Casali C - Search Results

1

Spastin recovery in hereditary spastic paraplegia by preventing neddylation-dependent degradation.

Sardina F, Pisciottani A, Ferrara M, Valente D, Casella M, Crescenzi M, Peschiaroli A, Casali C, Soddu S, Grierson AJ, Rinaldo C. Sardina F, et al. Among authors: casali c. Life Sci Alliance. 2020 Oct 26;3(12):e202000799. doi: 10.26508/lsa.202000799. Print 2020 Dec. Life Sci Alliance. 2020. PMID: 33106322 Free PMC article.

2

'When atlastin meets spastin'.

Di Fabio R, Tessa A, Marcotulli C, Leonardi L, Pierelli F, Santorelli FM, Casali C. Di Fabio R, et al. Among authors: casali c. Clin Genet. 2014 Nov;86(5):504-5. doi: 10.1111/cge.12331. Epub 2014 Jan 13. Clin Genet. 2014. PMID: 24417445 No abstract available.

3

Autosomal dominant hereditary spastic paraplegia: DHPLC-based mutation analysis of SPG4 reveals eleven novel mutations.

Patrono C, Scarano V, Cricchi F, Melone MA, Chiriaco M, Napolitano A, Malandrini A, De Michele G, Petrozzi L, Giraldi C, Santoro L, Servidei S, Casali C, Filla A, Santorelli FM. Patrono C, et al. Among authors: casali c. Hum Mutat. 2005 May;25(5):506. doi: 10.1002/humu.9340. Hum Mutat. 2005. PMID: 15841487

4

Missense and splice site mutations in SPG4 suggest loss-of-function in dominant spastic paraplegia.

Patrono C, Casali C, Tessa A, Cricchi F, Fortini D, Carrozzo R, Siciliano G, Bertini E, Santorelli FM. Patrono C, et al. Among authors: casali c. J Neurol. 2002 Feb;249(2):200-5. doi: 10.1007/pl00007865. J Neurol. 2002. PMID: 11985387

5

Intrafamilial variability in hereditary spastic paraplegia associated with an SPG4 gene mutation.

Santorelli FM, Patrono C, Fortini D, Tessa A, Comanducci G, Bertini E, Pierallini A, Amabile GA, Casali C. Santorelli FM, et al. Among authors: casali c. Neurology. 2000 Sep 12;55(5):702-5. doi: 10.1212/wnl.55.5.702. Neurology. 2000. PMID: 10980739

6

Differential changes in the spinal segmental locomotor output in Hereditary Spastic Paraplegia.

Martino G, Ivanenko Y, Serrao M, Ranavolo A, Draicchio F, Rinaldi M, Casali C, Lacquaniti F. Martino G, et al. Among authors: casali c. Clin Neurophysiol. 2018 Mar;129(3):516-525. doi: 10.1016/j.clinph.2017.11.028. Epub 2017 Dec 23. Clin Neurophysiol. 2018. PMID: 29353180

7

Locomotor coordination in patients with Hereditary Spastic Paraplegia.

Martino G, Ivanenko Y, Serrao M, Ranavolo A, Draicchio F, Casali C, Lacquaniti F. Martino G, et al. Among authors: casali c. J Electromyogr Kinesiol. 2019 Apr;45:61-69. doi: 10.1016/j.jelekin.2019.02.006. Epub 2019 Feb 19. J Electromyogr Kinesiol. 2019. PMID: 30836301

8

Hereditary Spastic Paraplegia: Beyond Clinical Phenotypes toward a Unified Pattern of Central Nervous System Damage.

Agosta F, Scarlato M, Spinelli EG, Canu E, Benedetti S, Bassi MT, Casali C, Sessa M, Copetti M, Pagani E, Comi G, Ferrari M, Falini A, Filippi M. Agosta F, et al. Among authors: casali c. Radiology. 2015 Jul;276(1):207-18. doi: 10.1148/radiol.14141715. Epub 2015 Jan 22. Radiology. 2015. PMID: 25611737

9

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. Among authors: casali c. J Neurol. 2014 Jan;261(1):52-9. doi: 10.1007/s00415-013-7151-4. Epub 2013 Oct 20. J Neurol. 2014. PMID: 24141732

10

Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum.

Casali C, Valente EM, Bertini E, Montagna G, Criscuolo C, De Michele G, Villanova M, Damiano M, Pierallini A, Brancati F, Scarano V, Tessa A, Cricchi F, Grieco GS, Muglia M, Carella M, Martini B, Rossi A, Amabile GA, Nappi G, Filla A, Dallapiccola B, Santorelli FM. Casali C, et al. Neurology. 2004 Jan 27;62(2):262-8. doi: 10.1212/wnl.62.2.262. Neurology. 2004. PMID: 14745065

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