1MORCOS J J. SPETZLER RF .Classification of AVMs [J ]. J Neurosurg, 1995,83(4):761-762.
2ABDALLA S A, GEISTHOFF U W,BONNEAU D,et al. Visceral manifestations in hereditary haemorrhagic telang- iectasia type 2[J]. J Med Genet,2003,40(7):494-502.
3PEREZ DEL MOLINO A,ZARRABEITIA R,FERNAN- DEZ A.Hereditary hemorrhagic telangiectasia [J]. Med Clin (Barc), 2005,124( 15 ):583-587.
4FAUGHNAN M E, PALDA V A, GARCIA-TSAO G,et al. International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia [J]. J Med Genet, 2011,48 (2) :73 - 87.
5宋勰.肝脏遗传性出血I生毛细血管扩张症的临床基础研究[D].济南:山东大学医学院,2007.
6MO J Q,DIMASHKIEH H H,BOVE K E.GLUT1 endothe- lial reactivity distinguishes hepatic infantile hemangioma from Congenital hepatic vascular malformation with associ- ated capillary proliferation [ J ]. Hum Pathol, 2004,35 (2): 200-209.
7REITZ M, SCHMIDT N O, VUKOVIC Z, et al. How to de- al with incompletely treated AVMs: experience of 67 cases and review of the literature [ J ]. Acta Neurochir Suppl, 2011,112( 1 ):123- 129.
8MEI-ZAHAV M. Osler-Weber-Rendu-a life-threatening disease in adults and children [J]. Harefuah,2003,142 (12):852-876.
