期刊文献+

单侧延髓梗死伴发Ondine’s curse综合征一例 被引量:3

暂未订购
导出
摘要 0ndine’s curse综合征是中枢性睡眠呼吸暂停综合征(central sleep apnea syndrome)的一种特殊类型,主要表现为睡眠状态时出现的二氧化碳潴留、低氧血症及呼吸暂停。该命名来源于德国的一个古老传说,
出处 《中国卒中杂志》 2010年第10期841-845,共5页 Chinese Journal of Stroke
  • 相关文献

参考文献12

  • 1钱甜,曹云.先天性中枢性低通气综合征的研究进展[J].中华儿科杂志,2007,45(10):755-759. 被引量:3
  • 2黄如训.延脑梗死继发Ondine's curse综合征[J].中国神经精神疾病杂志,2004,30(6):419-422. 被引量:14
  • 3Javaheri S.Central sleep apnea[].Clinics in Chest Medicine.2010
  • 4Javaheri S.Central sleep apnea[].Sleep medicine essentials.2009
  • 5Plum F.Breathing is controlled independently by voluntary, emotional, and metabolically related pathways[].Archives of Neurology.1992
  • 6Vingerhoets F,Bogousslavsky J.Respiratory dysfunction[].Stroke syndromes.2001
  • 7Takehara M,Ishikawa K,Hiroi T, et al.Central type of sleep apnea syndrome caused by unilateral lateral medullary infarction[].Rinsho Shinkeiga.1992
  • 8Van Euler C,Marttila I,Remmers JE,hppenbach T.Effects of lesions on the parabrachialis nucleus on the mechanisms for central and reflex termination of inspiration in the cat[].Acta Physiologica Scandinavica.1976
  • 9.Idiopathic congenital central hypoventilation syndrome: diagnosis and management. American Thoracic Society[].American Journal of Respiratory and Critical Care Medicine.1999
  • 10Flageole H.Central hypoventilation and diaphragmatic eventration: diagnosis and management[].Seminars in Pediatric Surgery.2003

二级参考文献27

  • 1许志飞,江载芳.先天性中枢性低通气综合征一例[J].中华儿科杂志,2005,43(8):636-637. 被引量:12
  • 2BogouSSlavsky J, Khurana R, Deruaz JP, et al. Respiratory failure andunilateral caudal brainstem infarction. Ann Neurol, 1990,28(5):668.
  • 3Vingerhoets F, Bogousslavsky J. Respiratory dysfunction in stroke. ClinChest Med, 1994,15(4) :729.
  • 4Morrell MJ, HeyWood P, Moosavi SH, et al. Unilateral focal lesions inthe rostrolateral medulla influence chemosensitivity and breathing mea-sured during wakefulness, sleep and exercise. J Neurol Neurosury Psychi-atry, 1999,67(5) :637.
  • 5Trang H, Dehan M, Beaufils F, et al. The french congenital central hypoventilation syndrome registry: general data, phenotype, and genotype. Chest, 2005, 127: 72-79.
  • 6Bajaj R, Smith J, Trochet D, et al. Congenital central hypoventilation syndrome and Hirsehsprung' s disease in an extremely preterm infant. Pediatrics, 2005, 115:e737-e738
  • 7Verloes A, Elmer C, Lacombe D, et al. Ondine-Hirschsprung syndrome (Haddad syndrome). Further delineation in two cases and review of the literature. Eur J Pediatr, 1993, 152: 75-77.
  • 8Sritippayawan S, Hamutcu R, Kun SS, et al. Mother-daughter transmission of congenital central hypoventilation syndrome. Am J Respir Care Med, 2002, 166: 367-369.
  • 9Amiel J, Laudier B, Attie-Bitach T, et al. Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome. Nat Genet, 2003, 33: 459-461.
  • 10Trochet D, O' Brien LM, Gozal D, et al. PHOX2B genotype allows for prediction of tumor risk in congenital central hypoventilation syndrome. Am J Hum Genet, 2005, 76: 421- 426.

共引文献15

同被引文献10

引证文献3

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部