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713 related items for PubMed ID: 19616813
1. 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]
12. 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. PubMed ID: 19222544 [Abstract] [Full Text] [Related]
16. Absence of linkage to 8q23.3-q24.1 and 2p11.1-q12.2 in a new BAFME pedigree in China: indication of a third locus for BAFME. Deng FY, Gong J, Zhang YC, Wang K, Xiao SM, Li YN, Lei SF, Chen XD, Xiao B, Deng HW. Epilepsy Res; 2005 Jul; 65(3):147-52. PubMed ID: 16029945 [Abstract] [Full Text] [Related]
18. Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3. Hedera P, Blair MA, Andermann E, Andermann F, D'Agostino D, Taylor KA, Chahine L, Pandolfo M, Bradford Y, Haines JL, Abou-Khalil B. Neurology; 2007 Jun 12; 68(24):2107-12. PubMed ID: 17377072 [Abstract] [Full Text] [Related]
19. [A case of familial essential myoclonus and epilepsy with suspected focus in the hemisphere ipsilateral to myoclonus limbs]. Asai H, Udaka F, Oishi N, Kubori T, Kameyama M. No To Shinkei; 2004 Jun 12; 56(6):509-13. PubMed ID: 15328840 [Abstract] [Full Text] [Related]
20. Pattern-sensitive epilepsy: electroclinical characteristics, natural history, and delineation of the epileptic syndrome. Radhakrishnan K, St Louis EK, Johnson JA, McClelland RL, Westmoreland BF, Klass DW. Epilepsia; 2005 Jan 12; 46(1):48-58. PubMed ID: 15660768 [Abstract] [Full Text] [Related] Page: [Next] [New Search]