13 results on '"Leroy, B. P."'
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2. Photophobia in inherited retinal disease
3. Retinal dystrophies & dysfunctions
4. A common NYX mutation in Flemish patients with X linked CSNB
5. Authors’ response
6. High β-trace protein concentration in the fluid of an orbital cyst associated with bilateral colobomatous microphthalmos
7. Intrafamilial phenotypic variability in families with RDS mutations: exclusion of ROM1 as a genetic modifier for those with retinitis pigmentosa
8. Using the EOG as a detective tool: 4463
9. Conditions that may mimic non-organic visual loss: 4262
10. ERGs in acquired retinal disease: 1333
11. Retinal vessel dilation following repletion of vitamin A deficiency
12. Rapid recovery of night blindness due to obesity surgery after vitamin A repletion therapy
13. The contribution of USH1C mutations to syndromic and non-syndromic deafness in the UK
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