Identification of 13 new mutations in the ACVRL1 gene in a group of 52 unselected Italian patients affected by hereditary haemorrhagic telangiectasia

Những quyển sách tương tự

• Hereditary Hemorrhagic Telangiectasia: Breakpoint Characterization of a Novel Large Deletion in ACVRL1 Suggests the Causing Mechanism
  Bằng: Boeri, Laura, et al.
  Được phát hành: (2013)
• Immunohistochemical analysis of a merkeloma observed in a patient affected by hereditary haemorrhagic telangiectasia
  Bằng: Rossi, Elisa, et al.
  Được phát hành: (2010)
• Hereditary haemorrhagic telangiectasia with extensive liver involvement is not caused by either HHT1 or HHT2.
  Bằng: Piantanida, M, et al.
  Được phát hành: (1996)
• Variceal haemorrhage in hereditary haemorrhagic telangiectasia.
  Bằng: Zentler-Munro, P L, et al.
  Được phát hành: (1989)
• Endoscopic surgical treatment of epistaxis in hereditary haemorrhagic telangiectasia: our experience
  Bằng: Pagella, Fabio, et al.
  Được phát hành: (2021)