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Contribution of ATXN2 intermediary polyQ expansions in a spectrum of neurodegenerative disorders.
Neurology. 2014 Sep 9;83(11):990-5. doi: 10.1212/WNL.0000000000000778. Epub 2014 Aug 6.
Neurology. 2014.
PMID: 25098532
Free PMC article.
Novel UBQLN2 mutations linked to amyotrophic lateral sclerosis and atypical hereditary spastic paraplegia phenotype through defective HSP70-mediated proteolysis.
Teyssou E, Chartier L, Amador MD, Lam R, Lautrette G, Nicol M, Machat S, Da Barroca S, Moigneu C, Mairey M, Larmonier T, Saker S, Dussert C, Forlani S, Fontaine B, Seilhean D, Bohl D, Boillée S, Meininger V, Couratier P, Salachas F, Stevanin G, Millecamps S.
Teyssou E, et al. Among authors: da barroca s.
Neurobiol Aging. 2017 Oct;58:239.e11-239.e20. doi: 10.1016/j.neurobiolaging.2017.06.018. Epub 2017 Jun 24.
Neurobiol Aging. 2017.
PMID: 28716533
Free article.
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Questioning on the role of D amino acid oxidase in familial amyotrophic lateral sclerosis.
Millecamps S, Da Barroca S, Cazeneuve C, Salachas F, Pradat PF, Danel-Brunaud V, Vandenberghe N, Lacomblez L, Le Forestier N, Bruneteau G, Camu W, Brice A, Meininger V, LeGuern E.
Millecamps S, et al. Among authors: da barroca s.
Proc Natl Acad Sci U S A. 2010 Jun 29;107(26):E107; author reply E108. doi: 10.1073/pnas.1006190107. Epub 2010 Jun 10.
Proc Natl Acad Sci U S A. 2010.
PMID: 20538972
Free PMC article.
No abstract available.
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Aggregation of Engineered Human β-Cells Into Pseudoislets: Insulin Secretion and Gene Expression Profile in Normoxic and Hypoxic Milieu.
Lecomte MJ, Pechberty S, Machado C, Da Barroca S, Ravassard P, Scharfmann R, Czernichow P, Duvillié B.
Lecomte MJ, et al. Among authors: da barroca s.
Cell Med. 2016 Aug 12;8(3):99-112. doi: 10.3727/215517916X692843. eCollection 2016 Dec 3.
Cell Med. 2016.
PMID: 28003935
Free PMC article.
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