Urashima M - Search Results

1

ABCC6 Gene Analysis in 20 Japanese Patients with Angioid Streaks Revealing Four Frequent and Two Novel Variants and Pseudodominant Inheritance.

Katagiri S, Negishi Y, Mizobuchi K, Urashima M, Nakano T, Hayashi T. Katagiri S, et al. Among authors: urashima m. J Ophthalmol. 2017;2017:1079687. doi: 10.1155/2017/1079687. Epub 2017 Aug 20. J Ophthalmol. 2017. PMID: 28912966 Free PMC article.

2

BUN/Cr ratio as an index of gastrointestinal bleeding mass in children.

Urashima M, Toyoda S, Nakano T, Matsuda S, Kobayashi N, Kitajima H, Tokushige A, Horita H, Akatsuka J, Maekawa K. Urashima M, et al. J Pediatr Gastroenterol Nutr. 1992 Jul;15(1):89-92. doi: 10.1097/00005176-199207000-00014. J Pediatr Gastroenterol Nutr. 1992. PMID: 1403455

3

A novel mutation (Cys83Tyr) in the second zinc finger of NR2E3 in enhanced S-cone syndrome.

Rocha-Sousa A, Hayashi T, Gomes NL, Penas S, Brandão E, Rocha P, Urashima M, Yamada H, Tsuneoka H, Falcão-Reis F. Rocha-Sousa A, et al. Among authors: urashima m. Graefes Arch Clin Exp Ophthalmol. 2011 Feb;249(2):201-8. doi: 10.1007/s00417-010-1482-y. Epub 2010 Aug 20. Graefes Arch Clin Exp Ophthalmol. 2011. PMID: 20725840

4

Macular Dysfunction in Oguchi Disease with the Frequent Mutation 1147delA in the SAG Gene.

Hayashi T, Tsuzuranuki S, Kozaki K, Urashima M, Tsuneoka H. Hayashi T, et al. Among authors: urashima m. Ophthalmic Res. 2011 Oct;46(4):175-80. doi: 10.1159/000325024. Epub 2011 Mar 29. Ophthalmic Res. 2011. PMID: 21447990

5

Evaluation of Quality of Life in Japanese Glaucoma Patients and its Relationship With Visual Function.

Takahashi G, Otori Y, Urashima M, Kuwayama Y; Quality of Life Improvement Committee. Takahashi G, et al. Among authors: urashima m. J Glaucoma. 2016 Mar;25(3):e150-6. doi: 10.1097/IJG.0000000000000221. J Glaucoma. 2016. PMID: 25827300

6

Homozygous deletions of UGT2B17 modifies effects of smoking on TP53-mutations and relapse of head and neck carcinoma.

Mafune A, Hama T, Suda T, Suzuki Y, Ikegami M, Sakanashi C, Imai S, Nakashima A, Yokoo T, Wada K, Kojima H, Urashima M. Mafune A, et al. Among authors: urashima m. BMC Cancer. 2015 Mar 31;15:205. doi: 10.1186/s12885-015-1220-2. BMC Cancer. 2015. PMID: 25886176 Free PMC article.

7

L-type voltage-dependent calcium channel alpha subunit 1C is a novel candidate gene associated with secondary hyperparathyroidism: an application of haplotype-based analysis for multiple linked single nucleotide polymorphisms.

Yokoyama K, Urashima M, Ohkido I, Kono T, Yoshida T, Muramatsu M, Niu T, Hosoya T. Yokoyama K, et al. Among authors: urashima m. Nephron Clin Pract. 2010;115(4):c237-43. doi: 10.1159/000313481. Epub 2010 Apr 28. Nephron Clin Pract. 2010. PMID: 20424473

8

Evaluating the Quality of Life of Glaucoma Patients Using the State-Trait Anxiety Inventory.

Otori Y, Takahashi G, Urashima M, Kuwayama Y; Quality of Life Improvement Committee. Otori Y, et al. Among authors: urashima m. J Glaucoma. 2017 Nov;26(11):1025-1029. doi: 10.1097/IJG.0000000000000761. J Glaucoma. 2017. PMID: 28858160

9

Associations Between Low Serum Testosterone and All-Cause Mortality and Infection-Related Hospitalization in Male Hemodialysis Patients: A Prospective Cohort Study.

Nakashima A, Ohkido I, Yokoyama K, Mafune A, Urashima M, Yokoo T. Nakashima A, et al. Among authors: urashima m. Kidney Int Rep. 2017 Aug 4;2(6):1160-1168. doi: 10.1016/j.ekir.2017.07.015. eCollection 2017 Nov. Kidney Int Rep. 2017. PMID: 29270524 Free PMC article.

10

Dysfunctional ABCG2 gene polymorphisms are associated with serum uric acid levels and all-cause mortality in hemodialysis patients.

Nakashima A, Ichida K, Ohkido I, Yokoyama K, Matsuo H, Ohashi Y, Takada T, Nakayama A, Suzuki H, Shinomiya N, Urashima M, Yokoo T. Nakashima A, et al. Among authors: urashima m. Hum Cell. 2020 Jul;33(3):559-568. doi: 10.1007/s13577-020-00342-w. Epub 2020 Mar 16. Hum Cell. 2020. PMID: 32180207 Free PMC article.

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