuyama t. Am J Med Genet A. 2008 Aug 15;146A(16):2145-51. doi: 10.1002/ajmg.a.32433. Am J Med Genet A. 2008. PMID: 18629876

7

Enzyme replacement therapy attenuates disease progression in two Japanese siblings with mucopolysaccharidosis type VI.

Furujo M, Kubo T, Kosuga M, Okuyama T. Furujo M, et al. Among authors: okuyama t. Mol Genet Metab. 2011 Dec;104(4):597-602. doi: 10.1016/j.ymgme.2011.08.029. Epub 2011 Aug 28. Mol Genet Metab. 2011. PMID: 21930407

8

Newborn screening for Pompe disease in Japan.

Oda E, Tanaka T, Migita O, Kosuga M, Fukushi M, Okumiya T, Osawa M, Okuyama T. Oda E, et al. Among authors: okuyama t. Mol Genet Metab. 2011 Dec;104(4):560-5. doi: 10.1016/j.ymgme.2011.09.002. Epub 2011 Sep 10. Mol Genet Metab. 2011. PMID: 21963784

9

Current diagnosis and management of mucopolysaccharidosis VI in the Asia-Pacific region.

Hwu WL, Okuyama T, But WM, Estrada S, Gu X, Hui J, Kosuga M, Lin SP, Ngu LH, Shi H, Tanaka A, Thong MK, Wattanasirichaigoon D, Wasant P, McGill J. Hwu WL, et al. Among authors: okuyama t. Mol Genet Metab. 2012 Sep;107(1-2):136-44. doi: 10.1016/j.ymgme.2012.07.019. Epub 2012 Jul 20. Mol Genet Metab. 2012. PMID: 22864057

10

Effects of idursulfase enzyme replacement therapy for Mucopolysaccharidosis type II when started in early infancy: comparison in two siblings.

Tajima G, Sakura N, Kosuga M, Okuyama T, Kobayashi M. Tajima G, et al. Among authors: okuyama t. Mol Genet Metab. 2013 Mar;108(3):172-7. doi: 10.1016/j.ymgme.2012.12.010. Epub 2013 Jan 9. Mol Genet Metab. 2013. PMID: 23375472

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

1,376 results

Search Page