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pro vyhledávání: '"Patrick Lundquist"'
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101646- (2024)
Externí odkaz:
https://doaj.org/article/83b2cb71bb50435682a240e94b145b1e
Autor:
Lauren Choate, Amber McDonald, Patrick Lundquist, Francis Hoffman, Angela Pickart, Emily Lauer, Sarah Thieke, Rebecca Hofmeister, Erik Thorland, Cherisse Marcou
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100489- (2023)
Externí odkaz:
https://doaj.org/article/ddf5e4f799834c94b3c503adb0224bdf
Autor:
Jaime Lopes, Noemi Vidal‐Folch, Patrick Lundquist, Lisa A. Schimmenti, Nadir Demirel, Vicki Dean, Janelle Olson, Tom Auth, Malinda Butz, Katelyn Reed, Mark Wylam, Jessica Balcom, Nicole J. Boczek, Linda Hasadsri
Publikováno v:
Pediatric Pulmonology. 58:819-824
MT-RNR1 variants are a well-known cause of aminoglycoside-induced hearing loss (AIHL). Individuals with cystic fibrosis (CF) routinely receive aminoglycosides and are at high risk of AIHL. However, genetic testing before treatment is not routinely pe