Nakamura M - Search Results

1

Different mutation of the XLRS1 gene causes juvenile retinoschisis with retinal white flecks.

Hotta Y, Nakamura M, Okamoto Y, Nomura R, Terasaki H, Miyake Y. Hotta Y, et al. Among authors: nakamura m. Br J Ophthalmol. 2001 Feb;85(2):238-9. doi: 10.1136/bjo.85.2.238. Br J Ophthalmol. 2001. PMID: 11225572 Free PMC article. No abstract available.

2

Polypoidal choroidal vasculopathy treated with macular translocation: clinical pathological correlation.

Terasaki H, Miyake Y, Suzuki T, Nakamura M, Nagasaka T. Terasaki H, et al. Among authors: nakamura m. Br J Ophthalmol. 2002 Mar;86(3):321-7. doi: 10.1136/bjo.86.3.321. Br J Ophthalmol. 2002. PMID: 11864892 Free PMC article.

3

Japanese X-linked juvenile retinoschisis: conflict of phenotype and genotype with novel mutations in the XLRS1 gene.

Nakamura M, Ito S, Terasaki H, Miyake Y. Nakamura M, et al. Arch Ophthalmol. 2001 Oct;119(10):1553-4. Arch Ophthalmol. 2001. PMID: 11594966 No abstract available.

4

Novel CACNA1F mutations in Japanese patients with incomplete congenital stationary night blindness.

Nakamura M, Ito S, Terasaki H, Miyake Y. Nakamura M, et al. Invest Ophthalmol Vis Sci. 2001 Jun;42(7):1610-6. Invest Ophthalmol Vis Sci. 2001. PMID: 11381068

5

A high association with cone dystrophy in Fundus albipunctatus caused by mutations of the RDH5 gene.

Nakamura M, Hotta Y, Tanikawa A, Terasaki H, Miyake Y. Nakamura M, et al. Invest Ophthalmol Vis Sci. 2000 Nov;41(12):3925-32. Invest Ophthalmol Vis Sci. 2000. PMID: 11053295

6

Focal electroretinogram and visual field defect in multiple evanescent white dot syndrome.

Horiguchi M, Miyake Y, Nakamura M, Fujii Y. Horiguchi M, et al. Among authors: nakamura m. Br J Ophthalmol. 1993 Jul;77(7):452-5. doi: 10.1136/bjo.77.7.452. Br J Ophthalmol. 1993. PMID: 8343478 Free PMC article. No abstract available.

7

High frequency of mitochondrial ND4 gene mutation in Japanese pedigrees with Leber hereditary optic neuropathy.

Nakamura M, Ara F, Yamada M, Hotta Y, Hayakawa M, Fujiki K, Kanai A, Sakai J, Inoue M, Yamamoto M, et al. Nakamura M, et al. Jpn J Ophthalmol. 1992;36(1):56-61. Jpn J Ophthalmol. 1992. PMID: 1635296

8

Triple anterior chamber after full-thickness lamellar keratoplasty for lattice corneal dystrophy.

Hirano K, Kojima T, Nakamura M, Hotta Y. Hirano K, et al. Among authors: nakamura m. Cornea. 2001 Jul;20(5):530-3. doi: 10.1097/00003226-200107000-00018. Cornea. 2001. PMID: 11413412

9

Late-onset form of lattice corneal dystrophy caused by leu527Arg mutation of the TGFBI gene.

Hirano K, Hotta Y, Nakamura M, Fujiki K, Kanai A, Yamamoto N. Hirano K, et al. Among authors: nakamura m. Cornea. 2001 Jul;20(5):525-9. doi: 10.1097/00003226-200107000-00017. Cornea. 2001. PMID: 11413411

10

Surface topology of collagen fibrils associated with proteoglycans in mouse cornea and sclera.

Miyagawa A, Kobayashi M, Fujita Y, Nakamura M, Hirano K, Kobayashi K, Miyake Y. Miyagawa A, et al. Among authors: nakamura m. Jpn J Ophthalmol. 2000 Nov-Dec;44(6):591-5. doi: 10.1016/s0021-5155(00)00272-0. Jpn J Ophthalmol. 2000. PMID: 11094171

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