Fujinami K - Search Results

1

Stargardt disease with preserved central vision: identification of a putative novel mutation in ATP-binding cassette transporter gene.

Fujinami K, Akahori M, Fukui M, Tsunoda K, Iwata T, Miyake Y. Fujinami K, et al. Acta Ophthalmol. 2011 May;89(3):e297-8. doi: 10.1111/j.1755-3768.2009.01848.x. Acta Ophthalmol. 2011. PMID: 20163366 Free article. No abstract available.

2

Transient macular dysfunction determined by focal macular electroretinogram.

Terauchi N, Fujinami K, Shinoda K, Tsunoda K, Hanazono G, Miyake Y, Inomata K. Terauchi N, et al. Among authors: fujinami k. Br J Ophthalmol. 2007 Dec;91(12):1709-10. doi: 10.1136/bjo.2006.113373. Br J Ophthalmol. 2007. PMID: 18024815 Free PMC article. No abstract available.

3

Fundus autofluorescence in autosomal dominant occult macular dystrophy.

Fujinami K, Tsunoda K, Hanazono G, Shinoda K, Ohde H, Miyake Y. Fujinami K, et al. Arch Ophthalmol. 2011 May;129(5):597-602. doi: 10.1001/archophthalmol.2011.96. Arch Ophthalmol. 2011. PMID: 21555613

4

Selective abnormality of cone outer segment tip line in acute zonal occult outer retinopathy as observed by spectral-domain optical coherence tomography.

Tsunoda K, Fujinami K, Miyake Y. Tsunoda K, et al. Among authors: fujinami k. Arch Ophthalmol. 2011 Aug;129(8):1099-101. doi: 10.1001/archophthalmol.2011.217. Arch Ophthalmol. 2011. PMID: 21825201 No abstract available.

5

Case of acute zonal occult outer retinopathy with abnormal pattern visual evoked potentials.

Chai Y, Yamazaki H, Fujinami K, Tsunoda K, Yamamoto S. Chai Y, et al. Among authors: fujinami k. Clin Ophthalmol. 2011;5:1235-41. doi: 10.2147/OPTH.S23194. Epub 2011 Sep 6. Clin Ophthalmol. 2011. PMID: 21966193 Free PMC article.

6

Oguchi disease with unusual findings associated with a heterozygous mutation in the SAG gene.

Fujinami K, Tsunoda K, Nakamura M, Oguchi Y, Miyake Y. Fujinami K, et al. Arch Ophthalmol. 2011 Oct;129(10):1375-6. doi: 10.1001/archophthalmol.2011.300. Arch Ophthalmol. 2011. PMID: 21987685 No abstract available.

7

Clinical characteristics of occult macular dystrophy in family with mutation of RP1l1 gene.

Tsunoda K, Usui T, Hatase T, Yamai S, Fujinami K, Hanazono G, Shinoda K, Ohde H, Akahori M, Iwata T, Miyake Y. Tsunoda K, et al. Among authors: fujinami k. Retina. 2012 Jun;32(6):1135-47. doi: 10.1097/IAE.0b013e318232c32e. Retina. 2012. PMID: 22466457

8

A longitudinal study of stargardt disease: clinical and electrophysiologic assessment, progression, and genotype correlations.

Fujinami K, Lois N, Davidson AE, Mackay DS, Hogg CR, Stone EM, Tsunoda K, Tsubota K, Bunce C, Robson AG, Moore AT, Webster AR, Holder GE, Michaelides M. Fujinami K, et al. Am J Ophthalmol. 2013 Jun;155(6):1075-1088.e13. doi: 10.1016/j.ajo.2013.01.018. Epub 2013 Mar 15. Am J Ophthalmol. 2013. PMID: 23499370

9

The clinical effect of homozygous ABCA4 alleles in 18 patients.

Fujinami K, Sergouniotis PI, Davidson AE, Mackay DS, Tsunoda K, Tsubota K, Robson AG, Holder GE, Moore AT, Michaelides M, Webster AR. Fujinami K, et al. Ophthalmology. 2013 Nov;120(11):2324-31. doi: 10.1016/j.ophtha.2013.04.016. Epub 2013 Jun 12. Ophthalmology. 2013. PMID: 23769331

10

Molecular characteristics of four Japanese cases with KCNV2 retinopathy: report of novel disease-causing variants.

Fujinami K, Tsunoda K, Nakamura N, Kato Y, Noda T, Shinoda K, Tomita K, Hatase T, Usui T, Akahori M, Itabashi T, Iwata T, Ozawa Y, Tsubota K, Miyake Y. Fujinami K, et al. Mol Vis. 2013 Jul 20;19:1580-90. Print 2013. Mol Vis. 2013. PMID: 23885164 Free PMC article.

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