Zobrazeno 1 - 4
of 4
pro vyhledávání: '"J C M, Herrero"'
Autor:
Renan Garcia de Oliveira, Lidiane de Souza Torres, J. C. M. Herrero, E. V. Patussi, Edis Belini-Junior, Eliana Litsuko Tomimatsu Shimauti, Claudia Regina Bonini-Domingos, Danilo Gruenig Humberto da Silva, Jéssika Viviani Okumura
Publikováno v:
Genetics and molecular research : GMR. 15(2)
Hemoglobin (Hb) variants involving alpha-chains are less common in the global population than Hb variants resulting from beta-chain alterations. Generally, alpha-chain Hb variants are caused by point mutations affecting alpha-1 and/or alpha-2 genes o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed780ed02b475f36fa60ff485f218e84
https://pubmed.ncbi.nlm.nih.gov/27421014
https://pubmed.ncbi.nlm.nih.gov/27421014
Autor:
M F, De Barros, J C M, Herrero, A M, Sell, F C, De Melo, M A, Braga, C B, Pelissari, J, Machado, S, De Souza Schiller, L, De Souza Hirle, J E L, Visentainer
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 18(3)
Congenital haemophilia A is a chromosome-linked recessive disorder caused by the deficiency or reduction of factor VIII (FVIII) pro-coagulant activity. During treatment, some patients develop alloantibodies (FVIII inhibitors) that neutralize the acti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::29039a13d1bbeb4fc319b0eb77961e6e
https://pubmed.ncbi.nlm.nih.gov/21726358
https://pubmed.ncbi.nlm.nih.gov/21726358
Autor:
DE BARROS, M. F.1, HERRERO, J. C. M.1, SELL, A. M.2, De MELO, F. C.2, BRAGA, M. A.2, PELISSARI, C. B.3, MACHADO, J.3, De SOUZA SCHILLER, S.4, De SOUZA HIRLE, L.3, VISENTAINER, J. E. L.2
Publikováno v:
Haemophilia. May2012, Vol. 18 Issue 3, pe236-e240. 5p. 3 Charts.
Publikováno v:
Haemophilia. May2012, Vol. 18 Issue 3, p476-481. 6p.