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Page 1
Complex phenotype in an Italian family with a novel mutation in SPG3A.
de Leva MF, Filla A, Criscuolo C, Tessa A, Pappatà S, Quarantelli M, Bilo L, Peluso S, Antenora A, Longo D, Santorelli FM, De Michele G. de Leva MF, et al. Among authors: antenora a. J Neurol. 2010 Mar;257(3):328-31. doi: 10.1007/s00415-009-5311-3. Epub 2009 Sep 19. J Neurol. 2010. PMID: 19768483
Antiphospholipid-related chorea.
Peluso S, Antenora A, De Rosa A, Roca A, Maddaluno G, Brescia Morra V, De Michele G. Peluso S, et al. Among authors: antenora a. Front Neurol. 2012 Oct 22;3:150. doi: 10.3389/fneur.2012.00150. eCollection 2012. Front Neurol. 2012. PMID: 23097646 Free PMC article.
Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data.
Jacobi H, Reetz K, du Montcel ST, Bauer P, Mariotti C, Nanetti L, Rakowicz M, Sulek A, Durr A, Charles P, Filla A, Antenora A, Schöls L, Schicks J, Infante J, Kang JS, Timmann D, Di Fabio R, Masciullo M, Baliko L, Melegh B, Boesch S, Bürk K, Peltz A, Schulz JB, Dufaure-Garé I, Klockgether T. Jacobi H, et al. Among authors: antenora a. Lancet Neurol. 2013 Jul;12(7):650-8. doi: 10.1016/S1474-4422(13)70104-2. Epub 2013 May 22. Lancet Neurol. 2013. PMID: 23707147
Parkinsonism may be part of the symptom complex of DOOR syndrome.
Bilo L, Peluso S, Antenora A, De Rosa A, Auletta G, Pappatà S, De Michele G. Bilo L, et al. Among authors: antenora a. Parkinsonism Relat Disord. 2014 Apr;20(4):463-5. doi: 10.1016/j.parkreldis.2014.01.014. Epub 2014 Jan 23. Parkinsonism Relat Disord. 2014. PMID: 24486243 No abstract available.
Metabolic Ataxias in Adults.
Antenora A, Filla A, Santorelli FM, Peluso S, Sacca F, De Michele G. Antenora A, et al. Curr Mol Med. 2014;14(8):959-970. doi: 10.2174/1566524014666141010131213. Curr Mol Med. 2014. PMID: 25323876
42 results