Michael P. Backlund
Helsinki, Finland
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 9 publications
A retrospective longitudinal study of 52 Finnish patients with X-linked retinoschisis.
Journal: Acta ophthalmologica
Published: July 05, 2024
Errors and Delays in Diagnosing Keratitis Fugax Hereditaria.
Journal: American journal of ophthalmology
Published: May 23, 2024
Characterisation of a LINE-1 Insertion in the RP1 Gene by Targeted Adaptive Nanopore Sequencing in a Family with Retinitis Pigmentosa.
Journal: Human mutation
Published: December 11, 2023
Functional assay for assessment of pathogenicity of BAP1 variants.
Journal: Human molecular genetics
Published: September 01, 2023
Analysis of glaucoma genes in Finnish patients with juvenile open-angle glaucoma.
Journal: Acta ophthalmologica
Published: December 22, 2022
Functional consequences of pathogenic variant c.61G>C in the inflammasome gene NLRP3 underlying keratitis fugax hereditaria.
Journal: The British journal of ophthalmology
Published: May 30, 2022
Endoplasmic reticulum stress increases AT1R mRNA expression via TIA-1-dependent mechanism.
Journal: Nucleic acids research
Published: July 12, 2015
Regulation of AT1R expression through HuR by insulin.
Journal: Nucleic acids research
Published: February 25, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026