Aridon P - Search Results

1

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.

2

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

3

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

4

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

5

Linkage mapping of a nonspecific form of X-linked mental retardation (MRX53) in a large Pakistani family.

Ahmad W, Noci S, Faiyaz ul Haque M, Sarno T, Aridon P, Ahmad MM, Amin-Ud-Din M, Rafiq MA, ul Haque S, De Fusco M, Ballabio A, Franco B, Casari G. Ahmad W, et al. Among authors: aridon p. Am J Med Genet. 2001 Apr 15;100(1):62-5. doi: 10.1002/1096-8628(20010415)100:1<62::aid-ajmg1190>3.0.co;2-h. Am J Med Genet. 2001. PMID: 11337751

6

Autosomal dominant cortical myoclonus and epilepsy (ADCME) with complex partial and generalized seizures: A newly recognized epilepsy syndrome with linkage to chromosome 2p11.1-q12.2.

Guerrini R, Bonanni P, Patrignani A, Brown P, Parmeggiani L, Grosse P, Brovedani P, Moro F, Aridon P, Carrozzo R, Casari G. Guerrini R, et al. Among authors: aridon p. Brain. 2001 Dec;124(Pt 12):2459-75. doi: 10.1093/brain/124.12.2459. Brain. 2001. PMID: 11701600

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. 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

Elusive amines and cluster headache: mutational analysis of trace amine receptor cluster on chromosome 6q23.

Aridon P, D'Andrea G, Rigamonti A, Leone M, Casari G, Bussone G. Aridon P, et al. Neurol Sci. 2004 Oct;25 Suppl 3:S279-80. doi: 10.1007/s10072-004-0309-1. Neurol Sci. 2004. PMID: 15549560

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: 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.

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

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