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8 results
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Characterization of RHD locus polymorphism in D negative and D variant donors from Northwestern Argentina.
Transfusion. 2019 Oct;59(10):3236-3242. doi: 10.1111/trf.15504. Epub 2019 Sep 10.
Transfusion. 2019.
PMID: 31503349
Clinical Trial.
Molecular structures identified in serologically D- samples of an admixed population.
Trucco Boggione C, Luján Brajovich ME, Tarragó M, Mattaloni SM, Biondi CS, Muñiz-Díaz E, Nogués N, Cotorruelo CM.
Trucco Boggione C, et al.
Transfusion. 2014 Oct;54(10):2456-62. doi: 10.1111/trf.12691. Epub 2014 May 12.
Transfusion. 2014.
PMID: 24819281
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Weak D antigen expression caused by a novel RHD allele in Argentineans.
Trucco Boggione C, Luján Brajovich ME, Gaspardi AC, Sippert E, Mattaloni SM, Leri M, Biondi C, Castilho L, Cotorruelo CM.
Trucco Boggione C, et al.
Transfusion. 2016 Nov;56(11):2895-2896. doi: 10.1111/trf.13790. Epub 2016 Sep 9.
Transfusion. 2016.
PMID: 27611815
No abstract available.
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Extensive clinical, serologic and molecular studies lead to the first reported Rhmod phenotype in Argentina.
Mufarrege N, Franco N, Trucco Boggione C, Arnoni C, de Paula Vendrame T, Bartoli S, Ensinck A, Principi C, Lujan Brajovich M, Mattaloni S, Riquelme B, Biondi C, Castilho L, Cotorruelo C.
Mufarrege N, et al. Among authors: trucco boggione c.
Transfusion. 2020 Jul;60(7):1373-1377. doi: 10.1111/trf.15792. Epub 2020 May 6.
Transfusion. 2020.
PMID: 32378229
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The novel RHD c.325A>G single nucleotide variation found in Argentineans leads to a partial D phenotype.
Mufarrege N, Trucco Boggione C, Puppo M, Ensinck A, Príncipi C, Brajovich ML, Mattaloni S, Biondi C, Kuperman S, Cotorruelo C.
Mufarrege N, et al. Among authors: trucco boggione c.
Transfusion. 2020 Nov;60(11):E43-E44. doi: 10.1111/trf.16050. Epub 2020 Sep 13.
Transfusion. 2020.
PMID: 32924170
No abstract available.
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Clinical Significance of an Alloantibody against the Kell Blood Group Glycoprotein.
Mattaloni SM, Arnoni C, Céspedes R, Nonaka C, Trucco Boggione C, Luján Brajovich ME, Trejo A, Zani N, Biondi CS, Castilho L, Cotorruelo CM.
Mattaloni SM, et al. Among authors: trucco boggione c.
Transfus Med Hemother. 2017 Jan;44(1):53-57. doi: 10.1159/000448381. Epub 2016 Nov 2.
Transfus Med Hemother. 2017.
PMID: 28275334
Free PMC article.
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A novel SNV on a previously reported hybrid RHCE background is responsible for an Rh haplotype potentially involved in the generation of an Rh null phenotype.
Principi C, Trucco Boggione C, Mestra Campo B, Posner V, Zani N, Luján Brajovich M, Villanueva M, Mattaloni SM, Ensinck A, Biondi C, Cotorruelo C.
Principi C, et al. Among authors: trucco boggione c.
Transfusion. 2022 Nov;62(11):E70-E72. doi: 10.1111/trf.17126. Epub 2022 Oct 17.
Transfusion. 2022.
PMID: 36251003
No abstract available.
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D-- phenotype caused by a novel RHCE null allele.
Principi C, Trucco Boggione C, Ensinck A, Posner V, Luján Brajovich M, Stettler S, Mattaloni S, Biondi C, Cotorruelo C.
Principi C, et al. Among authors: trucco boggione c.
Transfusion. 2024 Feb;64(2):E3-E5. doi: 10.1111/trf.17698. Epub 2024 Jan 5.
Transfusion. 2024.
PMID: 38180234
No abstract available.
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