Dig Dis Sci (2011) 56:2166–2178 DOI 10.1007/s10620-011-1585-2 ORIGINAL ARTICLE Natural History and Outcome of Hepatic Vascular Malformations in a Large Cohort of Patients with Hereditary Hemorrhagic
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G. Inama | E. Buscarini | E. Daina | A. Perna | D. Conte | G. Pongiglione | E. Boccardi | G. Leandro | C. Olivieri | C. Danesino | A. Zambelli | M. Grosso | F. Pagella | G. Rossi | P. Blotta | P. Gazzaniga | G. Manfredi | F. De Grazia | G. Brambilla | G. Lupinacci | F. Menozzi | Roberto Bonardi | P. Forner
[1] Liang‐Kung Chen,et al. Hereditary hemorrhagic telangiectasia. , 2020, Zhonghua yi xue za zhi = Chinese medical journal; Free China ed.
[2] J. Saurin,et al. Long‐term outcome of patients with hereditary hemorrhagic telangiectasia and severe hepatic involvement after orthotopic liver transplantation: A single‐center study , 2010, Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society.
[3] M. Daccarett,et al. Hereditary Hemorrhagic Telangiectasia Presenting as High Output Cardiac Failure during Pregnancy , 2009, Cardiology research and practice.
[4] A. Guttmacher,et al. International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia , 2009, Journal of Medical Genetics.
[5] D. Valla,et al. Vascular disorders of the liver , 2009, Hepatology.
[6] C. Shovlin,et al. Hereditary haemorrhagic telangiectasia: a clinical and scientific review , 2009, European Journal of Human Genetics.
[7] J. Saurin,et al. Evaluation of previously nonscreened hereditary hemorrhagic telangiectasia patients shows frequent liver involvement and early cardiac consequences , 2008, Hepatology.
[8] E. Buscarini,et al. Bevacizumab to treat complicated liver vascular malformations in hereditary hemorrhagic telangiectasia: A word of caution , 2008, Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society.
[9] Michael Böhm,et al. Kommentar zu den ESC-Guidelines for the Diagnosis and Treatment of Acute and Chronic Heart Failure 2008 , 2008, European journal of heart failure.
[10] M. Abramowicz,et al. Detection of a significant association between mutations in the ACVRL1 gene and hepatic involvement in German patients with hereditary haemorrhagic telangiectasia , 2008, Clinical genetics.
[11] C. Shovlin,et al. Estimates of maternal risks of pregnancy for women with hereditary haemorrhagic telangiectasia (Osler–Weber–Rendu syndrome): suggested approach for obstetric services , 2008, BJOG : an international journal of obstetrics and gynaecology.
[12] G. Garcia‐Tsao,et al. Hepatic vascular malformations in hereditary hemorrhagic telangiectasia. , 2008, Seminars in liver disease.
[13] C. Shovlin,et al. Embolisation of pulmonary arteriovenous malformations: no consistent effect on pulmonary artery pressure , 2008, European Respiratory Journal.
[14] R. Stefanov,et al. Interobserver agreement in diagnosing liver involvement in hereditary hemorrhagic telangiectasia by Doppler ultrasound. , 2008, Ultrasound in medicine & biology.
[15] F. d’Ovidio,et al. Liver involvement in a large cohort of patients with hereditary hemorrhagic telangiectasia: echo-color-Doppler vs multislice computed tomography study. , 2008, Journal of hepatology.
[16] L. Adams,et al. Bevacizumab reverses need for liver transplantation in hereditary hemorrhagic telangiectasia , 2008, Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society.
[17] A. Sanyal,et al. Prevention and management of gastroesophageal varices and variceal hemorrhage in cirrhosis. , 2007, The American journal of gastroenterology.
[18] A. Sanyal,et al. Prevention and Management of Gastroesophageal Varices and Variceal Hemorrhage in Cirrhosis , 2007, The American Journal of Gastroenterology.
[19] C. Sabbà,et al. Hereditary hemorrhagic telangiectasia: clinical features in ENG and ALK1 mutation carriers , 2007, Journal of thrombosis and haemostasis : JTH.
[20] G. Garcia‐Tsao. Liver involvement in hereditary hemorrhagic telangiectasia (HHT). , 2007, Journal of hepatology.
[21] Robert I. White,et al. Liver involvement in hereditary hemorrhagic telangiectasia: consensus recommendations , 2006, Liver international : official journal of the International Association for the Study of the Liver.
[22] P. Bayrak-Toydemir,et al. A fourth locus for hereditary hemorrhagic telangiectasia maps to chromosome 7 , 2006, American journal of medical genetics. Part A.
[23] P. Bayrak-Toydemir,et al. Genotype–phenotype correlation in hereditary hemorrhagic telangiectasia: Mutations and manifestations * , 2006, American journal of medical genetics. Part A.
