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212 results

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Page 1
Audiological phenotyping evaluation in KBG syndrome: Description of a multicenter review.
Rhamati L, Marcolla A, Guerrot AM, Lerosey Y, Goldenberg A, Serey-Gaut M, Rio M, Cormier Daire V, Baujat G, Lyonnet S, Rubinato E, Jonard L, Rondeau S, Rouillon I, Couloignier V, Jacquemont ML, Dupin Deguine D, Moutton S, Vincent M, Isidor B, Ziegler A, Marie JP, Marlin S. Rhamati L, et al. Among authors: marlin s. Int J Pediatr Otorhinolaryngol. 2023 Aug;171:111606. doi: 10.1016/j.ijporl.2023.111606. Epub 2023 Jun 11. Int J Pediatr Otorhinolaryngol. 2023. PMID: 37336020
A particular case of deafness-oligodontia syndrome.
Marlin S, Denoyelle F, Busquet D, Garabedian N, Petit C. Marlin S, et al. Int J Pediatr Otorhinolaryngol. 1998 Jun 1;44(1):63-9. doi: 10.1016/s0165-5876(98)00029-9. Int J Pediatr Otorhinolaryngol. 1998. PMID: 9720683
Auditory neuropathy or endocochlear hearing loss?
Loundon N, Marcolla A, Roux I, Rouillon I, Denoyelle F, Feldmann D, Marlin S, Garabedian EN. Loundon N, et al. Among authors: marlin s. Otol Neurotol. 2005 Jul;26(4):748-54. doi: 10.1097/01.mao.0000169044.63970.4a. Otol Neurotol. 2005. PMID: 16015179
Results of cochlear implantation in two children with mutations in the OTOF gene.
Rouillon I, Marcolla A, Roux I, Marlin S, Feldmann D, Couderc R, Jonard L, Petit C, Denoyelle F, Garabédian EN, Loundon N. Rouillon I, et al. Among authors: marlin s. Int J Pediatr Otorhinolaryngol. 2006 Apr;70(4):689-96. doi: 10.1016/j.ijporl.2005.09.006. Epub 2005 Oct 13. Int J Pediatr Otorhinolaryngol. 2006. PMID: 16226319
[Velopharyngeal insufficiency in children].
Rouillon I, Leboulanger N, Roger G, Marlin S, Garabédian EN. Rouillon I, et al. Among authors: marlin s. Ann Otolaryngol Chir Cervicofac. 2009 Jun;126(3):155-61. doi: 10.1016/j.aorl.2009.03.006. Epub 2009 May 20. Ann Otolaryngol Chir Cervicofac. 2009. PMID: 19467645 Review. French. No abstract available.
[Genetic deafness in adults].
Marlin S, Jonard L, Feldmann D, Loundon N, Rouillon I, Couderc R, Denoyelle F. Marlin S, et al. Rev Prat. 2009 May 20;59(5):630-1. Rev Prat. 2009. PMID: 19552200 French. No abstract available.
Bilateral implantation in children with cochleovestibular nerve hypoplasia.
Oker N, Loundon N, Marlin S, Rouillon I, Leboulanger N, Garabédian EN. Oker N, et al. Among authors: marlin s. Int J Pediatr Otorhinolaryngol. 2009 Oct;73(10):1470-3. doi: 10.1016/j.ijporl.2009.06.017. Epub 2009 Aug 7. Int J Pediatr Otorhinolaryngol. 2009. PMID: 19665238
Phenotype and genotype in females with POU3F4 mutations.
Marlin S, Moizard MP, David A, Chaissang N, Raynaud M, Jonard L, Feldmann D, Loundon N, Denoyelle F, Toutain A. Marlin S, et al. Clin Genet. 2009 Dec;76(6):558-63. doi: 10.1111/j.1399-0004.2009.01215.x. Clin Genet. 2009. PMID: 19930154
212 results