Progress in research on cystic fibrosis.
作者信息
Geddes D
出版信息
Thorax. 1984 Oct;39(10):721-5. doi: 10.1136/thx.39.10.721.
Abstract
摘要
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Thorax. 1984 Oct;39(10):721-5. doi: 10.1136/thx.39.10.721.
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本文引用的文献
1
Increased bioelectric potential difference across respiratory epithelia in cystic fibrosis.囊性纤维化患者呼吸上皮细胞跨膜生物电位差增加。
N Engl J Med. 1981 Dec 17;305(25):1489-95. doi: 10.1056/NEJM198112173052502.
2
Renal function in cystic fibrosis with special reference to the renal sodium handling.囊性纤维化患者的肾功能，特别涉及肾脏对钠的处理。
Acta Paediatr Scand. 1982 Sep;71(5):833-8. doi: 10.1111/j.1651-2227.1982.tb09528.x.
3
Relative ion permeability of normal and cystic fibrosis nasal epithelium.正常和囊性纤维化鼻上皮的相对离子通透性。
J Clin Invest. 1983 May;71(5):1410-7. doi: 10.1172/jci110894.
4
Higher bioelectric potentials due to decreased chloride absorption in the sweat glands of patients with cystic fibrosis.囊性纤维化患者汗腺中氯化物吸收减少导致生物电位升高。
N Engl J Med. 1983 May 19;308(20):1185-9. doi: 10.1056/NEJM198305193082002.
5
Chloride impermeability in cystic fibrosis.囊性纤维化中的氯离子不渗透性
Nature. 1983 Feb 3;301(5899):421-2. doi: 10.1038/301421a0.
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Improved growth and clinical, nutritional, and respiratory changes in response to nutritional therapy in cystic fibrosis.囊性纤维化患者在接受营养治疗后生长改善以及临床、营养和呼吸方面的变化。
J Pediatr. 1980 Sep;97(3):351-7. doi: 10.1016/s0022-3476(80)80180-6.
7
Abnormal ion permeation through cystic fibrosis respiratory epithelium.异常离子透过囊性纤维化呼吸道上皮。
Science. 1983 Sep 9;221(4615):1067-70. doi: 10.1126/science.6308769.
8
Amniotic fluid alkaline phosphatase isoenzymes in early prenatal diagnosis of cystic fibrosis.羊水碱性磷酸酶同工酶在囊性纤维化产前早期诊断中的应用
Lancet. 1983 Oct 22;2(8356):941-3. doi: 10.1016/s0140-6736(83)90454-3.
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Airway transepithelial electric potential in vivo: species and regional differences.体内气道跨上皮电势：物种和区域差异
J Appl Physiol Respir Environ Exerc Physiol. 1980 Jan;48(1):169-76. doi: 10.1152/jappl.1980.48.1.169.
10
Studies on cystic fibrosis using isoelectric focusing. I. An assay for detection of cystic fibrosis homozygotes and heterozygote carriers from serum.
Pediatr Res. 1975 Aug;9(8):635-40. doi: 10.1203/00006450-197508000-00005.
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