参考文献
|
-
Berg, JN,Gallione, CJ,Stenzel, TT(1997).The activing receptor-like kinase 1 gene: genomic structure and mutations in hereditary hemorrhagic telangiectasia type 2.Am J Hum Genet,61,60-67.
-
Bosher, LH, Jr,Blake, DA,Byrd, BR(1959).An analysis of the pathologic anatomy of pulmonary arteriovenous aneurysms with particular reference to the applicability of local excision.Surgery,45,91-104.
-
Cottin, V,Chinet, T,Lavolé, A(2007).Groupe d'Etudes et de Recherche sur les Maladies "Orphelines" Pulmonaires (GERM"O"P). Pulmonary arteriovenous malformations in hereditary hemorrhagic telangiectasia: a series of 126 patients.Medicine,86,1-17.
-
Cottin, V,Dupuis-Girod, S,Lesca, G(2007).Pulmonary vascular manifestations of hereditary hemorrhagic telangiectasia (rendu-osler disease).Respiration,74,361-378.
-
de Faria, JL,Czapski, K,Ribierto(1957).Cyanosis in Manson´s schistosomiasis: role of pulmonary schistosomatic arteriovenous fistulas.Am Heart J,54,196-204.
-
Dines, DE,Arms, RA,Bernatz, PE(1974).Pulmonary arteriovenous fistulas.Mayo Clin Proc,49,460-465.
-
Faughnan, ME,Palda, VA,Garcia-Tsao, G(2011).HHT Foundation International - Guidelines Working Group. International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia.J Med Genet,48,73-87.
-
Ference, BA,Shannon, TM,White, RI, Jr,Zawin, M,Burdge, CM(1994).Life-threatening pulmonary hemorrhage with pulmonary arteriovenous malformations and hereditary hemorrhagic telangiectasia.Chest,106,1387-1390.
-
Gomes, MR,Bernatz, PE,Dines, DE(1969).Pulmonary arteriovenous fistulas.Ann Thorac Surg,7,582-593.
-
Gossage, JR(2010).Role of contrast echocardiography in screening for pulmonary arteriovenous malformation in patients with hereditary hemorrhagic telangiectasia.Chest,138,769-771.
-
Gossage, JR,Kanj, G(1998).Pulmonary arteriovenous malformations. A state of the art review.Am J Respir Crit Care Med,158,643-661.
-
Govani, FS,Shovlin, CL(2009).Hereditary haemorrhagic telangiectasia: a clinical and scientific review.Eur J Hum Genet,17,860-871.
-
Haitjema, T,Disch, F,Overtoom, TT(1995).Screening family members of patients with hereditary hemorrhagic telangiectasia.Am J Med,99,519-524.
-
Johnson, DW,Berg, JN,Baldwin, MA(1996).Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2.Nat Genet,13,189-195.
-
Lacombe, P,Lagrange, C,Beauchet, A(2009).Diffuse pulmonary arteriovenous malformations in hereditary hemorrhagic telangiectasia: long-term results of embolization according to the extent of lung involvement.Chest,135,1031-1037.
-
Lange, PA,Stoller, JK(1995).The hepatopulmonary syndrome.Ann Intern Med,122,521-529.
-
Marchuk, DA(1997).The molecular genetics of hereditary hemorrhagic telangiectasia.Chest,111,79S-82S.
-
McAllister, KA,Grogg, KM,Johnson, DW(1994).Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1.Nat Genet,8,345-351.
-
Nakayama, M,Nawa, T,Chonan, T(2012).Prevalence of pulmonary arteriovenous malformations asestimated by low-dose thoracic CT screening.Intern Med,51,1677-1681.
-
Papagiannis, J,Apostolopoulou, S,Sarris, G(2002).Diagnosis and management of pulmonary arteriovenous malformations.Images Paediatr Cardiol,4,33-49.
-
Pierce, JA,Reagan, WP,Kimball, RW(1959).Unusual cases of pulmonary arteriovenous fistulas with a note on thyroid carcinoma as a cause.N Engl J Med,18,901-907.
-
Plauchu, H,de Chadarévian, JP,Bideau, A(1989).Agerelated clinical profile of hereditary hemorrhagic telangiectasia in an epidemiologically recruited population.Am J Med Genet,32,291-297.
-
Pollak, JS,Saluja, S,Thabet, A(2006).Clinical and anatomic outcomes after embolotherapy of pulmonary arteriovenous malformations.J Vasc Interv Radiol,17,35-44.
-
Prager, RL,Laws, KH,Bender, HW, Jr(1983).Arteriovenous fistula of the lung.Ann Thorac Surg,36,231-239.
-
Sluiter-Eringa, H,Orie, NG,Sluiter, HJ(1969).Pulmonary arteriovenous fistula. Diagnosis and prognosis in noncomplainant patients.Am Rev Respir Dis,100,177-188.
-
Taxman, RM,Halloran, MJ,Parker, BM(1973).Multiple pulmonary arteriovenous malformations in association with Fanconi’s syndrome.Chest,64,118-120.
-
Terry, PB,White, RI, Jr,Barth, KH(1983).Pulmonary arteriovenous malformations. Physiologic observations and results of therapeutic balloon embolization.N Engl J Med,308,1197-1200.
-
Vase, P,Holm, M,Arendrup, H.(1985).Pulmonary arteriovenous fistulas in hereditary hemorrhagic telangiectasia.Acta Med Scand,218,105-109.
-
Wong, HH,Chan, RP,Klatt, R(2011).Idiopathic Pulmonary Arteriovenous Malformations: Clinical and Imaging Characteristics.Eur Respir,38,368-375.
-
Woodward, CS,Pyeritz, RE,Chittams, JL(2013).Treated pulmonary arteriovenous malformations: patterns of persistence and associated retreatment success.Radiology,269,919-926.
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