Výsledky vyhledávání - "C.R.E. Grignoli"

Akademický článek

Thalassemia intermedia as a result of heterozygosis for ß0-thalassemia and aaaanti-3.7/aa genotype in a Brazilian patient

Autor: E.M. Kimura, C.R.E. Grignoli, V.R.P. Pinheiro, F.F. Costa, M.F. Sonati

Publikováno v: Brazilian Journal of Medical and Biological Research, Vol 36, Iss 6, Pp 699-701 (2003)

We report a case in which the interaction of heterozygosis for both the ß0-IVS-II-1 (G->A) mutation and the aaaanti-3.7 allele was the probable cause for the clinical occurrence of thalassemia intermedia. The propositus, a 6-year-old Caucasian Brazi

Externí odkaz: https://doaj.org/article/77c4bc104f894b429fe6e142284a61ed

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Increased risk for acute myeloid leukaemia in individuals with glutathione S -transferase mu 1 (GSTM1) and theta 1 (GSTT1) gene defects

Autor: Carmen Silvia Passos Lima, Fernando Ferreira Costa, Sara T.O. Saad, Valder R. Arruda, Irene Lorand-Metze, Fernando Lopes Alberto, M B Melo, C.R.E. Grignoli

Publikováno v: European Journal of Haematology. 66:383-388

Objectives: Glutathione S-transferases (GST) modulate the effects of exposure to various cytotoxic and genotoxic agents, including those associated with increased risks of the myelodysplastic syndrome (MDS), acute myeloid leukaemia (AML) and aplastic

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4234be710433754dbef6c5b65862f031
https://doi.org/10.1034/j.1600-0609.2001.066006383.x

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Hb rio claro [β34(B16)Va1→Met]: A novel electrophoretically silent variant found in association with Hb hasharon [α47(CE5)Asp→His] and α-thalassemia-2 (-α3.7)

Autor: Sara T.O. Saad, V. R. Arruda, Maria de Fátima Sonati, E. M. Kimura, C.R.E. Grignoli, M.R.S.C. Wenning, F. F. Costa

Publikováno v: Hemoglobin. 23:177-182

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::294f4e57a495fc10dbf49ef36ee36ad0
https://doi.org/10.3109/03630269908996162

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Thalassemia intermedia as a result of heterozygosis for ß0-thalassemia and aaaanti-3.7/aa genotype in a Brazilian patient

Autor: F. F. Costa, Vitória Régia Pereira Pinheiro, E. M. Kimura, Maria de Fátima Sonati, C.R.E. Grignoli

Publikováno v: Brazilian Journal of Medical and Biological Research. 36:699-701

We report a case in which the interaction of heterozygosis for both the 0-IVS-II-1 (G->A) mutation and the alpha alpha alpha anti-3,7 allele was the probable cause for the clinical occurrence of thalassemia intermedia. The propositus, a 6-year-old Ca

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::476a78119daf015f98b3f3d31c085ff2
https://doi.org/10.1590/s0100-879x2003000600003

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Thalassemia intermedia as a result of heterozygosis for ß0-thalassemia and aaaanti-3.7/aa genotype in a Brazilian patient

Autor: E.M. Kimura, C.R.E. Grignoli, V.R.P. Pinheiro, F.F. Costa, M.F. Sonati

Publikováno v: Brazilian Journal of Medical and Biological Research, Volume: 36, Issue: 6, Pages: 699-701, Published: JUN 2003
Brazilian Journal of Medical and Biological Research, Vol 36, Iss 6, Pp 699-701 (2003)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4edecb25784b2940070413c70b44045c
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2003000600003&lng=en&tlng=en

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