[24] R. Hebbel,et al. Blood outgrowth endothelial cells from Hereditary Haemorrhagic Telangiectasia patients reveal abnormalities compatible with vascular lesions. , 2005, Cardiovascular research.
[25] D. Lindhout,et al. Genotype-phenotype relationship in hereditary haemorrhagic telangiectasia , 2005, Journal of Medical Genetics.
[26] E. Buscarini,et al. Liver involvement in hereditary haemorrhagic telangiectasia or Rendu-Osler-Weber disease. , 2005, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.
[27] C. Shovlin,et al. A new locus for hereditary haemorrhagic telangiectasia (HHT3) maps to chromosome 5 , 2005, Journal of Medical Genetics.
[28] C. Sempoux,et al. Extensive ischemic liver necrosis complicating hereditary hemorrhagic telangiectasia: a rare indication for liver transplantation , 2005, Liver international : official journal of the International Association for the Study of the Liver.
[29] A. Hoes,et al. Guidelines for the diagnosis and treatment of chronic heart failure: executive summary (update 2005): The Task Force for the Diagnosis and Treatment of Chronic Heart Failure of the European Society of Cardiology. , 2005, European heart journal.
[30] M. Letarte,et al. Hereditary haemorrhagic telangiectasia: current views on genetics and mechanisms of disease , 2005, Journal of Medical Genetics.
[31] E. Buscarini,et al. Doppler ultrasonographic grading of hepatic vascular malformations in hereditary hemorrhagic telangiectasia -- results of extensive screening. , 2004, Ultraschall in der Medizin.
[32] E. Buscarini,et al. High prevalence of hepatic focal nodular hyperplasia in subjects with hereditary hemorrhagic telangiectasia. , 2004, Ultrasound in medicine & biology.
[33] A. Rustgi,et al. A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4) , 2004, The Lancet.
[34] M. Manns,et al. Sonographic criteria for the diagnosis of hepatic involvement in hereditary hemorrhagic telangiectasia (HHT) , 2003, Hepatology.
[35] D. Conte,et al. Severe liver fibrosis or cirrhosis: accuracy of US for detection--analysis of 300 cases. , 2003, Radiology.
[36] J. Wyatt,et al. The pathology of acute hepatic disintegration in hereditary haemorrhagic telangiectasia , 2003, Histopathology.
[37] T. Shioya,et al. Genetic epidemiology of hereditary hemorrhagic telangiectasia in a local community in the northern part of Japan , 2002, Human mutation.
[38] R. Kassab,et al. A word of caution. , 2000, International journal of cardiology.
[39] D. Jain,et al. Liver disease in patients with hereditary hemorrhagic telangiectasia. , 2000, The New England journal of medicine.
[40] A. Guttmacher,et al. Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). , 2000, American journal of medical genetics.
[41] A. Kjeldsen,et al. Hereditary haemorrhagic telangiectasia: a population‐based study of prevalence and mortality in Danish patients , 1999, Journal of internal medicine.
[42] A. Pinna,et al. Biliary necrosis due to hepatic involvement with hereditary hemorrhagic telangiectasia. , 1998, AJR. American journal of roentgenology.
[43] D. W. Johnson,et al. Mutations in the activin receptor–like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2 , 1996, Nature Genetics.
[44] J. Hughes,et al. Medical complications of pregnancy in hereditary haemorrhagic telangiectasia. , 1995, QJM : monthly journal of the Association of Physicians.
[45] J. Weissenbach,et al. A third locus for hereditary haemorrhagic telangiectasia maps to chromosome 12q. , 1995, Human molecular genetics.
[46] E. Buscarini,et al. Hepatic vascular malformations in hereditary hemorrhagic telangiectasia: imaging findings. , 1994, AJR. American journal of roentgenology.
[47] F. Collins,et al. A disease locus for hereditary haemorrhagic telangiectasia maps to chromosome 9q33–34 , 1994, Nature Genetics.
[48] J. Hughes,et al. A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3 , 1994, Nature Genetics.
[49] E. Heyer,et al. An abnormal concentration of cases of Rendu-Osler disease in the Valserine valley of the French Jura: a genealogical and demographic study. , 1992, Annals of human biology.
[50] J. Honnorat,et al. Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: Data from the French-Italian HHT network , 2007, Genetics in Medicine.
[51] A. Rotondo,et al. Hereditary hemorrhagic telangiectasia: multi-detector row helical CT assessment of hepatic involvement. , 2004, Radiology.
[52] S. Rossi,et al. Hepatic vascular malformations in hereditary hemorrhagic telangiectasia: Doppler sonographic screening in a large family. , 1997, Journal of hepatology.