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Issue DateTitleAuthor(s)
2003a-Thalassemia 2, 3.7 kb deletion and hemoglobin AC heterozygosity in pregnancy: a molecular and hematological analysisCouto, Fábio David; Albuquerque, Arlete Barreto Lins de; Adorno, Elisângela Vitória; Moura Neto, José Pereira de; Abbehusen, Luciana de Freitas; Oliveira, J. L. B. de; Reis, M. G. dos; Gonçalves, M. de Souza
1-Jun-2017Caracterização fenotípica e genotípica (FvW VNTR1, VNTR2 e VNTR3 intron 40) da Doença de Von Willebrand em indivíduos da BahiaAdorno, Elisângela Vitória; Laranjeira, Débora Santana; Moura Neto, José Pereira de; Gonçalves, Marilda de Souza
2005Hemoglobinopathies in newborns from Salvador, Bahia, Northeast BrazilAdorno, Elisângela Vitória; Couto, Fábio David; Moura Neto, José Pereira de; Menezes, Joelma Figueiredo; Rêgo, Marco Antônio Vasconcelos; Reis, Mitermayer Galvão dos; Gonçalves, Marilda Souza
2008Methylenetetrahydrofolate reductase polymorphisms in myeloid leukemia patients from Northeastern BrazilBarbosa, Cynara Gomes; Souza, Claudio Lima; Moura Neto, José Pereira de; Arruda, Maria da Glória Bomfim; Barreto, José Henrique Silva; Reis, Mitermayer Galvão; Goncalves, Marilda Souza
2008Sequence change in the HS2-LCR and Gγ-globin gene promoter region of sickle cell anemia patientsAdorno, Elisângela Vitória; Moura Neto, José Pereira de; Lyra, Isa Menezes; Zanette, Angela Maria Dias; Santos, L. F. O.; Seixas, Magda Oliveira; Reis, M. G.; Goncalves, M. S.
2011The association of infection and clinical severity in sickle cell anaemia patientsMoura Neto, José Pereira de; Lyra, Isa Menezes; Reis, Mitermayer Galvão dos; Goncalvesa, Marilda Souza
2011TNF-alpha and IL-8: Serum levels and gene polymorphisms (ÿ308G>A and ÿ251A>T) are associated with classical biomarkers and medical history in children with sickle cell anemiaLyra, Isa Menezes; Moura Neto, José Pereira de; Reis, Mitermayer Galvão dos; Barbosa, Cynara Gomes; Gonçalves, Marilda de Souza; Cerqueira, Bruno Antonio Veloso; Couto, Fábio David; Cajado, C.; Santos, Wendell Vilas Boas; Dorea, M. J.
2003α-Thalassemia 2, 3.7 kb deletion and hemoglobin AC heterozygosity in pregnancy: a molecular and hematological analysisGonçalves, M. de Souza; Couto, Fábio David; Albuquerque, Arlete Barreto Lins de; Adorno, Elisângela Vitória; Moura Neto, José Pereira de; Abbehusen, Luciana de Freitas; Oliveira, J. L. B. de; Reis, M. G. dos
Showing results 1 to 8 of 8

 

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