Anzahl der Einträge: 6.
Artikel
Gersch, Julia,
Hufendiek, Katerina ,
Delarocque, Julien ,
Framme, Carsten,
Jacobsen, Christina ,
Stöhr, Heidi,
Kellner, Ulrich und
Hufendiek, Karsten
(2022)
Investigation of Structural Alterations in Inherited Retinal Diseases: A Quantitative SD-OCT-Analysis of Retinal Layer Thicknesses in Light of Underlying Genetic Mutations.
International Journal of Molecular Sciences 23 (24), S. 16007.
Volltext nicht vorhanden.
Hufendiek, Karsten ,
Hufendiek, Katerina ,
Jägle, Herbert,
Stöhr, Heidi,
Book, Marius ,
Spital, Georg,
Rustambayova, Günay,
Framme, Carsten,
Weber, Bernhard H. F.,
Renner, Agnes B. und
Kellner, Ulrich
(2020)
Clinical Heterogeneity in Autosomal Recessive Bestrophinopathy with Biallelic Mutations in the BEST1 Gene.
International Journal of Molecular Sciences 21 (24), S. 9353.
Volltext nicht vorhanden.
Khan, Mubeen,
Cornelis, Stéphanie S.,
Pozo-Valero, Marta Del,
Whelan, Laura,
Runhart, Esmee H.,
Mishra, Ketan ,
Bults, Femke,
AlSwaiti, Yahya,
AlTalbishi, Alaa,
De Baere, Elfride,
Banfi, Sandro,
Banin, Eyal,
Bauwens, Miriam,
Ben-Yosef, Tamar,
Boon, Camiel J. F.,
van den Born, L. Ingeborgh,
Defoort, Sabine,
Devos, Aurore,
Dockery, Adrian ,
Dudakova, Lubica ,
Fakin, Ana,
Farrar, G. Jane,
Sallum, Juliana Maria Ferraz,
Fujinami, Kaoru,
Gilissen, Christian ,
Glavač, Damjan,
Gorin, Michael B.,
Greenberg, Jacquie,
Hayashi, Takaaki,
Hettinga, Ymkje M.,
Hoischen, Alexander ,
Hoyng, Carel B.,
Hufendiek, Karsten,
Jägle, Herbert,
Kamakari, Smaragda,
Karali, Marianthi,
Kellner, Ulrich,
Klaver, Caroline C. W.,
Kousal, Bohdan ,
Lamey, Tina M.,
MacDonald, Ian M.,
Matynia, Anna,
McLaren, Terri L.,
Mena, Marcela D. ,
Meunier, Isabelle,
Miller, Rianne,
Newman, Hadas,
Ntozini, Buhle,
Oldak, Monika ,
Pieterse, Marc,
Podhajcer, Osvaldo L.,
Puech, Bernard,
Ramesar, Raj,
Rüther, Klaus,
Salameh, Manar,
Salles, Mariana Vallim,
Sharon, Dror,
Simonelli, Francesca,
Spital, Georg,
Steehouwer, Marloes,
Szaflik, Jacek P.,
Thompson, Jennifer A.,
Thuillier, Caroline,
Tracewska, Anna M. ,
van Zweeden, Martine,
Vincent, Andrea L.,
Zanlonghi, Xavier,
Liskova, Petra ,
Stöhr, Heidi,
Roach, John N. De,
Ayuso, Carmen,
Roberts, Lisa ,
Weber, Bernhard H. F.,
Dhaenens, Claire‐Marie und
Cremers, Frans P. M.
(2020)
Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics.
Genetics in Medicine 22 (7), S. 1235-1246.
Volltext nicht vorhanden.
Rosengarth, Katharina,
Keck, Ingo,
Brandl-Rühle, Sabine,
Frolo, Jozef,
Hufendiek, Karsten,
Greenlee, Mark W. und
Plank, Tina
(2013)
Functional and structural brain modifications induced by oculomotor training in patients with age-related macular degeneration.
Frontiers in psychology : Perception Sience 4, S. 428.
Plank, Tina,
Frolo, Jozef,
Brandl-Rühle, Sabine,
Renner, Agnes B.,
Hufendiek, Karsten,
Helbig, Horst und
Greenlee, Mark W.
(2011)
Gray matter alterations in visual cortex of patients with loss of central vision due to hereditary retinal dystrophies.
NeuroImage 56 (3), S. 1556-1565.
Volltext nicht vorhanden.
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