@article {6416,
	title = {Ataxia telangiectasia-like disorder: A child with a novel variant in MRE11A gene},
	journal = {Revista de Neurologia},
	volume = {65},
	year = {2017},
	note = {Export Date: 19 March 2018},
	month = {2017},
	pages = {143 - 144},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-85032496864\&partnerID=40\&md5=dd9ca729be1100b4d12ea5fb4b36375d},
	author = {Aquino, J. and Ribeiro, V. and Alonso, I. and Ramos, F. and Vasconcelos, M.}
}
@article {6505,
	title = {Familial amyloid polyneuropathy in Portugal: New genes modulating age-at-onset},
	journal = {Annals of Clinical and Translational Neurology},
	volume = {4},
	year = {2017},
	note = {Cited By :2Export Date: 19 March 2018},
	month = {2017},
	pages = {98 - 105},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-85026195015\&doi=10.1002\%2facn3.380\&partnerID=40\&md5=88410e23b9aa42087de01ab56e0522b4},
	author = {Santos, D. and Coelho, T. and Alves-Ferreira, M. and Sequeiros, J. and Mendon{\c c}a, D. and Alonso, I. and Lemos, C. and Sousa, A.}
}
@article {6521,
	title = {Genetic contributors to intergenerational CAG repeat instability in Huntington{\textquoteright}s disease knock-in mice},
	journal = {Genetics},
	volume = {205},
	year = {2017},
	note = {Export Date: 19 March 2018},
	month = {2017},
	pages = {503 - 516},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-85021849174\&doi=10.1534\%2fgenetics.116.195578\&partnerID=40\&md5=2f2a2665eaff4874bc5dbea3ce3bd103},
	author = {Neto, J.L. and Lee, J.-M. and Afridi, A. and Gillis, T. and Guide, J.R. and Dempsey, S. and Lager, B. and Alonso, I. and Wheeler, V.C. and Pinto, R.M.}
}
@article {6368,
	title = {Massive sequencing of 70 genes reveals a myriad of missing genes or mechanisms to be uncovered in hereditary spastic paraplegias},
	journal = {European Journal of Human Genetics},
	volume = {25},
	year = {2017},
	note = {Cited By :2Export Date: 19 March 2018},
	month = {2017},
	pages = {1217 - 1228},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-85031283104\&doi=10.1038\%2fejhg.2017.124\&partnerID=40\&md5=2298efd24f5ae5c8b7667b041a4360d6},
	author = {Morais, S. and Raymond, L. and Mairey, M. and Coutinho, P. and Brand{\~a}o, E. and Ribeiro, P. and Loureiro, J.L. and Sequeiros, J. and Brice, A. and Alonso, I. and Stevanin, G.}
}
@article {6398,
	title = {A Portuguese rapid-onset dystonia-parkinsonism case with atypical features},
	journal = {Neurological Sciences},
	volume = {38},
	year = {2017},
	note = {Export Date: 19 March 2018},
	month = {2017},
	pages = {1713 - 1714},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-85019260495\&doi=10.1007\%2fs10072-017-2996-4\&partnerID=40\&md5=959bd7568381e28122c9c61a1767beb7},
	author = {Sousa, A.L. and Alonso, I. and Magalh{\~a}es, M.}
}
@book {6552,
	title = {Rare neurodegenerative diseases: Clinical and genetic update},
	series = {Advances in Experimental Medicine and Biology},
	volume = {1031},
	year = {2017},
	note = {Export Date: 19 March 2018},
	month = {2017},
	pages = {443 - 496},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-85037621160\&doi=10.1007\%2f978-3-319-67144-4_25\&partnerID=40\&md5=9b095ebb6ea8c1a3b3b40f970878a058},
	author = {Matilla-Duenas, A. and Corral-Juan, M. and Rodr{\'\i}guez-Palmero Seuma, A. and Vilas, D. and Ispierto, L. and Morais, S. and Sequeiros, J. and Alonso, I. and Volpini, V. and Serrano-Munuera, C. and Pintos-Morell, G. and Alvarez, R. and S{\'a}nchez, I.}
