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Silva, J., Pinto, R., Carvalho, T., Botelho, F., et al. (2009). Intraprostatic Botulinum Toxin Type A injection in patients with benign prostatic enlargement: Duration of the effect of a single treatment. BMC Urology, 9(1).
Silva, J., Pinto, R., Carvalho, T., Botelho, F., et al. (2011). Intraprostatic botulinum toxin type A administration: Evaluation of the effects on sexual function. BJU International, 107(12), 1950 - 1954.
Silva, D. S. P., Reis, M. I. R., Nascimento, D. S., Vale, A. D., et al. (2007). Sea bass (Dicentrarchus labrax) invariant chain and class II major histocompatibility complex: Sequencing and structural analysis using 3D homology modelling. Molecular Immunology, 44(15), 3758 - 3776.
Silles, E., Osorio, H., Maia, R., Günther Sillero, M. A., & Sillero, A. (2005). Micromolar HgCl2 concentrations transitorily duplicate the ATP level in Saccharomyces cerevisiae cells. FEBS Letters, 579(19), 4044 - 4048.
Sillero, N., Reis, M., Vieira, C. P., Vieira, J., & Morales-Hojas, R. (2014). Niche evolution and thermal adaptation in the temperate species Drosophila americana. Journal of Evolutionary Biology.
Siebert, M., Donis, K. C., Socal, M., Rieder, C. R. M., et al. (2012). Glucocerebrosidase gene variants in parkinsonian patients with Machado Joseph/spinocerebellar ataxia 3. Parkinsonism and Related Disorders, 18(2), 185 - 190.
Shinde, A. B., Baboota, R. K., Denis, S., Loizides-Mangold, U., et al. (2018). Mitochondrial disruption in peroxisome deficient cells is hepatocyte selective but is not mediated by common hepatic peroxisomal metabolites. Mitochondrion, 39, 51 - 59.
Sherwin, C. M., & Olsson, I. A. S. (2004). Housing conditions affect self-administration of anxiolytic by laboratory mice. Animal Welfare, 13(1), 33 - 38.
Serrano, I. D., Ramu, V. G., Pinto, A. R. T., Freire, J. M., et al. (2015). Correlation between membrane translocation and analgesic efficacy in kyotorphin derivatives. Biopolymers - Peptide Science Section, 104(1), 1 - 10.
Sereno, D., Monte Alegre, A., Silvestre, R., Vergnes, B., & Ouaissi, A. (2005). In vitro antileishmanial activity of nicotinamide. Antimicrobial Agents and Chemotherapy, 49(2), 808 - 812.
Sereno, D., Cordeiro Da Silva, A., Mathieu-Daude, F., & Ouaissi, A. (2007). Advances and perspectives in Leishmania cell based drug-screening procedures. Parasitology International, 56(1), 3 - 7.
Sereno, D., Vergnes, B., Mathieu-Daude, F., Cordeiro Da Silva, A., & Ouaissi, A. (2006). Looking for putative functions of the Leishmania cytosolic SIR2 deacetylase. Parasitology Research, 100(1), 1 - 9.
Sequeiros, J., Martins, S., & Silveira, I. (2011). Epidemiology and population genetics of degenerative ataxias. Handbook of Clinical Neurology (Vol. 103, pp. 227 - 251).
Sequeiros, J., Paneque, M., Guimarães, B., Rantanen, E., et al. (2012). The wide variation of definitions of genetic testing in international recommendations, guidelines and reports. Journal of Community Genetics, 3(2), 113 - 124.
Sequeiros, J., Ramos, E. M., Cerqueira, J., Costa, M. C., et al. (2010). Large normal and reduced penetrance alleles in Huntington disease: Instability in families and frequency at the laboratory, at the clinic and in the population. Clinical Genetics, 78(4), 381 - 387.
Sequeiros, J., Seneca, S., & Martindale, J. (2010). Consensus and controversies in best practices for molecular genetic testing of spinocerebellar ataxias. European Journal of Human Genetics, 18(11), 1188 - 1195.
Sequeiros, J., Santos, C., & Jardim, L. B. (2009). Response to Tumas et al. Clinical Genetics, 75(2), 208.
Sequeiros, J. (2006). Corino Andrade (1906-2005): a clinical geneticist before its own time. Clinical genetics, 69(2), 194 - 196.
Sequeiros, J., Martindale, J., & Seneca, S. (2010). EMQN Best Practice Guidelines for molecular genetic testing of SCAs. European Journal of Human Genetics, 18(11), 1173 - 1176.
Sequeiros, J., Gibbon, S., & Clarke, A. (2015). Genetics and ethics in Latin America. Journal of Community Genetics, 6(3), 185 - 187.
Seneca, S., Morris, M. A., Patton, S., Elles, R., & Sequeiros, J. (2008). Experience and outcome of 3 years of a European EQA scheme for genetic testing of the spinocerebellar ataxias. European Journal of Human Genetics, 16(8), 913 - 920.
Seixas, D., Galhardo, V., Sá, M. J., Guimarães, J., & Lima, D. (2009). Pain in multiple sclerosis: Characterization of a Portuguese population of 85 patients. Dor na esclerose múltipla: Caracterização de uma população Portuguesa de 85 doentesActa Medica Portuguesa, 22(3), 233 - 240.
Seixas, A. I., Loureiro, J. R., Costa, C., Ordóñez-Ugalde, A., et al. (2017). A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar Ataxia. American Journal of Human Genetics, 101(1), 87 - 103.
Seixas, A. I., Vale, J., Jorge, P., Marques, I., et al. (2011). FXTAS is rare among Portuguese patients with movement disorders: FMR1 premutations may be associated with a wider spectrum of phenotypes. Behavioral and Brain Functions, 7.
Seixas, D., & Lima, D. (2011). Accuracy, reliability, validity and limitations of functional and structural magnetic resonance imaging data. Cortex, 47(10), 1266 - 1269.

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