- Language
-
Englisch
- Identifier
-
1160600562
Subject
Augenheilkunde ; Sehschärfe ; Retinopathia pigmentosa
Contributor
Prokofyeva, Elena
Troeger, Eric
Bernd, Antje
Zrenner, Eberhart
Troeger, Eric
Bernd, Antje
Zrenner, Eberhart
- URN
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
26.01.2023, 1:57 PM CET
Object type
- Monografie
Associated
- Prokofyeva, Elena
- Troeger, Eric
- Bernd, Antje
- Zrenner, Eberhart
Other Objects (12)
Mechanism of Photoreceptor Cell Death in Rhodopsin mutant Rat Models (S334ter-3 and P23H-1) of Autosomal Dominant Retinitis Pigmentosa
Early Visual Symptom Patterns in Inherited Retinal Dystrophies
Kopplungsanalyse und Kandidatengenansatz auf Chromosom 14 zur Identifikation des ursächlichen Gens in einer Familie mit Leberscher kongenitaler Amaurose (LCA)
Etablierung eines Testsystems zum Studium der Mutationsreparatur von XLRP in vitro
The Role of PARP1 in cGMP Mediated Photoreceptor Degeneration
Epidemiology of Major Eye Diseases Leading to Blindness in Europe : A Literature Review.
Optimising Gene Therapy for X-linked Retinitis Pigmentosa
An epidemiological approach for the estimation of disease onset in Central Europe in central and peripheral monogenic retinal dystrophies
Multi-scale segmentation of retinal images
"Development of Cell-based Therapeutic Approaches for the Treatment of Inherited Retinal Dystrophies" and "Experimental Myelination of the Lamina Cribrosa by Cell Transplantation"
Retinal degeneretaion in Arylsulfatase G-deficient mice and neural stem cell-based neuroprotective approaches in mouse models of retinal degeneration.
Interim results of a multicenter trial with the new electronic subretinal implant alpha AMS in 15 patients blind from inherited retinal degenerations
Mechanism of Photoreceptor Cell Death in Rhodopsin mutant Rat Models (S334ter-3 and P23H-1) of Autosomal Dominant Retinitis Pigmentosa
Early Visual Symptom Patterns in Inherited Retinal Dystrophies
Kopplungsanalyse und Kandidatengenansatz auf Chromosom 14 zur Identifikation des ursächlichen Gens in einer Familie mit Leberscher kongenitaler Amaurose (LCA)
Etablierung eines Testsystems zum Studium der Mutationsreparatur von XLRP in vitro
The Role of PARP1 in cGMP Mediated Photoreceptor Degeneration
Epidemiology of Major Eye Diseases Leading to Blindness in Europe : A Literature Review.
Optimising Gene Therapy for X-linked Retinitis Pigmentosa
An epidemiological approach for the estimation of disease onset in Central Europe in central and peripheral monogenic retinal dystrophies
Multi-scale segmentation of retinal images
"Development of Cell-based Therapeutic Approaches for the Treatment of Inherited Retinal Dystrophies" and "Experimental Myelination of the Lamina Cribrosa by Cell Transplantation"
Retinal degeneretaion in Arylsulfatase G-deficient mice and neural stem cell-based neuroprotective approaches in mouse models of retinal degeneration.
Interim results of a multicenter trial with the new electronic subretinal implant alpha AMS in 15 patients blind from inherited retinal degenerations
Mechanism of Photoreceptor Cell Death in Rhodopsin mutant Rat Models (S334ter-3 and P23H-1) of Autosomal Dominant Retinitis Pigmentosa
Early Visual Symptom Patterns in Inherited Retinal Dystrophies
Kopplungsanalyse und Kandidatengenansatz auf Chromosom 14 zur Identifikation des ursächlichen Gens in einer Familie mit Leberscher kongenitaler Amaurose (LCA)
Etablierung eines Testsystems zum Studium der Mutationsreparatur von XLRP in vitro
The Role of PARP1 in cGMP Mediated Photoreceptor Degeneration
Epidemiology of Major Eye Diseases Leading to Blindness in Europe : A Literature Review.
Optimising Gene Therapy for X-linked Retinitis Pigmentosa
An epidemiological approach for the estimation of disease onset in Central Europe in central and peripheral monogenic retinal dystrophies
Multi-scale segmentation of retinal images
"Development of Cell-based Therapeutic Approaches for the Treatment of Inherited Retinal Dystrophies" and "Experimental Myelination of the Lamina Cribrosa by Cell Transplantation"
Retinal degeneretaion in Arylsulfatase G-deficient mice and neural stem cell-based neuroprotective approaches in mouse models of retinal degeneration.