Recent advances in cystic fibrosis research.
作者信息
Bowman B H, Barnett D R
出版信息
Birth Defects Orig Artic Ser. 1976;12(6):197-212.
PMID:61772
Abstract
摘要
相似文献
1
Recent advances in cystic fibrosis research.囊性纤维化研究的最新进展。
Birth Defects Orig Artic Ser. 1976;12(6):197-212.
2
Research in cystic fibrosis (second of three parts).
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[Research on cystic fibrosis--1983].
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Sweat chloride concentration in cystic fibrosis patients varies with KM.19 genotype but not with the presence of the common F508 deletion.囊性纤维化患者的汗液氯化物浓度随KM.19基因型而变化，但不随常见的F508缺失的存在而变化。
Am J Med Genet. 1991 May 1;39(2):230-1. doi: 10.1002/ajmg.1320390227.
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The CF-CIRC study: a French collaborative study to assess the accuracy of cystic fibrosis diagnosis in neonatal screening.CF-CIRC研究：一项法国合作研究，旨在评估新生儿筛查中囊性纤维化诊断的准确性。
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Total intra-individual variation in sweat sodium and chloride concentrations for the diagnosis of cystic fibrosis.用于诊断囊性纤维化的汗液钠和氯浓度的个体内总变异
Clin Chim Acta. 2008 Jul 17;393(2):128-9. doi: 10.1016/j.cca.2008.02.022. Epub 2008 Mar 5.
7
Research in cystic fibrosis: a review.
Tex Rep Biol Med. 1973 Winter;31(4):615-29.
8
Diagnosis of cystic fibrosis by sweat testing: age-specific reference intervals.通过汗液测试诊断囊性纤维化：特定年龄的参考区间
J Pediatr. 2008 Dec;153(6):758-63. doi: 10.1016/j.jpeds.2008.04.067. Epub 2008 Jun 27.
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Prognostic value of sweat-chloride levels in cystic fibrosis: a negative report.囊性纤维化中汗液氯化物水平的预后价值：一项否定性报告。
Eur J Respir Dis. 1983 Aug;64(6):434-6.
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CFTR activity and mitochondrial function.囊性纤维化跨膜传导调节因子活性与线粒体功能。
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