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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. Among authors: trang h. Nat Genet. 2003 Apr;33(4):459-61. doi: 10.1038/ng1130. Epub 2003 Mar 17. Nat Genet. 2003. PMID: 12640453
[Spotlight on the congenital central hypoventilation syndrome (Ondine's curse) and its management].
Trang H, Amiel J, Straus C. Trang H, et al. Rev Mal Respir. 2013 Oct;30(8):609-12. doi: 10.1016/j.rmr.2013.07.007. Epub 2013 Aug 29. Rev Mal Respir. 2013. PMID: 24182648 French. No abstract available.
[Ondine's syndrome].
Trang H. Trang H. Arch Pediatr. 2001 May;8 Suppl 2:380s-381s. doi: 10.1016/s0929-693x(01)80082-8. Arch Pediatr. 2001. PMID: 11394124 French. No abstract available.
Abnormal esophageal motility in children with congenital central hypoventilation syndrome.
Faure C, Viarme F, Cargill G, Navarro J, Gaultier C, Trang H. Faure C, et al. Among authors: trang h. Gastroenterology. 2002 May;122(5):1258-63. doi: 10.1053/gast.2002.33062. Gastroenterology. 2002. PMID: 11984512
Intermittent hyperglycemia due to autonomic nervous system dysfunction: a new feature in patients with congenital central hypoventilation syndrome.
Gelwane G, Trang H, Carel JC, Dauger S, Léger J. Gelwane G, et al. Among authors: trang h. J Pediatr. 2013 Jan;162(1):171-6.e2. doi: 10.1016/j.jpeds.2012.06.036. Epub 2012 Aug 3. J Pediatr. 2013. PMID: 22863257
Proceedings of the fourth international conference on central hypoventilation.
Trang H, Brunet JF, Rohrer H, Gallego J, Amiel J, Bachetti T, Fischbeck KH, Similowski T, Straus C, Ceccherini I, Weese-Mayer DE, Frerick M, Bieganowska K, Middleton L, Morandi F, Ottonello G; European Central Hypoventilation Syndrome Consortium. Trang H, et al. Orphanet J Rare Dis. 2014 Dec 5;9:194. doi: 10.1186/s13023-014-0194-5. Orphanet J Rare Dis. 2014. PMID: 25928806 Free PMC article. Review.
Abnormal auditory pathways in PHOX2B mutation positive congenital central hypoventilation syndrome.
Trang H, Masri Zada T, Heraut F. Trang H, et al. BMC Neurol. 2015 Mar 22;15:41. doi: 10.1186/s12883-015-0299-z. BMC Neurol. 2015. PMID: 25886294 Free PMC article.
Delineation of late onset hypoventilation associated with hypothalamic dysfunction syndrome.
De Pontual L, Trochet D, Caillat-Zucman S, Abou Shenab OA, Bougneres P, Crow Y, Cunningham S, Esteva B, Heberle LC, Leger J, Pinto G, Polak M, Shafik MH, Straus C, Trang H, Munnich A, Lyonnet S, Desguerre I, Amiel J. De Pontual L, et al. Among authors: trang h. Pediatr Res. 2008 Dec;64(6):689-94. doi: 10.1203/PDR.0b013e318187dd0e. Pediatr Res. 2008. PMID: 18670370
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: trang h. 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
[Ondine syndrome or central congenital hypoventilation syndrome].
Trang H. Trang H. Rev Prat. 2006 Jan 31;56(2):125-8. Rev Prat. 2006. PMID: 16584036 Review. French.
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