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227 results

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Page 1
Evaluation of cytomegalovirus (CMV) DNA quantification in dried blood spots: retrospective study of CMV congenital infection.
Vauloup-Fellous C, Ducroux A, Couloigner V, Marlin S, Picone O, Galimand J, Loundon N, Denoyelle F, Grangeot-Keros L, Leruez-Ville M. Vauloup-Fellous C, et al. Among authors: denoyelle f. J Clin Microbiol. 2007 Nov;45(11):3804-6. doi: 10.1128/JCM.01654-07. Epub 2007 Sep 26. J Clin Microbiol. 2007. PMID: 17898161 Free PMC article.
A particular case of deafness-oligodontia syndrome.
Marlin S, Denoyelle F, Busquet D, Garabedian N, Petit C. Marlin S, et al. Among authors: denoyelle f. 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
[Hereditary sensorineural deafness].
Denoyelle F, Marlin S, Petit C, Garabédian EN. Denoyelle F, et al. Rev Prat. 2000 Jan 15;50(2):146-9. Rev Prat. 2000. PMID: 10737085 French.
Usher syndrome and cochlear implantation.
Loundon N, Marlin S, Busquet D, Denoyelle F, Roger G, Renaud F, Garabedian EN. Loundon N, et al. Among authors: denoyelle f. 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. Among authors: denoyelle f. 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: denoyelle f. 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: denoyelle f. Clin Genet. 2004 Oct;66(4):333-40. doi: 10.1111/j.1399-0004.2004.00296.x. Clin Genet. 2004. PMID: 15355436
227 results