A case of hereditary hemorrhagic telangiectasia with hepatic encephalopathy due to portal hepatic venous shunt
Author:
Affiliation:
1. Department of Geriatric Medicine, Kyorin Medical University
Publisher
The Japan Geriatrics Society
Subject
Geriatrics and Gerontology
Link
https://www.jstage.jst.go.jp/article/geriatrics/54/2/54_179/_pdf
Reference17 articles.
1. 2) Shovlin CL, Guttmacher AE, Buscarini E, Faughnan ME, Hyland RH, Westermann CJ, et al.: Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). American Journal of Medical Genetics 2000; 91: 66-67.
2. 3) Tuente und genetik der Oslerschen krankheit. Z Menschl Vererb Konstitutionsl 1964; 37: 221-250.
3. 4) Dakeishi M, Shioya T, Wada Y, Shindo T, Otaka K, Manabe M, et al.: Genetic epidemiology of hereditary hemorrhagic telangiectasia in a local community in the northern part of Japan. Human Mutation 2002; 19: 140-148.
4. 6) Cottin V, Dupuis-Girod S, Lesca G, Cordier J: Pulmonary vascular manifestations of hereditary hemorrhagic telangiectasia (rendu-osler disease). Respiration 2007; 74: 361-378.
5. 7) Komiyama M, Terada A, Ishiguro T, Watanabe Y, Nakajima H, Yamada O, et al.: Neuroradiological Manifestations of Hereditary Hemorrhagic Telangiectasia in 139 Japanese Patients. Neurologia medico-chirurgica 2015; 55: 479-486.
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