• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Progressive pulmonary hypertension in children with portal hypertension.

作者信息

Levine O R, Harris R C, Blanc W A, Mellins R B

出版信息

J Pediatr. 1973 Dec;83(6):964-72. doi: 10.1016/s0022-3476(73)80530-x.

DOI:10.1016/s0022-3476(73)80530-x
PMID:4757535
Abstract
摘要

相似文献

1
Progressive pulmonary hypertension in children with portal hypertension.
J Pediatr. 1973 Dec;83(6):964-72. doi: 10.1016/s0022-3476(73)80530-x.
2
Patterns of cardiovascular dysfunction in chronic obstructive lung disease.
N Engl J Med. 1972 Apr 27;286(17):912-8. doi: 10.1056/NEJM197204272861703.
3
Clinical recognition of cor pulmonale in cystic fibrosis.囊性纤维化中肺心病的临床识别
J Pediatr. 1971 May;78(5):794-805. doi: 10.1016/s0022-3476(71)80350-5.
4
Cor pulmonale as a result of chronic nasopharyngeal obstruction due to hypertrophied tonsils and adenoids.因扁桃体和腺样体肥大导致慢性鼻咽部阻塞而引起的肺心病。
Arch Dis Child. 1969 Oct;44(237):585-92. doi: 10.1136/adc.44.237.585.
5
Editorial: Progressive pulmonary hypertension in children with portal hypertension.社论:门静脉高压症患儿的进行性肺动脉高压
J Pediatr. 1974 May;84(5):783-5. doi: 10.1016/s0022-3476(74)80044-2.
6
Pulmonary dysfunction and hepatopulmonary syndrome in cirrhosis and portal hypertension.肝硬化和门静脉高压症中的肺功能障碍和肝肺综合征。
Liver Int. 2009 Nov;29(10):1528-37. doi: 10.1111/j.1478-3231.2009.02103.x. Epub 2009 Sep 2.
7
Distinctive clinical features of portopulmonary hypertension.门肺高压的独特临床特征。
Chest. 1997 Oct;112(4):980-6. doi: 10.1378/chest.112.4.980.
8
Hyperdynamic states and the physiologic determinants of survival in patients with cirrhosis and portal hypertension.
Arch Surg. 1974 Mar;108(3):282-92. doi: 10.1001/archsurg.1974.01350270016004.
9
Blood gas changes and pulmonary hemodynamics in portal hypertension due to schistosomiasis mansoni.
Rev Inst Med Trop Sao Paulo. 1977 Mar-Apr;19(2):80-93.
10
Chronic cor pulmonale due to loss of altitude acclimatization (chronic mountain sickness).
Am J Med. 1971 Jun;50(6):728-43. doi: 10.1016/0002-9343(71)90181-1.

引用本文的文献

1
A consensus approach to the classification of pediatric pulmonary hypertensive vascular disease: Report from the PVRI Pediatric Taskforce, Panama 2011.小儿肺动脉高压性血管疾病分类的共识方法:PVRI儿科特别工作组报告,巴拿马,2011年
Pulm Circ. 2011;1(2):286-298. doi: 10.4103/2045-8932.83456.
2
Medical and surgical management of portal hypertension in children.儿童门静脉高压症的内科及外科治疗
Curr Treat Options Gastroenterol. 2006 Sep;9(5):432-43. doi: 10.1007/BF02738533.
3
Pulmonary hypertension in glycogen storage disease type I.
J Inherit Metab Dis. 1996;19(2):213-6. doi: 10.1007/BF01799432.
4
Pulmonary vascular disease in a child with atrial septal defect of the secundum type and type I glycogen storage disease.
Pediatr Cardiol. 1996 Jul-Aug;17(4):265-7. doi: 10.1007/BF02524807.
5
Plexogenic pulmonary arteriopathy and liver cirrhosis.多灶性肺血管病与肝硬化
Thorax. 1980 Feb;35(2):133-6. doi: 10.1136/thx.35.2.133.
6
The biochemical properties of the pulmonary circulation.肺循环的生化特性。
Lung. 1981;159(5):231-42. doi: 10.1007/BF02713921.
7
The Eck fistula in animals and humans.动物和人类的艾克瘘管。
Curr Probl Surg. 1983 Nov;20(11):687-752. doi: 10.1016/s0011-3840(83)80010-0.
8
Polymorphic debrisoquine and mephenytoin hydroxylation in patients with pulmonary hypertension of vascular origin after aminorex fumarate.富马酸氨基苯唑后血管性肺动脉高压患者中多态性异喹胍和美芬妥因的羟基化作用
Eur J Clin Pharmacol. 1986;31(4):437-42. doi: 10.1007/BF00613521.
9
Pulmonary hypertension in type I glycogen storage disease.I型糖原贮积病中的肺动脉高压。
Pediatr Cardiol. 1990 Jan;11(1):54-6. doi: 10.1007/BF02239550.
10
Type I glycogen storage disease with vasoconstrictive pulmonary hypertension.
J Inherit Metab Dis. 1990;13(1):102-7. doi: 10.1007/BF01799337.