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Intravitreal aflibercept for the treatment of patients with neovascular age-related macular degeneration in routine clinical practice in Latin America: the AQUILA study.
Wu L, Bordon AF, Charles M, Rodríguez FJ, Lee J, Machewitz T, Mueller M, Del Carmen Gay G, Fromow-Guerra J; AQUILA investigators. Wu L, et al. Among authors: mueller m. Int J Retina Vitreous. 2022 Oct 18;8(1):76. doi: 10.1186/s40942-022-00425-w. Int J Retina Vitreous. 2022. PMID: 36258240 Free PMC article.
Challenges in the Development and Evaluation of Pediatric Heart Valve Technologies.
Hofferberth SC, Kelley T, Armstrong AK, Heyninck-Jantz C, Maiorano A, Colson M, Schoen FJ, Wu C, Ibrahim N, Tretter JT, Mueller MD, Bianco RW, Carney JP, Behr L, Breuer CK, Beith J, Cox M, Feins EN, Vang E, Wood L, Tranquillo RT, Lim DS, Taylor AM, Redington A, Cheatham JP, McElhinney DB, Del Nido PJ, Yoganathan A. Hofferberth SC, et al. Among authors: mueller md. Ann Thorac Surg. 2024 Dec 12:S0003-4975(24)01045-2. doi: 10.1016/j.athoracsur.2024.11.024. Online ahead of print. Ann Thorac Surg. 2024. PMID: 39674526 Review.
Considerations for building and using integrated single-cell atlases.
Hrovatin K, Sikkema L, Shitov VA, Heimberg G, Shulman M, Oliver AJ, Mueller MF, Ibarra IL, Wang H, Ramírez-Suástegui C, He P, Schaar AC, Teichmann SA, Theis FJ, Luecken MD. Hrovatin K, et al. Among authors: mueller mf. Nat Methods. 2024 Dec 13. doi: 10.1038/s41592-024-02532-y. Online ahead of print. Nat Methods. 2024. PMID: 39672979 Review.
Copy-number analysis from genome sequencing data of 11,754 rare-disease parent-child trios: A model for identifying autosomal recessive human gene knockouts including a novel gene for autosomal recessive retinopathy.
Olinger E, Wilson IJ, Orr S, Barroso-Gil M, Neatu R; Genomics England Research Consortium; Atan D, Sayer JA. Olinger E, et al. Genet Med Open. 2024 Feb 29;2:101834. doi: 10.1016/j.gimo.2024.101834. eCollection 2024. Genet Med Open. 2024. PMID: 39669628 Free PMC article.
2,789 results