Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ana Carolina Cabañas-Pedro"'
Autor:
Ana Carolina Cabañas-Pedro, Josefina A. P. Braga, Roberta F Camilo-Araújo, Ana I. M. Silva, Perla Vicari, Maria Figueiredo
Publikováno v:
Haematologica, Vol 98, Iss 1 (2013)
Externí odkaz:
https://doaj.org/article/d5d6d03a019641b4a4985de3b5b0479a
Autor:
Ana Carolina Cabañas-Pedro, Thais Priscila Biassi, Maria Stella Figueiredo, Elvira Maria Guerra-Shinohara, Gisele W. B. Colleoni, Valeria de Freitas Dutra, Grazielle Mecabo, Patricia Moretti
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Identification of biomarkers associated with severity in sickle cell anemia is desirable. Circulating serum microRNAs (miRNA) are targets studied as diagnostic or prognostic markers, but few studies have been conducted in sickle cell anemia. The purp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6794d29fe0d01badb2c85fd56fe46df9
Autor:
Carolinne Thaisa de Oliveira Fernandes, Miranda, Karina Marques, Vermeulen-Serpa, Ana Carolina Cabañas, Pedro, José, Brandão-Neto, Sancha Helena de Lima, Vale, Maria Stella, Figueiredo
Publikováno v:
Journal of Trace Elements in Medicine and Biology. 72:126980
Sickle cell disease (SCD) is an inherited disease caused by hemoglobin S mutated hemoglobin S. It is characterized by chronic hemolysis, intermittent vaso-occlusive crises followed by ischemia-reperfusion, and organ damage. These patients have an inc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c64334962c744cba2658f6fca73e0b6e
https://doi.org/10.1016/j.jtemb.2022.126980
https://doi.org/10.1016/j.jtemb.2022.126980
Publikováno v:
British Journal of Haematology. 191
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2b1dad2ac8dec2c0712adc18845657a
https://doi.org/10.1111/bjh.16952
https://doi.org/10.1111/bjh.16952
Autor:
Sergio Tufik, Suely Roizenblatt, Maria Stella Figueiredo, Altay Alves Lino de Souza, Ana Carolina Cabañas-Pedro
Publikováno v:
British Journal of Haematology. 179:154-157
Summary High frequency of periodic limb movements in sleep (PLMS) has been described among children with sickle cell disease (SCD), but there is little information about PLMS among adults with SCD. We aim to determine the frequency of PLMS among adul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29fee4a618aea75e5541c4f59d490785
https://doi.org/10.1111/bjh.14811
https://doi.org/10.1111/bjh.14811
Autor:
Ana Carolina Cabañas-Pedro, Maria Stella Figueiredo, Olga Maria Silverio Amancio, Roberta Faria Camilo-Araújo, Josefina Aparecida Pellegrini Braga
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia v.36 n.5 2014
Revista brasileira de hematologia e hemoterapia
Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular (ABHHTC)
instacron:ABHHTC
Revista Brasileira de Hematologia e Hemoterapia, Volume: 36, Issue: 5, Pages: 334-339, Published: OCT 2014
Revista Brasileira de Hematologia e Hemoterapia
Revista Brasileira de Hematologia e Hemoterapia, Vol 36, Iss 5, Pp 334-339 (2014)
Revista brasileira de hematologia e hemoterapia
Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular (ABHHTC)
instacron:ABHHTC
Revista Brasileira de Hematologia e Hemoterapia, Volume: 36, Issue: 5, Pages: 334-339, Published: OCT 2014
Revista Brasileira de Hematologia e Hemoterapia
Revista Brasileira de Hematologia e Hemoterapia, Vol 36, Iss 5, Pp 334-339 (2014)
Objectives: To analyze the frequency of βS-globin haplotypes and alpha-thalassemia, and their influence on clinical manifestations and the hematological profile of children with sickle cell anemia. Method: The frequency of βS-globin haplotypes and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbe236624cbc6bc0171d068d93fbbadf
https://doi.org/10.1016/j.bjhh.2014.06.002
https://doi.org/10.1016/j.bjhh.2014.06.002
Autor:
Patricia Moretti, Maria Stella Figueiredo, Elvira Maria Guerra-Shinohara, Thais Priscila Biassi, Grazielle Mecabo, Ana Carolina Cabañas-Pedro, Valeria de Freitas Dutra, Gisele W. B. Colleoni
Publikováno v:
Blood. 132:3647-3647
Background: Sickle cell anemia (SCA) is a complex disease, associated with hemolysis, vaso-occlusion, vascular inflammation and endothelial activation. Significant morbidity and premature mortality are hallmarks of the disease and elevation of tricus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50a78856ccb67ff14fbf5a613e50bddd
https://doi.org/10.1182/blood-2018-99-115315
https://doi.org/10.1182/blood-2018-99-115315
Autor:
Roberta Faria Camilo-Araújo, Olga Maria Silverio Amancio, Maria Stella Figueiredo, Ana Carolina Cabanãs-Pedro, Josefina Aparecida Pellegrini Braga
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 36, Iss 5, Pp 334-339 (2014)
Objectives: To analyze the frequency of βS-globin haplotypes and alpha-thalassemia, and their influence on clinical manifestations and the hematological profile of children with sickle cell anemia. Method: The frequency of βS-globin haplotypes and
Externí odkaz:
https://doaj.org/article/790526d1f2d5456bb446ef0d9239f80d