Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Ana Claudia Mendonça Dos Anjos"'
Autor:
Taciana Furtado de Mendonça Belmont, Kleyton Palmeira do Ó, Andreia Soares da Silva, Kamila de Melo Vilar, Fernanda Silva Medeiros, Luydson Richardson Silva Vasconcelos, Ana Claudia Mendonça Dos Anjos, Betânia Lucena Domingues Hatzlhofer, Maíra Galdino da Rocha Pitta, Marcos André Cavalcanti Bezerra, Aderson da Silva Araújo, Moacyr Jesus Barreto de Melo Rego, Patrícia Moura, Maria do Socorro Mendonça Cavalcanti
Publikováno v:
PLoS ONE, Vol 11, Iss 9, p e0162297 (2016)
INTRODUCTION:Patients with sickle cell anemia (SCA) may present chronic hemolytic anemia, vaso-occlusion and respiratory tract infection (RTI) episodes. Galectin-3 (GAL-3) is a multifunctional protein involved in inflammation, apoptosis, adhesion and
Externí odkaz:
https://doaj.org/article/b76fc6fdf9364d74b98985bbdfab4927
Autor:
Clarisse Lopes de Castro Lobo, Rodolfo Delfini Cançado, Ana Claudia Celestino Bezerra Leite, Ana Claudia Mendonça dos Anjos, Ana Cristina Silva Pinto, Andre Palma da Cunha Matta, Célia Maria Silva, Gisele Sampaio Silva, João Ricardo Friedrisch, Josefina Aparecida Pellegrini Braga, Marcos Christiano Lange, Maria Stella Figueiredo, Marília Álvares Rugani, Orlando Veloso, Patrícia Gomes Moura, Paulo Ivo Cortez, Robert Adams, Sandra Fátima Menosi Gualandro, Shirley Lopes de Castilho, Ursula Thomé, Viviane Flumignan Zetola
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 33, Iss 1, Pp 43-48 (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://doaj.org/article/419146d56716416796ca8cf81fec6e0a
Autor:
Manuela F. Hazin, Thais Helena Chaves Batista, Gabriela da Silva Arcanjo, Aderson S Araujo, Betânia Lucena Domingues Hatzlhofer, Antonio R. Lucena-Araujo, Diego Arruda Falcão, Jéssica Vitória Gadelha de Freitas Batista, Pablo Ramon Gualberto Cardoso, Maira Galdino da Rocha Pitta, Marcos André Cavalcanti Bezerra, Diego A Pereira-Martins, Igor de Farias Domingos, Fernando Ferreira Costa, Ana Claudia Mendonça dos Anjos, Isabel Weinhäuser
Publikováno v:
Annals of Hematology. 100:1921-1927
The clinical and phenotypic heterogeneity of patients with sickle cell anemia (SCA) is influenced by environmental and genetic factors. Several genetic modifiers, such as the KLOTHO (KL) gene, have been associated with SCA clinical outcomes. The KL g
Autor:
Marcondes José de Vasconcelos Costa Sobreira, Aderson S Araujo, Antonio R. Lucena-Araujo, Flávia Peixoto Albuquerque, Isabela Cristina Cordeiro Farias, Danízia Menezes de Lima Silva, Diego A Pereira-Martins, Manuela Albuquerque de Melo, Bruna Vasconcelos de Ancântara, Gabriela da Silva Arcanjo, Diego Arruda Falcão, Ana Claudia Mendonça dos Anjos, A. S. Araújo, Magnun N. N. Santos, Rodrigo Marcionilo Santana, Thais Helena Chaves Batista, Isabel Weinhäuser, Jéssica Vitória Gadelha de Freitas Batista, Betânia Lucena Domingues Hatzlhofer, Ana Beatriz Lucas de Moura Rafael, Luana Priscilla Laranjeira Prado, Igor de Farias Domingos, Fernando Ferreira Costa, Marcos André Cavalcanti Bezerra, Juan L Coelho-Silva, Jéssica Maria Florencio Oliveira
Publikováno v:
Annals of Hematology. 100:921-931
Alpha thalassemia and beta-globin haplotype are considered classical genetic disease modifiers in sickle cell anemia (SCA) causing clinical heterogeneity. Nevertheless, their functional impact on SCA disease emergence and progression remains elusive.
