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Page 1
Linkage exclusion in Italian families with hereditary essential tremor.
Novelletto A, Gulli R, Ciotti P, Vitale C, Malaspina P, Blasi P, Pippucci T, Seri M, Cozzolino A, Bilo L, Abbruzzese G, Martinelli P, Bellone E, Barone P, Mandich P. Novelletto A, et al. Among authors: ciotti p. Eur J Neurol. 2011 Sep;18(9):e118-20. doi: 10.1111/j.1468-1331.2011.03458.x. Eur J Neurol. 2011. PMID: 21834898 No abstract available.
Contribution of copy number variations in CMT1X: a retrospective study.
Capponi S, Geroldi A, Pezzini I, Gulli R, Ciotti P, Ursino G, Lamp M, Reni L, Schenone A, Grandis M, Mandich P, Bellone E. Capponi S, et al. Among authors: ciotti p. Eur J Neurol. 2015 Feb;22(2):406-9. doi: 10.1111/ene.12434. Epub 2014 Apr 12. Eur J Neurol. 2015. PMID: 24724718
Enlarging the clinical spectrum associated with C9orf 72 repeat expansions: findings in an Italian cohort of patients with parkinsonian syndromes and relevance for genetic counselling.
Origone P, Verdiani S, Ciotti P, Gulli R, Bellone E, Marchese R, Abbruzzese G, Mandich P. Origone P, et al. Among authors: ciotti p. Amyotroph Lateral Scler Frontotemporal Degener. 2013 Sep;14(5-6):479-80. doi: 10.3109/21678421.2013.774020. Epub 2013 Mar 19. Amyotroph Lateral Scler Frontotemporal Degener. 2013. PMID: 23509957 No abstract available.
70 results