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A case series of a rare tendon rupture.
Weber S, Zimmermann B, Bühler G, Stillhard PF. Weber S, et al. J Surg Case Rep. 2021 Mar 29;2021(3):rjab058. doi: 10.1093/jscr/rjab058. eCollection 2021 Mar. J Surg Case Rep. 2021. PMID: 33815751 Free PMC article.
Newborn screening for common genetic variants associated with permanent hearing loss: Implementation in Ontario and a review of the first 3 years.
Kernohan KD, Gallagher L, Pigeon M, Yeh E, Lacaria M, Axford MM, MacCormick J, Papaioannou V, Quercia N, Rupar C, Zimmerman K, Weber S, Cushing SL, Chakraborty P. Kernohan KD, et al. Among authors: weber s. Genet Med. 2025 Jan 19:101364. doi: 10.1016/j.gim.2025.101364. Online ahead of print. Genet Med. 2025. PMID: 39846246
Outcomes of a Population-Based Congenital Cytomegalovirus Screening Program.
Dunn JKE, Chakraborty P, Reuvers E, Gallagher L, Kernohan KD, Lacaria M, Barton M, Leifso K, Pernica JM, Santander E, Pigeon M, Cushing SL, MacCormick J, Gantt S, Weber S, Bitnun A, Brophy J. Dunn JKE, et al. Among authors: weber s. JAMA Pediatr. 2025 Jan 21. doi: 10.1001/jamapediatrics.2024.5562. Online ahead of print. JAMA Pediatr. 2025. PMID: 39836409
Multi-Institutional Analysis of Pancreatoduodenectomy for Nonfamilial Periampullary Adenoma: A Novel Risk Score to Guide Shared Decision-Making.
Mavani PT, Sok C, Eng N, Marra A, Foroutani L, Alseidi A, Hariri H, Wilson G, Ahmad SA, Scoggins C, Hester C, Datta J, Merchant N, LeCompte M, Kim HJ, Sigler G, Zafar N, Weber S, Prela O, Carpizo D, Kasting C, Fields R, Sarmiento JM, Russell MC, Shah MM, Maithel SK, Kooby DA. Mavani PT, et al. Among authors: weber s. J Am Coll Surg. 2025 Jan 20. doi: 10.1097/XCS.0000000000001289. Online ahead of print. J Am Coll Surg. 2025. PMID: 39831703
3,631 results