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Investigative Ophthalmology & Visual Science|August 2, 2017
C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel MutationsChristina Gerth-Kahlert, Amit Tiwari, James V M Hanson, et al.
ESMO Gastrointestinal Oncology|February 6, 2026
Novel blood signature for hepatocellular carcinoma screeningK-M Chueng, K-N Kwok, S J-L Lam, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|May 26, 2025
Safety and Sample Adequacy for Comprehensive Biomarker Testing of Bronchoscopic Biopsies: An American Association of Bronchology and Interventional Pulmonology and International Association for the Study of Lung Cancer Clinical Practice GuidelineUdit Chaddha, Abhinav Agrawal, Uzair Ghori, et al.
Retina (Philadelphia, Pa.)|February 2, 2017
REPEATABILITY AND LONGITUDINAL ASSESSMENT OF FOVEAL CONE STRUCTURE IN CNGB3-ASSOCIATED ACHROMATOPSIAChristopher S Langlo, Laura R Erker, Maria Parker, et al.
The Journal of Urology|June 18, 2013
Validation of a genomic classifier that predicts metastasis following radical prostatectomy in an at risk patient populationR Jeffrey Karnes, Eric J Bergstralh, Elai Davicioni, et al.
Eye (London, England)|September 17, 2016
Ophthalmic presentation of giant cell arteritis in African-AmericansS T Garrity, M Pistilli, M S Vaphiades, et al.
Plos One|June 1, 2019
MicroRNA modulated networks of adaptive and innate immune response in pancreatic ductal adenocarcinomaTainara F Felix, Rainer M Lopez Lapa, Márcio de Carvalho, et al.
Genome Research|August 6, 2009
Population genomics in a disease targeted primary cell modelElin Grundberg, Tony Kwan, Bing Ge, et al.
Investigative Ophthalmology & Visual Science|August 7, 2020
Possible Modifying Effect of Hemoglobin A1c on Genetic Susceptibility to Severe Diabetic Retinopathy in Patients With Type 2 DiabetesKelvin K K Ng, Chloe Y Y Cheung, Chi-Ho Lee, 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.
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