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Author Title [ Type(Desc)] Year
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Journal Article
Lemos, C., Mendonça, D., Pereira-Monteiro, J., Barros, J., et al. (2010). BDNF and CGRP interaction: Implications in migraine susceptibility. Cephalalgia, 30(11), 1375 - 1382.
Ferro, A., Castro, M. - J., Lemos, C., Santos, M., et al. (2008). The C677T polymorphism in MTHFR is not associated with migraine in Portugal. Disease Markers, 25(2), 107 - 113.
Mota, A., Silva, P., Neves, D., Lemos, C., et al. (2008). Characterization of rat heart alkaline phosphatase isoenzymes and modulation of activity. Brazilian Journal of Medical and Biological Research, 41(7), 600 - 609.
Rosas, S., Paço, M., Lemos, C., & Pinho, T. (2017). Comparison between the Visual Analog Scale and the Numerical Rating Scale in the perception of esthetics and pain. International Orthodontics, 15(4), 543 - 560.
Rosas, S., Paço, M., Lemos, C., & Pinho, T. (2017). Comparison between the Visual Analog Scale and the Numerical Rating Scale in the perception of esthetics and pain. International Orthodontics, 15(4), 543 - 560.
Lemos, C., Azevedo, I., & Martel, F. (2005). Effect of red wine on the intestinal absorption of thiamine and folate in the rat: Comparison with the effect of ethanol alone. Alcoholism: Clinical and Experimental Research, 29(4), 664 - 671.
Lemos, C., Pereira-Monteiro, J., Mendonça, D., Ramos, E. M., et al. (2010). Evidence of syntaxin 1A involvement in migraine susceptibility: A Portuguese study. Archives of Neurology, 67(4), 422 - 427.
Pinho, T., MacIel, P., Lemos, C., & Sousa, A. (2010). Familial aggregation of maxillary lateral incisor agenesis. Journal of Dental Research, 89(6), 621 - 625.
Santos, D., Coelho, T., Alves-Ferreira, M., Sequeiros, J., et al. (2017). Familial amyloid polyneuropathy in Portugal: New genes modulating age-at-onset. Annals of Clinical and Translational Neurology, 4(2), 98 - 105.
Lemos, C., Castro, M. - J., Barros, J., Sequeiros, J., et al. (2009). Familial clustering of migraine: Further evidence from a portuguese study. Headache, 49(3), 404 - 411.
Castro, M. - J., Stam, A. H., Lemos, C., De Vries, B., et al. (2009). First mutation in the voltage-gated NaV1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy. Cephalalgia, 29(3), 308 - 313.
Beirão, J. M., Malheiro, J., Lemos, C., Matos, E., et al. (2015). Impact of liver transplantation on the natural history of oculopathy in Portuguese patients with transthyretin (V30M) amyloidosis. Amyloid, 22(1), 31 - 35.
Martel, F., Monteiro, R., Lemos, C., & Vieira-Coelho, M. A. (2004). In vitro and in vivo effect of fluoxetine on the permeability of 3H-serotonin across rat intestine. Canadian Journal of Physiology and Pharmacology, 82(11), 940 - 950.
Castro, A., Lemos, C., Falcão, A., Glass, N. L., & Videira, A. (2008). Increased resistance of complex I mutants to phytosphingosine-induced programmed cell death. Journal of Biological Chemistry, 283(28), 19314 - 19321.
Quintas, M., Neto, J. L., Pereira-Monteiro, J., Barros, J., et al. (2013). Interaction between γ-Aminobutyric Acid A Receptor Genes: New Evidence in Migraine Susceptibility. PLoS ONE, 8(9).
Ramos, E. M., Cerqueira, J., Lemos, C., Pinto-Basto, J., et al. (2012). Intergenerational instability in Huntington disease: Extreme repeat changes among 134 transmissions. Movement Disorders, 27(4), 583 - 585.
Paneque, M., Lemos, C., Escalona, K., Prieto, L., et al. (2007). Psychological follow-up of presymptomatic genetic testing for spinocerebellar ataxia type 2 (SCA2) in Cuba. Journal of Genetic Counseling, 16(4), 469 - 479.
Castro, M. - J., Stam, A. H., Lemos, C., Barros, J., et al. (2007). Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine. Journal of Human Genetics, 52(12), 990 - 998.
Lemos, C., Neto, J. L., Pereira-Monteiro, J., Mendonça, D., et al. (2011). A role for endothelin receptor type A in migraine without aura susceptibility? A study in Portuguese patients. European Journal of Neurology, 18(4), 649 - 655.
Paneque, M., Lemos, C., Sousa, A., Velázquez, L., et al. (2009). Role of the disease in the psychological impact of pre-symptomatic testing for SCA2 and FAP ATTRV30M: Experience with the disease, kinship and gender of the transmitting parent. Journal of Genetic Counseling, 18(5), 483 - 493.
Castro, A., Lemos, C., Falcão, A., Fernandes, A. S., et al. (2010). Rotenone enhances the antifungal properties of staurosporine. Eukaryotic Cell, 9(6), 906 - 914.
Videira, A., Kasuga, T., Tian, C., Lemos, C., et al. (2009). Transcriptional analysis of the response of Neurospora crassa to phytosphingosine reveals links to mitochondrial function. Microbiology, 155(9), 3134 - 3141.
Castro, M. - J., Nunes, B., De Vries, B., Lemos, C., et al. (2008). Two novel functional mutations in the Na+, K+ -ATPase α2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes. Clinical Genetics, 73(1), 37 - 43.
Santos, D., Coelho, T., Alves-Ferreira, M., Sequeiros, J., et al. (2016). Variants in RBP4 and AR genes modulate age at onset in familial amyloid polyneuropathy (FAP ATTRV30M). European Journal of Human Genetics, 24(5), 756 - 760.

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