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118 results

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Page 1
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. Among authors: loundon n. Clin Genet. 2009 Dec;76(6):558-63. doi: 10.1111/j.1399-0004.2009.01215.x. Clin Genet. 2009. PMID: 19930154
Analysis of specific risk factors of neurodevelopmental disorder in hearing-impaired infants under ten months of age: "EnTNDre" an opening research stemming from a transdisciplinary partnership.
Akrich S, Parlato de Oliveira E, Favrot-Meunier C, Rebichon C, de Clerck A, Ettori S, Rouillon I, Prang I, Loundon N. Akrich S, et al. Among authors: loundon n. Int J Pediatr Otorhinolaryngol. 2023 Mar;166:111453. doi: 10.1016/j.ijporl.2023.111453. Epub 2023 Jan 21. Int J Pediatr Otorhinolaryngol. 2023. PMID: 36746056
Current approach of primary tracheal dyskinesia.
Loundon N, Brugel L, Roger C, Denoyelle F, Coiffier T, Garabédian EN. Loundon N, et al. Pediatr Pulmonol Suppl. 1999;18:67-70. Pediatr Pulmonol Suppl. 1999. PMID: 10093100 No abstract available.
Usher syndrome and cochlear implantation.
Loundon N, Marlin S, Busquet D, Denoyelle F, Roger G, Renaud F, Garabedian EN. Loundon N, et al. Otol Neurotol. 2003 Mar;24(2):216-21. doi: 10.1097/00129492-200303000-00015. Otol Neurotol. 2003. PMID: 12621335
[Cochlear implantation in the child: results and perspectives].
Loundon N, Busquet D, Denoyelle F, Roger G, Garabedian EN. Loundon N, et al. Arch Pediatr. 2003 May;10 Suppl 1:161s-163s. doi: 10.1016/s0929-693x(03)90423-4. Arch Pediatr. 2003. PMID: 14509783 French. No abstract available.
Clinical evidence of the nonpathogenic nature of the M34T variant in the connexin 26 gene.
Feldmann D, Denoyelle F, Loundon N, Weil D, Garabedian EN, Couderc R, Joannard A, Schmerber S, Delobel B, Leman J, Journel H, Catros H, Ferrec C, Drouin-Garraud V, Obstoy MF, Moati L, Petit C, Marlin S. Feldmann D, et al. Among authors: loundon n. Eur J Hum Genet. 2004 Apr;12(4):279-84. doi: 10.1038/sj.ejhg.5201147. Eur J Hum Genet. 2004. PMID: 14694360
Screening of SLC26A4 (PDS) gene in Pendred's syndrome: a large spectrum of mutations in France and phenotypic heterogeneity.
Blons H, Feldmann D, Duval V, Messaz O, Denoyelle F, Loundon N, Sergout-Allaoui A, Houang M, Duriez F, Lacombe D, Delobel B, Leman J, Catros H, Journel H, Drouin-Garraud V, Obstoy MF, Toutain A, Oden S, Toublanc JE, Couderc R, Petit C, Garabédian EN, Marlin S. Blons H, et al. Among authors: loundon n. Clin Genet. 2004 Oct;66(4):333-40. doi: 10.1111/j.1399-0004.2004.00296.x. Clin Genet. 2004. PMID: 15355436
GJB2 and GJB6 mutations: genotypic and phenotypic correlations in a large cohort of hearing-impaired patients.
Marlin S, Feldmann D, Blons H, Loundon N, Rouillon I, Albert S, Chauvin P, Garabédian EN, Couderc R, Odent S, Joannard A, Schmerber S, Delobel B, Leman J, Journel H, Catros H, Lemarechal C, Dollfus H, Eliot MM, Delaunoy JL, David A, Calais C, Drouin-Garraud V, Obstoy MF, Goizet C, Duriez F, Fellmann F, Hélias J, Vigneron J, Montaut B, Matin-Coignard D, Faivre L, Baumann C, Lewin P, Petit C, Denoyelle F. Marlin S, et al. Among authors: loundon n. Arch Otolaryngol Head Neck Surg. 2005 Jun;131(6):481-7. doi: 10.1001/archotol.131.6.481. Arch Otolaryngol Head Neck Surg. 2005. PMID: 15967879
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. Otol Neurotol. 2005 Jul;26(4):748-54. doi: 10.1097/01.mao.0000169044.63970.4a. Otol Neurotol. 2005. PMID: 16015179
118 results