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Results: 1-13 |
Results: 13
Tracheal dyskinesia associated with midline abnormality: Embryological hypotheses and therapeutic implications
Authors: Corre, A Chaudre, F Roger, G Denoyelle, F Garabedian, EN
Citation: A. Corre et al., Tracheal dyskinesia associated with midline abnormality: Embryological hypotheses and therapeutic implications, PEDIAT PULM, 2001, pp. 10-12
Episodic laryngeal dysfunction.
Authors: Roger, G Denoyelle, F Garabedian, EN
Citation: G. Roger et al., Episodic laryngeal dysfunction., ARCH PED, 8, 2001, pp. 650S-654S
Connexin 26 gene mutations in congenitally deaf children - Pitfalls for genetic counseling
Authors: Marlin, S Garabedian, EN Roger, G Moatti, L Matha, N Lewin, P Petit, C Denoyelle, F
Citation: S. Marlin et al., Connexin 26 gene mutations in congenitally deaf children - Pitfalls for genetic counseling, ARCH OTOLAR, 127(8), 2001, pp. 927-933
Use of the carbon dioxide laser for tracheobronchial pathology in children
Authors: Ayache, D Wagner, I Denoyelle, F Garabedian, EN
Citation: D. Ayache et al., Use of the carbon dioxide laser for tracheobronchial pathology in children, EUR ARCH OT, 257(5), 2000, pp. 287-289
A simple and reliable method for the detection of the 30delG mutation of the CX26 gene
Authors: Casademont, I Chevrier, D Denoyelle, F Petit, C Guesdon, JL
Citation: I. Casademont et al., A simple and reliable method for the detection of the 30delG mutation of the CX26 gene, MOL CELL PR, 14(3), 2000, pp. 149-152
Extensive lymphangioma presenting with upper airway obstruction
Authors: Hartl, DM Roger, G Denoyelle, F Nicollas, R Triglia, JM Garabedian, EN
Citation: Dm. Hartl et al., Extensive lymphangioma presenting with upper airway obstruction, ARCH OTOLAR, 126(11), 2000, pp. 1378-1382
DFNA3
Authors: Denoyelle, F Weil, D Levilliers, J Petit, C
Citation: F. Denoyelle et al., DFNA3, ADV OTO-RH, 56, 2000, pp. 78-83
Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates
Authors: Ben Arab, S Hmani, M Denoyelle, F Boulila-Elgaied, A Chardenoux, S Hachicha, S Petit, C Ayadi, H
Citation: S. Ben Arab et al., Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates, CLIN GENET, 57(6), 2000, pp. 439-443
Current approach of primary tracheal dyskinesia
Authors: Loundon, N Brugel, L Roger, C Denoyelle, F Coiffier, T Garabedian, EN
Citation: N. Loundon et al., Current approach of primary tracheal dyskinesia, PEDIAT PULM, 1999, pp. 67-70
Townes-Brocks syndrome: Detection of a SALL1 mutation hot spot and evidence for a position effect in one patient
Authors: Marlin, S Blanchard, S Slim, R Lacombe, D Denoyelle, F Alessandri, JL Calzolari, E Drouin-Garraud, V Ferraz, FG Fourmaintraux, A Philip, N Toublanc, JE Petit, C
Citation: S. Marlin et al., Townes-Brocks syndrome: Detection of a SALL1 mutation hot spot and evidence for a position effect in one patient, HUM MUTAT, 14(5), 1999, pp. 377-386
Nasal fossa malformations and paramedian facial cleft: New perspectives
Authors: Garabedian, EN Ducroz, V Roger, G Denoyelle, F Catala, M
Citation: En. Garabedian et al., Nasal fossa malformations and paramedian facial cleft: New perspectives, J CRAN GENE, 19(1), 1999, pp. 12-19
Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling
Authors: Denoyelle, F Marlin, S Weil, D Moatti, L Chauvin, P Garabedian, EN Petit, C
Citation: F. Denoyelle et al., Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling, LANCET, 353(9161), 1999, pp. 1298-1303
Myringoplasty in children: Predictive factors of outcome
Authors: Denoyelle, F Roger, G Chauvin, P Garabedian, EN
Citation: F. Denoyelle et al., Myringoplasty in children: Predictive factors of outcome, LARYNGOSCOP, 109(1), 1999, pp. 47-51
Risultati: 1-13 |