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Polimorfismo C677T no gene da MTHFR e hemoglobinas variantes: um estudo em recém-nascidos de Salvador, Bahia, Brasil

Autor: Elisângela Vitória Adorno, F. D. Couto, Marco Antônio Vasconcelos Rêgo, Joelma Figueiredo Menezes, Mitermayer G. Reis, Marilda Souza Goncalves, José Pereira de Moura Neto

Publikováno v: Cadernos de Saúde Pública v.20 n.2 2004
Cadernos de Saúde Pública
Fundação Oswaldo Cruz (FIOCRUZ)
instacron:FIOCRUZ
Cadernos de Saúde Pública, Vol 20, Iss 2, Pp 529-533 (2004)
Cadernos de Saúde Pública, Volume: 20, Issue: 2, Pages: 529-533, Published: APR 2004
Cadernos de Saúde Pública, Vol 20, Iss 2, Pp 529-533

The C677T polymorphism in the methylenetetrahydrofolate reductase gene (MTHFR) is associated with an increase in total homocysteine serum levels (tHcy), described as a risk factor for cardiovascular disease. Eight hundred forty-three neonates from tw

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::caacb783b1e0b777a5332c56243597c9
https://doi.org/10.1590/s0102-311x2004000200021

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α-Thalassemia 2, 3.7 kb deletion and hemoglobin AC heterozygosity in pregnancy: a molecular and hematological analysis

Autor: M.G. dos Reis, M. De Souza Gonçalves, Elisângela Vitória Adorno, A. B. L. De Albuquerque, F. D. Couto, J. P. De Moura Neto, L. De Freitas Abbehusen, J. L. B. De Oliveira

Publikováno v: Clinical & Laboratory Haematology. 25:29-34

alpha-Thalassemia is a synthesis hemoglobinopathy with a worldwide distribution. alpha-thalassemia-23.7kb (alpha-Thal23.7kb) was investigated by PCR and standard hematologic analysis techniques in 106 pregnant women - 53 heterozygous for hemoglobin (

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::46371222d7dbcf8707192455712826ad
https://doi.org/10.1046/j.1365-2257.2003.00487.x

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Folate, vitamin B12 and total homocysteine levels in neonates from Brazil

Autor: F. D. Couto, Marilda Souza Goncalves, Leandro Marcio Moreira, D B Dos Santos, Mitermayer G. Reis

Publikováno v: European journal of clinical nutrition. 61(3)

To determine folates, vitamin B12 and total homocysteine levels among neonates from mothers of low or high socioeconomic status.We carried out a cross-sectional transversal study comprising 143 neonates from two maternity hospitals in the city of Sal

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::671be85008321c2f862e512c47fc85b2
https://pubmed.ncbi.nlm.nih.gov/16988650

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Hemoglobinopathies in newborns from Salvador, Bahia, Northeast Brazil

Autor: F. D. Couto, Elisângela Vitória Adorno, Marilda Souza Goncalves, Marco Antônio Vasconcelos Rêgo, José Pereira de Moura Neto, Joelma Figueiredo Menezes, Mitermayer G. Reis

Publikováno v: Cadernos de Saúde Pública v.21 n.1 2005
Cadernos de Saúde Pública
Fundação Oswaldo Cruz (FIOCRUZ)
instacron:FIOCRUZ
Cadernos de Saúde Pública, Vol 21, Iss 1, Pp 292-298 (2005)
Cadernos de Saúde Pública, Volume: 21, Issue: 1, Pages: 292-298, Published: FEB 2005

Hemoglobinopathies are hereditary disorders of the hemoglobin molecule with a high prevalence worldwide. Brazil has a prevalence of 0.1 to 0.3% of newborns with sickle cell anemia and 20.0 to 25.0% of heterozygous alpha2 thalassemia among African Bra

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20d54ec913a7e19f47fff2fe1d8eee05
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-311X2005000100032

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alpha-Thalassemia 2, 3.7 kb deletion and hemoglobin AC heterozygosity in pregnancy: a molecular and hematological analysis

Autor: F D, Couto, A B L, De Albuquerque, E V, Adorno, J P, De Moura Neto, L, De Freitas Abbehusen, J L B, De Oliveira, M G, Dos Reis, M, De Souza Gonçalves

Publikováno v: Clinical and laboratory haematology. 25(1)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::71ffb030ffcb1d3cff5d3a85c600fc59
https://pubmed.ncbi.nlm.nih.gov/12542439

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TNF-alpha and IL-8: Serum levels and gene polymorphisms (−308G>A and −251A>T) are associated with classical biomarkers and medical history in children with sickle cell anemia

Autor: Cynara Gomes Barbosa, J.P. Moura-Neto, Cyntia Cajado, Marilda Souza Goncalves, Isa Menezes Lyra, Wendell Vilas-Boas, M.J. Dorea, Bruno A. V. Cerqueira, F. D. Couto, Mitermayer G. Reis

Publikováno v: Cytokine. (2):312-317

Sickle cell anemia (SCA) is a disorder characterized by a heterogeneous clinical outcome. In the present study, we investigated the associations between Tumor Necrosis Factor-alpha (TNF-alpha) −308G>A and Interleukin 8 (IL-8) −251A>T gene polymor

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0475eb4148db41a24b0fc2b25929f44

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