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Items: 1 to 20 of 1238

1.

FAME 3: a novel form of progressive myoclonus and epilepsy.

Carr JA, van der Walt PE, Nakayama J, Fu YH, Corfield V, Brink P, Ptacek L.

Neurology. 2007 Apr 24;68(17):1382-9.

PMID:
17452583
2.

Absence of linkage to 8q24 in a European family with familial adult myoclonic epilepsy (FAME).

Labauge P, Amer LO, Simonetta-Moreau M, Attané F, Tannier C, Clanet M, Castelnovo G, An-Gourfinkel I, Agid Y, Brice A, Ducros A, LeGuern E.

Neurology. 2002 Mar 26;58(6):941-4.

PMID:
11914412
3.

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.

Brain. 2001 Dec;124(Pt 12):2459-75.

4.

Familial cortical myoclonic tremor with epilepsy (FCMTE): Clinical characteristics and exclusion of linkages to 8q and 2p in a large French family.

Magnin E, Vidailhet M, Depienne C, Saint-Martin C, Bouteiller D, LeGuern E, Apartis E, Rumbach L, Labauge P.

Rev Neurol (Paris). 2009 Oct;165(10):812-20. doi: 10.1016/j.neurol.2009.05.014. Epub 2009 Jul 18.

PMID:
19616813
5.

Genetic localization of the familial adult myoclonic epilepsy (FAME) gene to chromosome 8q24.

Plaster NM, Uyama E, Uchino M, Ikeda T, Flanigan KM, Kondo I, Ptácek LJ.

Neurology. 1999 Oct 12;53(6):1180-3.

PMID:
10522869
6.

Familial adult myoclonic epilepsy: recognition of mild phenotypes and refinement of the 2q locus.

Crompton DE, Sadleir LG, Bromhead CJ, Bahlo M, Bellows ST, Arsov T, Harty R, Lawrence KM, Dunne JW, Berkovic SF, Scheffer IE.

Arch Neurol. 2012 Apr;69(4):474-81. doi: 10.1001/archneurol.2011.584.

PMID:
22491192
7.

Familial benign myoclonus epilepsy of adult onset: a previously unrecognized myoclonic disorder.

Okino S.

J Neurol Sci. 1997 Jan;145(1):113-8. Erratum in: J Neurol Sci 1997 Nov 25;152(2):233.

PMID:
9073039
8.

Autosomal dominant early-onset cortical myoclonus, photic-induced myoclonus, and epilepsy in a large pedigree.

Gardella E, Tinuper P, Marini C, Guerrini R, Parrini E, Bisulli F, Liguori R, Montagna P, Lugaresi E.

Epilepsia. 2006 Oct;47(10):1643-9.

9.

Clinical, neuropsychological, neurophysiologic, and genetic features of a new Italian pedigree with familial cortical myoclonic tremor with epilepsy.

Suppa A, Berardelli A, Brancati F, Marianetti M, Barrano G, Mina C, Pizzuti A, Sideri G.

Epilepsia. 2009 May;50(5):1284-8. doi: 10.1111/j.1528-1167.2008.01976.x. Epub 2009 Feb 13.

10.

A novel pedigree with familial cortical myoclonic tremor and epilepsy (FCMTE): clinical characterization, refinement of the FCMTE2 locus, and confirmation of a founder haplotype.

Licchetta L, Pippucci T, Bisulli F, Cantalupo G, Magini P, Alvisi L, Baldassari S, Martinelli P, Naldi I, Vanni N, Liguori R, Seri M, Tinuper P.

Epilepsia. 2013 Jul;54(7):1298-306. doi: 10.1111/epi.12216. Epub 2013 May 11. Erratum in: Epilepsia. 2013 Sep;54(9):1709.

11.

Cortical tremor (FCMTE: familial cortical myoclonic tremor with epilepsy).

Regragui W, Gerdelat-Mas A, Simonetta-Moreau M.

Neurophysiol Clin. 2006 Sep-Dec;36(5-6):345-9. Epub 2007 Jan 19. Review.

PMID:
17336780
12.

Clinical and genetic analysis of a large pedigree with juvenile myoclonic epilepsy.

Serratosa JM, Delgado-Escueta AV, Medina MT, Zhang Q, Iranmanesh R, Sparkes RS.

Ann Neurol. 1996 Feb;39(2):187-95.

PMID:
8967750
13.

Familial adult myoclonic epilepsy (FAME).

Uyama E, Fu YH, Ptácek LJ.

Adv Neurol. 2005;95:281-8. Review. No abstract available.

PMID:
15508931
14.

Description of a family with a novel progressive myoclonus epilepsy and cognitive impairment.

Ferlazzo E, Italiano D, An I, Calarese T, Laguitton V, Bramanti P, Di Bella P, Genton P.

Mov Disord. 2009 May 15;24(7):1016-22. doi: 10.1002/mds.22489.

PMID:
19243074
15.

Familial cortical myoclonic tremor as a unique form of cortical reflex myoclonus.

Terada K, Ikeda A, Mima T, Kimura M, Nagahama Y, Kamioka Y, Murone I, Kimura J, Shibasaki H.

Mov Disord. 1997 May;12(3):370-7.

PMID:
9159732
16.

Clinical and neurophysiologic features of progressive myoclonus epilepsy without renal failure caused by SCARB2 mutations.

Rubboli G, Franceschetti S, Berkovic SF, Canafoglia L, Gambardella A, Dibbens LM, Riguzzi P, Campieri C, Magaudda A, Tassinari CA, Michelucci R.

Epilepsia. 2011 Dec;52(12):2356-63. doi: 10.1111/j.1528-1167.2011.03307.x. Epub 2011 Nov 2.

18.

Localization of a gene for benign adult familial myoclonic epilepsy to chromosome 8q23.3-q24.1.

Mikami M, Yasuda T, Terao A, Nakamura M, Ueno S, Tanabe H, Tanaka T, Onuma T, Goto Y, Kaneko S, Sano A.

Am J Hum Genet. 1999 Sep;65(3):745-51.

19.

[Familial progressive myoclonus epilepsy (Unverricht/Lundborg)].

Herbst A.

Psychiatr Neurol Med Psychol Beih. 1967;6:18-39. German. No abstract available.

PMID:
5006319
20.

Juvenile myoclonic epilepsy locus in chromosome 6p21.2-p11: linkage to convulsions and electroencephalography trait.

Liu AW, Delgado-Escueta AV, Serratosa JM, Alonso ME, Medina MT, Gee MN, Cordova S, Zhao HZ, Spellman JM, Peek JR, et al.

Am J Hum Genet. 1995 Aug;57(2):368-81.

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