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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1989 2
1991 1
1992 2
1993 5
1994 3
1995 9
1996 2
1997 3
1998 6
1999 3
2001 3
2002 4
2003 5
2004 4
2005 3
2006 1
2007 3
2008 5
2009 3
2010 8
2011 4
2012 6
2013 5
2014 13
2015 9
2016 9
2017 9
2018 8
2019 7
2020 8
2021 9
2022 4
2023 2
2024 2
2025 0

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152 results

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Page 1
KMT2B-related disorders: expansion of the phenotypic spectrum and long-term efficacy of deep brain stimulation.
Cif L, Demailly D, Lin JP, Barwick KE, Sa M, Abela L, Malhotra S, Chong WK, Steel D, Sanchis-Juan A, Ngoh A, Trump N, Meyer E, Vasques X, Rankin J, Allain MW, Applegate CD, Attaripour Isfahani S, Baleine J, Balint B, Bassetti JA, Baple EL, Bhatia KP, Blanchet C, Burglen L, Cambonie G, Seng EC, Bastaraud SC, Cyprien F, Coubes C, d'Hardemare V; Deciphering Developmental Disorders Study; Doja A, Dorison N, Doummar D, Dy-Hollins ME, Farrelly E, Fitzpatrick DR, Fearon C, Fieg EL, Fogel BL, Forman EB, Fox RG; Genomics England Research Consortium; Gahl WA, Galosi S, Gonzalez V, Graves TD, Gregory A, Hallett M, Hasegawa H, Hayflick SJ, Hamosh A, Hully M, Jansen S, Jeong SY, Krier JB, Krystal S, Kumar KR, Laurencin C, Lee H, Lesca G, François LL, Lynch T, Mahant N, Martinez-Agosto JA, Milesi C, Mills KA, Mondain M, Morales-Briceno H; NIHR BioResource; Ostergaard JR, Pal S, Pallais JC, Pavillard F, Perrigault PF, Petersen AK, Polo G, Poulen G, Rinne T, Roujeau T, Rogers C, Roubertie A, Sahagian M, Schaefer E, Selim L, Selway R, Sharma N, Signer R, Soldatos AG, Stevenson DA, Stewart F, Tchan M; Undiagnosed Diseases Network; Verma IC, de Vries BBA, Wilson JL, Wong DA, Zaitoun R, Zhen D… See abstract for full author list ➔ Cif L, et al. Among authors: mondain m. Brain. 2020 Dec 5;143(11):3242-3261. doi: 10.1093/brain/awaa304. Brain. 2020. PMID: 33150406 Free PMC article.
GJB2 mutations and degree of hearing loss: a multicenter study.
Snoeckx RL, Huygen PL, Feldmann D, Marlin S, Denoyelle F, Waligora J, Mueller-Malesinska M, Pollak A, Ploski R, Murgia A, Orzan E, Castorina P, Ambrosetti U, Nowakowska-Szyrwinska E, Bal J, Wiszniewski W, Janecke AR, Nekahm-Heis D, Seeman P, Bendova O, Kenna MA, Frangulov A, Rehm HL, Tekin M, Incesulu A, Dahl HH, du Sart D, Jenkins L, Lucas D, Bitner-Glindzicz M, Avraham KB, Brownstein Z, del Castillo I, Moreno F, Blin N, Pfister M, Sziklai I, Toth T, Kelley PM, Cohn ES, Van Maldergem L, Hilbert P, Roux AF, Mondain M, Hoefsloot LH, Cremers CW, Löppönen T, Löppönen H, Parving A, Gronskov K, Schrijver I, Roberson J, Gualandi F, Martini A, Lina-Granade G, Pallares-Ruiz N, Correia C, Fialho G, Cryns K, Hilgert N, Van de Heyning P, Nishimura CJ, Smith RJ, Van Camp G. Snoeckx RL, et al. Among authors: mondain m. Am J Hum Genet. 2005 Dec;77(6):945-57. doi: 10.1086/497996. Epub 2005 Oct 19. Am J Hum Genet. 2005. PMID: 16380907 Free PMC article.
Management of laryngomalacia.
