Characterization of polymeric nanoparticles for intravenous delivery: Focus on stability - Oliveira, C.L.; Veiga, F.; Varela, C.; Roleira, F.; Tavares, E.; Silveira, I.; Ribeiro, A.J. (Colloids and Surfaces B: Biointerfaces, 2017)

A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar Ataxia - Seixas, A.I.; Loureiro, J.R.; Costa, C.; Ordóñez-Ugalde, A.; Marcelino, H.; Oliveira, C.L.; Loureiro, J.L.; Dhingra, A.; Brandão, E.; Cruz, V.T.; Timóteo, A.; Quintáns, B.; et al. (American Journal of Human Genetics, 2017)

Recent advances in nucleic acid-based delivery: From bench to clinical trials in genetic diseases - Oliveira, C.; Ribeiro, A.J.; Veiga, F.; Silveira, I. (Journal of Biomedical Nanotechnology, 2016)

Unstable repeat expansions in neurodegenerative diseases: Nucleocytoplasmic transport emerges on the scene - Loureiro, J.R.; Oliveira, C.L.; Silveira, I. (Neurobiology of Aging, 2016)

Recent advances in characterization of nonviral vectors for delivery of nucleic acids: Impact on their biological performance - Oliveira, C.; Silveira, I.; Veiga, F.; Ribeiro, A.J. (Expert Opinion on Drug Delivery, 2015)

Autosomal dominant spastic paraplegias: A review of 89 families resulting from a Portuguese survey - Loureiro, J.L.; Brandão, E.; Ruano, L.; Brandão, A.F.; Lopes, A. M.; Thieleke-Matos, C.; Miller-Fleming, L.; Cruz, V.T.; Barbosa, M.; Silveira, I.; Stevanin, G.; Pinto-Basto, J.; et al. (JAMA Neurology, 2013)

Cerebellar ataxia, hemiplegic migraine, and related phenotypes due to a CACNA1A missense mutation: 12-year follow-up of a large portuguese family - Barros, J.; Damásio, J.; Tuna, A.; Alves, I.; Silveira, I.; Pereira-Monteiro, J.; Sequeiros, J.; Alonso, I.; Sousa, A.; Coutinho, P. (JAMA Neurology, 2013)

The Prevalence of Familial Hemiplegic Migraine With Cerebellar Ataxia and Spinocerebellar Ataxia Type 6 in Portugal - Barros, J.; Ruano, L.; Domingos, J.; Tuna, A.; Damásio, J.; Alonso, I.; Silveira, I.; Sequeiros, J.; Coutinho, P. (Headache, 2013)

'Costa da Morte' ataxia is spinocerebellar ataxia 36: Clinical and genetic characterization - García-Murias, M.; Quintáns, B.; Arias, M.; Seixas, A.I.; Cacheiro, P.; Tarrío, R.; Pardo, J.; Millán, M. J.; Arias-Rivas, S.; Blanco-Arias, P.; Dapena, D.; Moreira, R.; et al. (Brain, 2012)

Loss of junctophilin-3 contributes to huntington disease-like 2 pathogenesis - Seixas, A.I.; Holmes, S.E.; Takeshima, H.; Pavlovich, A.; Sachs, N.; Pruitt, J. L.; Silveira, I.; Ross, C.A.; Margolis, R.L.; Rudnicki, D. D. (Annals of Neurology, 2012)

Epidemiology and population genetics of degenerative ataxias - Sequeiros, J.; Martins, S.; Silveira, I. (Handbook of Clinical Neurology, 2011)

FXTAS is rare among Portuguese patients with movement disorders: FMR1 premutations may be associated with a wider spectrum of phenotypes - Seixas, A.I.; Vale, J.; Jorge, P.; Marques, I.; Santos, R.; Alonso, I.; Fortuna, A.M.; Pinto-Basto, J.; Coutinho, P.; Margolis, R.L.; Sequeiros, J.; Silveira, I. (Behavioral and Brain Functions, 2011)

Autosomal dominant cerebellar ataxia: Frequency analysis and clinical characterization of 45 families from Portugal - Vale, J.; Bugalho, P.; Silveira, I.; Sequeiros, J.; Guimarães, J.; Coutinho, P. (European Journal of Neurology, 2010)

Common origin of pure and interrupted repeat expansions in spinocerebellar ataxia type 2 (SCA2) - Ramos, E.M.; Martins, S.; Alonso, I.; Emmel, V.E.; Saraiva-Pereira, M.L.; Jardim, L.B.; Coutinho, P.; Sequeiros, J.; Silveira, I. (American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 2010)

Ancestral origin of the ATTCT repeat expansion in spinocerebellar ataxia type 10 (SCA10) - Almeida, T.; Alonso, I.; Martins, S.; Ramos, E.M.; Azevedo, L.; Ohno, K.; Amorim, A.; Saraiva-Pereira, M.L.; Jardim, L.B.; Matsuura, T.; Sequeiros, J.; Silveira, I. (PLoS ONE, 2009)

