Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Dulcinéia M, Albuquerque"'
Autor:
Mirta T. Ito, Sueli M. da Silva Costa, Letícia C. Baptista, Gabriela Q. Carvalho‐Siqueira, Dulcinéia M. Albuquerque, Vinicius M. Rios, Stephanie Ospina‐Prieto, Roberta C. Saez, Karla P. Vieira, Fernando Cendes, Margareth C. Ozelo, Sara Teresinha O. Saad, Fernando F. Costa, Mônica B. Melo
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 9, Iss 3 (2020)
Background The clinical aspects of sickle cell anemia (SCA) are heterogeneous, and different patients may present significantly different clinical evolutions. Almost all organs can be affected, particularly the central nervous system. Transient ische
Externí odkaz:
https://doaj.org/article/fec76e66829e42eeb575a253264ce95b
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:
Elza M. Kimura, Denise M. Oliveira, Susan E. D. C. Jorge, Cristina F. Abreu, Dulcinéia M. Albuquerque, Fernando F. Costa, Maria de Fátima Sonati
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 30, Iss 4, Pp 316-319 (2008)
As anormalidades estruturais da hemoglobina estão entre as doenças genéticas mais comumente encontradas nas populações humanas. O Laboratório de Hemoglobinopatias do Departamento de Patologia Clínica da Faculdade de Ciências Médicas da Unive
Externí odkaz:
https://doaj.org/article/58e7492183284a3e896568fd82a014a8
Autor:
Daniela P Leonardo, Dulcinéia M Albuquerque, Carolina Lanaro, Letícia C Baptista, José G Cecatti, Fernanda G Surita, Mary A Parpinelli, Fernando F Costa, Carla F Franco-Penteado, Kleber Y Fertrin, Maria Laura Costa
Publikováno v:
PLoS ONE, Vol 10, Iss 8, p e0136693 (2015)
Preeclampsia is one of the leading causes of maternal and neonatal morbidity and mortality in the world, but its appearance is still unpredictable and its pathophysiology has not been entirely elucidated. Genetic studies have associated single nucleo
Externí odkaz:
https://doaj.org/article/2c2ce5b846c74c2a90a260123d6c6f76
Autor:
Jéssica V G F, Batista, Gabriela S, Arcanjo, Thais H C, Batista, Marcondes J, Sobreira, Rodrigo M, Santana, Igor F, Domingos, Betânia L, Hatzlhofer, Diego A, Falcão, Diego A, Pereira-Martins, Jéssica M, Oliveira, Amanda S, Araujo, Luana P M, Laranjeira, Fernanda S, Medeiros, Flávia P, Albuquerque, Dulcinéia M, Albuquerque, Magnun N, Santos, Manuela F, Hazin, Ana C, Dos Anjos, Fernando F, Costa, Aderson S, Araujo, Antonio R, Lucena-Araujo, Marcos A, Bezerra
Publikováno v:
Annals of hematology. 100(4)
Hyperbilirubinemia in patients with sickle cell anemia (SCA) as a result of enhanced erythrocyte destruction, lead to cholelithiasis development in a subset of patients. Evidence suggests that hyperbilirubinemia may be related to genetic variations,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ab5c0c999aaa0fc6412b3440e44768ab
https://pubmed.ncbi.nlm.nih.gov/33523291
https://pubmed.ncbi.nlm.nih.gov/33523291
Autor:
Pamella A, Malagrino, Carlos H G, Sponton, Rodrigo D, Esposti, Carla F, Franco-Penteado, Romulo A, Fernandes, Marcos André C, Bezerra, Dulcinéia M, Albuquerque, Cynara M, Rodovalho, Maurício, Bacci, Angelina, Zanesco
Publikováno v:
Arquivos brasileiros de endocrinologia e metabologia. 57(1)
To evaluate the influence of the interaction between endothelial nitric oxide synthase gene (NOS3) polymorphisms at positions -786TC, Glu298Asp and intron 4b/a, and cardiorespiratory fitness on plasma nitrite/nitrate levels, blood pressure, lipid pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c692d4343a4c91f11450f8378132c8ec
https://pubmed.ncbi.nlm.nih.gov/23440097
https://pubmed.ncbi.nlm.nih.gov/23440097
Autor:
Susan E Costa, Jorge, Elza M, Kimura, Denise M, Oliveira, Satie, Ogo, Dulcinéia M, Albuquerque, Fernando F, Costa, Maria de Fátima, Sonati
Publikováno v:
Hemoglobin. 31(2)
Three novel alpha-globin variants were found during a screening program for hemoglobinopathies in blood donors at the UNICAMP Hematology and Hemotherapy Center, Campinas, State of São Paulo, Southeastern Brazil. They were named for the town of origi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f4be37d59a1060dc43b00e5007450816
https://pubmed.ncbi.nlm.nih.gov/17486496
https://pubmed.ncbi.nlm.nih.gov/17486496