CYSTIC FIBROSIS MUTATION AND PRIMARY CILIARY DYSKINESIA PATHOLOGY PRESENTING AS RECURRENT SINOPULMONARY INFECTIONS AND AZOOSPERMIA

Feldman E.; Parikh P.

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CYSTIC FIBROSIS MUTATION AND PRIMARY CILIARY DYSKINESIA PATHOLOGY PRESENTING AS RECURRENT SINOPULMONARY INFECTIONS AND AZOOSPERMIA

机译：囊性纤维化突变和原发性睫状运动障碍病理表现为反复发生的肺肺部感染和无精子症。

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《Annals of allergy, asthma, and immunology》 |2016年第1期|共1页
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Feldman E.; Parikh P.;
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正文语种 eng
中图分类医学免疫学;
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1. CYSTIC FIBROSIS MUTATION AND PRIMARY CILIARY DYSKINESIA PATHOLOGY PRESENTING AS RECURRENT SINOPULMONARY INFECTIONS AND AZOOSPERMIA [J] . Feldman E., Parikh P. Annals of allergy, asthma, and immunology . 2016,第5Suppla1期

机译：囊性纤维化突变和原发性睫状运动障碍病理表现为反复发生的肺肺部感染和无精子症。
2. Cystic fibrosis, primary ciliary dyskinesia and non-cystic fibrosis bronchiectasis: Update 2008-11 [J] . FlightW.G., JonesA.M. Thorax: The Journal of the British Thoracic Society . 2012,第7期

机译：囊性纤维化，原发性睫状运动障碍和非囊性纤维化支气管扩张：更新2008-11
3. The clinical effect and the effect on the ciliary motility of oral N-acetylcysteine in patients with cystic fibrosis and primary ciliary dyskinesia [J] . C Koch, E Morkassel, G Stafanger, The European respiratory journal : . 1988,第2期

机译：N-乙酰半胱氨酸对囊性纤维化合并原发性睫状运动障碍的临床疗效及对口腔睫状运动的影响
4. Cystic fibrosis transmembrane conductance regulator gene mutations cause 'black' pigment gallstone formation: new insights from mouse models and implications for therapeutic interventions in cystic fibrosis [C] . A. L. BRODERICK, H. WITTENBURG, M. A. LYONS, Falk Symposium . 2004

机译：囊性纤维化跨膜电导调节剂基因突变引起'黑色'颜料胆结石形成：来自小鼠模型的新见解，以及对囊性纤维化治疗干预的影响
5. Effects of Deletion Mutations in Agua on Fitness and Survival of Pseudomonas aeruginosa Cystic Fibrosis Isolates [D] . McCurtain, Jennifer Lynn 2018

机译：阿瓜缺失突变对铜绿假单胞菌囊性纤维化分离株适应性和存活的影响
6. Primary ciliary dyskinesia caused by a large homozygous deletion including exons 1–4 of DRC1 in Japanese patients with recurrent sinopulmonary infection [O] . Naoto Keicho, Minako Hijikata, Kozo Morimoto, 2020

机译：日本复发性肺肺感染患者大纯合子缺失（包括DRC1的外显子1-4）引起的原发性睫状运动障碍
7. Primary ciliary dyskinesia caused by a large homozygous deletion including exons 1–4 of DRC1 in Japanese patients with recurrent sinopulmonary infection [O] . Naoto Keicho, Minako Hijikata, Kozo Morimoto, 2019

机译：主要睫状体缺乏症引起的大型纯合缺失，包括日本患者的DRC1的外显子1-4患者复发性中断尿液感染

CYSTIC FIBROSIS MUTATION AND PRIMARY CILIARY DYSKINESIA PATHOLOGY PRESENTING AS RECURRENT SINOPULMONARY INFECTIONS AND AZOOSPERMIA

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