Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Luana Priscilla Laranjeira Prado"'
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:
Betânia Lucena Domingues, Hatzlhofer, Diego Antonio, Pereira-Martins, Igor, de Farias Domingos, Gabriela da Silva, Arcanjo, Isabel, Weinhäuser, Diego Arruda, Falcão, Isabela Cristina Cordeiro, Farias, Jéssica Vitória Gadelha, de Freitas Batista, Luana Priscilla Laranjeira, Prado, Jéssica Maria Florencio, Oliveira, Thais Helena Chaves, Batista, Marcondes José de Vasconcelos Costa, Sobreira, Rodrigo Marcionilo, de Santana, Amanda Bezerra de Sá, Araújo, Manuela Albuquerque, de Melo, Bruna Vasconcelos, de Ancântara, Juan Luiz, Coelho-Silva, Ana Beatriz Lucas, de Moura Rafael, Danízia Menezes, de Lima Silva, Flávia Peixoto, Albuquerque, Magnun Nueldo Nunes, Santos, Ana Cláudia, Dos Anjos, Fernando Ferreira, Costa, Aderson, da Silva Araújo, Antonio Roberto, Lucena-Araújo, Marcos André Cavalcanti, Bezerra
Publikováno v:
Annals of hematology. 100(4)
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:
Luana Priscilla Laranjeira Prado, Marcos André Cavalcanti Bezerra, Isabela Cristina Farias, Igor de Farias Domingos, Taciana Furtado de Mendonça, Maria do Socorro Cavalcanti, PatrÃcia Moura, Luydson Richardson Silva Vasconcelos, Diego Arruda Falcão, Mariana R. B. Mello, Aderson S Araujo, Kleber Yotsumoto Fertrin, A.R.L. Araújo, Fernando Ferreira Costa
Publikováno v:
Blood. 124:4912-4912
Leg ulcers are the most common clinical manifestations of sickle cell anemia (SCA), a monogenic disease with huge clinical diversity among patients. They affect 8% to 10% of SCA patients, reaching a percentage greater than 50% in patients residing in
Autor:
Hatzlhofer, Betânia Lucena Domingues, Pereira-Martins, Diego Antonio, de Farias Domingos, Igor, Arcanjo, Gabriela da Silva, Weinhäuser, Isabel, Falcão, Diego Arruda, Farias, Isabela Cristina Cordeiro, de Freitas Batista, Jéssica Vitória Gadelha, Prado, Luana Priscilla Laranjeira, Oliveira, Jéssica Maria Florencio, Batista, Thais Helena Chaves, Sobreira, Marcondes José de Vasconcelos Costa, de Santana, Rodrigo Marcionilo, Araújo, Amanda Bezerra de Sá, de Melo, Manuela Albuquerque, de Ancântara, Bruna Vasconcelos, Coelho-Silva, Juan Luiz, de Moura Rafael, Ana Beatriz Lucas, de Lima Silva, Danízia Menezes, Albuquerque, Flávia Peixoto
Publikováno v:
Annals of Hematology; Apr2021, Vol. 100 Issue 4, p921-931, 11p