Casari G - Search Results

1

Restless legs syndrome: epidemiological and clinicogenetic study in a South Tyrolean population isolate.

Vogl FD, Pichler I, Adel S, Pinggera GK, Bracco S, De Grandi A, Volpato CB, Aridon P, Mayer T, Meitinger T, Klein C, Casari G, Pramstaller PP. Vogl FD, et al. Among authors: casari g. Mov Disord. 2006 Aug;21(8):1189-95. doi: 10.1002/mds.20922. Mov Disord. 2006. PMID: 16685686

2

Linkage analysis identifies a novel locus for restless legs syndrome on chromosome 2q in a South Tyrolean population isolate.

Pichler I, Marroni F, Volpato CB, Gusella JF, Klein C, Casari G, De Grandi A, Pramstaller PP. Pichler I, et al. Among authors: casari g. Am J Hum Genet. 2006 Oct;79(4):716-23. doi: 10.1086/507875. Epub 2006 Aug 14. Am J Hum Genet. 2006. PMID: 16960808 Free PMC article.

3

Autosomal dominant restless legs syndrome maps on chromosome 14q.

Bonati MT, Ferini-Strambi L, Aridon P, Oldani A, Zucconi M, Casari G. Bonati MT, et al. Among authors: casari g. Brain. 2003 Jun;126(Pt 6):1485-92. doi: 10.1093/brain/awg137. Brain. 2003. PMID: 12764067

4

Genetics in restless legs syndrome.

Ferini-Strambi L, Bonati MT, Oldani A, Aridon P, Zucconi M, Casari G. Ferini-Strambi L, et al. Among authors: casari g. Sleep Med. 2004 May;5(3):301-4. doi: 10.1016/j.sleep.2004.01.005. Sleep Med. 2004. PMID: 15165539 Review.

5

ParkScreen: a low-cost rapid linkage marker panel for Parkinson's disease.

De Grandi A, Volpato CB, Bedin E, Pattaro C, Marroni F, Pichler I, Hicks AA, Casari G, Pramstaller PP. De Grandi A, et al. Among authors: casari g. J Mol Neurosci. 2009 Sep;39(1-2):235-41. doi: 10.1007/s12031-009-9193-8. Epub 2009 Mar 25. J Mol Neurosci. 2009. PMID: 19319700

6

A TRAPPC6B splicing variant associates to restless legs syndrome.

Aridon P, De Fusco M, Winkelmann JW, Zucconi M, Arnao V, Ferini-Strambi L, Casari G. Aridon P, et al. Among authors: casari g. Parkinsonism Relat Disord. 2016 Oct;31:135-138. doi: 10.1016/j.parkreldis.2016.08.016. Epub 2016 Aug 18. Parkinsonism Relat Disord. 2016. PMID: 27569842

7

Further evidence of genetic heterogeneity in familial essential tremor.

Aridon P, Ragonese P, De Fusco M, Salemi G, Casari G, Savettieri G. Aridon P, et al. Among authors: casari g. Parkinsonism Relat Disord. 2008;14(1):15-8. doi: 10.1016/j.parkreldis.2007.05.002. Epub 2007 Aug 20. Parkinsonism Relat Disord. 2008. PMID: 17703985

8

Importance of different types of prior knowledge in selecting genome-wide findings for follow-up.

Minelli C, De Grandi A, Weichenberger CX, Gögele M, Modenese M, Attia J, Barrett JH, Boehnke M, Borsani G, Casari G, Fox CS, Freina T, Hicks AA, Marroni F, Parmigiani G, Pastore A, Pattaro C, Pfeufer A, Ruggeri F, Schwienbacher C, Taliun D, Pramstaller PP, Domingues FS, Thompson JR. Minelli C, et al. Among authors: casari g. Genet Epidemiol. 2013 Feb;37(2):205-13. doi: 10.1002/gepi.21705. Genet Epidemiol. 2013. PMID: 23307621 Free PMC article.

9

Identification of a new locus for medullary cystic disease, on chromosome 16p12.

Scolari F, Puzzer D, Amoroso A, Caridi G, Ghiggeri GM, Maiorca R, Aridon P, De Fusco M, Ballabio A, Casari G. Scolari F, et al. Among authors: casari g. Am J Hum Genet. 1999 Jun;64(6):1655-60. doi: 10.1086/302414. Am J Hum Genet. 1999. PMID: 10330352 Free PMC article.

10

Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23.

Marconi R, De Fusco M, Aridon P, Plewnia K, Rossi M, Carapelli S, Ballabio A, Morgante L, Musolino R, Epifanio A, Micieli G, De Michele G, Casari G. Marconi R, et al. Among authors: casari g. Ann Neurol. 2003 Mar;53(3):376-81. doi: 10.1002/ana.10464. Ann Neurol. 2003. PMID: 12601705

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