}
@article {6349,
	title = {A recessive ataxia diagnosis algorithm for the next generation sequencing era},
	journal = {Annals of Neurology},
	volume = {82},
	year = {2017},
	note = {Export Date: 19 March 2018},
	month = {2017},
	pages = {892 - 899},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-85034584658\&doi=10.1002\%2fana.25084\&partnerID=40\&md5=270469524dd28bfd7f7641b23cc44c16},
	author = {Renaud, M. and Tranchant, C. and Martin, J.V.T. and Mochel, F. and Synofzik, M. and van de Warrenburg, B. and Pandolfo, M. and Koenig, M. and Kolb, S.A. and Anheim, M. and Alonso, I. and Azzedine, H. and Barbot, C. and Bereau, M. and Berkovic, S. and Bernard, G. and Bindoff, L.A. and Bompaire, F. and Bonneau, D. and Bonneau, P. and Boycott, K.M. and Bras, J. and Brais, B. and Brigatti, K.W. and Cameron, J. and Chamova, T. and Choquet, K. and Delague, V. and Denizeau, P. and Dotti, M.T. and El-Euch, G. and Elmalik, S.A. and Federico, A. and Fiskerstrand, T. and Gagnon, C. and Guerreiro, R. and Guissart, C. and Hassin-Baer, S. and Heimdal, K.R. and H{\'e}ron, B. and Isohanni, P. and Kalaydijeva, L. and Kawarai, T. and Koht, J.A. and Lai, S.-C. and Piana, R.L. and Lecocq, C. and Linnankivi, T. and L{\"o}nnqvist, T. and Lu, C.-S. and Maas, R. and Mahlaoui, N. and Mallaret, M. and Marelli, C. and Mariotti, C. and Mathieu, J. and M{\'e}neret, A. and Mignarri, A. and Monin, M.L. and Montaut, S. and Nanetti, L. and Nadjar, Y. and Poujois, A. and Salih, M.A. and Sousa, S. and Stanier, P. and Stoppa-Lyonnet, D. and Strauss, K. and Tallaksen, C. and Tarnopolsky, M. and Tinant, N. and Tournev, I. and Topaloglu, H. and Varhaug, K.N. and Woimant, F. and Wolf, N.I. and Yahalom, G. and Yoon, G. and Young, M.}
}
@article {6431,
	title = {Spinocerebellar ataxia type 10: common haplotype and disease progression rate in Peru and Brazil},
	journal = {European Journal of Neurology},
	volume = {24},
	year = {2017},
	note = {Cited By :1Export Date: 19 March 2018},
	month = {2017},
	pages = {892 - e36},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-85019672148\&doi=10.1111\%2fene.13281\&partnerID=40\&md5=73fa63f802fb2d0e9e9a533fa3674c4f},
	author = {Gheno, T.C. and Furtado, G.V. and Saute, J.A.M. and Donis, K.C. and Fontanari, A.M.V. and Emmel, V.E. and Pedroso, J.L. and Barsottini, O. and Godeiro-Junior, C. and van der Linden, H. and Ternes Pereira, E. and Cintra, V.P. and Marques, W. and de Castilhos, R.M. and Alonso, I. and Sequeiros, J. and Cornejo-Olivas, M. and Mazzetti, P. and Leotti, V.B. and Jardim, L.B. and Saraiva-Pereira, M.L.}
}
@booklet {6450,
	title = {A Trans-acting Factor May Modify Age at Onset in Familial Amyloid Polyneuropathy ATTRV30M in Portugal},
	howpublished = {Molecular Neurobiology},
	year = {2017},
	note = {Export Date: 19 March 2018Article in Press},
	month = {2017},
	pages = {1 - 8},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-85019539928\&doi=10.1007\%2fs12035-017-0593-4\&partnerID=40\&md5=bd96bc3385ca81c205b0d6f624ed662e},
	author = {Alves-Ferreira, M. and Coelho, T. and Santos, D. and Sequeiros, J. and Alonso, I. and Sousa, A. and Lemos, C.}
}
@article {6791,
	title = {DJ-1 linked parkinsonism (PARK7) is associated with Lewy body pathology},
	journal = {Brain},
	volume = {139},
	year = {2016},
	note = {Cited By :6Export Date: 19 March 2018},
	month = {2016},
	pages = {1680 - 1687},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-84978829850\&doi=10.1093\%2fbrain\%2faww080\&partnerID=40\&md5=4ffeedc877b1c7dcc2c0b341511213c6},
