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Large deletion of the GJB6 gene in deaf patients heterozygous for the GJB2 gene mutation: genotypic and phenotypic analysis.
Feldmann D, Denoyelle F, Chauvin P, Garabédian EN, Couderc R, Odent S, Joannard A, Schmerber S, Delobel B, Leman J, Journel H, Catros H, Le Maréchal C, Dollfus H, Eliot MM, Delaunoy JP, David A, Calais C, Drouin-Garraud V, Obstoy MF, Bouccara D, Sterkers O, Huy PT, Goizet C, Duriez F, Fellmann F, Hélias J, Vigneron J, Montaut B, Lewin P, Petit C, Marlin S. Feldmann D, et al. Among authors: schmerber s. Am J Med Genet A. 2004 Jun 15;127A(3):263-7. doi: 10.1002/ajmg.a.20588. Am J Med Genet A. 2004. PMID: 15150777
International consensus on Vibrant Soundbridge® implantation in children and adolescents.
Cremers CW, O'Connor AF, Helms J, Roberson J, Clarós P, Frenzel H, Profant M, Schmerber S, Streitberger C, Baumgartner WD, Orfila D, Pringle M, Cenjor C, Giarbini N, Jiang D, Snik AF. Cremers CW, et al. Among authors: schmerber s. Int J Pediatr Otorhinolaryngol. 2010 Nov;74(11):1267-9. doi: 10.1016/j.ijporl.2010.07.028. Epub 2010 Sep 15. Int J Pediatr Otorhinolaryngol. 2010. PMID: 20828837
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: schmerber s. Eur J Hum Genet. 2004 Apr;12(4):279-84. doi: 10.1038/sj.ejhg.5201147. Eur J Hum Genet. 2004. PMID: 14694360
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: schmerber s. 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
SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations.
Albert S, Blons H, Jonard L, Feldmann D, Chauvin P, Loundon N, Sergent-Allaoui A, Houang M, Joannard A, Schmerber S, Delobel B, Leman J, Journel H, Catros H, Dollfus H, Eliot MM, David A, Calais C, Drouin-Garraud V, Obstoy MF, Tran Ba Huy P, Lacombe D, Duriez F, Francannet C, Bitoun P, Petit C, Garabédian EN, Couderc R, Marlin S, Denoyelle F. Albert S, et al. Among authors: schmerber s. Eur J Hum Genet. 2006 Jun;14(6):773-9. doi: 10.1038/sj.ejhg.5201611. Eur J Hum Genet. 2006. PMID: 16570074
[Middle ear cholesteatoma surgery].
Charachon R, Schmerber S, Lavieille JP. Charachon R, et al. Among authors: schmerber s. Ann Otolaryngol Chir Cervicofac. 1999 Dec;116(6):322-40. Ann Otolaryngol Chir Cervicofac. 1999. PMID: 10615524 Review. French.
[Computer-assisted video-endoscopic endonasal surgery].
Schmerber S, Chen B, Lavallée S, Coulomb M, Chirossel JP, Lavieille JP, Reyt E. Schmerber S, et al. Ann Otolaryngol Chir Cervicofac. 2001 Feb;118(1):35-44. Ann Otolaryngol Chir Cervicofac. 2001. PMID: 11240435 Free article. French.
134 results