STREAMLINED NEWBORN SCREENING FOR CYSTIC FIBROSIS: CREATING THE NEW FACE OF CYSTIC FIBROSIS

Valletta D. L.

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STREAMLINED NEWBORN SCREENING FOR CYSTIC FIBROSIS: CREATING THE NEW FACE OF CYSTIC FIBROSIS

机译：进行囊性纤维化的流产新生儿筛查：开创囊性纤维化的新局面

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《Pediatric Pulmonology》 |2014年第38期|共1页
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Valletta D. L.;
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正文语种 eng
中图分类儿科学;
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1. STREAMLINED NEWBORN SCREENING FOR CYSTIC FIBROSIS: CREATING THE NEW FACE OF CYSTIC FIBROSIS [J] . Valletta D. L. Pediatric Pulmonology . 2014,第Suppla38期

机译：进行囊性纤维化的流产新生儿筛查：开创囊性纤维化的新局面
2. Cystic fibrosis newborn screening does not delay the identification of cystic fibrosis in children with negative results. [J] . Maclean JE, Solomon M, Corey M, Journal of cystic fibrosis: official journal of the European Cystic Fibrosis Society . 2011,第5期

机译：囊性纤维化新生儿筛查不会延迟对儿童囊性纤维化的鉴定，结果阴性。
3. New York State Cystic Fibrosis Consortium: The First 2.5 Years of Experience With Cystic Fibrosis Newborn Screening in an Ethnically Diverse Population [J] . Alejandro D. Iglesias, Ashley Badgwell, Robert Giusti Pediatrics: Official Publication of the American Academy of Pediatrics . 2007,第2期

机译：纽约州囊性纤维化财团：囊性纤维化新生儿筛查的前2.5年经验在不同种族的人群中
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. Cystic Fibrosis Transmembrane Conductance Regulator Modulator Therapies in Cystic Fibrosis: A Retrospective Evaluation of a Nationwide Specialty Pharmacy Database [D] . Mehta, Zumi . 2020

机译：囊性纤维化跨膜电导调节剂调节剂患者囊性纤维化：全国特色药房数据库的回顾性评估
6. Newborn screening for cystic fibrosis: Role of primary care providers in caring for infants with positive screening results [O] . June C. Carroll, Robin Z. Hayeems, Fiona A. Miller, 2021

机译：囊性纤维化的新生儿筛查：初级保健提供者在患有阳性筛查结果的关心中的作用
7. P019 Late diagnosis of cystic fibrosis as a consequence of normal IRT concentration in Newborn Screening for Cystic Fibrosis - false negative [O] . K. Zybert, U. Borawska-Kowalczyk, M. Dawidziuk, 2020

机译：P019晚期诊断囊性纤维化的正常IRT浓度在新生儿筛查中囊性纤维化 - 假阴性
8. Newborn Screening for Cystic Fibrosis: A Paradigm for Public Health Genetics211 Policy Development. Proceedings of a Workshop. Held in Atlanta, Georgia in 211 January 1997. Morbidity and Mortality Weekly Report, Vol. 46, No. RR-16, December 211 12, 1997 [R] . Cono, J., Qualls, N. L., Khoury, M. J., 1997

机译：新生儿囊性纤维化筛查：公共卫生遗传学的一种范例211政策制定。研讨会的会议记录。 1997年1月21日在佐治亚州亚特兰大市举行。发病率和死亡率周报，第一卷。 46，编号RR-16，1997年12月211日12

STREAMLINED NEWBORN SCREENING FOR CYSTIC FIBROSIS: CREATING THE NEW FACE OF CYSTIC FIBROSIS

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