Bastos EF - Search Results

1

Association of LRRK2 and GBA mutations in a Brazilian family with Parkinson's disease.

Spitz M, Pereira JS, Nicareta DH, Abreu Gde M, Bastos EF, Seixas TL, Pimentel MM. Spitz M, et al. Among authors: bastos ef. Parkinsonism Relat Disord. 2015 Jul;21(7):825-6. doi: 10.1016/j.parkreldis.2015.03.029. Epub 2015 May 2. Parkinsonism Relat Disord. 2015. PMID: 25952961 No abstract available.

2

Myelodysplastic syndrome without ring sideroblasts and with Janus kinase 2 gene mutation: An unusual case report.

Ornellas MH, De França Silva M, Solza C, De Lucena Gonçalves SB, Silva De Almeida L, De Paula Ayres-Silva J, Seixas TL, Bastos EF, Liehr T, Alves G. Ornellas MH, et al. Among authors: bastos ef. Mol Clin Oncol. 2016 Sep;5(3):227-230. doi: 10.3892/mco.2016.947. Epub 2016 Jul 1. Mol Clin Oncol. 2016. PMID: 27588186 Free PMC article.

3

Screening of mutations in the additional sex combs like 1, transcriptional regulator, tumor protein p53, and KRAS proto-oncogene, GTPase/NRAS proto-oncogene, GTPase genes of patients with myelodysplastic syndrome.

Leite C, Delmonico L, Alves G, Gomes RJ, Martino MR, da Silva AR, Moreira ADS, Maioli MC, Scherrer LR, Bastos EF, Irineu R, Ornellas MH. Leite C, et al. Among authors: bastos ef. Biomed Rep. 2017 Oct;7(4):343-348. doi: 10.3892/br.2017.965. Epub 2017 Aug 9. Biomed Rep. 2017. PMID: 28928972 Free PMC article.

4

Complex karyotype including ring chromosome 11 in a patient with acute myeloid leukemia: case report.

Ornellas MHF, Maioli MCP, Lucena SBSG, Bastos EF, Chaves TS, Melo KV, Ribeiro-Carvalho MM, Liehr T, Alves G. Ornellas MHF, et al. Among authors: bastos ef. Sao Paulo Med J. 2018 Jul-Aug;136(4):361-367. doi: 10.1590/1516-3180.2016.0252150217. Epub 2017 Aug 21. Sao Paulo Med J. 2018. PMID: 28832804 Free PMC article.

5

Trisomy 11 as an additional chromosome alteration in a child with acute promyelocytic leukemia with poor prognosis.

Bastos EF, Silva LA, Ramos MC, Pimenta G, Cortez PI, de Lucena SB, Fernandez Tde S. Bastos EF, et al. Case Rep Genet. 2012;2012:659016. doi: 10.1155/2012/659016. Epub 2012 Jul 5. Case Rep Genet. 2012. PMID: 23074691 Free PMC article.

6

A de novo complex chromosomal rearrangement with nine breakpoints characterized by FISH in a boy with mild mental retardation, developmental delay, short stature and microcephaly.

Joyce CA, Cabral de Almeida JC, Santa Rose AA, Correia P, Moraes L, Bastos E, Llerena J Jr. Joyce CA, et al. Clin Genet. 1999 Jul;56(1):86-92. doi: 10.1034/j.1399-0004.1999.560113.x. Clin Genet. 1999. PMID: 10466423

7

Angelman syndrome methylation screening of 15q11-q13 in institutionalized individuals with severe mental retardation.

Aquino NH, Bastos E, Fonseca LC, Llerena JC Jr. Aquino NH, et al. Genet Test. 2002 Summer;6(2):129-31. doi: 10.1089/10906570260199393. Genet Test. 2002. PMID: 12215253

8

Physical and chemical characterization of drill cuttings: A review.

Costa LC, Carvalho CF, Soares ASF, Souza ACP, Bastos EFT, Guimarães ECBT, Santos JC, Carvalho T, Calderari VH, Marinho LS, Marques MRC. Costa LC, et al. Among authors: bastos eft. Mar Pollut Bull. 2023 Sep;194(Pt A):115342. doi: 10.1016/j.marpolbul.2023.115342. Epub 2023 Aug 25. Mar Pollut Bull. 2023. PMID: 37634349 Review.

9

Fluoxetine-induced plasticity in the rodent visual system.

Bastos EF, Marcelino JL, Amaral AR, Serfaty CA. Bastos EF, et al. Brain Res. 1999 Apr 3;824(1):28-35. doi: 10.1016/s0006-8993(99)01184-1. Brain Res. 1999. PMID: 10095039

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