Marlin S - Search Results

1

Pycnodysostosis presenting as atypical stridor.

Manfredi L, Marlin S, Fauroux B, Garabedian N, Couloigner V, Leboulanger N. Manfredi L, et al. Among authors: marlin s. Eur Ann Otorhinolaryngol Head Neck Dis. 2016 Apr;133(2):87-90. doi: 10.1016/j.anorl.2015.06.005. Epub 2016 Feb 5. Eur Ann Otorhinolaryngol Head Neck Dis. 2016. PMID: 26856677 Free article. Review.

2

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

3

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: marlin s. 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.

4

Perrault syndrome: report of four new cases, review and exclusion of candidate genes.

Marlin S, Lacombe D, Jonard L, Leboulanger N, Bonneau D, Goizet C, de Villemeur TB, Cabrol S, Houang M, Moatti L, Feldmann D, Denoyelle F. Marlin S, et al. Am J Med Genet A. 2008 Mar 1;146A(5):661-4. doi: 10.1002/ajmg.a.32180. Am J Med Genet A. 2008. PMID: 18241061

5

Cochlear implant and inner ear malformation. Proposal for an hyperosmolar therapy at surgery.

Loundon N, Leboulanger N, Maillet J, Riggouzzo A, Richard P, Marlin S, Garabedian EN. Loundon N, et al. Among authors: marlin s. Int J Pediatr Otorhinolaryngol. 2008 Apr;72(4):541-7. doi: 10.1016/j.ijporl.2008.01.004. Epub 2008 Feb 20. Int J Pediatr Otorhinolaryngol. 2008. PMID: 18282614

6

Hallerman-Streiff-like syndrome presenting with laterality and cardiac defects.

Morice-Picard F, Marlin S, Rooryck C, Fayon M, Thambo JB, Demarquez JL, Fauroux B, Denoyelle F, Lacombe D. Morice-Picard F, et al. Among authors: marlin s. Clin Dysmorphol. 2009 Apr;18(2):116-119. doi: 10.1097/MCD.0b013e32831da7ab. Clin Dysmorphol. 2009. PMID: 19057381

7

[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.

8

Velopharyngoplasty for noncleft velopharyngeal insufficiency: results in relation to 22q11 microdeletion.

Rouillon I, Leboulanger N, Roger G, Maulet M, Marlin S, Loundon N, Portnoï MF, Denoyelle F, Garabédian EN. Rouillon I, et al. Among authors: marlin s. Arch Otolaryngol Head Neck Surg. 2009 Jul;135(7):652-6. doi: 10.1001/archoto.2009.64. Arch Otolaryngol Head Neck Surg. 2009. PMID: 19620585

9

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

10

Progressive hearing loss associated with a unique cervical node due to a homozygous SLC29A3 mutation: a very mild phenotype.

Jonard L, Couloigner V, Pierrot S, Louha M, Gherbi S, Denoyelle F, Marlin S. Jonard L, et al. Among authors: marlin s. Eur J Med Genet. 2012 Jan;55(1):56-8. doi: 10.1016/j.ejmg.2011.06.009. Epub 2011 Aug 23. Eur J Med Genet. 2012. PMID: 21888995

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