Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Thalassemia Clinical Research Network"'
Autor:
Walter, Patrick B, Porter, John, Evans, Patricia, Kwiatkowski, Janet L, Neufeld, Ellis J, Coates, Thomas, Giardina, Patricia J, Grady, Robert W, Vichinsky, Elliott, Olivieri, Nancy, Trachtenberg, Felicia, Alberti, Daniele, Fung, Ellen, Ames, Bruce, Higa, Annie, Harmatz, Paul, Thalassemia Clinical Research Network
Publikováno v:
British journal of haematology, vol 160, iss 3
This exploratory study assessed apoptosis in peripheral blood leucocytes (PBL) from β-thalassaemia patients receiving chronic transfusions and chelation therapy (deferasirox or deferoxamine) at baseline, 1, 6, and 12months. At baseline, thalassaemic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::6316c487d91149312a11693929bef950
https://escholarship.org/uc/item/6460j1q8
https://escholarship.org/uc/item/6460j1q8
Autor:
Thalassemia Clinical Research Network, Elliott Vichinsky, Charles Quinn, Brigitta U Mueller, Patricia J Giardina, Melody J. Cunningham, Susan Carson, Thomas D. Coates, Ashutosh Lal, Janet Kwiatkowski, Nancy F Olivieri, Hae-Young Kim, Titi Singer
Publikováno v:
Blood. 112:1880-1880
The α-globin Constant Spring (CS) mutation (α142 STOP → Gln; TAA → CAA) is the most prevalent non-deletional thalassemia in south East Asia and southern China. DNA diagnosis of Hb H Constant Spring (Hb H CS; 2 α-gene deletions and 1 CS mutatio