	author = {Taipa, R. and Pereira, C. and Reis, I. and Alonso, I. and Bastos-Lima, A. and Melo-Pires, M. and Magalh{\~a}es, M.}
}
@article {6726,
	title = {EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH)},
	journal = {European Journal of Human Genetics},
	volume = {24},
	year = {2016},
	note = {Cited By :14Export Date: 19 March 2018},
	month = {2016},
	pages = {479 - 495},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-84960397668\&doi=10.1038\%2fejhg.2015.128\&partnerID=40\&md5=aedb529de1d8bca3adccfd3b56da9190},
	author = {Porto, G. and Brissot, P. and Swinkels, D.W. and Zoller, H. and Kamarainen, O. and Patton, S. and Alonso, I. and Morris, M. and Keeney, S.}
}
@article {6742,
	title = {Large-scale functional RNAi Screen in C. elegans identifies TGF-β and notch signaling pathways as modifiers of CACNAIA},
	journal = {ASN Neuro},
	volume = {8},
	year = {2016},
	note = {Cited By :3Export Date: 19 March 2018},
	month = {2016},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-84961625995\&doi=10.1177\%2f1759091416637025\&partnerID=40\&md5=a7895635db89c0794f5dc80f94128bce},
	author = {da Concei{\c c}{\~a}o Pereira, M. and Morais, S. and Sequeiros, J. and Alonso, I.}
}
@article {6701,
	title = {Variants in RBP4 and AR genes modulate age at onset in familial amyloid polyneuropathy (FAP ATTRV30M)},
	journal = {European Journal of Human Genetics},
	volume = {24},
	year = {2016},
	note = {Cited By :9Export Date: 19 March 2018},
	month = {2016},
	pages = {756 - 760},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-84939553337\&doi=10.1038\%2fejhg.2015.180\&partnerID=40\&md5=009df72ca028815121e7b33f67ce7c11},
	author = {Santos, D. and Coelho, T. and Alves-Ferreira, M. and Sequeiros, J. and Mendon{\c c}a, D. and Alonso, I. and Lemos, C. and Sousa, A.}
}
@article {5448,
	title = {Chromosome substitution strain assessment of a Huntington{\textquoteright}s disease modifier locus},
	journal = {Mammalian Genome},
	volume = {26},
	year = {2015},
	note = {Cited By :2Export Date: 12 January 2016},
	month = {2015},
	pages = {119 - 130},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84940002551\&partnerID=40\&md5=20d3879276019934f325467f96a8c7a2},
	author = {Ramos, E.M. and Kovalenko, M. and Guide, J.R. and St. Claire, J. and Gillis, T. and Mysore, J. S. and Sequeiros, J. and Wheeler, V.C. and Alonso, I. and MacDonald, M. E.}
}
@booklet {5407,
	title = {EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH)},
	howpublished = {European Journal of Human Genetics},
	year = {2015},
	note = {Export Date: 12 January 2016Article in Press},
	month = {2015},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84936976676\&partnerID=40\&md5=3615d95c94f3beac334811fe5e75251d},
	author = {Porto, G. and Brissot, P. and Swinkels, D.W. and Zoller, H. and Kamarainen, O. and Patton, S. and Alonso, I. and Morris, M. and Keeney, S.}
}
@article {5497,
	title = {Haplotype analysis of the 4p16.3 region in Portuguese families with Huntington{\textquoteright}s disease},
	journal = {American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics},
	volume = {168},
	year = {2015},
	note = {Export Date: 12 January 2016},
	month = {2015},
	pages = {135 - 143},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84923108709\&partnerID=40\&md5=48fc86498a5c591ca8dcf19ff86b4c4d},
