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新生儿先天性肾上腺皮质增生症三例 被引量:2

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作者 王爱琼 马丽
出处 《中国新生儿科杂志》 CAS 2008年第1期53-53,共1页 Chinese Journal of Neonatology
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  • 1van der Kamp HJ,Wit JM.Neonatal screening for congenital adrenal hyperplasia[J].Eur J Endocrinol,2004,151(suppl 3):S71-S75.
  • 2Homma K,Hasegawa T,Takeshita E,et al.Elevated urine pregnanetriolone definitively establishes the diagnosis of classical 21-hydroxylase deficiency in term and preterm neonates[J].J Clin Endrocrinol Metab,2004,89(12):6087-6091.
  • 3Lane DE.Polycystic ovary syndrome and its differential diagnosis[J].Obs Gynecol Survey,2006,61(2):125-135.
  • 4van der Kamp HJ,Oudshoorn CG.Cutoff levels of 17-hydroxyprogesterone in neonatal screening for congenital adrenal hyperplasia should be based on gestational age rather than on birth weight[J].J Clin Endocrinol Metab,2005,90(7):3904-3907.
  • 5Speiser PW.Diagnosis and management of congenital adrenal hyperplasia[J].Expert Rev Endocrin Metab,2006,1(1):103-110.
  • 6Pang S,Pollack MS,Marshall RN,et al.Prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency[J].N Engl J Med,1990,322:111-115.
  • 7Joint LWPES/ESPE CAH Working Group.Consensus statement on 21-hydroxylase deficiency from the Lawson Wilkins pediatric endocrine society and the european society for paediatric endocrinology[J].J Clin Endocrinol Metab,20002,87(9):4048-4053.
  • 8New MI,Carison A,Obeid J,et al.Prenatal diagnosis for congenital adrenal hyperplasia in 532 pregnancies[J].J Clin Endrocrinol Metab,2001,86(12):5651-5657.
  • 9Lajic S,Wedell A,Bui TH,et al.Long-term somatic follow-up of prenatally treated children with congenital adrenal hyperplasia[J].J Clin Endocrinol Metab,1998,83 (11):3872-3880.
  • 10Khadilkar VV,Khadilkar AV,Maskati GB.Impact of availability of oral hydrocortisone on growth of children with CAH[J].India J Pediatr,2005,72(4):301-303.

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