Aridon P - Search Results

1

No evidence of ATP1A2 involvement in 12 multiplex Italian families with benign familial infantile seizures.

Martinelli Boneschi F, Aridon P, Zara F, Guerrini R, Marini C, De Fusco M, Comi G, Casari G. Martinelli Boneschi F, et al. Among authors: aridon p. Neurosci Lett. 2005 Nov 11;388(2):71-4. doi: 10.1016/j.neulet.2005.06.026. Neurosci Lett. 2005. PMID: 16026932

2

Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2.

De Fusco M, Marconi R, Silvestri L, Atorino L, Rampoldi L, Morgante L, Ballabio A, Aridon P, Casari G. De Fusco M, et al. Among authors: aridon p. Nat Genet. 2003 Feb;33(2):192-6. doi: 10.1038/ng1081. Epub 2003 Jan 21. Nat Genet. 2003. PMID: 12539047

3

ATP1A2 mutations in 11 families with familial hemiplegic migraine.

Riant F, De Fusco M, Aridon P, Ducros A, Ploton C, Marchelli F, Maciazek J, Bousser MG, Casari G, Tournier-Lasserve E. Riant F, et al. Among authors: aridon p. Hum Mutat. 2005 Sep;26(3):281. doi: 10.1002/humu.9361. Hum Mutat. 2005. PMID: 16088919

4

Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families.

Striano P, Lispi ML, Gennaro E, Madia F, Traverso M, Bordo L, Aridon P, Martinelli Boneschi F, Barone B, dalla Bernardina B, Bianchi A, Capovilla G, De Marco P, Dulac O, Gaggero R, Gambardella A, Nabbout R, Prud'homme JF, Day R, Vanadia F, Vecchi M, Veggiotti P, Vigevano F, Viri M, Minetti C, Zara F. Striano P, et al. Among authors: aridon p. Epilepsia. 2006 Jun;47(6):1029-34. doi: 10.1111/j.1528-1167.2006.00521.x. Epilepsia. 2006. PMID: 16822249 Free article.

5

Increased sensitivity of the neuronal nicotinic receptor alpha 2 subunit causes familial epilepsy with nocturnal wandering and ictal fear.

Aridon P, Marini C, Di Resta C, Brilli E, De Fusco M, Politi F, Parrini E, Manfredi I, Pisano T, Pruna D, Curia G, Cianchetti C, Pasqualetti M, Becchetti A, Guerrini R, Casari G. Aridon P, et al. Am J Hum Genet. 2006 Aug;79(2):342-50. doi: 10.1086/506459. Epub 2006 Jun 26. Am J Hum Genet. 2006. PMID: 16826524 Free PMC article.

6

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

7

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

8

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

9

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

10

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.

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