These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
8. 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. PubMed ID: 19616813 [TBL] [Abstract][Full Text] [Related]
9. 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. PubMed ID: 22491192 [TBL] [Abstract][Full Text] [Related]
10. Focal subcortical reflex myoclonus. A clinical and neurophysiological study. Cantello R; Gianelli M; Civardi C; Mutani R Arch Neurol; 1997 Feb; 54(2):187-96. PubMed ID: 9041860 [TBL] [Abstract][Full Text] [Related]
11. Familial cortical tremor with epilepsy: an under-recognized familial tremor. Okuma Y; Shimo Y; Shimura H; Hatori K; Hattori T; Tanaka S; Kondo T; Mizuno Y Clin Neurol Neurosurg; 1998 Mar; 100(1):75-8. PubMed ID: 9637212 [TBL] [Abstract][Full Text] [Related]
12. 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. PubMed ID: 23663087 [TBL] [Abstract][Full Text] [Related]
13. Clinical and neurophysiological features of familial cortical myoclonic tremor with epilepsy. Cen Z; Huang C; Yin H; Ding X; Xie F; Lu X; Ouyang Z; Lou Y; Qiu X; Wang Z; Xiao J; Ding M; Luo W Mov Disord; 2016 Nov; 31(11):1704-1710. PubMed ID: 27613677 [TBL] [Abstract][Full Text] [Related]
14. Familial paroxysmal exercise-induced dyskinesia, epilepsy, and mental retardation in a family with autosomal dominant inheritance. Perniola T; Margari L; de Iaco MG; Presicci A; Ventura P; Ferrannini E; Illiceto G Mov Disord; 2001 Jul; 16(4):724-30. PubMed ID: 11481699 [TBL] [Abstract][Full Text] [Related]
17. Natural history and long-term evolution in families with autosomal dominant cortical tremor, myoclonus, and epilepsy. Coppola A; Santulli L; Del Gaudio L; Minetti C; Striano S; Zara F; Striano P Epilepsia; 2011 Jul; 52(7):1245-50. PubMed ID: 21426326 [TBL] [Abstract][Full Text] [Related]
18. Familial cortical myoclonic tremor with epilepsy: a single syndromic classification for a group of pedigrees bearing common features. van Rootselaar AF; van Schaik IN; van den Maagdenberg AM; Koelman JH; Callenbach PM; Tijssen MA Mov Disord; 2005 Jun; 20(6):665-73. PubMed ID: 15747356 [TBL] [Abstract][Full Text] [Related]
19. Familial cortical myoclonic tremor and epilepsy: Description of a new South African pedigree with 30 year follow up. van Coller R; van Rootselaar AF; Schutte C; van der Meyden CH Parkinsonism Relat Disord; 2017 May; 38():35-40. PubMed ID: 28237853 [TBL] [Abstract][Full Text] [Related]
20. A Dutch family with 'familial cortical tremor with epilepsy'. Clinical characteristics and exclusion of linkage to chromosome 8q23.3-q24.1. van Rootselaar F; Callenbach PM; Hottenga JJ; Vermeulen FL; Speelman HD; Brouwer OF; Tijssen MA J Neurol; 2002 Jul; 249(7):829-34. PubMed ID: 12140665 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]