新生儿呼吸窘迫综合征ABCA3 基因遗传缺陷的研究

周熙惠, 惠智艳, 李媛, 宋红霞, 张葳, 肖谧, 王芳会… - 中华儿科杂志, 2012 - cqvip.com
目的探讨动脉自旋标记(arterial spin labeling, ASL) MR 灌注技术在新生儿缺氧缺血性脑病(HIE
) 诊断中的应用价值. 方法选用7 例无窒息病史以及无其他神经系统疾病的足月新生儿作为正常 …

Interstitial lung disease in children with Rubinstein‐Taybi syndrome

L Bradford, MK Ross, J Minso… - Pediatric …, 2022 - Wiley Online Library
Abstract Introduction Rubinstein‐Taybi syndrome (RSTS) is a rare genetic syndrome caused
primarily by a mutation in the CREBBP gene found on chromosome 16. Patients with RSTS …

Familial interstitial pneumonia

JL Talbert, DA Schwartz, MP Steele - Clinical pulmonary medicine, 2014 - journals.lww.com
On the basis of the vast amount of evidence presented, there leaves little doubt that familial
interstitial pneumonia (FIP) is a recognized entity. FIP may present clinically similar to …

Development of the pulmonary surfactant system

S Orgeig, CB Daniels, LC Sullivan - The Lung, 2004 - Elsevier
Publisher Summary This chapter focuses on the normal composition, function, and
development of the pulmonary surfactant system, and discusses the effects of genetic and …

新生儿呼吸窘迫综合征高危因素893 例分析

曲雯雯, 范含笑, 谢露, 韩笑, 尹晓娟 - 中国儿童保健杂志, 2013 - cqvip.com
目的探讨新生儿呼吸窘迫综合征(respiratorydistresssyndrome, RDS) 发病的高危因素,
为临床治疗提供参考依据. 方法对2007 年1 月-2012 年10 月在八一儿童医院新生儿监护病房 …

Autoimmune pulmonary alveolar proteinosis successfully treated with lung lavage in an adolescent patient: a case report

AM Alasiri, RA Alasbali, MA Alaqil, AM Alahmari… - Journal of Medical Case …, 2021 - Springer
Background Pulmonary alveolar proteinosis is a rare interstitial lung disease characterized
by accumulating surfactant materials in the alveoli. The autoimmune form is by far the most …

胎鼠肺泡Ⅱ 型上皮细胞的分离及原代培养

付红敏, 许峰, 黄波, 杨鸣, 符跃强, 方芳, 匡凤梧 - 重庆医科大学学报, 2009 - cqvip.com
目的: 探讨胎鼠肺泡Ⅱ 型上皮细胞(Alveolar epithelial cell type Ⅱ, AECⅡ) 的分离,
纯化及原代培养方法, 为有关胎儿肺发育及新生儿肺部疾病的研究奠定基础. 方法 …

Altered surfactant homeostasis and recurrent respiratory failure secondary to TTF-1 nuclear targeting defect

D Peca, S Petrini, C Tzialla, R Boldrini, F Morini… - Respiratory …, 2011 - Springer
Background Mutations of genes affecting surfactant homeostasis, such as SFTPB, SFTPC
and ABCA3, lead to diffuse lung disease in neonates and children. Haploinsufficiency of …

A non-BRICHOS surfactant protein c mutation disrupts epithelial cell function and intercellular signaling

M Woischnik, C Sparr, S Kern, T Thurm, A Hector… - BMC cell biology, 2010 - Springer
Background Heterozygous mutations of SFTPC, the gene encoding surfactant protein C (SP-
C), cause sporadic and familial interstitial lung disease (ILD) in children and adults. The …

[PDF][PDF] 构建原代分离培养与鉴定小鼠肺泡Ⅱ 型上皮细胞的方法及模型

郑金旭, 黄振杰, 汤艳, 丁明 - Journal of Clinical Rehabilitative Tissue …, 2010 - cjter.com
摘要背景: 肺泡Ⅱ 型上皮细胞在肺发育和肺功能调节中起重要作用, 它与肺纤维化和肺癌等疾病
的发生发展有密切联系, 为了对这些疾病进行体外实验研究, 必须对肺泡Ⅱ 型上皮细胞进行分离 …