1[1]Kerbl R,Litscher H,Grubbauer HM,et al. Congenital central hypoventilation syndrome (Ondine' s curse syndrome) in two siblings: delayed diagnosis and successful noninvasive treatment. Eur J Pediatr, 1996,155:977-980.
2[2]Strauser LM, Helikson MA, Tobias JD. Anesthetic care for the child with congenital central alveolar hypoventilation syndrome (Ondine' s curse). J Clin Anesth, 1999,11: 431-437.
3[3]American Thoracic Society. Idiopathic congenital central hypoventilation syndrome:diagnosis and management. Am J Respir Crit Care Med, 1999,160: 368-373.
4[4]Croaker GD,Shi E,Simpson E,et al. Congenital central hypoventilation syndrome and Hirschsprung' s disease. Arch Dis Child, 1998,78:316-322.
5[5]Nakamura A, Kuwaki T,Kuriyama T, et al. Normal ventilation and ventilatory responses to chemical stimuli in juvenile mutant mice deficient in endothelin-3. Respir Physiol, 2001,124:1-9.
6[6]Sakai T,Wakizaka A,Matsuda H,et al. Point mutation in exon 12 of the receptor tyrosine kinase proto-oncogene RET in OndineHirschsprung syndrome. Pediatrics, 1998,101: 924-926.
7[7]Renolleau S, Vardon G, Dauger S, et al. Ventilatory responses to hypercapnia and hypoxia in Mash-1 heterozygous newborn and adult mice. Pediatr Res, 1999,46: 535-542.
9[9]Shirasawa S,Arata A,Onimaru H,et al. Rnx deficiency results in congenital central hypoventilation. Nat Genet, 2000,24: 287-290.
10[10]Cutz E, Ma TK, Perrin DG, et al. Peripheral chemoreceptors in congenital central hypoventilation syndrome. Am J Respir Crit Care Med, 1997,155:358-363.