10 Einträge gefunden

1. Ongoing retinal degeneration despite intraventricular enzyme replacement therapy with cerliponase alfa in late-infantile neuronal ceroid lipofuscinosis type 2 (CLN2 disease)

   1. Dulz, Simon
   2. Schwering, C
   3. Wildner, Jan
   4. Spartalis, Christoph
   5. Schuettauf, Frank
   6. Bartsch, Udo
   7. Wibbeler, Eva

   2023 - Forschungsinformationssystem des UKE
2. Visual perception and macular integrity in non-classical CLN2 disease

   1. Atiskova, Yevgeniya
   2. Wildner, Jan
   3. Wibbeler, Eva
   4. Nickel, Miriam
   5. Spitzer, Martin Stephan
   6. Schwering, Christoph
   7. Schulz, Angela

   2022 - Forschungsinformationssystem des UKE - frei zugänglich
3. Ophthalmological manifestations of neuronal ceroid lipofuscinoses (NCL):NCL as diseases of brain and retina-the role of ophthalmologists, Ophthalmologische Manifestationen bei neuronalen Ceroid-Lipofuszinosen (NCL):NCL als Erkrankungen von Retina und Gehirn – Rolle der Augenärzte

   1. Atiskova, Yevgeniya
   2. Kohlschütter, Alfried
   3. Spitzer, Martin Stephan
   4. Dulz, Simon

   2021 - Forschungsinformationssystem des UKE
4. Retinal vessel tortuosity as a prognostic marker for disease severity in Fabry disease

   1. Atiskova, Yevgeniya
   2. Wildner, Jan
   3. Spitzer, Martin Stephan
   4. Aries, Charlotte
   5. Muschol, Nicole
   6. Dulz, Simon

   2021 - Forschungsinformationssystem des UKE - frei zugänglich
5. Retained visual function in a subset of patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD)

   1. Dulz, Simon
   2. Atiskova, Yevgeniya
   3. Engel, Peter
   4. Wildner, Jan
   5. Tsiakas, Konstantinos
   6. Santer, Rene

   2021 - Forschungsinformationssystem des UKE
6. An ophthalmic rating scale to assess ocular involvement in juvenile CLN3 disease

   1. Dulz, Simon
   2. Atiskova, Yevgeniya
   3. Wibbeler, Eva
   4. Wildner, Jan Einar
   5. Wagenfeld, Lars
   6. Schwering, Christoph
   7. Nickel, Miriam

   2020 - Forschungsinformationssystem des UKE
7. Mice deficient in the lysosomal enzyme palmitoyl-protein thioesterase 1 (PPT1) display a complex retinal phenotype

   1. Atiskova, Yevgeniya
   2. Bartsch, Susanne
   3. Danyukova, Tatyana
   4. Becker, Elke
   5. Hagel, Christian
   6. Storch, Stephan
   7. Bartsch, Udo

   2019 - Forschungsinformationssystem des UKE - frei zugänglich
8. Retinal hyperreflective foci in Fabry disease

   1. Atiskova, Yevgeniya
   2. Rassuli, Rahman
   3. Koehn, Anja Friederike
   4. Golsari, Amir
   5. Wagenfeld, Lars
   6. du Moulin, Marcel
   7. Muschol, Nicole

   2019 - Forschungsinformationssystem des UKE - frei zugänglich
9. The ocular phenotype in primary hyperoxaluria type 1

   1. Birtel, Johannes
   2. Herrmann, Philipp
   3. Garrelfs, Sander F
   4. Dulz, Simon
   5. Atiskova, Yevgeniya
   6. Diederen, Roselie M
   7. Gliem, Martin

   2019 - Forschungsinformationssystem des UKE
10. Oxalate retinopathy is irreversible despite early combined liver-kidney transplantation in primary hyperoxaluria type 1

    1. Atiskova, Yevgeniya
    2. Dulz, Simon
    3. Schmäschke, Kaja
    4. Oh, Jun
    5. Grabhorn, Enke
    6. Kemper, Markus J
    7. Brinkert, Florian

    2019 - Forschungsinformationssystem des UKE