422 results on '"Rudolph, Günther"'
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2. Kongenitale und kindliche Katarakt. Untersuchung und Indikationsstellung bei Neugeborenen und Kindern
3. Accessory heterozygous mutations in cone photoreceptor CNGA3 exacerbate CNG channel–associated retinopathy
4. Achromatopsia: Genetics and Gene Therapy
5. A pathological indicator for dysthyroid optic neuropathy: tritan color vision deficiency
6. Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia.
7. RPE65-assoziierte Netzhautdystrophie: Gentherapie kann das Sehen verbessern
8. Real-World Clinical Experience With Idebenone in the Treatment of Leber Hereditary Optic Neuropathy
9. Extraocular muscles involved in convergence are innervated by an additional set of palisade endings that may differ in their excitability: A human study
10. Assessment of retinopathy of prematurity regression and reactivation using an artificial intelligence–based vascular severity score
11. Erkrankungen im Schulalter
12. Erkrankungen im Kleinkind- und Vorschulalter
13. Erkrankungen im Neugeborenenalter
14. Konnatale Störungen
15. Evaluation of visual evoked potentials in dysthyroid optic neuropathy.
16. Gene Therapy with Voretigene Neparvovec Improves Vision and Partially Restores Electrophysiological Function in Pre-School Children with Leber Congenital Amaurosis
17. Evaluation of visual evoked potentials in dysthyroid optic neuropathy
18. Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia
19. Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia
20. Achromatopsia: Genetics and Gene Therapy
21. Gene Therapy with Voretigene Neparvovec Improves Vision and Partially Restores Electrophysiological Function in Pre-School Children with Leber Congenital Amaurosis.
22. Ferdinand Tönnies und die Lehre von Karl Marx Annäherung und Vorbehalt
23. Pediatric Lens Subluxation Surgery, Aphakic Glaucoma, Hemangioma and Dissociative Visual Loss
24. Real-World Clinical Experience With Idebenone in the Treatment of Leber Hereditary Optic Neuropathy—Response to Dr. Finsterer's Letter
25. Artificial iris implantation in a 9-year-old boy
26. Zur Staatsauffassung von Ferdinand Tönnies
27. Efficacy and Safety of Intravitreal Gene Therapy for Leber Hereditary Optic Neuropathy Treated within 6 Months of Disease Onset
28. A duplication on chromosome 16q12 affecting the IRXB gene cluster is associated with autosomal dominant cone dystrophy with early tritanopic color vision defect
29. Real-World Clinical Experience With Idebenone in the Treatment of Leber Hereditary Optic Neuropathy
30. Bilateral visual improvement with unilateral gene therapy injection for Leber hereditary optic neuropathy
31. X-linked ocular albinism (Nettleship-Falls): a novel 29-bp deletion in exon 1.: Carrier detection by ophthalmic examination and DNA analysis
32. North Carolina macular dystrophy: a hereditary macular dystrophy with good visual prognosis: Hereditäre Makulaerkrankung mit guter funktioneller Prognose*
33. CDHR1 mutations in retinal dystrophies
34. First-ever retinal gene therapy: Does real-world experience back its use? Recent reports of retinal atrophy have raised concerns on potential long-term safety.
35. Case-Control Genetic Association Study of Fibulin-6 (FBLN6 or HMCN1) Variants in Age-Related Macular Degeneration (AMD)
36. The multifocal pattern electroretinogram in glaucoma
37. Comparing alternative ranibizumab dosages for safety and efficacy in retinopathy of prematurity : a randomized clinical trial
38. Deep‐intronic variants in CNGB3 cause achromatopsia by pseudoexon activation
39. Hemifacial atrophy (Parry-Romberg syndrome, #141300) with papillitis, retinal alterations, and restriction of motility
40. Clinical Phenotype and Course of PDE6A-Associated Retinitis Pigmentosa Disease, Characterized in Preparation for a Gene Supplementation Trial.
41. The Clinical Phenotype of CNGA3 -Related Achromatopsia: Pretreatment Characterization in Preparation of a Gene Replacement Therapy Trial
42. Deep‐intronic variants in CNGB3 cause achromatopsia by pseudoexon activation.
43. The role of fixation for reliable mfERG results
44. Microprobe Measurements to Determine Phase Boundaries and Diffusion Paths in Ternary Phase Diagrams Taking a Cu-Ni-Al System as an Example
45. MITTELDEUTSCHE HALLENKIRCHEN UND DIĖ ERSTE STUFE DER SPÄTGOTIK
46. Multifocal ERG with the scanning laser ophthalmoscope: query on the ideal configuration for attaining high resolution and result stability
47. Real-World Clinical Experience With Idebenone in the Treatment of Leber Hereditary Optic Neuropathy—Response to Dr. Finsterer's Letter.
48. Ophthalmogenetik: Seltene Erkrankungen – Eine Herausforderung für Diagnose und Behandlung
49. Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing
50. Genetik als Grundlage für neue Erkenntnisse und Therapieoptionen in der Augenheilkunde
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