Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Claudia Cantarini"'
Publikováno v:
Pediatric Reports, Vol 15, Iss 1, Pp 129-142 (2023)
Hereditary Hemorrhagic Telangiectasia (HHT) or Rendu–Osler–Weber Syndrome (ROW) is an autosomal dominant vascular disease, with an estimated prevalence of 1:5000. Genes associated with HHT are ACVRL1, ENG, SMAD4, and GDF2, all encoding for protei
Externí odkaz:
https://doaj.org/article/a1c28f9b63144cd3a9ce844a7ba9544b
Autor:
Silvia Grignaschi, Anna Sbalchiero, Giuseppe Spinozzi, Bianca Lucia Palermo, Claudia Cantarini, Chantal Nardiello, Lorenzo Cavagna, Carla Olivieri
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
BackgroundSystemic Sclerosis (SSc) is a rare autoimmune disease whose pathogenesis is still poorly understood. The Transforming Growth Factor β superfamily is considered pivotal and a crucial role has been suggested for the type III receptor, Endogl
Externí odkaz:
https://doaj.org/article/ad2c6a68f6604cb0a210cbc3fd67a722