Petra M. Liskova

Prague, PR 12808, Czech Republic

Last Updated: 09/26/2026

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Found 138 publications

The AP5B1 p.(Leu785Pro) variant is a frequent cause of late-onset macular dystrophy with variable extraocular manifestations.

The AP5B1 p.(Leu785Pro) variant is a frequent cause of late-onset macular dystrophy with variable extraocular manifestations.

Journal: HGG advances
Published: June 23, 2026

The AP5B1 p.Leu785Pro variant is a frequent cause of late-onset macular dystrophy with variable extraocular manifestations.

The AP5B1 p.Leu785Pro variant is a frequent cause of late-onset macular dystrophy with variable extraocular manifestations.

Journal: HGG advances
Published: June 23, 2026

Paediatric Keratoconus: An ERN-EYE Clinical Consensus Statement on Diagnosis, Treatment and Follow-Up Care.

Paediatric Keratoconus: An ERN-EYE Clinical Consensus Statement on Diagnosis, Treatment and Follow-Up Care.

Journal: Ophthalmology and therapy
Published: May 15, 2026

Clinical and molecular features of PRCD-associated retinopathy.

Clinical and molecular features of PRCD-associated retinopathy.

Journal: Acta ophthalmologica
Published: May 07, 2026

Radial outer retina reflectivity (RORR) sign in LAMP2-associated retinopathy.

Radial outer retina reflectivity (RORR) sign in LAMP2-associated retinopathy.

Journal: Acta ophthalmologica
Published: March 02, 2026

Genetic Prediction of Keratoplasty in Fuchs Endothelial Corneal Dystrophy.

Genetic Prediction of Keratoplasty in Fuchs Endothelial Corneal Dystrophy.

Journal: Ophthalmology
Published: February 20, 2026

Genetic Prediction of Keratoplasty in Fuchs Endothelial Corneal Dystrophy.

Genetic Prediction of Keratoplasty in Fuchs Endothelial Corneal Dystrophy.

Journal: Ophthalmology
Published: February 20, 2026

Molecular characterization of CHST6 in Egyptian families with macular corneal dystrophy reveals recurrent and novel variants.

Molecular characterization of CHST6 in Egyptian families with macular corneal dystrophy reveals recurrent and novel variants.

Journal: Ophthalmic genetics
Published: January 22, 2026

Targeted antisense oligonucleotide therapy rescues PRPF31 expression in retinitis pigmentosa caused by a splicing mutation.

Targeted antisense oligonucleotide therapy rescues PRPF31 expression in retinitis pigmentosa caused by a splicing mutation.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: November 27, 2025

Decoding the Cornea-Glaucoma Association: Evidence From Mendelian Randomization.

Decoding the Cornea-Glaucoma Association: Evidence From Mendelian Randomization.

Journal: Investigative ophthalmology & visual science
Published: July 08, 2025

Recessive variants in mitochondrial complex I nuclear subunits are an underrated cause of optic atrophy.

Recessive variants in mitochondrial complex I nuclear subunits are an underrated cause of optic atrophy.

Journal: Brain : a journal of neurology
Published: June 13, 2025

Recessive variants in mitochondrial Complex I nuclear subunits are an underrated cause of optic atrophy.

Recessive variants in mitochondrial Complex I nuclear subunits are an underrated cause of optic atrophy.

Journal: Brain : a journal of neurology
Published: June 13, 2025
Showing 1-12 of 138

Last Updated: 09/26/2026