Sandra Valeina

Riga, RIX, Latvia

Last Updated: 09/26/2026

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Found 16 publications

Patient with two rare diseases-Renal coloboma syndrome and craniopharyngioma.

Patient with two rare diseases-Renal coloboma syndrome and craniopharyngioma.

Journal: Radiology case reports

Published: February 15, 2026

Guidance (challenges and priorities) in the assessment of children with low vision: ERN-EYE clinical consensus statement.

Guidance (challenges and priorities) in the assessment of children with low vision: ERN-EYE clinical consensus statement.

Journal: Survey of ophthalmology

Published: November 11, 2025

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.

Journal: Nature genetics

Published: June 02, 2025

Genetic Analysis of CYP1B1 and Other Anterior Segment Dysgenesis-Associated Genes in Latvian Cohort of Primary Congenital Glaucoma.

Genetic Analysis of CYP1B1 and Other Anterior Segment Dysgenesis-Associated Genes in Latvian Cohort of Primary Congenital Glaucoma.

Journal: Biomedicines

Published: April 03, 2025

De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.

De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.

Journal: medRxiv : the preprint server for health sciences

Published: January 20, 2025

Colour Vision Deficits in Children with Amblyopia: Impact of Angular Size of Stimuli on Detection.

Colour Vision Deficits in Children with Amblyopia: Impact of Angular Size of Stimuli on Detection.

Journal: Vision (Basel, Switzerland)

Published: October 28, 2024

Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes.

Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes.

Journal: Biomolecules

Published: January 29, 2024

Altered Splicing of LAMP2 in a Multigenerational Family from Latvia Affected by Danon Disease.

Altered Splicing of LAMP2 in a Multigenerational Family from Latvia Affected by Danon Disease.

Journal: Medicina (Kaunas, Lithuania)

Published: November 23, 2023

Preliminary Results of New Modification of Vertical Muscle Transposition to Enhance Abducting Force in Sixth Nerve Palsy.

Preliminary Results of New Modification of Vertical Muscle Transposition to Enhance Abducting Force in Sixth Nerve Palsy.

Journal: Biomedicine hub

Published: January 12, 2023

The Epidemiological and Clinical Findings from the Latvian Registry of Primary Congenital Glaucoma and Evaluation of Prognostic Factors.

The Epidemiological and Clinical Findings from the Latvian Registry of Primary Congenital Glaucoma and Evaluation of Prognostic Factors.

Journal: Medicina (Kaunas, Lithuania)

Published: November 08, 2020

Travel burden and clinical presentation of retinoblastoma: analysis of 1024 patients from 43 African countries and 518 patients from 40 European countries.

Travel burden and clinical presentation of retinoblastoma: analysis of 1024 patients from 43 African countries and 518 patients from 40 European countries.

Journal: The British journal of ophthalmology

Published: April 29, 2020

Global Retinoblastoma Presentation and Analysis by National Income Level.

Global Retinoblastoma Presentation and Analysis by National Income Level.

Journal: JAMA oncology

Published: February 28, 2020

Showing 1-12 of 16

Last Updated: 09/26/2026