Racis L - Search Results

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Large deletion mutation of SPAST in a multi-generation family from Sardinia.

Racis L, Di Fabio R, Tessa A, Guillot F, Storti E, Piccolo F, Nesti C, Tedde A, Pierelli F, Agnetti V, Santorelli FM, Casali C. Racis L, et al. Eur J Neurol. 2014 Jun;21(6):935-8. doi: 10.1111/ene.12290. Epub 2013 Nov 4. Eur J Neurol. 2014. PMID: 24824741

The high prevalence of hereditary spastic paraplegia in Sardinia, insular Italy.

Racis L, Tessa A, Di Fabio R, Storti E, Agnetti V, Casali C, Santorelli FM, Pugliatti M. Racis L, et al. J Neurol. 2014 Jan;261(1):52-9. doi: 10.1007/s00415-013-7151-4. Epub 2013 Oct 20. J Neurol. 2014. PMID: 24141732

Infantile-onset ascending hereditary spastic paralysis: a case report and brief literature review.

Racis L, Tessa A, Pugliatti M, Storti E, Agnetti V, Santorelli FM. Racis L, et al. Eur J Paediatr Neurol. 2014 Mar;18(2):235-9. doi: 10.1016/j.ejpn.2013.09.009. Epub 2013 Oct 9. Eur J Paediatr Neurol. 2014. PMID: 24144828 Review.

Novel SPAST deletion and reduced DPY30 expression in a Spastic Paraplegia type 4 kindred.

Racis L, Storti E, Pugliatti M, Agnetti V, Tessa A, Santorelli FM. Racis L, et al. BMC Med Genet. 2014 Apr 1;15:39. doi: 10.1186/1471-2350-15-39. BMC Med Genet. 2014. PMID: 24690193 Free PMC article.

Bridging Over the Troubled Heterogeneity of SPG-Related Pathologies: Mechanisms Unite What Genetics Divide.

Tessa A, Denora PS, Racis L, Storti E, Orlacchio A, Santorelli FM. Tessa A, et al. Among authors: racis l. Curr Mol Med. 2014;14(8):1034-1042. doi: 10.2174/1566524014666141010154526. Curr Mol Med. 2014. PMID: 25323869

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