Aridon P - 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: aridon p. Mov Disord. 2006 Aug;21(8):1189-95. doi: 10.1002/mds.20922. Mov Disord. 2006. PMID: 16685686

2

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: aridon p. Brain. 2003 Jun;126(Pt 6):1485-92. doi: 10.1093/brain/awg137. Brain. 2003. PMID: 12764067

3

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: aridon p. Sleep Med. 2004 May;5(3):301-4. doi: 10.1016/j.sleep.2004.01.005. Sleep Med. 2004. PMID: 15165539 Review.

4

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. 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

5

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. 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

6

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: aridon p. Am J Hum Genet. 1999 Jun;64(6):1655-60. doi: 10.1086/302414. Am J Hum Genet. 1999. PMID: 10330352 Free PMC article.

7

Autosomal recessive rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: delineation of the syndrome and gene mapping to chromosome 16p12-11.2.

Guerrini R, Bonanni P, Nardocci N, Parmeggiani L, Piccirilli M, De Fusco M, Aridon P, Ballabio A, Carrozzo R, Casari G. Guerrini R, et al. Among authors: aridon p. Ann Neurol. 1999 Mar;45(3):344-52. doi: 10.1002/1531-8249(199903)45:3<344::aid-ana10>3.0.co;2-9. Ann Neurol. 1999. PMID: 10072049

8

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: aridon p. Ann Neurol. 2003 Mar;53(3):376-81. doi: 10.1002/ana.10464. Ann Neurol. 2003. PMID: 12601705

9

Autosomal dominant hereditary spastic paraplegia: report of a large Italian family with R581X spastin mutation.

Aridon P, Ragonese P, De Fusco M, Lo Coco D, Salemi G, Casari G, Savettieri G. Aridon P, et al. Neurol Sci. 2007 Aug;28(4):171-4. doi: 10.1007/s10072-007-0815-z. Epub 2007 Aug 10. Neurol Sci. 2007. PMID: 17690846

10

Linkage mapping of a new syndromic form of X-linked mental retardation, MRXS7, associated with obesity.

Ahmad W, De Fusco M, Faiyaz ul Haque M, Aridon P, Sarno T, Sohail M, ul Haque S, Ahmad M, Ballabio A, Franco B, Casari G. Ahmad W, et al. Among authors: aridon p. Eur J Hum Genet. 1999 Oct-Nov;7(7):828-32. doi: 10.1038/sj.ejhg.5200376. Eur J Hum Genet. 1999. PMID: 10573017

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

78 results

Search Page