Ayari S, Aubertin G, Girschig H, Van Den Abbeele T, Denoyelle F, Couloignier V, Mondain M. Ayari S, et al. Among authors: mondain m. Eur Ann Otorhinolaryngol Head Neck Dis. 2013 Feb;130(1):15-21. doi: 10.1016/j.anorl.2012.04.003. Epub 2012 Jul 24. Eur Ann Otorhinolaryngol Head Neck Dis. 2013. PMID: 22835508 Free article. Review.
Cochlear Implantation and Other Treatments in Single-Sided Deafness and Asymmetric Hearing Loss: Results of a National Multicenter Study Including a Randomized Controlled Trial.
Marx M, Mosnier I, Venail F, Mondain M, Uziel A, Bakhos D, Lescanne E, N'Guyen Y, Bernardeschi D, Sterkers O, Deguine O, Lepage B, Godey B, Schmerber S, Bonne NX, Vincent C, Fraysse B. Marx M, et al. Among authors: mondain m. Audiol Neurootol. 2021;26(6):414-424. doi: 10.1159/000514085. Epub 2021 Mar 31. Audiol Neurootol. 2021. PMID: 33789270 Free PMC article. Clinical Trial.
[Introduction].
Groupe d'étude MACVIA-LR. Groupe d'étude MACVIA-LR. Presse Med. 2015 Nov;44 Suppl 1:S1-5. doi: 10.1016/j.lpm.2015.07.014. Epub 2015 Oct 18. Presse Med. 2015. PMID: 26476754 French. No abstract available.
Genetic Evaluation of Prelingual Hearing Impairment: Recommendations of an European Network for Genetic Hearing Impairment.
Jonard L, Brotto D, Moreno-Pelayo MA, Del Castillo I, Kremer H, Pennings R, Caria H, Fialho G, Boudewyns A, Van Camp G, Ołdak M, Oziębło D, Deggouj N, De Siati RD, Gasparini P, Girotto G, Verstreken M, Dossena S, Roesch S, Battelino S, Trebušak Podkrajšek K, Warnecke A, Lenarz T, Lesinski-Schiedat A, Mondain M, Roux AF, Denoyelle F, Loundon N, Serey Gaut M, Trevisi P, Rubinato E, Martini A, Marlin S. Jonard L, et al. Among authors: mondain m. Audiol Res. 2023 May 10;13(3):341-346. doi: 10.3390/audiolres13030029. Audiol Res. 2023. PMID: 37218840 Free PMC article.
Painful peripheral facial palsy.
Abramovici L, Akkari M, Mondain M, Uziel A, Venail F. Abramovici L, et al. Among authors: mondain m. Eur Ann Otorhinolaryngol Head Neck Dis. 2014 Jun;131(3):201-5. doi: 10.1016/j.anorl.2013.06.006. Epub 2014 Mar 19. Eur Ann Otorhinolaryngol Head Neck Dis. 2014. PMID: 24657186 Free article. No abstract available.
Role of the ENT specialist in the diagnosis of pediatric obstructive sleep apnea-hypopnea syndrome (POSAHS). Part 3: sleep recordings.
Akkari M, Yildiz S, Marianowski R, Monteyrol PJ, Chalumeau F, Fayoux P, Leboulanger N, Franco P, Couloigner V, Mondain M. Akkari M, et al. Among authors: mondain m. Eur Ann Otorhinolaryngol Head Neck Dis. 2020 Nov;137(5):405-410. doi: 10.1016/j.anorl.2020.02.001. Epub 2020 Feb 24. Eur Ann Otorhinolaryngol Head Neck Dis. 2020. PMID: 32107171 Free article. Review.
Cochlear Aqueduct Post-Natal Growth: A Computed Tomography Study.
Abbas M, Wang J, Leboucq N, Mondain M, Blanc F. Abbas M, et al. Among authors: mondain m. J Assoc Res Otolaryngol. 2024 Dec;25(6):611-617. doi: 10.1007/s10162-024-00963-0. Epub 2024 Sep 18. J Assoc Res Otolaryngol. 2024. PMID: 39294515
152 results