	author = {Ramos, E.M. and Gillis, T. and Mysore, J. S. and Lee, J. -M. and G{\"o}gele, M. and D{\textquoteright}Elia, Y. and Pichler, I. and Sequeiros, J. and Pramstaller, P.P. and Gusella, J. F. and MacDonald, M. E. and Alonso, I.}
}
@article {5512,
	title = {Mutations in PNKP cause recessive ataxia with oculomotor apraxia type 4},
	journal = {American Journal of Human Genetics},
	volume = {96},
	year = {2015},
	note = {Export Date: 12 January 2016},
	month = {2015},
	pages = {474 - 479},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84924246336\&partnerID=40\&md5=ced002f34161723078050509e0d874d9},
	author = {Bras, J. and Alonso, I. and Barbot, C. and Costa, M.M. and Darwent, L. and Orme, T. and Sequeiros, J. and Hardy, J. and Coutinho, P. and Guerreiro, R.}
}
@article {5516,
	title = {Paternal transmission of subcortical band heterotopia through DCX somatic mosaicism},
	journal = {Seizure},
	volume = {25},
	year = {2015},
	note = {Export Date: 12 January 2016},
	month = {2015},
	pages = {62 - 64},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84923228256\&partnerID=40\&md5=5dd4718a5933a1d42ed0bec34154769b},
	author = {Moreira, I. and Bastos-Ferreira, R. and Silva, J. and Ribeiro, C. and Alonso, I. and Chaves, J.}
}
@booklet {5396,
	title = {Variants in RBP4 and AR genes modulate age at onset in familial amyloid polyneuropathy (FAP ATTRV30M)},
	howpublished = {European Journal of Human Genetics},
	year = {2015},
	note = {Export Date: 12 January 2016Article in Press},
	month = {2015},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84939553337\&partnerID=40\&md5=3169865e6d7fcbdb14b5f766c8c54dfe},
	author = {Santos, D. and Coelho, T. and Alves-Ferreira, M. and Sequeiros, J. and Mendon{\c c}a, D. and Alonso, I. and Lemos, C. and Sousa, A.}
}
@article {4744,
	title = {Autosomal dominant spastic paraplegias: A review of 89 families resulting from a Portuguese survey},
	journal = {JAMA Neurology},
	volume = {70},
	year = {2013},
	note = {Cited By (since 1996):1Export Date: 8 April 2014Source: Scopus},
	month = {2013},
	pages = {481 - 487},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84876133160\&partnerID=40\&md5=f118e6988d2a0ce5c8565bd43234fba0},
	author = {Loureiro, J.L. and Brand{\~a}o, E. and Ruano, L. and Brand{\~a}o, A.F. and Lopes, A. M. and Thieleke-Matos, C. and Miller-Fleming, L. and Cruz, V.T. and Barbosa, M. and Silveira, I. and Stevanin, G. and Pinto-Basto, J. and Sequeiros, J. and Alonso, I. and Coutinho, P.}
}
@article {4721,
	title = {Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington{\textquoteright}s disease motor onset},
	journal = {Neurogenetics},
	volume = {14},
	year = {2013},
	note = {Cited By (since 1996):2Export Date: 8 April 2014Source: Scopus},
	month = {2013},
	pages = {173 - 179},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84888063832\&partnerID=40\&md5=10b47c0fd5922805d754454404213459},
	author = {Ramos, E.M. and Latourelle, J.C. and Gillis, T. and Mysore, J. S. and Squitieri, F. and Di Pardo, A. and Di Donato, S. and Gellera, C. and Hayden, M. R. and Morrison, P. J. and Nance, M. and Ross, C.A. and Margolis, R.L. and Gomez-Tortosa, E. and Ayuso, C. and Suchowersky, O. and Trent, R. J. and McCusker, E. and Novelletto, A. and Frontali, M. and Jones, R. and Ashizawa, T. and Frank, S. and Saint-Hilaire, M. -H. and Hersch, S. M. and Rosas, H. D. and Lucente, D. and Harrison, M. B. and Zanko, A. and Abramson, R. K. and Marder, K. and Gusella, J. F. and Lee, J. -M. and Alonso, I. and Sequeiros, J. and Myers, R. H. and MacDonald, M. E.}
