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Ophthalmic Research|November 28, 2019
Transcorneal Electrical Stimulation for the Treatment of Retinitis Pigmentosa: A Multicenter Safety Study of the OkuStim® System (TESOLA-Study)Jasleen K Jolly, Siegfried K Wagner, Peter Martus, et al.
Molecular Therapy. Nucleic Acids|July 13, 2020
Detailed Phenotyping and Therapeutic Strategies for Intronic ABCA4 Variants in Stargardt DiseaseMubeen Khan, Gavin Arno, Ana Fakin, et al.
The British Journal of Ophthalmology|October 10, 2018
Macular spatial distribution of preserved autofluorescence in patients with choroideremiaAmir H Hariri, Michael S Ip, Aniz Girach, et al.
Science (New York, N.Y.)|October 21, 1994
Removal of Stratospheric O3 by Radicals: In Situ Measurements of OH, HO2, NO, NO2, ClO, and BrOP O Wennberg, R C Cohen, R M Stimpfle, et al.
Pigment Cell & Melanoma Research|November 20, 2014
Wnt5A promotes an adaptive, senescent-like stress response, while continuing to drive invasion in melanoma cellsMarie R Webster, Mai Xu, Kathryn A Kinzler, et al.
Cancer Research|September 10, 2017
ATG5 Mediates a Positive Feedback Loop between Wnt Signaling and Autophagy in MelanomaAbibatou Ndoye, Anna Budina-Kolomets, Curtis H Kugel, et al.
Ophthalmic Genetics|July 5, 2021
Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndromeAustin D Igelman, Cristy Ku, Mariana Matioli da Palma, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 13, 2025
Biallelic null variants in C19orf44 cause a unique late-onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophyMiriam Ehrenberg, Maayan Avraham, Sandeep Sarma Asodu, et al.
American Journal of Ophthalmology|April 26, 2022
WFS1-Associated Optic Neuropathy: Genotype-Phenotype Correlations and Disease ProgressionAnna Majander, Neringa Jurkute, Florence Burté, et al.
Journal of Hypertension|October 30, 1998
Correlates of cognitive status of old patients with isolated systolic hypertension: the Syst-Eur Vascular Dementia ProjectM L Seux, L Thijs, F Forette, et al.
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