遗传性出血性毛细血管扩张症

有症状的遗传性出血性毛细血管扩张症患儿的临床和遗传学特征：来自儿科中心的经验

Symptomatic children with hereditary hemorrhagic telangiectasia : A pediatric center experience

目的：探讨遗传性出血性毛细血管扩张症所引起鼻出血的治疗方法。

Objective : To study the treatment of nosebleed caused by hereditary hemorrhagic telangiectasia ( HHT ) .

PVA微球栓塞肝脏遗传性出血性毛细血管扩张症1例

PVA microspheres embolization : a case of hepatic involvement in hereditary hemorrhagic telangiectasia

ALK-1基因无义突变Arg479Stop导致的遗传性出血性毛细血管扩张症

Hereditary hemorrhagic telangiectasia resulted from a nonsense mutation Arg 479 Stop in the ALK-1 gene

通过超声多普勒发现了3例遗传性出血性毛细血管扩张症（OslerWeberRendu综合征）患者的肝脏血管受累。

Three cases of Osler - Weber - Rendu disease or hereditary haemorrhagic telangiectasia with hepatic involvement diagnosed by Doppler ultrasound were described , showing an increased blood flow within the dilated common hepatic artery and multiple aneurysms of the intraparenchymal branches of the proper hepatic artery .

彩超诊断累及肝脏的遗传性出血性毛细血管扩张症

Color Doppler ultrasound in diagnosis of hereditary hemorrhagic telangiectasia with hepatic involvement

Ⅱ型遗传性出血性毛细血管扩张症血管生长发育相关蛋白质分析及意义

Analysis of angiogenesis related proteins and its implication in type-2 hereditary hemorrhagic telangiectasia

中西医结合治疗遗传性出血性毛细血管扩张症致鼻出血疗效观察

The Treatment of Nosebleed Caused by Hereditary Hemorrhagic Telangiectasia

超声在遗传性出血性毛细血管扩张症肝受累中的应用价值

Ultrasonographic Application in Diagnosing Hereditary Hemorrhagic Telangiectasia Involving Liver

目的定位一个中国汉族遗传性出血性毛细血管扩张症家系的致病基因。

Objective To localize the pathogenic gene of hereditary hemorrhagic telangiectasia ( HHT ) in a Chinese family of Han Nationality .