Cholestasis and meconium ileus in infants with cystic fibrosis and their clinical outcomes

Leeuwen Lisette; Magoffin Annabel K.; Fitzgerald Dominic A.; Cipolli Marco; Gaskin Kevin J.

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Cholestasis and meconium ileus in infants with cystic fibrosis and their clinical outcomes

机译：囊性纤维化婴儿的胆汁淤积和胎粪肠梗阻及其临床结果

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Objective To identify the incidence and outcomes of cholestasis and meconium ileus (MI) in infants with cystic fibrosis (CF).

机译：目的确定胆囊性纤维化（CF）婴儿胆汁淤积和胎粪肠梗阻（MI）的发生率和结局。

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《Archives of disease in childhood》 |2014年第5期|共5页
作者
Leeuwen Lisette; Magoffin Annabel K.; Fitzgerald Dominic A.; Cipolli Marco; Gaskin Kevin J.;
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正文语种 eng
中图分类儿科学;
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1. Cholestasis and meconium ileus in infants with cystic fibrosis and their clinical outcomes [J] . Leeuwen Lisette, Magoffin Annabel K., Fitzgerald Dominic A., Archives of disease in childhood . 2014,第5期

机译：囊性纤维化婴儿的胆汁淤积和胎粪肠梗阻及其临床结果
2. Risk factors for adverse outcome in infancy in meconium ileus cystic fibrosis infants: A multicentre Italian study [J] . Padoan Rita, Cirilli Natalia, Falchetti Diego, Journal of cystic fibrosis: official journal of the European Cystic Fibrosis Society . 2019,第6期

机译：术中初期患者患者缺乏症的危险因素：多期式意大利研究
3. Differences in clinical outcomes of paediatric cystic fibrosis patients with and without meconium ileus [J] . Tan Su Min Joyce, Coffey Michael J., Ooi Chee Y. Journal of cystic fibrosis: official journal of the European Cystic Fibrosis Society . 2019,第6期

机译：没有Meconium Ileus的小儿囊性纤维化患者临床结果的差异
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. Nutritional status and growth in infants with cystic fibrosis at diagnosis and at age two years and six years. [D] . Rich, Marianne. 2005

机译：诊断时以及两岁和六岁时患有囊性纤维化婴儿的营养状况和生长。
6. Cystic fibrosis patients bearing both the common missense mutation Gly→Asp at codon 551 and the ΔF508 mutation are clinically indistinguishable from ΔF508 homozygotes except for decreased risk of meconium ileus [O] . Ada Hamosh, Terri M. King, Beryl J. Rosenstein, 1992

机译：囊性纤维化患者同时患有常见的错义突变第551位密码子的Gly→Asp和ΔF508突变除了降低了胎粪肠梗阻的风险外在临床上与ΔF508纯合子没有区别。
7. THE CLINICAL AND GENETIC CHARACTERISTICS AND OUTCOMES OF MECONIUM ILEUS IN CYSTIC FIBROSIS [O] . E. I. Kondratyeva, V. D. Sherman, E. L. Amelina, 2016

机译：膀胱纤维化术中迁徙术的临床和遗传特征及成果

Cholestasis and meconium ileus in infants with cystic fibrosis and their clinical outcomes

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