BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

183 related articles for article (PubMed ID: 21850007)

  • 1. Remapping and mutation analysis of benign adult familial myoclonic epilepsy in a Japanese pedigree.
    Mori S; Nakamura M; Yasuda T; Ueno S; Kaneko S; Sano A
    J Hum Genet; 2011 Oct; 56(10):742-7. PubMed ID: 21850007
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. A newly identified locus for benign adult familial myoclonic epilepsy on chromosome 3q26.32-3q28.
    Yeetong P; Ausavarat S; Bhidayasiri R; Piravej K; Pasutharnchat N; Desudchit T; Chunharas C; Loplumlert J; Limotai C; Suphapeetiporn K; Shotelersuk V
    Eur J Hum Genet; 2013 Feb; 21(2):225-8. PubMed ID: 22713812
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Localization of a gene for benign adult familial myoclonic epilepsy to chromosome 8q23.3-q24.1.
    Mikami M; Yasuda T; Terao A; Nakamura M; Ueno S; Tanabe H; Tanaka T; Onuma T; Goto Y; Kaneko S; Sano A
    Am J Hum Genet; 1999 Sep; 65(3):745-51. PubMed ID: 10441581
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fine mapping and whole-exome sequencing of a familial cortical myoclonic tremor with epilepsy family.
    Cen ZD; Xie F; Lou DN; Lu XJ; Ouyang ZY; Liu L; Cao J; Li D; Yin HM; Wang ZJ; Xiao JF; Luo W
    Am J Med Genet B Neuropsychiatr Genet; 2015 Oct; 168(7):595-9. PubMed ID: 26130016
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. A Chinese benign adult familial myoclonic epilepsy pedigree suggesting linkage to chromosome 5p15.31-p15.1.
    Li J; Hu X; Chen Q; Zhang Y; Zhang Y; Hu G
    Cell Biochem Biophys; 2014 Jul; 69(3):627-31. PubMed ID: 24549855
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Intronic pentanucleotide TTTCA repeat insertion in the SAMD12 gene causes familial cortical myoclonic tremor with epilepsy type 1.
    Cen Z; Jiang Z; Chen Y; Zheng X; Xie F; Yang X; Lu X; Ouyang Z; Wu H; Chen S; Yin H; Qiu X; Wang S; Ding M; Tang Y; Yu F; Li C; Wang T; Ishiura H; Tsuji S; Jiao C; Liu C; Xiao J; Luo W
    Brain; 2018 Aug; 141(8):2280-2288. PubMed ID: 29939203
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Benign adult familial myoclonic epilepsy (BAFME): evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian families.
    Madia F; Striano P; Di Bonaventura C; de Falco A; de Falco FA; Manfredi M; Casari G; Striano S; Minetti C; Zara F
    Neurogenetics; 2008 May; 9(2):139-42. PubMed ID: 18231815
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. A new benign adult familial myoclonic epilepsy (BAFME) pedigree suggesting linkage to chromosome 2p11.1-q12.2.
    Striano P; Chifari R; Striano S; de Fusco M; Elia M; Guerrini R; Casari G; Canevini MP
    Epilepsia; 2004 Feb; 45(2):190-2. PubMed ID: 14738428
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Autosomal dominant cortical tremor, myoclonus and epilepsy: many syndromes, one phenotype.
    Striano P; Zara F; Striano S
    Acta Neurol Scand; 2005 Apr; 111(4):211-7. PubMed ID: 15740570
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Positional candidate approach for the gene responsible for benign adult familial myoclonic epilepsy.
    Sano A; Mikami M; Nakamura M; Ueno S; Tanabe H; Kaneko S
    Epilepsia; 2002; 43 Suppl 9():26-31. PubMed ID: 12383276
    [TBL] [Abstract][Full Text] [Related]  

  • 15. History of familial adult myoclonus epilepsy/benign adult familial myoclonic epilepsy around the world.
    Berkovic SF; Striano P; Tsuji S
    Epilepsia; 2023 Jun; 64 Suppl 1(Suppl 1):S3-S8. PubMed ID: 36707971
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic localization of the familial adult myoclonic epilepsy (FAME) gene to chromosome 8q24.
    Plaster NM; Uyama E; Uchino M; Ikeda T; Flanigan KM; Kondo I; Ptácek LJ
    Neurology; 1999 Oct; 53(6):1180-3. PubMed ID: 10522869
    [TBL] [Abstract][Full Text] [Related]  

  • 17. DNA analysis of benign adult familial myoclonic epilepsy reveals associations between the pathogenic TTTCA repeat insertion in SAMD12 and the nonpathogenic TTTTA repeat expansion in TNRC6A.
    Terasaki A; Nakamura M; Urata Y; Hiwatashi H; Yokoyama I; Yasuda T; Onuma T; Wada K; Kaneko S; Kan R; Niwa SI; Hashimoto O; Komure O; Goto YI; Yamagishi Y; Nakano M; Furusawa Y; Sano A
    J Hum Genet; 2021 Apr; 66(4):419-429. PubMed ID: 33040085
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Benign adult familial myoclonic epilepsy (BAFME) with night blindness.
    Manabe Y; Narai H; Warita H; Hayashi T; Shiro Y; Sakai K; Kashihara K; Shoji M; Abe K
    Seizure; 2002 Jun; 11(4):266-8. PubMed ID: 12027575
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.