Mondain M - Search Results

1

Combined genetic approaches yield a 48% diagnostic rate in a large cohort of French hearing-impaired patients.

Baux D, Vaché C, Blanchet C, Willems M, Baudoin C, Moclyn M, Faugère V, Touraine R, Isidor B, Dupin-Deguine D, Nizon M, Vincent M, Mercier S, Calais C, García-García G, Azher Z, Lambert L, Perdomo-Trujillo Y, Giuliano F, Claustres M, Koenig M, Mondain M, Roux AF. Baux D, et al. Among authors: mondain m. Sci Rep. 2017 Dec 1;7(1):16783. doi: 10.1038/s41598-017-16846-9. Sci Rep. 2017. PMID: 29196752 Free PMC article.

2

A large deletion including most of GJB6 in recessive non syndromic deafness: a digenic effect?

Pallares-Ruiz N, Blanchet P, Mondain M, Claustres M, Roux AF. Pallares-Ruiz N, et al. Among authors: mondain m. Eur J Hum Genet. 2002 Jan;10(1):72-6. doi: 10.1038/sj.ejhg.5200762. Eur J Hum Genet. 2002. PMID: 11896458

3

Evaluation of dHPLC for CX26 mutation screening in patients from southern France with sensorineural deafness.

Pallares-Ruiz N, Blanchet P, Mondain M, Low-Hong S, Demaille J, Claustres M, Roux AF. Pallares-Ruiz N, et al. Among authors: mondain m. Genet Test. 2001 Winter;5(4):339-43. doi: 10.1089/109065701753617507. Genet Test. 2001. PMID: 11960582

4

Molecular epidemiology of DFNB1 deafness in France.

Roux AF, Pallares-Ruiz N, Vielle A, Faugère V, Templin C, Leprevost D, Artières F, Lina G, Molinari N, Blanchet P, Mondain M, Claustres M. Roux AF, et al. Among authors: mondain m. BMC Med Genet. 2004 Mar 6;5:5. doi: 10.1186/1471-2350-5-5. BMC Med Genet. 2004. PMID: 15070423 Free PMC article.

5

Nonsyndromic 35 delG mutation of the connexin 26 gene associated with deafness in syndromic children: two case reports.

Venail F, Roux AF, Pallares-Ruiz N, Claustres M, Blanchet P, Gardiner Q, Mondain M. Venail F, et al. Among authors: mondain m. Laryngoscope. 2004 Mar;114(3):566-9. doi: 10.1097/00005537-200403000-00033. Laryngoscope. 2004. PMID: 15091236

6

[Usher type I syndrome in children: genotype/phenotype correlation and cochlear implant benefits].

Blanchet C, Roux AF, Hamel C, Ben Salah S, Artières F, Faugère V, Uziel A, Mondain M. Blanchet C, et al. Among authors: mondain m. Rev Laryngol Otol Rhinol (Bord). 2007;128(3):137-43. Rev Laryngol Otol Rhinol (Bord). 2007. PMID: 18323324 French.

7

Pure-tone threshold description of an elderly French screened population.

Blanchet C, Pommie C, Mondain M, Berr C, Hillaire D, Puel JL. Blanchet C, et al. Among authors: mondain m. Otol Neurotol. 2008 Jun;29(4):432-40. doi: 10.1097/MAO.0b013e3181719746. Otol Neurotol. 2008. PMID: 18520580

8

Nasal epithelial cells are a reliable source to study splicing variants in Usher syndrome.

Vaché C, Besnard T, Blanchet C, Baux D, Larrieu L, Faugère V, Mondain M, Hamel C, Malcolm S, Claustres M, Roux AF. Vaché C, et al. Among authors: mondain m. Hum Mutat. 2010 Jun;31(6):734-41. doi: 10.1002/humu.21255. Hum Mutat. 2010. PMID: 20513143

9

Management of infantile subglottic hemangioma: acebutolol or propranolol?

Blanchet C, Nicollas R, Bigorre M, Amedro P, Mondain M. Blanchet C, et al. Among authors: mondain m. Int J Pediatr Otorhinolaryngol. 2010 Aug;74(8):959-61. doi: 10.1016/j.ijporl.2010.05.013. Epub 2010 Jun 16. Int J Pediatr Otorhinolaryngol. 2010. PMID: 20557953

10

[Stridor or not stridor].

Mondain M, Blanchet C. Mondain M, et al. Arch Pediatr. 2010 Jun;17(6):602-3. doi: 10.1016/S0929-693X(10)70018-X. Arch Pediatr. 2010. PMID: 20654800 French. No abstract available.

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