Mendes CS - Search Results

1

Neuroprotection by BDNF against glutamate-induced apoptotic cell death is mediated by ERK and PI3-kinase pathways.

Almeida RD, Manadas BJ, Melo CV, Gomes JR, Mendes CS, Grãos MM, Carvalho RF, Carvalho AP, Duarte CB. Almeida RD, et al. Among authors: mendes cs. Cell Death Differ. 2005 Oct;12(10):1329-43. doi: 10.1038/sj.cdd.4401662. Cell Death Differ. 2005. PMID: 15905876 Free article.

2

Frontotemporal dementia and mitochondrial DNA transitions.

Grazina M, Silva F, Santana I, Santiago B, Mendes C, Simões M, Oliveira M, Cunha L, Oliveira C. Grazina M, et al. Neurobiol Dis. 2004 Mar;15(2):306-11. doi: 10.1016/j.nbd.2003.11.004. Neurobiol Dis. 2004. PMID: 15006700 Free article.

3

Metabolic effects of hypoxia in colorectal cancer by 13C NMR isotopomer analysis.

Abrantes AM, Tavares LC, Pires S, Casalta-Lopes J, Mendes C, Simões M, Grazina MM, Carvalho RA, Botelho MF. Abrantes AM, et al. Biomed Res Int. 2014;2014:759791. doi: 10.1155/2014/759791. Epub 2014 Jul 1. Biomed Res Int. 2014. PMID: 25093181 Free PMC article.

4

Genetic Variation of MT-ND Genes in Frontotemporal Lobar Degeneration: Biochemical Phenotype-Genotype Correlation.

Gaspar R, Santana I, Mendes C, Fernandes AS, Duro D, Simões M, Luís D, Santos MJ, Grazina M. Gaspar R, et al. Neurodegener Dis. 2015;15(2):70-80. doi: 10.1159/000380766. Epub 2015 Apr 3. Neurodegener Dis. 2015. PMID: 25871488

5

Antenatal manifestations of mitochondrial disorders.

Tavares MV, Santos MJ, Domingues AP, Pratas J, Mendes C, Simões M, Moura P, Diogo L, Grazina M. Tavares MV, et al. J Inherit Metab Dis. 2013 Sep;36(5):805-11. doi: 10.1007/s10545-012-9567-x. Epub 2013 Jan 30. J Inherit Metab Dis. 2013. PMID: 23361304

6

Identification of a novel deletion in SURF1 gene: Heterogeneity in Leigh syndrome with COX deficiency.

Ribeiro C, do Carmo Macário M, Viegas AT, Pratas J, Santos MJ, Simões M, Mendes C, Bacalhau M, Garcia P, Diogo L, Grazina M. Ribeiro C, et al. Mitochondrion. 2016 Nov;31:84-88. doi: 10.1016/j.mito.2016.10.004. Epub 2016 Oct 15. Mitochondrion. 2016. PMID: 27756633

7

Disclosing the functional changes of two genetic alterations in a patient with Chronic Progressive External Ophthalmoplegia: Report of the novel mtDNA m.7486G>A variant.

Bacalhau M, Simões M, Rocha MC, Hardy SA, Vincent AE, Durães J, Macário MC, Santos MJ, Rebelo O, Lopes C, Pratas J, Mendes C, Zuzarte M, Rego AC, Girão H, Wong LC, Taylor RW, Grazina M. Bacalhau M, et al. Neuromuscul Disord. 2018 Apr;28(4):350-360. doi: 10.1016/j.nmd.2017.11.006. Epub 2017 Nov 23. Neuromuscul Disord. 2018. PMID: 29398297 Free PMC article.

8

In silico analysis for predicting pathogenicity of five unclassified mitochondrial DNA mutations associated with mitochondrial cytopathies' phenotypes.

Bacalhau M, Pratas J, Simões M, Mendes C, Ribeiro C, Santos MJ, Diogo L, Macário MC, Grazina M. Bacalhau M, et al. Eur J Med Genet. 2017 Mar;60(3):172-177. doi: 10.1016/j.ejmg.2016.12.009. Epub 2016 Dec 24. Eur J Med Genet. 2017. PMID: 28027978

9

Response to "In silico prediction is insufficient to assess pathogenicity of mtDNA variants".

Bacalhau M, Pratas J, Simões M, Mendes C, Ribeiro C, Santos MJ, Diogo L, Macário MC, Grazina M. Bacalhau M, et al. Eur J Med Genet. 2018 Jan;61(1):46-47. doi: 10.1016/j.ejmg.2017.08.008. Epub 2017 Aug 12. Eur J Med Genet. 2018. PMID: 28807868 No abstract available.

10

Validation of control of allergic rhinitis and asthma test for children (CARATKids)--a prospective multicenter study.

Linhares DV, da Fonseca JA, Borrego LM, Matos A, Pereira AM, Sá-Sousa A, Gaspar A, Mendes C, Moreira C, Gomes E, Rebelo FF, Cidrais Rodrigues JC, Onofre JM, Azevedo LF, Alfaro M, Calix MJ, Amaral R, Rodrigues-Alves R, Correia de Sousa J, Morais-Almeida M; CARATKids study group. Linhares DV, et al. Pediatr Allergy Immunol. 2014 Mar;25(2):173-9. doi: 10.1111/pai.12218. Pediatr Allergy Immunol. 2014. PMID: 24628568

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