Autor:
Gabriela da Silva Arcanjo, Antonio R. Lucena-Araujo, Marcondes José de Vasconcelos Costa Sobreira, Jéssica Vitória Gadelha de Freitas Batista, Aderson S Araujo, Igor de Farias Domingos, A. S. Araújo, Magnun N. N. Santos, Thais Helena Chaves Batista, Jéssica Maricelly Deodato de Oliveira, Marcos André Cavalcanti Bezerra, Fernanda Silva Medeiros, Diego A Pereira-Martins, Diego Arruda Falcão, Flávia Peixoto Albuquerque, Ana Claudia Mendonça dos Anjos, Manuela F. Hazin, Dulcineia M. Albuquerque, Luana Priscilla Morais Laranjeira, Betânia Lucena Domingues Hatzlhofer, Fernando Ferreira Costa, Rodrigo Marcionilo Santana
Publikováno v:
Annals of Hematology. 100:903-911
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,
Autor:
Betânia Lucena Domingues Hatzlhofer, Taciana Furtado Mendonça-Belmont, Antonio R. Lucena-Araujo, Igor de Farias Domingos, João Victor Cordeiro Farias, Marcos André Cavalcanti Bezerra, Maria do Socorro de Mendonça Cavalcanti, Isabela Cristina Cordeiro Farias, Luydson Richardson Silva Vasconcelos, Patrícia Muniz Mendes Freire de Moura, Diego Arruda Falcão, Aderson S Araujo, Gabriela da Silva Arcanjo, Kleyton Palmeira do Ó, Andreia Soares da Silva, Ana Claudia Mendonça dos Anjos
Publikováno v:
Research, Society and Development, Vol 9, Iss 7, Pp e439974240-e439974240 (2020)
Research, Society and Development; Vol. 9 No. 7; e439974240
Research, Society and Development; Vol. 9 Núm. 7; e439974240
Research, Society and Development; v. 9 n. 7; e439974240
Research, Society and Development
Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
Research, Society and Development; Vol. 9 No. 7; e439974240
Research, Society and Development; Vol. 9 Núm. 7; e439974240
Research, Society and Development; v. 9 n. 7; e439974240
Research, Society and Development
Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
Objective: This study has as objective to verify whether MBL2 gene polymorphisms are related to the occurrence of cerebrovascular disease (CD) in sickle cell anemia (SCA) patients. Methods: Overall, 259 unrelated SCA patients were enrolled. The patie
Autor:
Taciana Furtado de Mendonça, Stephan Menzel, Fernando Ferreira Costa, John N. Brewin, Anderson F. Cunha, Betania Lucena Domingues Hatzlhofer, Rayssa L. Borges-Medeiros, Antonio R. Lucena-Araujo, Evandra Strazza Rodrigues, Simone Kashima, Pedro Rodrigues Souza Cruz, Aderson S Araujo, Igor de Farias Domingos, Diego Arruda Falcão, Kate Gardner, Ana Claudia Mendonça dos Anjos, Maria do Socorro de Mendonça Cavalcanti, Diego A Pereira-Martins, Mônica Barbosa de Melo, Marcos André Cavalcanti Bezerra
Publikováno v:
Journal of the neurological sciences. 414
Overt stroke in adults with sickle cell anemia (SCA) continues to be a major cause of morbidity and mortality, while no evidence-based strategy for prevention has been reached so far. Although transcranial Doppler ultrasonography represents the most
Autor:
Luydson Richardson Silva Vasconcelos, Fernanda Silva Medeiros, Marcos André Cavalcanti Bezerra, Aderson S Araujo, Maria do Carmo Valgueiro Costa de Oliveira, Patrícia Moura, Betânia Lucena Domingues Hatzlhofer, Taciana Furtado de Mendonça, Katiuscia Araújo de Miranda Lopes, Laís Medeiros da Câmara França, Andreia Soares da Silva, Ana Claudia Mendonça dos Anjos, Maria do Socorro de Mendonça Cavalcanti
Publikováno v:
Genetics and Molecular Biology v.40 n.3 2017
Genetics and Molecular Biology
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology, Volume: 40, Issue: 3, Pages: 600-603, Published: 21 AUG 2017
Genetics and Molecular Biology, Vol 40, Iss 3, Pp 600-603 (2017)
Genetics and Molecular Biology
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology, Volume: 40, Issue: 3, Pages: 600-603, Published: 21 AUG 2017
Genetics and Molecular Biology, Vol 40, Iss 3, Pp 600-603 (2017)
Sickle cell anemia (SCA) presents heterogenous clinical manifestations that cannot be explained solely by alterations to hemoglobin (Hb); other components such as endothelial adhesion, thrombosis and inflammation may be involved. The mannose-binding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85e9182c13d908ad354c8f0ccc963db5
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572017000400600
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572017000400600
Autor:
Diego A Pereira-Martins, Juan L Coelho-Silva, Antonio R. Lucena-Araujo, Maria do Socorro de Mendonça Cavalcanti, Aderson S Araujo, Renata C. Azevedo, Marcos André Cavalcanti Bezerra, Fernando Ferreira Costa, Diego Arruda Falcão, Ana Claudia Mendonça dos Anjos, Igor de Farias Domingos, Taciana Furtado de Mendonça, Rayssa L. Borges-Medeiros
Publikováno v:
British journal of haematology. 182(2)
Autor:
Kleyton Palmeira do Ó, Taciana Furtado Mendonça-Belmont, Isabela Cristina Cordeiro Farias, Patrícia Muniz Mendes Freire de Moura, Fernanda Silva Medeiros, Maria do Socorro de Mendonça Cavalcanti, Ana Claudia Mendonça dos Anjos, Betânia Lucena Domingues Hatzlhofer, Aderson S Araujo, Luydson Richardson Silva Vasconcelos, Felipe A. B. S. Ferreira, Marcos André Cavalcanti Bezerra, Andreia Soares da Silva
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 10, Iss 1, Pp e2018012-e2018012 (2018)
The SOD2 polymorphism Val16Ala TàC influences the antioxidative response. This study investigated the association of the SOD2 polymorphism and superoxide dismutase (SOD) activity with vaso-occlusive crisis (VOC) and acute splenic sequestration (ASS)