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1.
Electrophysiology-Guided Genetic Characterisation Maximises Molecular Diagnosis in an Irish Paediatric Inherited Retinal Degeneration Population.
Genes (Basel)
; 13(4)2022 03 29.
Article
in English
| MEDLINE | ID: mdl-35456422
2.
Coats-like exudative vitreoretinopathy (CLEVER) in CEP290 inherited retinal degeneration.
BMJ Case Rep
; 15(2)2022 Feb 15.
Article
in English
| MEDLINE | ID: mdl-35168937
3.
Ophthalmic manifestations of vitamin A and D deficiency in two autistic teenagers: case reports and a review of the literature.
Case Rep Ophthalmol
; 6(1): 24-9, 2015.
Article
in English
| MEDLINE | ID: mdl-25759666
4.
Revesz syndrome masquerading as bilateral cicatricial retinopathy of prematurity.
J AAPOS
; 17(6): 634-6, 2013 Dec.
Article
in English
| MEDLINE | ID: mdl-24321428
5.
Central corneal thickness and corneal diameter in premature infants.
Acta Ophthalmol Scand
; 83(6): 751-3, 2005 Dec.
Article
in English
| MEDLINE | ID: mdl-16396656
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