Anzahl der Einträge: 4.
2020
Runhart, Esmee H.,
Khan, Mubeen,
Cornelis, Stéphanie S.,
Roosing, Susanne,
Del Pozo-Valero, Marta,
Lamey, Tina M.,
Liskova, Petra ,
Roberts, Lisa ,
Stöhr, Heidi,
Klaver, Caroline C. W.,
Hoyng, Carel B.,
Cremers, Frans P. M.,
Dhaenens, Claire-Marie,
AlTabishi, Alaa,
Ayuso, Carmen,
Banfi, Sandro,
Ben-Yosef, Tamar,
van den Born, L. Ingeborgh,
Fakin, Ana,
Farrar, G. Jane,
Ferraz Sallum, Juliana Maria,
Fujinami, Kaoru,
Gorin, Michael B.,
Hlavata, Lucia,
Kamakari, Smaragda,
Kousal, Bohdan,
MacDonald, Ian M.,
McLaren, Terri L.,
Matynia, Anna,
Oldak, Monika,
Podhajcer, Osvaldo L.,
Ramesar, Raj,
De Roach, John N.,
Sharon, Dror,
Simonelli, Francesca,
Testa, Francesco,
Thompson, Jennifer A.,
Tracewska, Anna M.,
Vincent, Andrea L. und
Weber, Bernhard H. F.
(2020)
Association of Sex With Frequent and Mild ABCA4 Alleles in Stargardt Disease.
JAMA Ophthalmology 138 (10), S. 1035.
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.
2019
Sangermano, Riccardo ,
Garanto, Alejandro ,
Khan, Mubeen,
Runhart, Esmee H.,
Bauwens, Miriam,
Bax, Nathalie M.,
van den Born, L. Ingeborgh,
Khan, Muhammad Imran,
Cornelis, Stéphanie S.,
Verheij, Joke B. G. M.,
Pott, Jan-Willem R.,
Thiadens, Alberta A. H. J.,
Klaver, Caroline C. W.,
Puech, Bernard,
Meunier, Isabelle,
Naessens, Sarah,
Arno, Gavin,
Fakin, Ana,
Carss, Keren J.,
Raymond, F. Lucy,
Webster, Andrew R.,
Dhaenens, Claire-Marie,
Stöhr, Heidi,
Grassmann, Felix ,
Weber, Bernhard H. F.,
Hoyng, Carel B.,
De Baere, Elfride,
Albert, Silvia ,
Collin, Rob W. J. und
Cremers, Frans P. M.
(2019)
Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides.
Genetics in Medicine 21 (8), S. 1751-1760.
Volltext nicht vorhanden.
Jolly, Jasleen K. ,
Wagner, Siegfried K.,
Martus, Peter,
MacLaren, Robert E.,
Wilhelm, Barbara,
Webster, Andrew R.,
Downes, Susan M.,
Charbel Issa, Peter,
Kellner, Ulrich,
Jägle, Herbert,
Rüther, Klaus,
Bertelsen, Mette,
Bragadóttir, Ragnheiður,
Prener Holtan, Josephine,
van den Born, L. Ingeborgh,
Sodi, Andrea,
Virgili, Gianni,
Gosheva, Mariya,
Pach, Johanna,
Zündorf, Ida,
Zrenner, Eberhart und
Gekeler, Florian
(2019)
Transcorneal Electrical Stimulation for the Treatment of Retinitis Pigmentosa: A Multicenter Safety Study of the OkuStim® System (TESOLA-Study).
Ophthalmic Research 63 (3), S. 234-243.
Volltext nicht vorhanden.
Diese Liste wurde erzeugt am Thu Apr 25 16:27:45 2024 CEST.