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3. XOLARIS: A 24-Month, Prospective, Natural History Study of 201 Participants with Retinitis Pigmentosa GTPase Regulator-Associated X-Linked Retinitis Pigmentosa

4. Refractive Error in Inherited Retinal Disease

7. Assessment of Visual Function with Cotoretigene Toliparvovec in X-Linked Retinitis Pigmentosa in the Randomized XIRIUS Phase 2/3 Study

8. Loss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration

9. Factors affecting variability in vascular response to dietary (poly)phenols : role of gut microbial metabolism

10. The Neumann problem on the domain in 𝕊3 bounded by the Clifford torus

14. Three‐Year Safety Results of SAR422459 (EIAV‐ABCA4) Gene Therapy in Patients With ABCA4‐Associated Stargardt Disease: An Open‐Label Dose‐Escalation Phase I/IIa Clinical Trial, Cohorts 1‐5

18. Safety and efficacy of ATSN-101 in patients with Leber congenital amaurosis caused by biallelic mutations in GUCY2D: a phase 1/2, multicentre, open-label, unilateral dose escalation study.

26. The Natural History of Inherited Retinal Dystrophy Due to Biallelic Mutations in the RPE65 Gene

27. On the variation of the Einstein–Hilbert action in pseudohermitian geometry.

33. A proposal for an updated staging system for LCHADD retinopathy.

34. Expanding the phenotypic and genotypic spectrum of patients with HGSNAT-related retinopathy.

35. Stargardt macular dystrophy and therapeutic approaches.

40. On the variation of the Einstein-Hilbert action in pseudohermitian geometry

44. The Neumann problem on the Clifford torus in $\mathbb{S}^3$

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