Hatsukawa Y - Search Results

1

Clinical course of a Japanese girl with Leber congenital amaurosis associated with a novel nonsense pathogenic variant in NMNAT1: a case report and mini review.

Kayazawa T, Kuniyoshi K, Hatsukawa Y, Fujinami K, Yoshitake K, Tsunoda K, Shimojo H, Iwata T, Kusaka S. Kayazawa T, et al. Among authors: hatsukawa y. Ophthalmic Genet. 2022 Jun;43(3):400-408. doi: 10.1080/13816810.2021.2023195. Epub 2022 Jan 13. Ophthalmic Genet. 2022. PMID: 35026968 Review.

2

Novel nonsense and splice site mutations in CRB1 gene in two Japanese patients with early-onset retinal dystrophy.

Kuniyoshi K, Ikeo K, Sakuramoto H, Furuno M, Yoshitake K, Hatsukawa Y, Nakao A, Tsunoda K, Kusaka S, Shimomura Y, Iwata T. Kuniyoshi K, et al. Among authors: hatsukawa y. Doc Ophthalmol. 2015 Feb;130(1):49-55. doi: 10.1007/s10633-014-9464-8. Epub 2014 Oct 17. Doc Ophthalmol. 2015. PMID: 25323024

3

Acute Bilateral Photoreceptor Degeneration in an Infant After Vaccination Against Measles and Rubella.

Kuniyoshi K, Hatsukawa Y, Kimura S, Fujino T, Ohguro H, Nakai R, Sunami K, Mishima SI, Sato T, Kusaka S, Suzuki Y, Shimomura Y. Kuniyoshi K, et al. Among authors: hatsukawa y. JAMA Ophthalmol. 2017 May 1;135(5):478-482. doi: 10.1001/jamaophthalmol.2017.0380. JAMA Ophthalmol. 2017. PMID: 28358967 Free PMC article.

4

Favorable outcomes of adequate laser photocoagulation and salvage bevacizumab treatment for aggressive posterior retinopathy of prematurity.

Fukushima Y, Fujino T, Kusaka S, Hatsukawa Y, Nishida K. Fukushima Y, et al. Among authors: hatsukawa y. Am J Ophthalmol Case Rep. 2018 May 22;11:66-71. doi: 10.1016/j.ajoc.2018.05.006. eCollection 2018 Sep. Am J Ophthalmol Case Rep. 2018. PMID: 29998205 Free PMC article.

5

Siblings with optic neuropathy and RTN4IP1 mutation.

Okamoto N, Miya F, Hatsukawa Y, Suzuki Y, Kawato K, Yamamoto Y, Tsunoda T, Kato M, Saitoh S, Yamasaki M, Kanemura Y, Kosaki K. Okamoto N, et al. Among authors: hatsukawa y. J Hum Genet. 2017 Oct;62(10):927-929. doi: 10.1038/jhg.2017.68. Epub 2017 Jun 22. J Hum Genet. 2017. PMID: 28638143

6

Deep intronic GPR143 mutation in a Japanese family with ocular albinism.

Naruto T, Okamoto N, Masuda K, Endo T, Hatsukawa Y, Kohmoto T, Imoto I. Naruto T, et al. Among authors: hatsukawa y. Sci Rep. 2015 Jun 10;5:11334. doi: 10.1038/srep11334. Sci Rep. 2015. PMID: 26061757 Free PMC article.

7

The effect of early treatment at the initial stage 3 moderate phase of retinopathy of prematurity on severe retinal changes.

Hatsukawa Y, Ueki N, Yamagishi T, Kitajima H. Hatsukawa Y, et al. Jpn J Ophthalmol. 2005 Sep-Oct;49(5):391-6. doi: 10.1007/s10384-004-0216-2. Jpn J Ophthalmol. 2005. PMID: 16187040

8

Cancer-associated retinopathy in a child with Langerhans cell histiocytosis.

Hayashi M, Hatsukawa Y, Yasui M, Yanagihara I, Ohguro H, Fujikado T. Hayashi M, et al. Among authors: hatsukawa y. Jpn J Ophthalmol. 2007 Sep-Oct;51(5):393-396. doi: 10.1007/s10384-007-0457-y. Epub 2007 Oct 5. Jpn J Ophthalmol. 2007. PMID: 17926119 No abstract available.

9

Progression and timing of treatment of zone I retinopathy of prematurity.

Soh Y, Fujino T, Hatsukawa Y. Soh Y, et al. Among authors: hatsukawa y. Am J Ophthalmol. 2008 Sep;146(3):369-374. doi: 10.1016/j.ajo.2008.05.010. Epub 2008 Jul 7. Am J Ophthalmol. 2008. PMID: 18602081

10

A case of intraocular yolk sac tumor in a child and its pathogenesis.

Fujino T, Okamura A, Hatsukawa Y, Nakayama K, Inoue M, Nakayama M. Fujino T, et al. Among authors: hatsukawa y. J AAPOS. 2009 Dec;13(6):613-5. doi: 10.1016/j.jaapos.2009.09.016. J AAPOS. 2009. PMID: 20006831

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

47 results

Search Page