Successful Pregnancy of a Patient with Cystic Fibrosis Genotype F508del/ F508del and Progressed Pulmonary Destruction on lumacaftor/ivacaftor

Mainz Jochen G.; Michl Ruth Katharina; Beiersdorf Natalie; Lorenz Michael; Schneider Uwe; Groten Tanja; Jaudszus Anke

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Successful Pregnancy of a Patient with Cystic Fibrosis Genotype F508del/ F508del and Progressed Pulmonary Destruction on lumacaftor/ivacaftor

机译：患有囊性纤维化基因型F508DEL / F508DEL的患者的成功怀孕，并在Lumacaftor / Ivacafacer上进行了肺部破坏

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来源
《Klinische Paediatrie》 |2019年第5期|共3页
作者
Mainz Jochen G.; Michl Ruth Katharina; Beiersdorf Natalie; Lorenz Michael; Schneider Uwe; Groten Tanja; Jaudszus Anke;
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作者单位

Univ Jena Cyst Fibrosis Ctr Ped Pneumol Jena Germany;

Univ Jena Cyst Fibrosis Ctr Ped Pneumol Jena Germany;

Univ Jena Cyst Fibrosis Ctr Ped Pneumol Jena Germany;

Univ Jena Cyst Fibrosis Ctr Ped Pneumol Jena Germany;

Univ Jena Obstet Jena Germany;

Univ Jena Obstet Jena Germany;

Univ Jena Cyst Fibrosis Ctr Ped Pneumol Jena Germany;

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原文格式 PDF
正文语种 ger
中图分类儿科学;
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入库时间 2022-08-20 04:17:34

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专利

1. Successful Pregnancy of a Patient with Cystic Fibrosis Genotype F508del/ F508del and Progressed Pulmonary Destruction on lumacaftor/ivacaftor [J] . Mainz Jochen G., Michl Ruth Katharina, Beiersdorf Natalie, Klinische Paediatrie . 2019,第5期

机译：患有囊性纤维化基因型F508DEL / F508DEL的患者的成功怀孕，并在Lumacaftor / Ivacafacer上进行了肺部破坏
2. EFFECTS OF LUMACAFTOR/IVACAFTOR IN CYSTIC FIBROSIS PATIENTS HOMOZYGOUS FOR F508DEL CFTR MUTATION [J] . Melotti P., Tridello G., Pintani E., Pediatric Pulmonology . 2018,第Suppla2期

机译：Lumacafacer / IVAcaftor在囊性纤维化患者纯合的F508del CFTR突变的影响
3. FEASIBILITY OF ULTRASHORT ECHO TIME (UTE) MRI TO EVALUATE THE EFFECT OF LUMACAFTOR/IVACAFTOR THERAPY IN CHILDREN WITH CYSTIC FIBROSIS (CF) HOMOZYGOUS FOR F508DEL [J] . Nagle S., Brody A. S., Woods J., Thorax: The Journal of the British Thoracic Society . 2017,第Suppla3期

机译：超超声回声时间（UTE）MRI评估Lumacafactor / Ivacafactor治疗在囊性纤维化儿童（CF）纯合的F508del纯合作的影响
4. Impact of air pollution on cystic fibrosis pulmonary exacerbations: a case-crossover analysis [C] . Pieter Goeminne, Michal Kicinski, Francois Vermeulen, Annual conference of the International Society of Exposure Science . 2014

机译：空气污染对囊性纤维化肺部加重的影响：病例交叉分析
5. Liposomal antimicrobial agent formulations for the treatment of pulmonary infection in cystic fibrosis patients. [D] . Halwani, Majed Abdulaziz. 2010

机译：脂质体抗微生物剂制剂，用于治疗囊性纤维化患者的肺部感染。
6. Treatment of Cystic Fibrosis Patients Homozygous for F508del with Lumacaftor-Ivacaftor (Orkambi®) Restores Defective CFTR Channel Function in Circulating Mononuclear Cells [O] . Maria Favia, Crescenzio Gallo, Lorenzo Guerra, 2020

机译：用Lumacaftor-Ivacaftor（Orkambi®）治疗F508del纯合的囊性纤维化患者恢复循环单核细胞中CFTR通道功能的缺陷。
7. Functional Respiratory Imaging to Assess the Short-Term Effects of Orkambi (Lumacaftor/Ivacaftor) on Lung Function in Patients with Cystic Fibrosis Homozygous for F508del [O] . E. Lauwers, D. Belmans, B. Mignot, 2020

机译：功能性呼吸成像，评估Orkambi（Lumacafer / Ivacafacter）对F508del纯合型囊性纤维化患者肺功能的短期效应

Successful Pregnancy of a Patient with Cystic Fibrosis Genotype F508del/ F508del and Progressed Pulmonary Destruction on lumacaftor/ivacaftor

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