Pereira, M., Valério-Bolas, A., Santos-Mateus, D., Alexandre-Pires, G., et al. (2017). Canine neutrophils activate effector mechanisms in response to Leishmania infantum. Veterinary Parasitology, 248, 10 - 20.

Rodrigues, A., Santos-Mateus, D., Alexandre-Pires, G., Valério-Bolas, A., et al. (2017). Leishmania infantum exerts immunomodulation in canine Kupffer cells reverted by meglumine antimoniate. Comparative Immunology, Microbiology and Infectious Diseases, 55, 42 - 52.

Oliveira, P., Martins, N. M., Santos, M., Pinto, F., et al. (2016). The versatile TolC-like Slr1270 in the cyanobacterium Synechocystis sp. PCC 6803. Environmental Microbiology, 18(2), 486 - 502.

Oliveira, P., Martins, N. M., Santos, M., Couto, N. A. S., et al. (2015). The anabaena sp. PCC 7120 exoproteome: Taking a peek outside the box. Life, 5(1), 130 - 163.

Castro, H., Teixeira, F., Romao, S., Santos, M., et al. (2011). Leishmania mitochondrial peroxiredoxin plays a crucial peroxidase-unrelated role during infection: Insight into its novel chaperone activity. PLoS Pathogens, 7(10).

Temudo, T., Santos, M., Ramos, E., Dias, K., et al. (2011). Rett syndrome with and without detected MECP2 mutations: An attempt to redefine phenotypes. Brain and Development, 33(1), 69 - 76.

Santos, M., Summavielle, T., Teixeira-Castro, A., Silva-Fernandes, A., et al. (2010). Monoamine deficits in the brain of methyl-CpG binding protein 2 null mice suggest the involvement of the cerebral cortex in early stages of Rett syndrome. Neuroscience, 170(2), 453 - 467.

Temudo, T., Rios, M., Prior, C., Carrilho, I., et al. (2009). Evaluation of CSF neurotransmitters and folate in 25 patients with Rett disorder and effects of treatment. Brain and Development, 31(1), 46 - 51.

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.

Oliveira, J., Santos, R., Soares-Silva, I., Jorge, P., et al. (2008). LAMA2 gene analysis in a cohort of 26 congenital muscular dystrophy patients. Clinical Genetics, 74(6), 502 - 512.

Temudo, T., Ramos, E., Dias, K., Barbot, C., et al. (2008). Movement disorders in Rett syndrome: An analysis of 60 patients with detected MECP2 mutation and correlation with mutation type. Movement Disorders, 23(10), 1384 - 1390.

Temudo, T., Oliveira, P., Santos, M., Dias, K., et al. (2007). Stereotypies in Rett syndrome: Analysis of 83 patients with and without detected MECP2 mutations. Neurology, 68(15), 1183 - 1187.

Santos, M., Coelho, P. A., & MacIel, P. (2006). Chromatin remodeling and neuronal function: Exciting links. Genes, Brain and Behavior, 5(SUPPL. 2), 80 - 91.

Santos, M., do Carmo Costa, M., Edite Rio, M., José Sá, M., et al. (2004). Genotypes at the APOE and SCA2 loci do not predict the course of multiple sclerosis in patients of Portuguese origin. Multiple Sclerosis, 10(2), 153 - 157.

Castro, H., Sousa, C., Novais, M., Santos, M., et al. (2004). Two linked genes of Leishmania infantum encode tryparedoxins localised to cytosol and mitochondrion. Molecular and Biochemical Parasitology, 136(2), 137 - 147.