BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

714 related articles for article (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
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 74(24):2000-3. PubMed ID: 20548044
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cortical tremor (FCMTE: familial cortical myoclonic tremor with epilepsy).
    Regragui W; Gerdelat-Mas A; Simonetta-Moreau M
    Neurophysiol Clin; 2006; 36(5-6):345-9. PubMed ID: 17336780
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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. PubMed ID: 17054686
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 58(6):941-4. PubMed ID: 11914412
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 68(17):1382-9. PubMed ID: 17452583
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 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. 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. PubMed ID: 11701600
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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. PubMed ID: 9159732
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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. PubMed ID: 8967750
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Oculomotor abnormalities in myoclonic tremor: a comparison with spinocerebellar ataxia type 6.
    Bour LJ; van Rootselaar AF; Koelman JH; Tijssen MA
    Brain; 2008 Sep; 131(Pt 9):2295-303. PubMed ID: 18687731
    [TBL] [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
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Myoclonic occipital photosensitive epilepsy with dystonia (MOPED): A familial epilepsy syndrome.
    Sadleir LG; Paterson S; Smith KR; Redshaw N; Ranta A; Kalnins R; Berkovic SF; Bahlo M; Hildebrand MS; Scheffer IE
    Epilepsy Res; 2015 Aug; 114():98-105. PubMed ID: 26088892
    [TBL] [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; 68(24):2107-12. PubMed ID: 17377072
    [TBL] [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; 56(6):509-13. PubMed ID: 15328840
    [TBL] [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; 46(1):48-58. PubMed ID: 15660768
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 36.