}
@article {2790,
	title = {Cerebellar ataxia, hemiplegic migraine, and related phenotypes due to a CACNA1A missense mutation: 12-year follow-up of a large portuguese family},
	journal = {JAMA Neurology},
	volume = {70},
	year = {2013},
	note = {Export Date: 18 March 2013Source: Scopus},
	month = {2013///},
	pages = {235 - 240},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84874027219\&partnerID=40\&md5=5a64eead07d106ec656c95b088883ef3},
	author = {Barros, J. and Dam{\'a}sio, J. and Tuna, A. and Alves, I. and Silveira, I. and Pereira-Monteiro, J. and Sequeiros, J. and Alonso, I. and Sousa, A. and Coutinho, P.}
}
@booklet {4634,
	title = {Huntington disease and Huntington disease-like in a case series from Brazil},
	howpublished = {Clinical Genetics},
	year = {2013},
	note = {Export Date: 8 April 2014Source: ScopusArticle in Press},
	month = {2013},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84885552918\&partnerID=40\&md5=eff40bda7191e4feb2df3fc8654c9ca5},
	author = {Castilhos, R. and Souza, A. and Furtado, G. and Gheno, T. and Silva, A. and Vargas, F. and Lima, M.-A. and Barsottini, O. and Pedroso, J. and Godeiro, C. and Salarini, D. and Pereira, E. and Lin, K. and Toralles, M.-B. and Saute, J. and Rieder, C. and Quintas, M. and Sequeiros, J. and Alonso, I. and Saraiva-Pereira, M. and Jardim, L.}
}
@article {4658,
	title = {Interaction between γ-Aminobutyric Acid A Receptor Genes: New Evidence in Migraine Susceptibility},
	journal = {PLoS ONE},
	volume = {8},
	year = {2013},
	note = {Export Date: 8 April 2014Source: ScopusArt. No.: e74087},
	month = {2013},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84883511876\&partnerID=40\&md5=184db90d5eef8fc3221a32fe1eeb3554},
	author = {Quintas, M. and Neto, J.L. and Pereira-Monteiro, J. and Barros, J. and Sequeiros, J. and Sousa, A. and Alonso, I. and Lemos, C.}
}
@booklet {4621,
	title = {The Prevalence of Familial Hemiplegic Migraine With Cerebellar Ataxia and Spinocerebellar Ataxia Type 6 in Portugal},
	howpublished = {Headache},
	year = {2013},
	note = {Export Date: 8 April 2014Source: ScopusArticle in Press},
	month = {2013},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84886743970\&partnerID=40\&md5=dfc1f06cc2e9ced02dc83f97f6703e26},
	author = {Barros, J. and Ruano, L. and Domingos, J. and Tuna, A. and Dam{\'a}sio, J. and Alonso, I. and Silveira, I. and Sequeiros, J. and Coutinho, P.}
}
@article {3007,
	title = {Alu elements mediate large SPG11 gene rearrangements: Further spatacsin mutations},
	journal = {Genetics in Medicine},
	volume = {14},
	year = {2012},
	note = {Export Date: 18 March 2013Source: Scopus},
	month = {2012///},
	pages = {143 - 151},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84855558170\&partnerID=40\&md5=cebfb723707752898768ab723a34f364},
	author = {Concei{\c c}o Pereira, M. and Loureiro, J.L. and Pinto-Basto, J. and Brando, E. and Margarida Lopes, A. and Neves, G. and Dias, P. and Geraldes, R. and Martins, I.P. and Cruz, V.T. and Kamsteeg, E.-J. and Brunner, H.G. and Coutinho, P. and Sequeiros, J. and Alonso, I.}
}
@article {2960,
	title = {Intergenerational instability in Huntington disease: Extreme repeat changes among 134 transmissions},
	journal = {Movement Disorders},
	volume = {27},
	year = {2012},
	note = {Cited By (since 1996): 1Export Date: 18 March 2013Source: Scopus},
	month = {2012///},
