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Publications by Michel Michaelides

Whole-Exome Sequencing in the Investigation of Retinal Dystrophy

The Lancet
Medicine
2016English

Bi-Allelic Loss-Of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

American Journal of Human Genetics
Genetics
2019English

Clinical and Genetic Features of Choroideremia in Childhood

Ophthalmology
Ophthalmology
2016English

Mutation in the Intracellular Chloride Channel CLCC1 Associated With Autosomal Recessive Retinitis Pigmentosa

PLoS Genetics
EvolutionEcologyGeneticsMolecular BiologyCancer ResearchSystematicsBehavior
2018English

Bullous X Linked Retinoschisis: Clinical Features and Prognosis

British Journal of Ophthalmology
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2017English

Inherited Cataracts: Molecular Genetics, Clinical Features, Disease Mechanisms and Novel Therapeutic Approaches

British Journal of Ophthalmology
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2020English

Stargardt Disease: Clinical Features, Molecular Genetics, Animal Models and Therapeutic Options

British Journal of Ophthalmology
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2016English

Functional and Anatomical Outcomes of Choroidal Neovascularization Complicating Best1-Related Retinopathy

Retina
MedicineOphthalmology
2017English

Adaptive Optics Retinal Imaging in CNGA3-Associated Achromatopsia: Retinal Characterization, Interocular Symmetry, and Intrafamilial Variability

Investigative Ophthalmology and Visual Science
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2019English

Residual Cone Structure in Patients With X-Linked Cone Opsin Mutations

Investigative Ophthalmology and Visual Science
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2018English

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