Kondo H - Search Results

1

A Japanese Family With Autosomal Dominant Oculocutaneous Albinism Type 4.

Oki R, Yamada K, Nakano S, Kimoto K, Yamamoto K, Kondo H, Kubota T. Oki R, et al. Among authors: kondo h. Invest Ophthalmol Vis Sci. 2017 Feb 1;58(2):1008-1016. doi: 10.1167/iovs.16-20612. Invest Ophthalmol Vis Sci. 2017. PMID: 28192564

2

Diagnosis of autosomal dominant retinitis pigmentosa by linkage-based exclusion screening with multiple locus-specific microsatellite markers.

Kondo H, Tahira T, Mizota A, Adachi-Usami E, Oshima K, Hayashi K. Kondo H, et al. Invest Ophthalmol Vis Sci. 2003 Mar;44(3):1275-81. doi: 10.1167/iovs.02-0895. Invest Ophthalmol Vis Sci. 2003. PMID: 12601059

3

A homozygosity-based search for mutations in patients with autosomal recessive retinitis pigmentosa, using microsatellite markers.

Kondo H, Qin M, Mizota A, Kondo M, Hayashi H, Hayashi K, Oshima K, Tahira T, Hayashi K. Kondo H, et al. Among authors: kondo m. Invest Ophthalmol Vis Sci. 2004 Dec;45(12):4433-9. doi: 10.1167/iovs.04-0544. Invest Ophthalmol Vis Sci. 2004. PMID: 15557452

4

Novel mutations in Norrie disease gene in Japanese patients with Norrie disease and familial exudative vitreoretinopathy.

Kondo H, Qin M, Kusaka S, Tahira T, Hasebe H, Hayashi H, Uchio E, Hayashi K. Kondo H, et al. Invest Ophthalmol Vis Sci. 2007 Mar;48(3):1276-82. doi: 10.1167/iovs.06-1042. Invest Ophthalmol Vis Sci. 2007. PMID: 17325173

5

Mutations in the TSPAN12 gene in Japanese patients with familial exudative vitreoretinopathy.

Kondo H, Kusaka S, Yoshinaga A, Uchio E, Tawara A, Hayashi K, Tahira T. Kondo H, et al. Am J Ophthalmol. 2011 Jun;151(6):1095-1100.e1. doi: 10.1016/j.ajo.2010.11.026. Epub 2011 Feb 19. Am J Ophthalmol. 2011. PMID: 21334594

6

Novel compound heterozygous mutations in the MFRP gene in a Japanese patient with posterior microphthalmos.

Matsushita I, Kondo H, Tawara A. Matsushita I, et al. Among authors: kondo h. Jpn J Ophthalmol. 2012 Jul;56(4):396-400. doi: 10.1007/s10384-012-0145-4. Epub 2012 May 9. Jpn J Ophthalmol. 2012. PMID: 22565643

7

Familial acorea, microphthalmia and cataract syndrome.

Kondo H, Tahira T, Yamamoto K, Tawara A. Kondo H, et al. Br J Ophthalmol. 2013 Sep;97(9):1155-60. doi: 10.1136/bjophthalmol-2013-303165. Epub 2013 Jul 5. Br J Ophthalmol. 2013. PMID: 23832966

8

Submicroscopic deletions at 13q32.1 cause congenital microcoria.

Fares-Taie L, Gerber S, Tawara A, Ramirez-Miranda A, Douet JY, Verdin H, Guilloux A, Zenteno JC, Kondo H, Moisset H, Passet B, Yamamoto K, Iwai M, Tanaka T, Nakamura Y, Kimura W, Bole-Feysot C, Vilotte M, Odent S, Vilotte JL, Munnich A, Regnier A, Chassaing N, De Baere E, Raymond-Letron I, Kaplan J, Calvas P, Roche O, Rozet JM. Fares-Taie L, et al. Among authors: kondo h. Am J Hum Genet. 2015 Apr 2;96(4):631-9. doi: 10.1016/j.ajhg.2015.01.014. Epub 2015 Mar 12. Am J Hum Genet. 2015. PMID: 25772937 Free PMC article.

9

Foveal Hypoplasia in Patients with Stickler Syndrome.

Matsushita I, Nagata T, Hayashi T, Kimoto K, Kubota T, Ohji M, Kusaka S, Kondo H. Matsushita I, et al. Among authors: kondo h. Ophthalmology. 2017 Jun;124(6):896-902. doi: 10.1016/j.ophtha.2017.01.046. Epub 2017 Mar 7. Ophthalmology. 2017. PMID: 28283280

10

RDH5-Related Fundus Albipunctatus in a Large Japanese Cohort.

Katagiri S, Hayashi T, Nakamura M, Mizobuchi K, Gekka T, Komori S, Ueno S, Terasaki H, Sakuramoto H, Kuniyoshi K, Kusaka S, Nagashima R, Kondo M, Fujinami K, Tsunoda K, Matsuura T, Kondo H, Yoshitake K, Iwata T, Nakano T. Katagiri S, et al. Among authors: kondo m, kondo h. Invest Ophthalmol Vis Sci. 2020 Mar 9;61(3):53. doi: 10.1167/iovs.61.3.53. Invest Ophthalmol Vis Sci. 2020. PMID: 32232344 Free PMC article.

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