Diversity of RH and transfusion support in Brazilian sickle cell disease patients with unexplained Rh antibodies

Autor: Carla Luana Dinardo, Maria do Carmo Valgueiro, Luciana C Schimidt, Ingrid Helena Ribeiro, Connie M. Westhoff, Ester Cerdeira Sabino, Marcia Regina Dezan, Nhlbi Recipient Epidemiology, Shannon Kelly, Shirley Lopes de Castilho, Brian Custer, Liliana Preiss

Publikováno v: Transfusion

Background Genetic diversity in the RH genes among sickle cell disease (SCD) patients is well described but not yet extensively explored in populations of racially diverse origin. Transfusion support is complicated in patients who develop unexpected

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9207a8fddb6f751f02458b82bff3a1c
https://doi.org/10.1111/trf.15479

Diversity of variant alleles encoding Kidd, Duffy, and Kell antigens in individuals with sickle cell disease using whole genome sequencing data from the NHLBI TOPMed Program

Autor: Marsha M. Wheeler, Carla Luana Dinardo, Alexandre C. Pereira, Shannon Kelly, Ester Cerdeira Sabino, Marilyn J. Telen, Jill M. Johnsen, Karla Melo, Brian Custer, Shirley Lopes de Castilho, Luciana Cayres Schmidt, Marcia Regina Dezan, Allison E. Ashley-Koch, Deborah A. Nickerson, Deepti Jain, Theo G M Oliveira

Publikováno v: TransfusionREFERENCES. 61(2)

Background Genetic variants in the SLC14A1, ACKR1, and KEL genes, which encode Kidd, Duffy, and Kell red blood cell antigens, respectively, may result in weakened expression of antigens or a null phenotype. These variants are of particular interest t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a16e2fc22ea7e3487a3927fab714536a
https://pubmed.ncbi.nlm.nih.gov/33231305

Brazilian Guidelines for transcranial doppler in children and adolescents with sickle cell disease

Autor: Maria Stella Figueiredo, Marcos Christiano Lange, Rodolfo D. Cançado, Robert J. Adams, Ana Claudia Mendonça dos Anjos, Marília A. Rugani, Andre Palma da Cunha Matta, Shirley Lopes de Castilho, Patrícia Moura, Joao Ricardo Friedrisch, Orlando Veloso, Viviane Flumignan Zétola, Ana Cristina Silva Pinto, Josefina Aparecida Pellegrini Braga, Ursula Thomé, Célia Maria Silva, Clarisse Lopes de Castro Lobo, Gisele Sampaio Silva, Sandra Fátima Menosi Gualandro, Paulo Ivo Cortez, Ana Claudia Celestino Bezerra Leite

Publikováno v: Revista Brasileira de Hematologia e Hemoterapia, Vol 33, Iss 1, Pp 43-48 (2011)
Revista Brasileira de Hematologia e Hemoterapia
Revista Brasileira de Hematologia e Hemoterapia v.33 n.1 2011
Revista brasileira de hematologia e hemoterapia
Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular (ABHHTC)
instacron:ABHHTC
Repositório Institucional da UNIFESP
Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
Revista Brasileira de Hematologia e Hemoterapia, Volume: 33, Issue: 1, Pages: 43-48, Published: FEB 2011

BACKGROUND: Sickle cell disease is the most common monogenic hereditary disease in Brazil. Although strokes are one of the main causes of morbidity and mortality in these patients, the use of transcranial Doppler to identify children at risk is not u

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::910b0340197eed3f8f1c46dead49a1db
https://doi.org/10.5581/1516-8484.20110014