@article {6512,
	title = {Contraction of fully expanded FMR1 alleles to the normal range: Predisposing haplotype or rare events?},
	journal = {Journal of Human Genetics},
	volume = {62},
	year = {2017},
	note = {Cited By :1Export Date: 19 March 2018},
	month = {2017},
	pages = {269 - 275},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-85010877200\&doi=10.1038\%2fjhg.2016.122\&partnerID=40\&md5=4946a5c9b805cc25f5616998a4735f69},
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}
@article {4711,
	title = {Bilirubin levels and redox status in a young healthy population},
	journal = {Acta Haematologica},
	volume = {130},
	year = {2013},
	note = {Export Date: 8 April 2014Source: Scopus},
	month = {2013},
	pages = {57 - 60},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84874801184\&partnerID=40\&md5=8b9ba9628bb3723adb3b77b3d3f2c922},
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}
@article {2973,
	title = {Impact of UGT1A1 gene variants on total bilirubin levels in Gilbert syndrome patients and in healthy subjects},
	journal = {Blood Cells, Molecules, and Diseases},
	volume = {48},
	year = {2012},
	note = {Cited By (since 1996): 2Export Date: 18 March 2013Source: Scopus},
	month = {2012///},
	pages = {166 - 172},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84857648817\&partnerID=40\&md5=a01b2773dc023e7acb417b80d7118b06},
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}
@article {2846,
	title = {Oxidized low-density lipoprotein and lipoprotein(a) levels in chronic kidney disease patients under hemodialysis: Influence of adiponectin and of a polymorphism in the apolipoprotein(a) gene},
	journal = {Hemodialysis International},
	volume = {16},
	year = {2012},
	note = {Export Date: 18 March 2013Source: Scopus},
	month = {2012///},
	pages = {481 - 490},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84867103661\&partnerID=40\&md5=61675c4a54bb2f44553bb6a7e435b24d},
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}
@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},
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}
@article {3138,
	title = {Novel ancestral Dysferlin splicing mutation which migrated from the Iberian peninsula to South America},
	journal = {Neuromuscular Disorders},
	volume = {21},
	year = {2011},
	note = {Cited By (since 1996): 1Export Date: 18 March 2013Source: Scopus},
	month = {2011///},
	pages = {328 - 337},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-79955480653\&partnerID=40\&md5=29da434ddc7e1a889d66c624a7c9b6f6},
	author = {Vernengo, L. and Oliveira, J. and Krahn, M. and Vieira, E. and Santos, R. and Carrasco, L. and Negr{\~a}o, L. and Panuncio, A. and Leturcq, F. and Labelle, V. and Bronze-da-Rocha, E. and Mesa, R. and Pizzarossa, C. and L{\'e}vy, N. and Rodriguez, M.-M.}
}
@article {3231,
	title = {Deep brain stimulation does not change neurovascular coupling in non-motor visual cortex: An autonomic and visual evoked blood flow velocity response study},
	journal = {Parkinsonism and Related Disorders},
	volume = {16},
	year = {2010},
	note = {Cited By (since 1996): 5Export Date: 18 March 2013Source: Scopus},
	month = {2010///},
	pages = {600 - 603},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-77958152153\&partnerID=40\&md5=bca2e564ec4797b62ddad756c38c8bfe},
	author = {Azevedo, E. and Santos, R. and Freitas, J. and Rosas, M.-J. and Gago, M. and Garrett, C. and Rosengarten, B.}
}
@article {3273,
	title = {Private dysferlin exon skipping mutation (c.5492G > A) with a founder effect reveals further alternative splicing involving exons 49-51},
	journal = {Journal of Human Genetics},
	volume = {55},
	year = {2010},
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	pages = {546 - 549},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-77957573173\&partnerID=40\&md5=56e960630ed13994451942d8518737d3},
	author = {Santos, R. and Oliveira, J. and Vieira, E. and Coelho, T. and Carneiro, A.L. and Evangelista, T. and Dias, C. and Fortuna, A. and Geraldo, A. and Negro, L. and Guimares, A. and Bronze-da-Rocha, E.}
}
@article {3577,
	title = {LAMA2 gene analysis in a cohort of 26 congenital muscular dystrophy patients},
	journal = {Clinical Genetics},
	volume = {74},
	year = {2008},
	note = {Cited By (since 1996): 9Export Date: 18 March 2013Source: Scopus},
	month = {2008///},
	pages = {502 - 512},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-56749104483\&partnerID=40\&md5=899cd1d17cace5ab35519345b1ef7913},
	author = {Oliveira, J. and Santos, R. and Soares-Silva, I. and Jorge, P. and Vieira, E. and Oliveira, M.E. and Moreira, A. and Coelho, T. and Ferreira, J.C. and Fonseca, M.J. and Barbosa, C. and Prats, I. and Ar{\'\i}ztegui, M.L. and Martins, M.L. and Moreno, T. and Heinimann, K. and Barbot, C. and Pascual-Pascual, S.I. and Cabral, A. and Fineza, I. and Santos, M. and Bronze-da-Rocha, E.}
}