	pages = {583 - 585},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84859436267\&partnerID=40\&md5=46d46683e6e658d82ca3bca14c1e929d},
	author = {Ramos, E.M. and Cerqueira, J. and Lemos, C. and Pinto-Basto, J. and Alonso, I. and Sequeiros, J.}
}
@article {2945,
	title = {Prevalence of Huntington{\textquoteright}s disease gene CAG repeat alleles in sporadic amyotrophic lateral sclerosis patients},
	journal = {Amyotrophic Lateral Sclerosis},
	volume = {13},
	year = {2012},
	note = {Cited By (since 1996): 1Export Date: 18 March 2013Source: Scopus},
	month = {2012///},
	pages = {265 - 269},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84860387378\&partnerID=40\&md5=1ab22611d3d944d5b39d2a200d3c5041},
	author = {Ramos, E.M. and Keagle, P. and Gillis, T. and Lowe, P. and Mysore, J. S. and Leclerc, A. L. and Ratti, A. and Ticozzi, N. and Gellera, C. and Gusella, J. F. and Silani, V. and Alonso, I. and Brown Jr., R. H. and MacDonald, M. E. and Landers, J. E.}
}
@article {3197,
	title = {Does DNA methylation in the promoter region of the ATXN3 gene modify age at onset in MJD (SCA3) patients?},
	journal = {Clinical Genetics},
	volume = {79},
	year = {2011},
	note = {Cited By (since 1996): 3Export Date: 18 March 2013Source: Scopus},
	month = {2011///},
	pages = {100 - 102},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-78650010388\&partnerID=40\&md5=69ab709285de64e581228fd1848c5c6c},
	author = {Emmel, V.E. and Alonso, I. and Jardim, L.B. and Saraiva-Pereira, M.L. and Sequeiros, J.}
}
@article {3111,
	title = {FXTAS is rare among Portuguese patients with movement disorders: FMR1 premutations may be associated with a wider spectrum of phenotypes},
	journal = {Behavioral and Brain Functions},
	volume = {7},
	year = {2011},
	note = {Export Date: 18 March 2013Source: ScopusArt. No.: 19},
	month = {2011///},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-79957829884\&partnerID=40\&md5=2be467541a40dac8980e300ecb23245a},
	author = {Seixas, A.I. and Vale, J. and Jorge, P. and Marques, I. and Santos, R. and Alonso, I. and Fortuna, A.M. and Pinto-Basto, J. and Coutinho, P. and Margolis, R.L. and Sequeiros, J. and Silveira, I.}
}
@article {3151,
	title = {A role for endothelin receptor type A in migraine without aura susceptibility? A study in Portuguese patients},
	journal = {European Journal of Neurology},
	volume = {18},
	year = {2011},
	note = {Cited By (since 1996): 4Export Date: 18 March 2013Source: Scopus},
	month = {2011///},
	pages = {649 - 655},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-79952721018\&partnerID=40\&md5=2c06712d4c8eb476a1024b9e336d28ad},
	author = {Lemos, C. and Neto, J.L. and Pereira-Monteiro, J. and Mendon{\c c}a, D. and Barros, J. and Sequeiros, J. and Alonso, I. and Sousa, A.}
}
@article {3366,
	title = {Ataxia and progressive encephalopathy in a 4-year-old girl},
	journal = {Laboratory Medicine},
	volume = {41},
	year = {2010},
	note = {Cited By (since 1996): 1Export Date: 18 March 2013Source: Scopus},
	month = {2010///},
	pages = {5 - 9},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-77952007680\&partnerID=40\&md5=f9fd1183d7acabe6845ec444967b5971},
	author = {Spears, M.D. and Melton, S. and Mao, Q. and Payne, D. and Rakheja, D. and Hatanpaa, K.J. and Burns, D.K. and Sequeiros, J. and Alonso, I.}
}
@article {3227,
	title = {BDNF and CGRP interaction: Implications in migraine susceptibility},
	journal = {Cephalalgia},
	volume = {30},
	year = {2010},
