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1. Faster Sensitivity Loss around Dense Scotomas than for Overall Macular Sensitivity in Stargardt Disease: ProgStar Report No. 14

10. Faster Sensitivity Loss around Dense Scotomas than for Overall Macular Sensitivity in Stargardt Disease: ProgStar Report No. 14

11. Germline large deletion ofBAP1and decreased expression in non‐tumor choroid in uveal melanoma patients with high risk for inherited cancer

12. Retinal Histopathology in Eyes from a Patient with Stargardt disease caused by Compound Heterozygous ABCA4 Mutations*

13. Longitudinal Changes of Fixation Location and Stability Within 12 Months in Stargardt Disease: ProgStar Report No. 12

17. GermlineBAP1alterations in familial uveal melanoma

19. Detailed genetic characteristics of an international large cohort of patients with Stargardt disease: ProgStar study report 8.

20. Visual Acuity Loss and Associated Risk Factors in the Retrospective Progression of Stargardt Disease Study (ProgStar Report No. 2)

22. Congenital uveal melanoma?

25. Detailed genetic characteristics of an international large cohort of patients with Stargardt disease: ProgStar study report 8

30. Effectiveness of Mirror Therapy on Function for Chronic Stroke Patients

33. Sequencing Analysis of the ATOH7 Gene in Individuals with Optic Nerve Hypoplasia

35. Retinal Histopathology in Eyes from a Patient with Stargardt disease caused by Compound Heterozygous ABCA4 Mutations.

36. Analysis of BAP1 Germline Gene Mutation in Young Uveal Melanoma Patients.

37. Predictors of visual acuity and genotype-phenotype correlates in a cohort of patients with Stargardt disease.

38. Sequencing Analysis of the ATOH7 Gene in Individuals with Optic Nerve Hypoplasia.

39. Autosomal Dominant Retinitis Pigmentosa Secondary to Pre-mRNA Splicing-Factor Gene PRPF31 (RP11): Review of Disease Mechanism and Report of a Family with a Novel 3-Base Pair Insertion.

40. Monogenic Diseases Masquerading as Multiple Sclerosis: A Systematic Review

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