Zobrazeno 1 - 10
of 26
pro vyhledávání: '"María de Fatima Sonati"'
Autor:
Ana María Soler, Bruna Facanali Piellusch, Lorena da Silveira, Gisele Audrei Pedroso, Pablo López, Enrique Savio, María de Fatima Sonati, Julio da Luz
Publikováno v:
Genetics and Molecular Biology, Vol 44, Iss 2 (2021)
Abstract Alpha thalassemia is the most common genetic disorder across the world, being the α-3.7 deletion the most frequent mutation. In order to analyze the spectrum and origin of alpha thalassemia mutations in Uruguay, we obtained a sample of 168
Externí odkaz:
https://doaj.org/article/38f2148b21d04941b808924cbc89c8f7
Autor:
Adekunle Emmanuel Alagbe, Gisele Audrei Pedroso, Beatriz Benedetti de Oliveira, Edivilson da Costa, Gisélia Aparecida Freire Maia, Bruna Facanali Piellusch, Susan Elisabeth Domingues Costa Jorge, Fernando Ferreira Costa, José Luiz Proença Modena, Angelica Zaninelli Schreiber, Maria de Fátima Sonati, Magnun Nueldo Nunes Santos
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss 1, Pp 14-21 (2024)
Introduction: The hemogram and hemogram-derivative ratios (HDRs) are becoming markers of the severity and mortality of COVID-19. We evaluated the hemograms and serial weekly HDRs [neutrophil-lymphocyte ratio (NLR), monocyte-lymphocyte ratio (MLR), pl
Externí odkaz:
https://doaj.org/article/5ae5a371a1b94ac59205079d3c6eada3
Autor:
Okeke Chinedu, Wouitchékpo Vincent Tonassé, Dulcinéia Martins Albuquerque, Igor de Farias Domingos, Aderson da Silva Araújo, Marcos André Cavalcanti Bezerra, Maria de Fátima Sonati, Magnun Nueldo Nunes dos Santos
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss 2, Pp 165-170 (2021)
Introduction: Mutations affecting genes involved in oxidative and signaling pathways may be associated with kidney disease in sickle cell anemia. We determined the allele and genotype frequencies of some polymorphisms in the promoter regions of the H
Externí odkaz:
https://doaj.org/article/874eebcef95940afb6c1fe7c4b2627a6
Autor:
Natália O. Mota, Elza M. Kimura, Roberta D. Ferreira, Gisele A. Pedroso, Dulcinéia M. Albuquerque, Daniela M. Ribeiro, Magnun N. N. Santos, Cristina M. Bittar, Fernando F. Costa, Maria de Fatima Sonati
Publikováno v:
Genetics and Molecular Biology, Vol 40, Iss 4, Pp 768-773 (2017)
Abstract Alpha-thalassemias are among the most common genetic diseases in the world. They are characterized by hypochromic and microcytic anemia and great clinical variability, ranging from a practically asymptomatic phenotype to severe anemia, which
Externí odkaz:
https://doaj.org/article/ab8203e372444ae2907faa5cc288cb62
Autor:
Thales Allyrio Araújo de Medeiros Fernandes, Tereza Maria Dantas de Medeiros, Jayra Juliana Paiva Alves, Christiane Medeiros Bezerra, José Veríssimo Fernandes, Édvis Santos Soares Serafim, Maria Zélia Fernandes, Maria de Fatima Sonati
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 37, Iss 3, Pp 172-177 (2015)
Objective: To characterize the socioeconomic and demographic aspects of sickle cell disease patients from the state of Rio Grande do Norte (RN), Northeast Brazil, and their adherence to the recommended treatment. Methods: This cross-sectional descrip
Externí odkaz:
https://doaj.org/article/6e9599c801b4444f9e5a087586970982
Autor:
Elza Miyuki Kimura, Denise Madureira Oliveira, Susan Elisabeth Jorge, Daniela Maria Ribeiro, Tânia Regina Zaccariotto, Magnun Nueldo Nunes Santos, Vanessa Almeida, Dulcinéia Martins Albuquerque, Fernando Ferreira Costa, Maria de Fátima Sonati
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 37, Iss 2, Pp 103-108 (2015)
Background: Brazil has a multiethnic population with a high diversity of hemoglobinopathies. While screenings for beta-globin mutations are far more common, alterations affecting alpha-globin genes are usually more silent and less well known. The aim
Externí odkaz:
https://doaj.org/article/26ced1cda486421d92d57652b39af210
Autor:
Julio Da Luz, Amalia Ávila, Sandra Icasuriaga, María Gongóra, Luis Castillo, Alejandra Serrón, Elza Miyuki Kimura, Fernando Ferreira Costa, Mónica Sans, Maria de Fátima Sonati
Publikováno v:
Genetics and Molecular Biology, Vol 36, Iss 3, Pp 316-322 (2013)
Hemoglobinopathies are the most common recessive diseases worldwide but their prevalence in Uruguay has not been investigated. In this study, 397 unrelated outpatient children from the Pereira Rosell Hospital Center (CHPR), as well as 31 selected pat
Externí odkaz:
https://doaj.org/article/601988c346994b18aa9b7f8d325b665c
Autor:
Gustavo Henrique de Medeiros Alcoforado, Christiane Medeiros Bezerra, Telma Maria Araújo Moura Lemos, Denise Madureira de Oliveira, Elza Miyuki Kimura, Fernando Ferreira Costa, Maria de Fátima Sonati, Tereza Maria Dantas de Medeiros
Publikováno v:
Genetics and Molecular Biology, Vol 35, Iss 3, Pp 594-598 (2012)
α-Thalassemia, arising from a defect in a-globin chain synthesis, is often caused by deletions involving one or both of the a-genes on the same allele. With the aim of investigating the prevalence of α-thalassemia 3.7 kb deletion in the adult popul
Externí odkaz:
https://doaj.org/article/ac24540af3e64bb687063e99225e6b8e
Autor:
Gustavo Henrique de Medeiros Alcoforado, Christiane Medeiros Bezerra, Telma Maria Araújo Moura Lemos, Denise Madureira de Oliveira, Elza Miyuki Kimura, Fernando Ferreira Costa, Maria de Fátima Sonati, Tereza Maria Dantas de Medeiros
Publikováno v:
Genetics and Molecular Biology, Vol 35, Iss 3, Pp 594-598 (2012)
α-Thalassemia, arising from a defect in a-globin chain synthesis, is often caused by deletions involving one or both of the a-genes on the same allele. With the aim of investigating the prevalence of α-thalassemia 3.7 kb deletion in the adult popul
Externí odkaz:
https://doaj.org/article/3acd163b117e49afb22ed238df4bfd4c
Autor:
Cynthia Hatsue Kitayama Cabral, Édvis Santos Soares Serafim, Waleska Rayane Dantas Bezerra de Medeiros, Thales Allyrio Araújo de Medeiros Fernandes, Elza Miyuki Kimura, Fernando Ferreira Costa, Maria de Fátima Sonati, Ivanise Marina Moretti Rebecchi, Tereza Maria Dantas de Medeiros
Publikováno v:
Genetics and Molecular Biology, Vol 34, Iss 3, Pp 421-424 (2011)
βS haplotypes were studied in 47 non-related patients with sickle-cell anemia from the state of Rio Grande do Norte, Brazil. Molecular analysis was conducted by PCR/RFLP using restriction endonucleases XmnI, HindIII, HincII and HinfI to analyze six
Externí odkaz:
https://doaj.org/article/d604977a95d0433eb890902e2f6df7d6