Výsledky vyhledávání - "J. C. M. Herrero"

Hemoglobin (Hb) Val de Marne (Hb Footscray) in Brazil: the first case report

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

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Influence of class I and II HLA alleles on inhibitor development in severe haemophilia A patients from the south of Brazil

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

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