	note = {Cited By (since 1996): 8Export Date: 18 March 2013Source: Scopus},
	month = {2010///},
	pages = {1375 - 1382},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-79751474283\&partnerID=40\&md5=230fb7a7d2d342cd685b6d72197f644a},
	author = {Lemos, C. and Mendon{\c c}a, D. and Pereira-Monteiro, J. and Barros, J. and Sequeiros, J. and Alonso, I. and Sousa, A.}
}
@article {3343,
	title = {Common origin of pure and interrupted repeat expansions in spinocerebellar ataxia type 2 (SCA2)},
	journal = {American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics},
	volume = {153},
	year = {2010},
	note = {Cited By (since 1996): 4Export Date: 18 March 2013Source: Scopus},
	month = {2010///},
	pages = {524 - 531},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-77349087351\&partnerID=40\&md5=bde1fb216daf4d250e900def52a9f35e},
	author = {Ramos, E.M. and Martins, S. and Alonso, I. and Emmel, V.E. and Saraiva-Pereira, M.L. and Jardim, L.B. and Coutinho, P. and Sequeiros, J. and Silveira, I.}
}
@article {3328,
	title = {Evidence of syntaxin 1A involvement in migraine susceptibility: A Portuguese study},
	journal = {Archives of Neurology},
	volume = {67},
	year = {2010},
	note = {Cited By (since 1996): 4Export Date: 18 March 2013Source: Scopus},
	month = {2010///},
	pages = {422 - 427},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-77950873164\&partnerID=40\&md5=55ea4d8062d60b0fb8f401afac3cb2e4},
	author = {Lemos, C. and Pereira-Monteiro, J. and Mendon{\c c}a, D. and Ramos, E.M. and Barros, J. and Sequeiros, J. and Alonso, I. and Sousa, A.}
}
@article {3252,
	title = {Large normal and reduced penetrance alleles in Huntington disease: Instability in families and frequency at the laboratory, at the clinic and in the population},
	journal = {Clinical Genetics},
	volume = {78},
	year = {2010},
	note = {Cited By (since 1996): 6Export Date: 18 March 2013Source: Scopus},
	month = {2010///},
	pages = {381 - 387},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-77956413099\&partnerID=40\&md5=49d07a08a3970dcd0cba57cb2e76bfeb},
	author = {Sequeiros, J. and Ramos, E.M. and Cerqueira, J. and Costa, M.C. and Sousa, A. and Pinto-Basto, J. and Alonso, I.}
}
@article {3223,
	title = {Sensory neuronopathy in ataxia with oculomotor apraxia type 2},
	journal = {Journal of the Neurological Sciences},
	volume = {298},
	year = {2010},
	note = {Cited By (since 1996): 1Export Date: 18 March 2013Source: Scopus},
	month = {2010///},
	pages = {118 - 120},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-77958153343\&partnerID=40\&md5=80f8c56e6db4b5802c4d210cca4486cd},
	author = {Gazulla, J. and Benavente, I. and L{\'o}pez-Fraile, I.P. and Tordesillas, C. and Modrego, P. and Alonso, I. and Pinto-Basto, J.}
}
@article {3535,
	title = {Ancestral origin of the ATTCT repeat expansion in spinocerebellar ataxia type 10 (SCA10)},
	journal = {PLoS ONE},
	volume = {4},
	year = {2009},
	note = {Cited By (since 1996): 8Export Date: 18 March 2013Source: ScopusArt. No.: e4553},
	month = {2009///},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-62349092631\&partnerID=40\&md5=c8b9608dcf3e879b501d34e20b01be07},
	author = {Almeida, T. and Alonso, I. and Martins, S. and Ramos, E.M. and Azevedo, L. and Ohno, K. and Amorim, A. and Saraiva-Pereira, M.L. and Jardim, L.B. and Matsuura, T. and Sequeiros, J. and Silveira, I.}
}
@article {3517,
	title = {The spatial learning phenotype of heterozygous leaner mice is robust to systematic variation of the housing environment},
