切换至 "中华医学电子期刊资源库"

中华妇幼临床医学杂志(电子版) ›› 2012, Vol. 08 ›› Issue (04) : 415 -417. doi: 10.3877/cma.j.issn.1673-5250.2012.04.001

所属专题: 文献

专家约稿

新生儿上呼吸道梗阻病因的早期识别
薛辛东1,*()   
  1. 1. 110004 沈阳,中国医科大学附属盛京医院儿科
  • 收稿日期:2012-06-24 修回日期:2012-06-28 出版日期:2012-08-01
  • 通信作者: 薛辛东
  • 基金资助:
    国家自然科学基金资助项目(30672253)
  • Received:2012-06-24 Revised:2012-06-28 Published:2012-08-01
引用本文:

薛辛东. 新生儿上呼吸道梗阻病因的早期识别[J]. 中华妇幼临床医学杂志(电子版), 2012, 08(04): 415-417.

[1]
Daniel SJ. The upper airway:congenital malformations[J]. Paediatr Respir Rev, 2006, 7:S260-263.
[2]
Dinwiddie R. Congenital upper airway obstruction[J]. Paediatr Respir Rev, 2004, 5:17-24.
[3]
Hammer J. Acquired upper airway obstruction[J]. Paediatr Respir Rev, 2004, 5:25-33.
[4]
Altman KW, Wetmore RF, Marsh RR. Congenital airway abnormalities in patients requiring hospitalization[J]. Arch Otolaryngol Head Neck Surg, 1999, 125:525-528.
[5]
Miller MJ, Martin RJ, Carlo WA, et al. Oral breathing in newborn infants[J]. J Pediatr, 1985, 107:465-491.
[6]
De Almeida V, Alvaro R, al-Alaiyan S, et al. Prevalence and charcaterization of spontaneous oral breathing in preterm infants[J]. Am J Perinatol, 1995, 12:185-188.
[7]
Marcellus L.The infant with Pierre Robin sequence: Review and implications for nursing practice[J]. J Pediatr Nurs, 2001, 16:23-34.
[8]
Jakobsen LP, Knudsen MA, Lespinasse J, et al. The genetic basis of the Pierre Robin sequence[J].Cleft Palate Craniofac J, 2006, 43:155-159.
[9]
Elluru RG. Treatment options for severe upper airway obstruction in Pierre-Robin sequence[J]. J Pediatr, 2005, 147:7-9.
[10]
Marques IL, de Sousa TV, Carneiro AF, et al. Robin sequence: A single treatment protocol[J]. J Pediatr, 2005, 81:14-22.
[11]
Wilson AC, Moore DJ, Moore MH, et al. Late presentation of upper airway obstruction in Pierre Robin sequence[J]. Arch Dis Child, 2000, 83:435-438.
[12]
Lidsky ME, Lander TA, Sidman JD. Resolving feeding difficulties with early airway intervention in Pierre Robin sequence[J]. Laryngoscope, 2008, 118:120-123.
[13]
Hsieh WS, Yang PH, Wong KS, et al. Vallecular cyst:An uncommon cause of stridor in newborn infants[J]. Eur J Pediatr, 2000, 159:79-81.
[14]
Kuint J, Horowitz Z, Kugel C, et al. Laryngeal obstruction caused by lingual thyroglossal duct cyst presenting at birth[J]. Am J Perinatol, 1997, 14:353-356.
[15]
Diaz MC, Stormorken A, Christopher NC, et al. A thyroglossal duct cyst causing apnea and cyanosis in a neonate[J]. Pediatr Emerg Care, 2005, 21:35-37.
[16]
Fu JH, Xue XD, Fan GG, et al. Early diagnosis of lingual thyroglossal duct cyst in newborns:Analysis of 10 cases previously misdiagnosed as laryngomalacia[J]. Chin J Pediar, 2009, 47(1):23-25.
[17]
Kanawaku Y, Funayama M, Sakai J, et al. Sudden infant death:Lingual thyroglossal duct cyst versus environmental factors[J]. Forensic Sci. Int, 2006, 156:158-160.
[18]
Zoumalan R, Maddalozzo J, Holinger LD. Etiology of stridor in infants[J]. Ann Otol Rhinol Laryngol, 2007, 116:329-334.
[19]
Chandra RK, Gerber ME, Holinger LD. Histological insight into the pathogenesis of severe laryngomalacia[J]. Int J Pediatr Otorhinolaryngol, 2001, 61:31-38.
[20]
Thompson DM. Abnormal sensorimotor integrative function of the larynx in congenital laryngomalacia:A new theory of etiology[J]. Laryngoscope, 2007, 117:1-33.
[21]
OIney DR, Greinwald JH, Jr Smith RJ, et al. Laryngotnalacia and its treatment[J]. Laryngoscope, 1999, 109:1770-1775.
[22]
Daniel SJ. The upper airway:Congenital malformations[J]. Paediatr Respirat Rev, 2006, 7:260-263.
[23]
Bedwell J, Surgical GZ. Treatment of laryngomalacia[J]. Cur Pediatr Rev, 2011, 7:33-41.
No related articles found!
阅读次数
全文


摘要