Author:
Delaney H M,Rooks V J,Wolfe S Q,Sawyer T L
Publisher
Springer Science and Business Media LLC
Subject
Obstetrics and Gynaecology,Pediatrics, Perinatology, and Child Health
Reference10 articles.
1. Giordano P, Nigro A, Lenato GM, Guanti G, Suppressa P, Lastella P et al. Screening for children from families with Rendu-Osler-Weber disease: from geneticist to clinician. J Thromb Haemost 2006; 4: 1237–1245.
2. Morgan T, McDonald J, Anderson C, Ismail M, Miller F, Mao R et al. Intracranial hemorrhage in infants and children with hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome). Pediatrics 2002; 109: E12.
3. Bourdeau A, Cymerman U, Paquet M-E, Meschino W, McKinnon WC, Guttmacher AE et al. Endoglin expression is reduced in normal vessels but is still detectable in arteriovenous malformations of patients with hereditary hemorrhagic telangiectasia type I. Am J Pathol 2000; 156: 911–923.
4. Kuo Y-H, Santoreneos S, Roos D, Brophy BP . Treatment of multiple arteriovenous malformations in pediatric patients with hereditary hemorrhagic telangiectasia and spontaneous hemorrhage. Report of two cases. J Neurosurg 2007; 107: 489–494.
5. Maher CO, Piepgras DG, Brough Jr RD, Friedman JA, Pollock BE . Cerebrovascular manifestations in 321 cases of hereditary hemorrhage telangiectasia. Stroke 2001; 32: 877–882.
Cited by
13 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献