17 results on '"de Zaeytijd J"'
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2. Phenotype of maculopathy in primary hyperoxaluria type 1
3. Oguchi disease due to a novel mutation in the GRK1 gene
4. Molecular study of the MFRP gene in patients with posterior microphthalmia (MCOP) supports its role in autosomal recessive MCOP pathogenesis
5. Sarcoidosis of orbita and central nervous system presenting as a non-arteritic ischemic optic neuropathy
6. Female heterozygotes of X-linked ocular disease in the era of molecular diagnostics
7. Diplopia as presenting sign of Turcot syndrome
8. Ampiginous choroiditis: heterogeneity in 2 cases
9. Novel and known FRMD7 mutations and copy number variation in Belgian patients with X-linked idiopathic infantile nystagmus
10. Leopard-spot pattern of yellow-orange subretinal deposits in central serous chorioretinopathy
11. Bilateral non-arteritic ischemic optic neuropathy due to excessive use of transdermal estrogen by transgender patient
12. Mechanisms & recovery of vitamin A deficiency
13. Pivotal role for SD‐OCT in the diagnosis of acute zonal occult outer retinopathy
14. Colour Vision in Stargardt Disease
15. Angioid streaks beyond pseudoxanthoma elasticum
16. A novel association of Cowden syndrome and combined hamartoma of retina and retinal pigment epithelium
17. Anterior scleral thickness in Marfan syndrome: A quantitative analysis.
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