@article {6421,
	title = {A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar Ataxia},
	journal = {American Journal of Human Genetics},
	volume = {101},
	year = {2017},
	note = {Cited By :2Export Date: 19 March 2018},
	month = {2017},
	pages = {87 - 103},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-85021415706\&doi=10.1016\%2fj.ajhg.2017.06.007\&partnerID=40\&md5=84985cdc99a86734726baafd72a2cdc3},
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@article {4686,
	title = {Alteration of ganglioside biosynthesis responsible for complex hereditary spastic paraplegia},
	journal = {American Journal of Human Genetics},
	volume = {93},
	year = {2013},
	note = {Cited By (since 1996):2Export Date: 8 April 2014Source: Scopus},
	month = {2013},
	pages = {118 - 123},
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@article {4744,
	title = {Autosomal dominant spastic paraplegias: A review of 89 families resulting from a Portuguese survey},
	journal = {JAMA Neurology},
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	year = {2013},
	note = {Cited By (since 1996):1Export Date: 8 April 2014Source: Scopus},
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@article {4682,
	title = {The potential of motion quantification systems in the automatic evaluation of motor function after stroke},
	journal = {International Journal of Stroke},
	volume = {8},
	year = {2013},
	note = {Export Date: 8 April 2014Source: Scopus},
	month = {2013},
	pages = { - },
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84881533066\&partnerID=40\&md5=c68656dca7829d336a103eb1ed794c59},
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@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},
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@article {3547,
	title = {Novel SPG3A and SPG4 mutations in dominant spastic paraplegia families},
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	year = {2009},
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	author = {Loureiro, J.L. and Miller-Fleming, L. and Thieleke-Matos, C. and Magalh{\~a}es, P. and Cruz, V.T. and Coutinho, P. and Sequeiros, J. and Silveira, I.}
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@article {3926,
	title = {Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum},
	journal = {Nature Genetics},
	volume = {39},
	year = {2007},
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	author = {Stevanin, G. and Santorelli, F.M. and Azzedine, H. and Coutinho, P. and Chomilier, J. and Denora, P.S. and Martin, E. and Ouvrard-Hernandez, A.-M. and Tessa, A. and Bouslam, N. and Lossos, A. and Charles, P. and Loureiro, J.L. and Elleuch, N. and Confavreux, C. and Cruz, V.T. and Ruberg, M. and Leguern, E. and Grid, D. and Tazir, M. and Fontaine, B. and Filla, A. and Bertini, E. and Durr, A. and Brice, A.}
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@article {3889,
	title = {A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21},
	journal = {Neurology},
	volume = {68},
	year = {2007},
	note = {Cited By (since 1996): 11Export Date: 18 March 2013Source: Scopus},
	month = {2007///},
	pages = {1837 - 1840},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-34249008076\&partnerID=40\&md5=9f42412553eb3cbcf47eb6117be00b4a},
	author = {Stevanin, G. and Paternotte, C. and Coutinho, P. and Klebe, S. and Elleuch, N. and Loureiro, J.L. and Denis, E. and Cruz, V.T. and D{\"u}rr, A. and Prud{\textquoteright}homme, J.-F. and Weissenbach, J. and Brice, A. and Hazan, J.}
}
@article {4068,
	title = {Cerebellar ataxia with spasmodic cough: A new form of dominant ataxia},
	journal = {Archives of Neurology},
	volume = {63},
	year = {2006},
	note = {Cited By (since 1996): 3Export Date: 18 March 2013Source: Scopus},
	month = {2006///},
	pages = {553 - 555},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-33645739135\&partnerID=40\&md5=ec27dd0408d7763d260d525bf110b6a4},
	author = {Coutinho, P. and Cruz, V.T. and Tuna, A. and Silva, S.E. and Guimar{\~a}es, J.}
}
@article {4153,
	title = {Neuroferritinopathy: Missense mutation in FTL causing early-onset bilateral pallidal involvement},
	journal = {Neurology},
	volume = {65},
	year = {2005},
	note = {Cited By (since 1996): 34Export Date: 18 March 2013Source: Scopus},
	month = {2005///},
	pages = {603 - 605},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-23844553465\&partnerID=40\&md5=bb8e13589c21c86197ce6d8411a2f0a8},
	author = {MacIel, P. and Cruz, V.T. and Constante, M. and Iniesta, I. and Costa, M.C. and Gallati, S. and Sousa, N. and Sequeiros, J. and Coutinho, P. and Santos, M.M.}
}
@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.}
}