Novel SPG3A and SPG4 mutations in dominant spastic paraplegia families - Loureiro, J.L.; Miller-Fleming, L.; Thieleke-Matos, C.; Magalhães, P.; Cruz, V.T.; Coutinho, P.; Sequeiros, J.; Silveira, I. (Acta Neurologica Scandinavica, 2009)

The spatial learning phenotype of heterozygous leaner mice is robust to systematic variation of the housing environment - Marques, J.M.; Alonso, I.; Santos, C.; Silveira, I.; Olsson, I.A.S. (Comparative Medicine, 2009)

Cis-acting factors promoting the CAG intergenerational instability in Machado-Joseph disease - Martins, S.; Coutinho, P.; Silveira, I.; Giunti, P.; Jardim, L.B.; Calafell, F.; Sequeiros, J.; Amorim, A. (American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 2008)

Machado-Joseph disease enhances genetic fitness: A comparison between affected and unaffected women and between MJD and the general population - Prestes, P.R.; Saraiva-Pereira, M.L.; Silveira, I.; Sequeiros, J.; Jardim, L.B. (Annals of Human Genetics, 2008)

Motor and cognitive deficits in the heterozygous leaner mouse, a Cav2.1 voltage-gated Ca2+ channel mutant - Alonso, I.; Marques, J.M.; Sousa, N.; Sequeiros, J.; Olsson, I.A.S.; Silveira, I. (Neurobiology of Aging, 2008)

Asian origin for the worldwide-spread mutational event in Machado-Joseph disease - Martins, S.; Calafell, F.; Gaspar, C.; Wong, V.C.N.; Silveira, I.; Nicholson, G.A.; Brunt, E.R.; Tranebjaerg, L.; Stevanin, G.; Hsieh, M.; Soong, B.-W.; Loureiro, L.; et al. (Archives of Neurology, 2007)

Depressive symptoms in Machado-Joseph disease (SCA3) patients and their relatives - Cecchin, C.R.; Pires, A.P.; Rieder, C.R.; Monte, T.L.; Silveira, I.; Carvalho, T.; Saraiva-Pereira, M.L.; Sequeiros, J.; Jardim, L.B. (Community Genetics, 2006)

A novel trinucleotide repeat expansion at chromosome 3q26.2 identified by a CAG/CTG repeat expansion detection array - Holmes, S.E.; Wentzell, J.S.; Seixas, A.I.; Callahan, C.; Silveira, I.; Ross, C.A.; Margolis, R.L. (Human Genetics, 2006)

Reduced penetrance of intermediate size alleles in spinocerebellar ataxia type 10 - Alonso, I.; Jardim, L.B.; Artigalas, O.; Saraiva-Pereira, M.L.; Matsuura, T.; Ashizawa, T.; Sequeiros, J.; Silveira, I. (Neurology, 2006)

Spinocerebellar ataxias in 114 Brazilian families: Clinical and molecular findings [3] - Trott, A.; Jardim, L.B.; Ludwig, H.T.; Saute, J.A.M.; Artigalás, O.; Kieling, C.; Wanderley, H.Y.C.; Rieder, C.R.M.; Monte, T.L.; Socal, M.; Alonso, I.; Ferro, A.; et al. (Clinical Genetics, 2006)

FXTAS, SCA10, and SCA17 in American patients with movement disorders [1] - Seixas, A.I.; Maurer, M.H.; Lin, M.; Callahan, C.; Ahuja, A.; Matsuura, T.; Ross, C.A.; Hisama, F.M.; Silveira, I.; Margolis, R.L. (American Journal of Medical Genetics, 2005)

Haplotype diversity and somatic instability in normal and expanded SCA8 alleles - Martins, S.; Seixas, A.I.; Magalhães, P.; Coutinho, P.; Sequeiros, J.; Silveira, I. (American Journal of Medical Genetics - Neuropsychiatric Genetics, 2005)

A novel H101Q mutation causes PKCγ loss in spinocerebellar ataxia type 14 - Alonso, I.; Costa, C.; Gomes, A.; Ferro, A.; Seixas, A.I.; Silva, S.; Cruz, V.T.; Coutinho, P.; Sequeiros, J.; Silveira, I. (Journal of Human Genetics, 2005)

A novel R1347Q mutation in the predicted voltage sensor segment of the P/Q-type calcium-channel α1A-subunit in a family with progressive cerebellar ataxia and hemiplegic migraine [6] - Alonso, I.; Barros, J.; Tuna, A.; Seixas, A.; Coutinho, P.; Sequeiros, J.; Silveira, I. (Clinical Genetics, 2004)