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2007
Karageorgos, L., Brooks, D. A., Pollard, A., Melville, E. L., et al. (2007). Mutational analysis of 105 mucopolysaccharidosis type VI patients. Human Mutation, 28(9), 897 - 903.
Mesquita, A. R., Pêgo, J. M., Summavielle, T., MacIel, P., et al. (2007). Neurodevelopment milestone abnormalities in rats exposed to stress in early life. Neuroscience, 147(4), 1022 - 1033.
Pinto, M., Lima, D., & Tavares, I. (2007). Neuronal activation at the spinal cord and medullary pain control centers after joint stimulation: A c-fos study in acute and chronic articular inflammation. Neuroscience, 147(4), 1076 - 1089.
Stevanin, G., Paternotte, C., Coutinho, P., Klebe, S., et al. (2007). A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21. Neurology, 68(21), 1837 - 1840.
Stevanin, G., Paternotte, C., Coutinho, P., Klebe, S., et al. (2007). A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21. Neurology, 68(21), 1837 - 1840.
Couto, A. R., Bruges-Armas, J., Peach, C. A., Chapman, K., et al. (2007). A novel LEMD3 mutation common to patients with osteopoikilosis with and without melorheostosis. Calcified Tissue International, 81(2), 81 - 84.
Arosa, F. A., Santos, S. G., & Powis, S. J. (2007). Open conformers: the hidden face of MHC-I molecules. Trends in Immunology, 28(3), 115 - 123.
Pons, S., Zanón-Moreno, V., Melo, P., Vila, V., et al. (2007). Optic neuropathy induced by prenatal drug or alcohol exposure. Neuropatía óptica inducida por exposición prenatal a drogas o alcoholArchivos de la Sociedad Espanola de Oftalmologia, 82(1), 21 - 26.
Pons, S., Zanón-Moreno, V., Melo, P., Vila, V., et al. (2007). Optic neuropathy induced by prenatal drug or alcohol exposure. Neuropatía óptica inducida por exposición prenatal a drogas o alcoholArchivos de la Sociedad Espanola de Oftalmologia, 82(1), 21 - 26.
Pais-Vieira, M., Lima, D., & Galhardo, V. (2007). Orbitofrontal cortex lesions disrupt risk assessment in a novel serial decision-making task for rats. Neuroscience, 145(1), 225 - 231.
Pinto, J. P., Ramos, P., & De Sousa, M. (2007). Overexpression of HFE in HepG2 cells reveals differences in intracellular distribution and co-localization of wt- and mutated forms. Blood Cells, Molecules, and Diseases, 39(1), 75 - 81.
Reis, F., Rocha-Pereira, P., Teixeira de Lemos, E., Parada, B., et al. (2007). Oxidative Stress in Cyclosporine-Induced Hypertension: Evidence of Beneficial Effects or Tolerance Development With Nitrate Therapy. Transplantation Proceedings, 39(8), 2494 - 2500.
Stendel, C., Roos, A., Deconinck, T., Pereira, J., et al. (2007). Peripheral nerve demyelination caused by a mutant Rho GTPase guanine nucleotide exchange factor, frabin/FGD4. American Journal of Human Genetics, 81(1), 158 - 164.
Stendel, C., Roos, A., Deconinck, T., Pereira, J., et al. (2007). Peripheral nerve demyelination caused by a mutant Rho GTPase guanine nucleotide exchange factor, frabin/FGD4. American Journal of Human Genetics, 81(1), 158 - 164.
Morales-Hojas, R., Cheke, R. A., & Post, R. J. (2007). A preliminary analysis of the population genetics and molecular phylogenetics of Onchocerca volvulus (Nematoda: Filarioidea) using nuclear ribosomal second internal transcribed spacer sequences. Memorias do Instituto Oswaldo Cruz, 102(7), 879 - 882.
Adriano, M. - A., Vergnes, B., Poncet, J., Mathieu-Daude, F., et al. (2007). Proof of interaction between Leishmania SIR2RP1 deacetylase and chaperone HSP83. Parasitology Research, 100(4), 811 - 818.
Paneque, H. M., Prieto, A. L., Reynaldo, R. R., Cruz, M. T., et al. (2007). Psychological aspects of presymptomatic diagnosis of spinocerebellar ataxia type 2 in Cuba. Community Genetics, 10(3), 132 - 139.
Paneque, H. M., Prieto, A. L., Reynaldo, R. R., Cruz, M. T., et al. (2007). Psychological aspects of presymptomatic diagnosis of spinocerebellar ataxia type 2 in Cuba. Community Genetics, 10(3), 132 - 139.
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.
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.
Vieira, J., Cardoso, C. S., Pinto, J., Patil, K., et al. (2007). A putative gene located at the MHC class I region around the D6S105 marker contributes to the setting of CD8+ T-lymphocyte numbers in humans. International Journal of Immunogenetics, 34(5), 359 - 367.
Vieira, J., Cardoso, C. S., Pinto, J., Patil, K., et al. (2007). A putative gene located at the MHC class I region around the D6S105 marker contributes to the setting of CD8+ T-lymphocyte numbers in humans. International Journal of Immunogenetics, 34(5), 359 - 367.
Vieira, J., Cardoso, C. S., Pinto, J., Patil, K., et al. (2007). A putative gene located at the MHC class I region around the D6S105 marker contributes to the setting of CD8+ T-lymphocyte numbers in humans. International Journal of Immunogenetics, 34(5), 359 - 367.
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.
Pais-Ribeiro, J., da Silva, A. M., Meneses, R. F., & Falco, C. (2007). Relationship between optimism, disease variables, and health perception and quality of life in individuals with epilepsy. Epilepsy and Behavior, 11(1), 33 - 38.

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