Preserved para-arteriole retinal pigment epithelium (PPRPE) in retinitis pigmentosa

exomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease causing SNVs/indels.

Genomics·2014

Establishing baseline rod electroretinogram values in achromatopsia and cone dystrophy.

Documenta ophthalmologica. Advances in ophthalmology·2012

Long-term follow-up of a family with dominant X-linked retinitis pigmentosa.

Eye (London, England)·2009

Two mouse retinal degenerations caused by missense mutations in the beta-subunit of rod cGMP phosphodiesterase gene.

Vision research·2007

Cortical visual function in the rd12 mouse model of Leber Congenital Amarousis (LCA) after gene replacement therapy to restore retinal function.

Vision research·2006

Mouse models of ocular diseases.

Visual neuroscience·2005

Limb anomalies from evolutionary, developmental, and genetic perspectives.

Birth defects original article series·1996

Multisite neural tube closure in humans.

Birth defects original article series·1996

Advancing nanomaterials for treatment of eye diseases: a review.

Experimental and molecular pathology·2026

Multimodal Imaging Characteristics of Sarcoid Retinal Granulomas.

Ocular immunology and inflammation·2026

Morphological changes in vernal keratoconjunctivitis over time: A confocal imaging perspective.

Indian journal of ophthalmology·2026

Outcomes of therapeutic penetrating keratoplasty and deep anterior lamellar keratoplasty in acanthamoeba keratitis: A systematic review and meta-analysis.

Acta ophthalmologica·2026

[Choroidal status in angle-closure glaucoma].

Vestnik oftalmologii·2026

[Functional and anatomical outcomes of various perioperative treatment strategies for diabetic macular edema after cataract phacoemulsification].

Vestnik oftalmologii·2026

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Preserved para-arteriole retinal pigment epithelium (PPRPE) in retinitis pigmentosa

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exomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease causing SNVs/indels.

Establishing baseline rod electroretinogram values in achromatopsia and cone dystrophy.

Long-term follow-up of a family with dominant X-linked retinitis pigmentosa.

Two mouse retinal degenerations caused by missense mutations in the beta-subunit of rod cGMP phosphodiesterase gene.

Cortical visual function in the rd12 mouse model of Leber Congenital Amarousis (LCA) after gene replacement therapy to restore retinal function.

Mouse models of ocular diseases.

Limb anomalies from evolutionary, developmental, and genetic perspectives.

Multisite neural tube closure in humans.

Advancing nanomaterials for treatment of eye diseases: a review.

Multimodal Imaging Characteristics of Sarcoid Retinal Granulomas.

Morphological changes in vernal keratoconjunctivitis over time: A confocal imaging perspective.

Outcomes of therapeutic penetrating keratoplasty and deep anterior lamellar keratoplasty in acanthamoeba keratitis: A systematic review and meta-analysis.

[Choroidal status in angle-closure glaucoma].

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Preserved para-arteriole retinal pigment epithelium (PPRPE) in retinitis pigmentosa

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