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L DiNardo

Showing results (21-30 of 37) with videos related to

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Frontiers in Cellular and Infection Microbiology|July 25, 2022
Different Transcriptomic Response to <i>T. cruzi</i> Infection in hiPSC-Derived Cardiomyocytes From Chagas Disease Patients With and Without Chronic CardiomyopathyTheo G M Oliveira, Gabriela Venturini, Juliana M Alvim, et al.
British Journal of Haematology|September 16, 2024
Genetic variants associated with white blood cell count amongst individuals with sickle cell diseaseMina Cintho Ozahata, Yuelong Guo, Isabel Gomes, et al.
Transfusion|July 19, 2020
FcγR2B B2.4 haplotype predicts increased risk of red blood cell alloimmunization in sickle cell disease patientsAbel Costa Neto, Flávia Santos, Ingrid Ribeiro, et al.
Transfusion|August 14, 2019
Diversity of RH and transfusion support in Brazilian sickle cell disease patients with unexplained Rh antibodiesCarla L Dinardo, Shannon Kelly, Marcia R Dezan, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|April 29, 2022
Impact of HLA-G +3142C>G on the development of antibodies to blood group systems other than the Rh and Kell among sensitized patients with sickle cell diseaseJuliana O Martins, Flavia Pagani, Marcia R Dezan, et al.
Journal of Clinical Laboratory Analysis|June 27, 2018
High frequency of variant RHD genotypes among donors and patients of mixed origin with serologic weak-D phenotypeMarcia Regina Dezan, Valéria B Oliveira, Çarolina Nunes Gomes, et al.
International Journal of Immunogenetics|August 18, 2017
-318C/T polymorphism of the CTLA-4 gene is an independent risk factor for RBC alloimmunization among sickle cell disease patientsV B Oliveira, M R Dezan, F C A Gomes, et al.
Transfusion Medicine (Oxford, England)|September 18, 2020
Accelerated erythrocyte destruction mimicking post-transfusion hyperhaemolysis in the course of uncomplicated vaso-occlusive crisis associated with sickle cell diseaseMarina C A V Conrado, Guilherme S V C Fonseca, Marcia R Dezan, et al.
Human Molecular Genetics|April 3, 2022
Genetic risk factors and COVID-19 severity in Brazil: results from BRACOVID studyAlexandre C Pereira, Taniela M Bes, Mariliza Velho, et al.
Journal of Clinical Laboratory Analysis|June 2, 2017
Defining the clinical relevance of red blood cell autoantibodies by Monocyte Monolayer AssayMarina C A V Conrado, Amanda N D'Avila, Juliana B Vieira, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

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Pageof 4
Frontiers in Cellular and Infection Microbiology|July 25, 2022
Different Transcriptomic Response to <i>T. cruzi</i> Infection in hiPSC-Derived Cardiomyocytes From Chagas Disease Patients With and Without Chronic CardiomyopathyTheo G M Oliveira, Gabriela Venturini, Juliana M Alvim, et al.
British Journal of Haematology|September 16, 2024
Genetic variants associated with white blood cell count amongst individuals with sickle cell diseaseMina Cintho Ozahata, Yuelong Guo, Isabel Gomes, et al.
Transfusion|July 19, 2020
FcγR2B B2.4 haplotype predicts increased risk of red blood cell alloimmunization in sickle cell disease patientsAbel Costa Neto, Flávia Santos, Ingrid Ribeiro, et al.
Transfusion|August 14, 2019
Diversity of RH and transfusion support in Brazilian sickle cell disease patients with unexplained Rh antibodiesCarla L Dinardo, Shannon Kelly, Marcia R Dezan, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|April 29, 2022
Impact of HLA-G +3142C>G on the development of antibodies to blood group systems other than the Rh and Kell among sensitized patients with sickle cell diseaseJuliana O Martins, Flavia Pagani, Marcia R Dezan, et al.
Journal of Clinical Laboratory Analysis|June 27, 2018
High frequency of variant RHD genotypes among donors and patients of mixed origin with serologic weak-D phenotypeMarcia Regina Dezan, Valéria B Oliveira, Çarolina Nunes Gomes, et al.
International Journal of Immunogenetics|August 18, 2017
-318C/T polymorphism of the CTLA-4 gene is an independent risk factor for RBC alloimmunization among sickle cell disease patientsV B Oliveira, M R Dezan, F C A Gomes, et al.
Transfusion Medicine (Oxford, England)|September 18, 2020
Accelerated erythrocyte destruction mimicking post-transfusion hyperhaemolysis in the course of uncomplicated vaso-occlusive crisis associated with sickle cell diseaseMarina C A V Conrado, Guilherme S V C Fonseca, Marcia R Dezan, et al.
Human Molecular Genetics|April 3, 2022
Genetic risk factors and COVID-19 severity in Brazil: results from BRACOVID studyAlexandre C Pereira, Taniela M Bes, Mariliza Velho, et al.
Journal of Clinical Laboratory Analysis|June 2, 2017
Defining the clinical relevance of red blood cell autoantibodies by Monocyte Monolayer AssayMarina C A V Conrado, Amanda N D'Avila, Juliana B Vieira, et al.
Pageof 4