[反复鼻出血、呼吸困难以及肺部和肝脏的明显异常表现] - Suppr

Suppr

超能文献

[Recurring nose bleeds, dyspnea and conspicuous findings in the lung and liver].

作者信息

Holzapfel K, von Beckerath N, Rummeny E J, Gaa J

机构信息

Institut für Röntgendiagnostik, Klinikum rechts der Isar der TU München, Ismaninger Strasse 22, 81675 Munich, Germany.

出版信息

Radiologe. 2007 Aug;47(8):716-20. doi: 10.1007/s00117-006-1424-1.

DOI:10.1007/s00117-006-1424-1

PMID:17028839

Abstract

摘要

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本文引用的文献

Hereditary hemorrhagic telangiectases: magnetic resonance imaging features in liver involvement.遗传性出血性毛细血管扩张症：肝脏受累的磁共振成像特征

J Comput Assist Tomogr. 2006 May-Jun;30(3):405-11. doi: 10.1097/00004728-200605000-00010.

Hereditary hemorrhagic telangiectasia: an update on clinical manifestations and diagnostic measures.遗传性出血性毛细血管扩张症：临床表现与诊断方法的最新进展

Wien Klin Wochenschr. 2006 Mar;118(3-4):72-80. doi: 10.1007/s00508-006-0561-x.

High prevalence of hepatic focal nodular hyperplasia in subjects with hereditary hemorrhagic telangiectasia.遗传性出血性毛细血管扩张症患者肝局灶性结节性增生的高患病率。

Ultrasound Med Biol. 2004 Sep;30(9):1089-97. doi: 10.1016/j.ultrasmedbio.2004.08.004.

Hepatic involvement in hereditary hemorrhagic telangiectasia: CT findings.遗传性出血性毛细血管扩张症的肝脏受累：CT表现

Abdom Imaging. 2004 Mar-Apr;29(2):211-20. doi: 10.1007/s00261-003-0101-3.

Hereditary hemorrhagic telangiectasia: multi-detector row helical CT assessment of hepatic involvement.遗传性出血性毛细血管扩张症：多层螺旋CT对肝脏受累情况的评估

Radiology. 2004 Jan;230(1):250-9. doi: 10.1148/radiol.2301021745. Epub 2003 Nov 26.

Genetic epidemiology of hereditary hemorrhagic telangiectasia in a local community in the northern part of Japan.日本北部某当地社区遗传性出血性毛细血管扩张症的遗传流行病学

Hum Mutat. 2002 Feb;19(2):140-8. doi: 10.1002/humu.10026.

Liver disease in patients with hereditary hemorrhagic telangiectasia.遗传性出血性毛细血管扩张症患者的肝脏疾病

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Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome).遗传性出血性毛细血管扩张症（伦杜-奥斯勒-韦伯综合征）的诊断标准。

Am J Med Genet. 2000 Mar 6;91(1):66-7. doi: 10.1002/(sici)1096-8628(20000306)91:1<66::aid-ajmg12>3.0.co;2-p.

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J Intern Med. 1999 Jan;245(1):31-9. doi: 10.1046/j.1365-2796.1999.00398.x.

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