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470 related items for PubMed ID: 15747356
1. 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 [Abstract] [Full Text] [Related]
2. Cortical tremor (FCMTE: familial cortical myoclonic tremor with epilepsy). Regragui W, Gerdelat-Mas A, Simonetta-Moreau M. Neurophysiol Clin; 2006 Jun; 36(5-6):345-9. PubMed ID: 17336780 [Abstract] [Full Text] [Related]
3. 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 [Abstract] [Full Text] [Related]
4. Familial benign nonprogressive myoclonic epilepsies. Striano P, de Falco FA, Minetti C, Zara F. Epilepsia; 2009 May; 50 Suppl 5():37-40. PubMed ID: 19469844 [Abstract] [Full Text] [Related]
5. 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. PubMed ID: 17452583 [Abstract] [Full Text] [Related]
7. 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 24; 54(7):1298-306. PubMed ID: 23663087 [Abstract] [Full Text] [Related]
8. Familial cortical myoclonic tremor with epilepsy: the third locus (FCMTE3) maps to 5p. Depienne C, Magnin E, Bouteiller D, Stevanin G, Saint-Martin C, Vidailhet M, Apartis E, Hirsch E, LeGuern E, Labauge P, Rumbach L. Neurology; 2010 Jun 15; 74(24):2000-3. PubMed ID: 20548044 [Abstract] [Full Text] [Related]
9. 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 15; 12(3):370-7. PubMed ID: 9159732 [Abstract] [Full Text] [Related]
10. 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 15; 69(4):474-81. PubMed ID: 22491192 [Abstract] [Full Text] [Related]
11. 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 15; 50(5):1284-8. PubMed ID: 19222544 [Abstract] [Full Text] [Related]
12. 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 15; 52(7):1245-50. PubMed ID: 21426326 [Abstract] [Full Text] [Related]
13. [Myoclonus and myoclonic epilepsies in childhood]. Nieto-Barrera M. Rev Neurol; 2011 Jul 15; 28(3):278-84. PubMed ID: 10714297 [Abstract] [Full Text] [Related]
14. 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 15; 38():35-40. PubMed ID: 28237853 [Abstract] [Full Text] [Related]
15. Clinical anticipation in Japanese families of benign adult familial myoclonus epilepsy. Hitomi T, Kondo T, Kobayashi K, Matsumoto R, Takahashi R, Ikeda A. Epilepsia; 2012 Feb 15; 53(2):e33-6. PubMed ID: 22150818 [Abstract] [Full Text] [Related]
16. Autosomal dominant cortical tremor, myoclonus, and epilepsy (ADCME) in a unique south Indian community. Mahadevan R, Viswanathan N, Shanmugam G, Sankaralingam S, Essaki B, Chelladurai RP. Epilepsia; 2016 Mar 15; 57(3):e56-9. PubMed ID: 26749494 [Abstract] [Full Text] [Related]
17. 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 15; 47(10):1643-9. PubMed ID: 17054686 [Abstract] [Full Text] [Related]
18. 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 15; 31(11):1704-1710. PubMed ID: 27613677 [Abstract] [Full Text] [Related]
19. 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 15; 249(7):829-34. PubMed ID: 12140665 [Abstract] [Full Text] [Related]
20. [Myoclonic epilepsies in infancy]. Palencia R. Rev Neurol; 2000 Jun 15; 30 Suppl 1():S15-24. PubMed ID: 10904965 [Abstract] [Full Text] [Related] Page: [Next] [New Search]