Amiel J - Search Results

1

Methylation-associated PHOX2B gene silencing is a rare event in human neuroblastoma.

de Pontual L, Trochet D, Bourdeaut F, Thomas S, Etchevers H, Chompret A, Minard V, Valteau D, Brugieres L, Munnich A, Delattre O, Lyonnet S, Janoueix-Lerosey I, Amiel J. de Pontual L, et al. Among authors: amiel j. Eur J Cancer. 2007 Nov;43(16):2366-72. doi: 10.1016/j.ejca.2007.07.016. Epub 2007 Aug 31. Eur J Cancer. 2007. PMID: 17765533 Free article.

2

Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome.

Amiel J, Laudier B, Attié-Bitach T, Trang H, de Pontual L, Gener B, Trochet D, Etchevers H, Ray P, Simonneau M, Vekemans M, Munnich A, Gaultier C, Lyonnet S. Amiel J, et al. Nat Genet. 2003 Apr;33(4):459-61. doi: 10.1038/ng1130. Epub 2003 Mar 17. Nat Genet. 2003. PMID: 12640453

3

Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma.

Trochet D, Bourdeaut F, Janoueix-Lerosey I, Deville A, de Pontual L, Schleiermacher G, Coze C, Philip N, Frébourg T, Munnich A, Lyonnet S, Delattre O, Amiel J. Trochet D, et al. Among authors: amiel j. Am J Hum Genet. 2004 Apr;74(4):761-4. doi: 10.1086/383253. Epub 2004 Mar 11. Am J Hum Genet. 2004. PMID: 15024693 Free PMC article.

4

Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma.

Bourdeaut F, Trochet D, Janoueix-Lerosey I, Ribeiro A, Deville A, Coz C, Michiels JF, Lyonnet S, Amiel J, Delattre O. Bourdeaut F, et al. Among authors: amiel j. Cancer Lett. 2005 Oct 18;228(1-2):51-8. doi: 10.1016/j.canlet.2005.01.055. Cancer Lett. 2005. PMID: 15949893 Review.

5

Molecular consequences of PHOX2B missense, frameshift and alanine expansion mutations leading to autonomic dysfunction.

Trochet D, Hong SJ, Lim JK, Brunet JF, Munnich A, Kim KS, Lyonnet S, Goridis C, Amiel J. Trochet D, et al. Among authors: amiel j. Hum Mol Genet. 2005 Dec 1;14(23):3697-708. doi: 10.1093/hmg/ddi401. Epub 2005 Oct 25. Hum Mol Genet. 2005. PMID: 16249188

6

PHOX2B germline and somatic mutations in late-onset central hypoventilation syndrome.

Trochet D, de Pontual L, Straus C, Gozal D, Trang H, Landrieu P, Munnich A, Lyonnet S, Gaultier C, Amiel J. Trochet D, et al. Among authors: amiel j. Am J Respir Crit Care Med. 2008 Apr 15;177(8):906-11. doi: 10.1164/rccm.200707-1079OC. Epub 2007 Dec 13. Am J Respir Crit Care Med. 2008. PMID: 18079495

7

Homozygous mutation of the PHOX2B gene in congenital central hypoventilation syndrome (Ondine's Curse).

Trochet D, de Pontual L, Estêvao MH, Mathieu Y, Munnich A, Feingold J, Goridis C, Lyonnet S, Amiel J. Trochet D, et al. Among authors: amiel j. Hum Mutat. 2008 May;29(5):770. doi: 10.1002/humu.20727. Hum Mutat. 2008. PMID: 18407552

8

Mutations of the RET gene in isolated and syndromic Hirschsprung's disease in human disclose major and modifier alleles at a single locus.

de Pontual L, Pelet A, Trochet D, Jaubert F, Espinosa-Parrilla Y, Munnich A, Brunet JF, Goridis C, Feingold J, Lyonnet S, Amiel J. de Pontual L, et al. Among authors: amiel j. J Med Genet. 2006 May;43(5):419-23. doi: 10.1136/jmg.2005.040113. Epub 2006 Jan 27. J Med Genet. 2006. PMID: 16443855 Free PMC article.

9

Exclusion of RNX as a major gene in congenital central hypoventilation syndrome (CCHS, Ondine's curse).

Amiel J, Pelet A, Trang H, de Pontual L, Simonneau M, Munnich A, Gaultier C, Lyonnet S. Amiel J, et al. Am J Med Genet A. 2003 Feb 15;117A(1):18-20. doi: 10.1002/ajmg.a.10934. Am J Med Genet A. 2003. PMID: 12548735

10

PHOX2B gene mutation in a patient with late-onset central hypoventilation.

Trang H, Laudier B, Trochet D, Munnich A, Lyonnet S, Gaultier C, Amiel J. Trang H, et al. Among authors: amiel j. Pediatr Pulmonol. 2004 Oct;38(4):349-51. doi: 10.1002/ppul.20074. Pediatr Pulmonol. 2004. PMID: 15334515

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