	journal = {Comparative Medicine},
	volume = {59},
	year = {2009},
	note = {Cited By (since 1996): 3Export Date: 18 March 2013Source: Scopus},
	month = {2009///},
	pages = {129 - 138},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-65549099531\&partnerID=40\&md5=c5dcd6e11bae50ba6905e7b8b35b7897},
	author = {Marques, J.M. and Alonso, I. and Santos, C. and Silveira, I. and Olsson, I.A.S.}
}
@article {3599,
	title = {Motor and cognitive deficits in the heterozygous leaner mouse, a Cav2.1 voltage-gated Ca2+ channel mutant},
	journal = {Neurobiology of Aging},
	volume = {29},
	year = {2008},
	note = {Cited By (since 1996): 9Export Date: 18 March 2013Source: Scopus},
	month = {2008///},
	pages = {1733 - 1743},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-51449092440\&partnerID=40\&md5=fc7020a27ed6c42f8d360e2351bfca9b},
	author = {Alonso, I. and Marques, J.M. and Sousa, N. and Sequeiros, J. and Olsson, I.A.S. and Silveira, I.}
}
@article {4057,
	title = {Reduced penetrance of intermediate size alleles in spinocerebellar ataxia type 10},
	journal = {Neurology},
	volume = {66},
	year = {2006},
	note = {Cited By (since 1996): 12Export Date: 18 March 2013Source: Scopus},
	month = {2006///},
	pages = {1602 - 1604},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-33745373901\&partnerID=40\&md5=087d4c80f899d3cf338536ce9df81f9d},
	author = {Alonso, I. and Jardim, L.B. and Artigalas, O. and Saraiva-Pereira, M.L. and Matsuura, T. and Ashizawa, T. and Sequeiros, J. and Silveira, I.}
}
@article {4023,
	title = {Spinocerebellar ataxias in 114 Brazilian families: Clinical and molecular findings [3]},
	journal = {Clinical Genetics},
	volume = {70},
	year = {2006},
	note = {Cited By (since 1996): 14Export Date: 18 March 2013Source: Scopus},
	month = {2006///},
	pages = {173 - 176},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-33745827039\&partnerID=40\&md5=de22af828de5b88d785286755acdfa57},
	author = {Trott, A. and Jardim, L.B. and Ludwig, H.T. and Saute, J.A.M. and Artigal{\'a}s, O. and Kieling, C. and Wanderley, H.Y.C. and Rieder, C.R.M. and Monte, T.L. and Socal, M. and Alonso, I. and Ferro, A. and Carvalho, T. and do C{\'e}u Moreira, M. and Mendon{\c c}a, P. and Ferreirinha, F. and Silveira, I. and Sequeiros, J. and Giugliani, R. and Saraiva-Pereira, M.L.}
}
@article {4133,
	title = {A novel H101Q mutation causes PKCγ loss in spinocerebellar ataxia type 14},
	journal = {Journal of Human Genetics},
	volume = {50},
	year = {2005},
	note = {Cited By (since 1996): 21Export Date: 18 March 2013Source: Scopus},
	month = {2005///},
	pages = {523 - 529},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-27644562111\&partnerID=40\&md5=240f114c28312907498c1576c7a34fd9},
	author = {Alonso, I. and Costa, C. and Gomes, A. and Ferro, A. and Seixas, A.I. and Silva, S. and Cruz, V.T. and Coutinho, P. and Sequeiros, J. and Silveira, I.}
}
@article {4345,
	title = {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]},
	journal = {Clinical Genetics},
	volume = {65},
	year = {2004},
	note = {Cited By (since 1996): 22Export Date: 18 March 2013Source: Scopus},
	month = {2004///},
	pages = {70 - 72},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-1642555626\&partnerID=40\&md5=f014842055e4d200d0b0849d28739b8d},
	author = {Alonso, I. and Barros, J. and Tuna, A. and Seixas, A. and Coutinho, P. and Sequeiros, J. and Silveira, I.}
}
