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Journal Abstract Search
203 related items for PubMed ID: 21426326
1. 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 [Abstract] [Full Text] [Related]
6. 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]
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]
14. 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]
15. Autosomal dominant cortical tremor, myoclonus and epilepsy: many syndromes, one phenotype. Striano P, Zara F, Striano S. Acta Neurol Scand; 2005 Apr 15; 111(4):211-7. PubMed ID: 15740570 [Abstract] [Full Text] [Related]
18. Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2. Stogmann E, Reinthaler E, Eltawil S, El Etribi MA, Hemeda M, El Nahhas N, Gaber AM, Fouad A, Edris S, Benet-Pages A, Eck SH, Pataraia E, Mei D, Brice A, Lesage S, Guerrini R, Zimprich F, Strom TM, Zimprich A. Brain; 2013 Apr 15; 136(Pt 4):1155-60. PubMed ID: 23518707 [Abstract] [Full Text] [Related]
19. Familial benign nonprogressive myoclonic epilepsies. Striano P, de Falco FA, Minetti C, Zara F. Epilepsia; 2009 May 15; 50 Suppl 5():37-40. PubMed ID: 19469844 [Abstract] [Full Text] [Related]