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Reticular crack lesion in the ocular fundus

Japanese journal of ophthalmology, 2009-01, Vol.53 (1), p.72-73

Isashiki, Yasushi

2009

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Reduced N-Acetylaspartate Levels in Mice Lacking Aralar, a Brain- and Muscle-type Mitochondrial Aspartate-glutamate Carrier

The Journal of biological chemistry, 2005-09, Vol.280 (35), p.31333-31339

2005

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A novel truncating mutation of cytochrome P4501B1 (CYP1B1) gene in primary infantile glaucoma

American journal of ophthalmology, 1999-09, Vol.128 (3), p.370-372

1999

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Phylogenetic evaluation of the CYP1B1 gene in patients with primary congenital glaucoma

Acta ophthalmologica (Oxford, England), 2008-02, Vol.86 (1), p.114-115

2008

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RNA world/pseudogene/non-coding RNA

Nippon Ganka Gakkai zasshi, 2009-12, Vol.113 (12), p.1172

2009

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Reply

American journal of ophthalmology, 2008-07, Vol.146 (1), p.146

2008

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American journal of ophthalmology, 2008-07, Vol.146 (1), p.146-147

2008

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Identification of a Novel Splice Site Mutation of the CSPG2 Gene in a Japanese Family with Wagner Syndrome

Investigative ophthalmology & visual science, 2005-08, Vol.46 (8), p.2726-2735

2005

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American journal of ophthalmology, 2008, Vol.146 (1), p.146-147

2008

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Genetic association of manganese superoxide dismutase with exudative age-related macular degeneration

American journal of ophthalmology, 2000-12, Vol.130 (6), p.769-773

2000

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Notes on ophthalmological terminology 19. Pseudological terminology

Nippon Ganka Gakkai zasshi, 2008-10, Vol.112 (10), p.910

2008

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Histopathological and ultrastructural features of feline hereditary cerebellar cortical atrophy : a novel animal model of human spinocerebellar degeneration

Acta neuropathologica, 1998-10, Vol.96 (4), p.379-387

1998

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Sorsby's Fundus Dystrophy in Two Japanese Families With Unusual Clinical Features

Japanese journal of ophthalmology, 1999-11, Vol.43 (6), p.472-480

1999

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Medical record/electronic medical record

Nippon Ganka Gakkai zasshi, 2007-02, Vol.111 (2), p.108

2007

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The 100 most frequently cited articles in ophthalmology journals

Archives of ophthalmology (1960), 2007-07, Vol.125 (7), p.952

2007

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Manganese Superoxide Dismutase Gene (SOD2) Polymorphism and Exudative Age-related Macular Degeneration in the Japanese Population. Authors' reply

American journal of ophthalmology, 2008, Vol.146 (1), p.146-147

2008

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Novel mutation at the initiation codon in the Norrie disease gene in two Japanese families

Human genetics, 1995, Vol.95 (1), p.105-108

1995

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Cytochrome P450 1B1 gene mutations in Japanese patients with primary congenital glaucoma

American journal of ophthalmology, 2001-03, Vol.131 (3), p.345-350

2001

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HTLV-I associated retinochoroidal degeneration

Japanese journal of ophthalmology, 1996, Vol.40 (1), p.71-78

1996

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Two patients with severe corneal disease in KID syndrome

American journal of ophthalmology, 2004, Vol.137 (1), p.181-183

2004

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Analysis of Peripherin/ Rds Gene for Japanese Retinal Dystrophies

Japanese journal of ophthalmology, 1998-05, Vol.42 (3), p.186-192

1998

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A novel splice site mutation in the tissue inhibitor of the metalloproteinases-3 gene in Sorsby’s fundus dystrophy with unusual clinical features

Human genetics, 1998-08, Vol.103 (2), p.179

1998

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Retinopathy associated with Machado–Joseph disease (spinocerebellar ataxia 3) with CAG trinucleotide repeat expansion

American journal of ophthalmology, 2001-06, Vol.131 (6), p.808-810

2001

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Assessment of mitochondrial gene in proliferative vitreoretinal tissues from patients with familial diabetes mellitus

Japanese journal of ophthalmology, 1996, Vol.40 (1), p.66-70

1996

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Optic neuropathy and cerebellar ataxia associated with a rare missense variation (A14510G) of mitochondrial DNA

British journal of ophthalmology, 2001-08, Vol.85 (8), p.1007-1007

2001

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Reticular crack lesion in the ocular fundus

Reduced N-Acetylaspartate Levels in Mice Lacking Aralar, a Brain- and Muscle-type Mitochondrial Aspartate-glutamate Carrier

A novel truncating mutation of cytochrome P4501B1 (CYP1B1) gene in primary infantile glaucoma

Phylogenetic evaluation of the CYP1B1 gene in patients with primary congenital glaucoma

RNA world/pseudogene/non-coding RNA

Reply

Reply

Identification of a Novel Splice Site Mutation of the CSPG2 Gene in a Japanese Family with Wagner Syndrome

Reply

Genetic association of manganese superoxide dismutase with exudative age-related macular degeneration

Notes on ophthalmological terminology 19. Pseudological terminology

Histopathological and ultrastructural features of feline hereditary cerebellar cortical atrophy : a novel animal model of human spinocerebellar degeneration

Sorsby's Fundus Dystrophy in Two Japanese Families With Unusual Clinical Features

Medical record/electronic medical record

The 100 most frequently cited articles in ophthalmology journals

Manganese Superoxide Dismutase Gene (SOD2) Polymorphism and Exudative Age-related Macular Degeneration in the Japanese Population. Authors' reply

Novel mutation at the initiation codon in the Norrie disease gene in two Japanese families

Cytochrome P450 1B1 gene mutations in Japanese patients with primary congenital glaucoma

HTLV-I associated retinochoroidal degeneration

Two patients with severe corneal disease in KID syndrome

Analysis of Peripherin/ Rds Gene for Japanese Retinal Dystrophies

A novel splice site mutation in the tissue inhibitor of the metalloproteinases-3 gene in Sorsby’s fundus dystrophy with unusual clinical features

Retinopathy associated with Machado–Joseph disease (spinocerebellar ataxia 3) with CAG trinucleotide repeat expansion

Assessment of mitochondrial gene in proliferative vitreoretinal tissues from patients with familial diabetes mellitus

Optic neuropathy and cerebellar ataxia associated with a rare missense variation (A14510G) of mitochondrial DNA

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