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Hereditary haemorrhagic telangiectasia

Johnson DW, Berg JN, Baldwin MA et al. Mutations in the activin receptor-like kinase I gene in hereditary haemorrhagic telangiectasia type 2. Nat. Genet. 13, 189-195, 1996. [Pg.393]

TGF-P receptor II Receptor for MIS/AMH ACK 1 (activin-receptor-like kinase) Gastrointestinal cancel PMDS Hereditary haemorrhagic telangiectasia (HHT)... [Pg.109]

Ocran, K., Rldres, S., Henkamp, I., Wermke, W. Sonography findings in hepatic involvement of hereditary haemorrhagic telangiectasia. Ultrasound. Med. 2004 25 191-194... [Pg.841]

Kjeldsen AD, Vase P, Green A (1999) Hereditary haemorrhagic telangiectasia a population-hased study of prevalence and mortality in Danish patients. J Intern Med 245 31-39... [Pg.116]

Pollock BE, Flickinger JC, Lunsford LD et al. (1998) Factors associated with successful arteriovenous malformation radiosurgery. Radiosurgery 42 1239-1247 Porteous ME, Brun J, Proctor SJ (1992) Hereditary haemorrhagic telangiectasia a clinical analysis. J Med Genet 29 527-530... [Pg.118]

See other pages where Hereditary haemorrhagic telangiectasia is mentioned: [Pg.109]    [Pg.359]    [Pg.825]    [Pg.826]    [Pg.841]    [Pg.115]    [Pg.134]    [Pg.109]    [Pg.359]    [Pg.825]    [Pg.826]    [Pg.841]    [Pg.115]    [Pg.134]    [Pg.106]    [Pg.838]   
See also in sourсe #XX -- [ Pg.838 ]



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