Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Letícia C Baptista"'
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:
Mônica Barbosa de Melo, Letícia C. Baptista, Fernando Ferreira Costa, Fernanda Garanhani Surita, Maria Laura Costa, Bruno Batista de Souza, Cristiane S. Rocha, Iscia Lopes-Cendes
Publikováno v:
Blood cells, moleculesdiseases. 84
Sickle cell disease (SCD) is a group of disorders whose common characteristic is the presence of hemoglobin (Hb) S in erythrocytes. The main consequence of this abnormality is vaso-occlusion, which can affect almost all organs including the placenta.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd950cacfa9a4a6ad5f610759098c0c8
https://pubmed.ncbi.nlm.nih.gov/32562953
https://pubmed.ncbi.nlm.nih.gov/32562953
Autor:
Sara T.O. Saad, Fernando Ferreira Costa, Fernando Cendes, Mirta Tomie Ito, Margareth C. Ozelo, Roberta Casagrande Saez, Letícia C. Baptista, Mônica Barbosa de Melo, Stephanie Ospina-Prieto, Sueli Matilde da Silva Costa, Vinicius Mandolesi Rios, Dulcineia M. Albuquerque, Gabriela Queila de Carvalho-Siqueira, Karla Priscila Vieira
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
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 isc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef6bca44792c12fc707fcd36a8eca4e7
https://doi.org/10.1161/jaha.119.014143
https://doi.org/10.1161/jaha.119.014143
Autor:
Galina Ananina, Maria Helena Costa, Letícia C. Baptista, Mônica Barbosa de Melo, Sueli Matilde da Silva Costa, G.I.S.L.E.N.E. Gil, Mariana Maschietto, Fernando Pestana da Costa
Publikováno v:
Placenta. 83:e82-e83
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b567d1ad6efa2eb716084ad17247b81a
https://doi.org/10.1016/j.placenta.2019.06.263
https://doi.org/10.1016/j.placenta.2019.06.263
Autor:
Mônica Barbosa de Melo, Maria Laura Costa, Kleber Yotsumoto Fertrin, Fernanda Garanhani Surita, Regiane Ferreira, Mary Angela Parpinelli, Letícia C. Baptista, Fernando Ferreira Costa, Dulcineia M. Albuquerque, Carolina Lanaro
Publikováno v:
Annals of hematology. 95(11)
Sickle cell disease (SCD) is a complex disease that is characterized by the polymerization of deoxyhemoglobin S, altered red blood cell membrane biology, endothelial activation, hemolysis, a procoagulant state, acute and chronic inflammation, and vas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7792269d93301bc4ccbf094703c0e9f6
https://pubmed.ncbi.nlm.nih.gov/27546026
https://pubmed.ncbi.nlm.nih.gov/27546026
Autor:
Letícia C. Baptista, Daniela Pinheiro Leonardo, José Guilherme Cecatti, Carolina Lanaro, Carla F. Franco-Penteado, Kleber Yotsumoto Fertrin, Fernanda Garanhani Surita, Maria Laura Costa, Mary Angela Parpinelli, Dulcineia M. Albuquerque, Fernando Ferreira Costa
Publikováno v:
PLoS ONE
PLoS ONE, Vol 10, Iss 8, p e0136693 (2015)
PLoS ONE, Vol 10, Iss 8, p e0136693 (2015)
Background 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 si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::967556af50c549685c4e1e0d9c4ca01f
http://europepmc.org/articles/PMC4552660
http://europepmc.org/articles/PMC4552660
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