Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Carolina Trucco, Boggione"'
Autor:
Cintia Principi, Carolina Trucco Boggione, Bleidy Mestra Campo, Victoria Posner, Nestor Zani, Melina Luján Brajovich, Mariana Villanueva, Stella Maris Mattaloni, Alejandra Ensinck, Claudia Biondi, Carlos Cotorruelo
Publikováno v:
TransfusionREFERENCES. 62(11)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22808359938b95c29988c19e1f58eec8
https://pubmed.ncbi.nlm.nih.gov/36251003
https://pubmed.ncbi.nlm.nih.gov/36251003
Autor:
Bibiana D. Riquelme, Cintia Principi, Sonia Bartoli, Carine Prisco Arnoni, Noelia Franco, Claudia Biondi, Tatiane Aparecida de Paula Vendrame, Alejandra Ensinck, Lilian Castilho, Carlos Cotorruelo, Stella Maris Mattaloni, Carolina Trucco Boggione, Nicolás Mufarrege, Melina Eliana Luján Brajovich
Publikováno v:
Transfusion. 60:1373-1377
Background A highly reduced expression of Rh antigens in the erythrocyte membrane is the main feature of Rhmod , an extremely rare phenotype. Mutations within RHAG gene, which encodes RhAG glycoprotein and modulates Rh antigen expression and Rh compl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4dca7a6560ba6d5dda7d56c41682c50e
https://doi.org/10.1111/trf.15792
https://doi.org/10.1111/trf.15792
Autor:
Núria Nogués, Carolina Trucco Boggione, Nicolás Mufarrege, Melina Eliana Luján Brajovich, Cecilia González-Santesteban, Carlos Cotorruelo, Eduardo Muñiz-Diaz, Claudia Biondi, Lilian Castilho, Stella Maris Mattaloni, Mónica Leri
Publikováno v:
Transfusion. 59:3236-3242
Background A notable RHD variability has been observed in Central Argentina's current population attributed to the intermixing of different ethnic groups. The Northwestern region of the country is characterized by a markedly Amerindian genetic contri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88dc59c5e49887e6d8158ed989de82a5
https://doi.org/10.1111/trf.15504
https://doi.org/10.1111/trf.15504
Autor:
Cintia Principi, Carlos Cotorruelo, Silvina Kuperman, Alejandra Ensinck, Stella Maris Mattaloni, Carolina Trucco Boggione, Nicolás Mufarrege, Mónica Puppo, Claudia Biondi, Melina Eliana Luján Brajovich
Publikováno v:
TransfusionREFERENCES. 60(11)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27336260c7839f31de4c87e3dc4ea326
https://pubmed.ncbi.nlm.nih.gov/32924170
https://pubmed.ncbi.nlm.nih.gov/32924170
Autor:
Nicolás, Mufarrege, Noelia, Franco, Carolina, Trucco Boggione, Carine, Arnoni, Tatiane, de Paula Vendrame, Sonia, Bartoli, Alejandra, Ensinck, Cintia, Principi, Melina, Lujan Brajovich, Stella, Mattaloni, Bibiana, Riquelme, Claudia, Biondi, Lilian, Castilho, Carlos, Cotorruelo
Publikováno v:
TransfusionREFERENCES. 60(7)
A highly reduced expression of Rh antigens in the erythrocyte membrane is the main feature of RhRh antigens, RhAG and CD47 glycoproteins were studied by serologic methods in the proband, her parents and sister. Osmotic fragility and viscoelastic para
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5868a99e01a7eb2059270675aaf1f46a
https://pubmed.ncbi.nlm.nih.gov/32378229
https://pubmed.ncbi.nlm.nih.gov/32378229
Autor:
Rosario Céspedes, Néstor Zani, Carine Prisco Arnoni, Stella Maris Mattaloni, Claudia Nonaka, Andrea Trejo, Melina Eliana Luján Brajovich, Carolina Trucco Boggione, Lilian Castilho, Claudia Biondi, C. Cotorruelo
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Background: Kell null (K0) individuals can produce anti-Ku, an antibody against many epitopes in the Kell glycoprotein, after transfusion and/or pregnancy. Since sensitized K0 patients are rare, little is known about anti-Ku clinical relevance and in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40fe9e46bb340a561131caab092f3248
https://www.karger.com/Article/FullText/448381
https://www.karger.com/Article/FullText/448381
Autor:
Núria Nogués, Carolina Trucco Boggione, Eduardo Muñiz-Diaz, Marcel Tarragó, Carlos Cotorruelo, Stella Maris Mattaloni, Claudia Biondi, Melina Eliana Luján Brajovich
Publikováno v:
Transfusion. 54:2456-2462
Background 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. Study Design and Methods A cohort
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8b64e1d2cfd7144d0bd8bed0bab330d
https://doi.org/10.1111/trf.12691
https://doi.org/10.1111/trf.12691
Autor:
Carolina, Trucco Boggione, Melina Eliana, Luján Brajovich, Ane Caroline, Gaspardi, Emilia, Sippert, Stella Maris, Mattaloni, Mónica, Leri, Claudia, Biondi, Lilian, Castilho, Carlos Miguel, Cotorruelo
Publikováno v:
Transfusion. 56(11)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3f1059d608b1d9d4cde8d8165e0d94f7
https://pubmed.ncbi.nlm.nih.gov/27611815
https://pubmed.ncbi.nlm.nih.gov/27611815
Autor:
Núria Nogués, Marcel Tarragó, Carolina Trucco Boggione, Amelia Racca, Eduardo Muñiz-Diaz, Claudia Biondi, Carlos Cotorruelo, Melina Eliana Luján Brajovich
Publikováno v:
Transfusion. 52:389-396
BACKGROUND: 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 strat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94dfcbea9e421d142ca93f9eb3070c2a
https://doi.org/10.1111/j.1537-2995.2011.03297.x
https://doi.org/10.1111/j.1537-2995.2011.03297.x
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