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Association between hearing loss and hereditary ATTR amyloidosis.
Bartier S, Bodez D, Kharoubi M, Guellich A, Canouï-Poitrine F, Chatelin V, Coste A, Damy T, Béquignon E. Bartier S, et al. Among authors: coste a. Amyloid. 2019 Dec;26(4):234-242. doi: 10.1080/13506129.2019.1663814. Epub 2019 Sep 10. Amyloid. 2019. PMID: 31502881
Mutations in DNAJB13, Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male Infertility.
El Khouri E, Thomas L, Jeanson L, Bequignon E, Vallette B, Duquesnoy P, Montantin G, Copin B, Dastot-Le Moal F, Blanchon S, Papon JF, Lorès P, Yuan L, Collot N, Tissier S, Faucon C, Gacon G, Patrat C, Wolf JP, Dulioust E, Crestani B, Escudier E, Coste A, Legendre M, Touré A, Amselem S. El Khouri E, et al. Among authors: coste a. Am J Hum Genet. 2016 Aug 4;99(2):489-500. doi: 10.1016/j.ajhg.2016.06.022. Am J Hum Genet. 2016. PMID: 27486783 Free PMC article.
Emergency Department care of childhood epistaxis.
Béquignon E, Teissier N, Gauthier A, Brugel L, De Kermadec H, Coste A, Prulière-Escabasse V. Béquignon E, et al. Among authors: coste a. Emerg Med J. 2017 Aug;34(8):543-548. doi: 10.1136/emermed-2015-205528. Epub 2016 Aug 19. Emerg Med J. 2017. PMID: 27542804 Review.
How your ears can tell what is hidden in your heart: wild-type transthyretin amyloidosis as potential cause of sensorineural hearing loss inelderly-AmyloDEAFNESS pilot study.
Béquignon E, Guellich A, Bartier S, Raynal M, Prulière-Escabasse V, Canouï-Poitrine F, Coste A, Damy T. Béquignon E, et al. Among authors: coste a. Amyloid. 2017 Jun;24(2):96-100. doi: 10.1080/13506129.2017.1330744. Epub 2017 Jun 9. Amyloid. 2017. PMID: 28598686 Clinical Trial.
515 results