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News

Research

Confirmation of the existence of "Shilca" syndrome and the first case of coexistent hereditary corneal dystrophies
28 April 2021
Research

Confirmation of the existence of "Shilca" syndrome and the first case of coexistent hereditary corneal dystrophies

Finding by IMO Foundation new type of Usher Syndrome
19 January 2021
Research

A finding by the IMO Foundation strengthens the hypothesis of a new type of Usher Syndrome

Picture of a sample of induced pluripotent stem cells.
2 October 2020
Research

The IMO Foundation provides two unique cellular models to the international scientific community

New progress of the IMO Foundation for the treatment of retinal diseases without cure
28 February 2020
Research

New progress of the IMO Foundation for the treatment of retinal diseases without cure

Human Eye Fundación IMO
18 December 2019
Research

The IMO Foundation leads a European Clinical Research Project for the first time

Identification of 3 novel genetic variants causing vision loss
24 October 2019
Research

Identification of 3 novel genetic variants causing vision loss

Pilot project with CRISPR to treat hereditary retinal diseases
26 September 2019
Research

Pilot project with CRISPR to treat hereditary retinal diseases

research team
4 June 2019
Research

A mutation linked to macular dystrophy found for the first time

new cell culture area - IMO Barcelona
25 August 2017
Research

IMO opts for translational medicine with the new cell culture area

Francisco Mulet
20 July 2017
Research

After being blind for the past 30 years, the first Spanish recipient of the IRIS®II retinal chip has begun to locate objects

4 December 2013
Research

The IMO Foundation leads a clinical study about genetic and AMD

11 March 2013
Research / Prevention

The study of genes enables molecular abnormalities to be identified in cases of hereditary glaucoma

16 November 2012
Research

The IMO is taking part in a study on intravitreal drugs used to treat diabetic macular oedema

31 May 2012
Research

The IMO Foundation to study new genetic markers for predisposition to AMD