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Partial lipodystrophy associated with muscular dystrophy of unknown genetic origin.
Carboni N, Brancati F, Cocco E, Solla E, D'Apice MR, Mateddu A, McIntyre A, Fadda E, Mura M, Lattanzi G, Piras R, Maioli MA, Marrosu G, Novelli G, Marrosu MG, Hegele RA. Carboni N, et al. Among authors: piras r. Muscle Nerve. 2014 Jun;49(6):928-30. doi: 10.1002/mus.24157. Muscle Nerve. 2014. PMID: 24375490 No abstract available.
Influence of treatments in multiple sclerosis disability: a cohort study.
Cocco E, Sardu C, Spinicci G, Musu L, Massa R, Frau J, Lorefice L, Fenu G, Coghe G, Massole S, Maioli MA, Piras R, Melis M, Porcu G, Mamusa E, Carboni N, Contu P, Marrosu MG. Cocco E, et al. Among authors: piras r. Mult Scler. 2015 Apr;21(4):433-41. doi: 10.1177/1352458514546788. Epub 2014 Sep 25. Mult Scler. 2015. PMID: 25257611
The cohort of the multiple sclerosis center of Cagliari.
Marrosu MG, Lorefice L, Frau J, Coghe G, Fenu G, Piras R, Melis M, Cocco E. Marrosu MG, et al. Among authors: piras r. Neurol Sci. 2011 Jan;31 Suppl 3:309-12. doi: 10.1007/s10072-010-0470-7. Neurol Sci. 2011. PMID: 21267619
Large genotype-phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosis.
Ricci G, Mele F, Govi M, Ruggiero L, Sera F, Vercelli L, Bettio C, Santoro L, Mongini T, Villa L, Moggio M, Filosto M, Scarlato M, Previtali SC, Tripodi SM, Pegoraro E, Telese R, Di Muzio A, Rodolico C, Bucci E, Antonini G, D'Angelo MG, Berardinelli A, Maggi L, Piras R, Maioli MA, Siciliano G, Tomelleri G, Angelini C, Tupler R. Ricci G, et al. Among authors: piras r. Sci Rep. 2020 Dec 10;10(1):21648. doi: 10.1038/s41598-020-78578-7. Sci Rep. 2020. PMID: 33303865 Free PMC article.
128 results