Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Constanze Kortuem"'
Publikováno v:
Der Ophthalmologe. 119:403-406
Autor:
Friederike C. Kortuem, Melanie Kempf, Laura Kuehlewein, Fadi Nasser, Constanze Kortuem, Michel Paques, Susanne Kohl, Marius Ueffing, Bernd Wissinger, Eberhart Zrenner, Katarina Stingl
Publikováno v:
Acta Ophthalmologica. 100
Autor:
Elke Karin Altpeter, Constanze Kortuem, Susanne Trauzettel-Klosinski, Tobias Marx, Stephan Kuester-Gruber
Publikováno v:
Ophthalmic Research. 64:512-522
Introduction: The purpose of this study was to compare reading speeds (RS) of either paragraphs of text or single sentences in patients with maculopathy by investigating the repeatability of RS to decide which text type to use in studies on patients
Autor:
Saskia Ott, Friederike Kortüm, Constanze Kortuem, Ronja Jung, Susanne Kohl, Melanie Kempf, Krunoslav Sting, Katarina Stingl
Publikováno v:
Acta Ophthalmologica. 100
Purpose Leber congenital amaurosis type 2 (LCA2) and early-onset severe retinal dystrophy (EOSRD) are linked to visual impairment with nyctalopia and visual acuity reduction in early childhood. In 2017, the first gene therapy voretigene neparvovec (L
Publikováno v:
Clinical Ophthalmology (Auckland, N.Z.)
Purpose The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic forced ophthalmologists to adjust their working conditions to ensure patient and staff safety, while still providing effective and timely treatment. This international
Autor:
Elke Karin Altpeter, Tobias Marx, Stephan Kuester-Gruber, Susanne Trauzettel-Klosinski, Constanze Kortuem
Publikováno v:
Ophthalmic research, 65(2):237238
Publikováno v:
Acta Ophthalmologica
Autor:
Tobias Peters, Benjamin Beier, Nadine Kahle, Felix F L Reichel, Yousof Vaheb, G. Alex Ochakovski, Robert E MacLaren, Marius Ueffing, Constanze Kortuem, Immanuel P. Seitz, M. Dominik Fischer, Karl Ulrich Bartz-Schmidt, Aniz Girach, Laura Kuehlewein, Barbara Wilhelm, Eberhart Zrenner
Publikováno v:
JAMA Ophthalmol
IMPORTANCE: Choroideremia (CHM) is a rare, degenerative, genetic retinal disorder resulting from mutation of the CHM gene, leading to an absence of functional ras-associated binding escort protein 1 (REP1). There is currently no approved treatment fo