Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Carlos M, Cotorruelo"'
Autor:
Carolina Trucco, Boggione, Melina E, Luján Brajovich, Stella M, Mattaloni, René A, Di Mónaco, Silvia E, García Borrás, Claudia S, Biondi, Carlos M, Cotorruelo
Publikováno v:
Blood transfusion = Trasfusione del sangue. 15(1)
Non-invasive foetal RHD genotyping can predict haemolytic disease of the foetus and the newborn in pregnancies with anti-D alloantibodies and also avoid antenatal anti-D prophylaxis in pregnant women carrying an RHD negative foetus. Considering that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cc62541ac318baa2a0d570613e202017
https://pubmed.ncbi.nlm.nih.gov/27136431
https://pubmed.ncbi.nlm.nih.gov/27136431
Autor:
Carolina, Trucco Boggione, Melina E, Luján Brajovich, Marcel, Tarragó, Stella M, Mattaloni, Claudia S, Biondi, Eduardo, Muñiz-Díaz, Núria, Nogués, Carlos M, Cotorruelo
Publikováno v:
Transfusion. 54(10)
The D- phenotype is mainly caused by the complete deletion of the RHD gene in Caucasians. However, a plethora of allelic variants have been described among D- individuals from different ethnic groups.A cohort of 1314 routine serologically D- samples
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::21a9734cad01cbbd1142e85cc0ea3074
https://pubmed.ncbi.nlm.nih.gov/24819281
https://pubmed.ncbi.nlm.nih.gov/24819281
Autor:
Melina E Luján, Brajovich, Carolina Trucco, Boggione, Claudia S, Biondi, Amelia L, Racca, Marcel, Tarragó, Núria, Nogués, Eduardo, Muñiz-Díaz, Carlos M, Cotorruelo
Publikováno v:
Transfusion. 52(2)
The serologic assignment of the RhD status may be hindered in patients with weak D expression. A comprehensive study of RHD alleles occurring in the mixed population of Argentina is necessary to evaluate the most suitable DNA typing strategy.A total
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::06061521ef47f89b49888fc61e2f0f4a
https://pubmed.ncbi.nlm.nih.gov/21883261
https://pubmed.ncbi.nlm.nih.gov/21883261
Publikováno v:
Encyclopedia of Medical Genomics and Proteomics ISBN: 0203997352
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b390b0d898f3bb1ddd2cbcbe62e9538
https://doi.org/10.3109/9780203997352.232
https://doi.org/10.3109/9780203997352.232
Autor:
Claudia S, Biondi, Carlos M, Cotorruelo, Alejandra, Ensinck, Liliana L, Racca, Amelia L, Racca
Publikováno v:
Clinical laboratory. 50(5-6)
The erythrophagocytosis assay is a useful parameter to evaluate the immune erythrocyte destruction occurring in vivo. The aim of this work was to use this assay in: a) the diagnostic and therapeutic assessment of autoimmune haemolytic anaemia (AIHA),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::17939dcbfbee5575c315ce4489e84963
https://pubmed.ncbi.nlm.nih.gov/15209434
https://pubmed.ncbi.nlm.nih.gov/15209434
Publikováno v:
Clinical laboratory. 48(5-6)
The Rh antigens are encoded by the RHD and RHCE genes. In RhD negative individuals the RHD gene is absent or grossly deleted. Routinely, Rh typing is performed by haemagglutination. However, there are some clinical situations in which serological tec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ca7f6d11a116faca379a827f911688a2
https://pubmed.ncbi.nlm.nih.gov/12071577
https://pubmed.ncbi.nlm.nih.gov/12071577