Accessibility and reading comfort

Text size

Light/Dark mode

Lines vertical spacing

Trouble using our website?
Contact us

Dr Robert REJDAK

In this page

Member info

Dr Robert REJDAK

Substitute

Poland

Team

Dr Katarzyna Nowomiejska

Poland

National Integration (TWG9), Neuro-Ophthalmology Rare Diseases (WG2), Pediatric Ophthalmology Rare Diseases (WG3), Research (TWG8), Retinal Rare Eye Diseases (WG1)
See more

HCP Center

Medical University of Lublin has its origins in the year 1944 in Lublin, Poland. The university gained its autonomy in 1950. As the years passed, new...

contact

Medical University of Lublin, Lublin, Poland

Department of General OphthalmologyMedical University in Lublinul. Chmielna 1
20-079 Lublin
Poland

Scientific publications

Multirater Validation of Peripapillary Hyperreflective Ovoid Mass-like Structures (PHOMS)

We performed a Delphi consensus process to develop a consistent and refined definition of PHOMS with clear principles around the nature of PHOMS...

Diagnosis and classification of optic neuritis

There is no consensus regarding the classification of optic neuritis, and precise diagnostic criteria are not...

Residual Attention Network for distinction between visible optic disc drusen and healthy optic discs

In this study the authors propose a new solution for distinguish healthy cases and those with optic disc drusen (ODD) utilizing Residual Attention...

Identification of the RPGR Gene Pathogenic Variants in a Cohort of Polish Male Patients with Retinitis Pigmentosa Phenotype

This is the first RPGR mutation screening in Poland showing a prevalence of 18% of RPGR pathogenic mutations and likely pathogenic variants in the...

DNAJC30 Gene Variants Are a Frequent Cause of a Rare Disease: Leber Hereditary Optic Neuropathy in Polish Patients

The results of our study suggest that Sanger sequencing of the single-exon DNAJC30 gene should be a method of choice applied to identify a...

Vascular Changes in the Macula of Patients after Previous Episodes of Vision Loss Due to Leber Hereditary Optic Neuropathy and Non-Arteritic Ischemic Optic Neuropathy

The superficial perfusion and structure of the macula assessed with OCT-A are affected both in chronic LHON and NA-AION, but more in LHON eyes,...

CENTRAL RETINAL VEIN OCCLUSION IN OTHERWISE HEALTHY CHILDREN AND ADOLESCENTS: Association With Multigenetic Variants of Thrombophilia

The genotyping analysis identified combined genetic variants of thrombophilia in each patient. Mutations for MTHFR (C677T) and GPIIIa PlA1/A2 were...