Joao P. Marques
Coimbra, Portugal
Last Updated: 09/26/2026
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Found 158 publications
PCARE-associated inherited retinal diseases: clinical and molecular insights from a Portuguese population.
Journal: Ophthalmic genetics
Published: September 01, 2026
Defining a Novel RPGR Phenotype of Sector Retinitis Pigmentosa With Cone Dystrophy.
Journal: Investigative ophthalmology & visual science
Published: August 10, 2026
Recommendations for quality care indicators in severe asthma multidisciplinary units in Portugal (PRECISION project): A nationwide consensus.
Journal: Pulmonology
Published: July 31, 2026
Temporal Sparing and Involvement Across Retinal Disorders: A Multimodal Imaging Perspective.
Journal: Retina (Philadelphia, Pa.)
Published: July 27, 2026
Macular holes in inherited retinal dystrophies and vitreoretinopathies.
Journal: Survey of ophthalmology
Published: June 08, 2026
Pigmented paravenous retinochoroidal atrophy: a spectrum of phenotypes.
Journal: Eye (London, England)
Published: April 13, 2026
PRPH2-associated retinal disease: dual inheritance and broad phenotypic spectrum in a Portuguese cohort.
Journal: Eye (London, England)
Published: March 15, 2026
Inherited retinal disease genes with dual inheritance patterns: insights from the IRD-PT registry.
Journal: Journal of medical genetics
Published: March 12, 2026
Clinical and Genetic Landscape of RPGR-Associated Retinal Dystrophies in Portugal: Insights From the Nationwide IRD-PT Registry.
Journal: Clinical & experimental ophthalmology
Published: February 10, 2026
Enhancing Molecular Diagnostic Accuracy in Genetic Eye Disorders Through a Personalized Re-Evaluation Strategy.
Journal: Investigative ophthalmology & visual science
Published: January 30, 2026
Last Updated: 09/26/2026