The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
MeSH Review

Epilepsies, Myoclonic

Welcome! If you are familiar with the subject of this article, you can contribute to this open access knowledge base by deleting incorrect information, restructuring or completely rewriting any text. Read more.

Disease relevance of Epilepsies, Myoclonic


High impact information on Epilepsies, Myoclonic


Chemical compound and disease context of Epilepsies, Myoclonic


Biological context of Epilepsies, Myoclonic


Gene context of Epilepsies, Myoclonic


  1. Adult-onset idiopathic generalized epilepsy: clinical and behavioral features. Cutting, S., Lauchheimer, A., Barr, W., Devinsky, O. Epilepsia (2001) [Pubmed]
  2. Late-onset myoclonic epilepsy in Down's syndrome (LOMEDS). Möller, J.C., Hamer, H.M., Oertel, W.H., Rosenow, F. Seizure : the journal of the British Epilepsy Association. (2002) [Pubmed]
  3. Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndrome. Campos, Y., Garcia-Silva, T., Barrionuevo, C.R., Cabello, A., Muley, R., Arenas, J. Pediatric neurology. (1995) [Pubmed]
  4. SCN1A mutation analysis in myoclonic astatic epilepsy and severe idiopathic generalized epilepsy of infancy with generalized tonic-clonic seizures. Ebach, K., Joos, H., Doose, H., Stephani, U., Kurlemann, G., Fiedler, B., Hahn, A., Hauser, E., Hundt, K., Holthausen, H., Müller, U., Neubauer, B.A. Neuropediatrics. (2005) [Pubmed]
  5. Audiological findings in patients with myoclonic epilepsy associated with ragged-red fibres. Tsutsumi, T., Nishida, H., Noguchi, Y., Komatsuzaki, A., Kitamura, K. The Journal of laryngology and otology. (2001) [Pubmed]
  6. Bismuth absorption and myoclonic encephalopathy during bismuth subsalicylate therapy. Mendelowitz, P.C., Hoffman, R.S., Weber, S. Ann. Intern. Med. (1990) [Pubmed]
  7. The role of vigabatrin in the management of infantile epileptic syndromes. Appleton, R.E. Neurology (1993) [Pubmed]
  8. Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+? Singh, R., Andermann, E., Whitehouse, W.P., Harvey, A.S., Keene, D.L., Seni, M.H., Crossland, K.M., Andermann, F., Berkovic, S.F., Scheffer, I.E. Epilepsia (2001) [Pubmed]
  9. The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndrome. Fabrizi, G.M., Cardaioli, E., Grieco, G.S., Cavallaro, T., Malandrini, A., Manneschi, L., Dotti, M.T., Federico, A., Guazzi, G. J. Neurol. Neurosurg. Psychiatr. (1996) [Pubmed]
  10. Arylsulfatase A pseudodeficiency and Lafora bodies in a patient with progressive myoclonic epilepsy. Tinuper, P., Plazzi, G., Monari, L., Sangiorgi, S., Pellissier, J.F., Cerullo, A., Provini, F., Capellari, S., Baruzzi, A., Lugaresi, E. Epilepsia (1994) [Pubmed]
  11. Platelet GABA-transaminase in epileptic children: influence of epilepsy and anticonvulsants. Arteaga, R., Herranz, J.L., Armijo, J.A. Epilepsy Res. (1993) [Pubmed]
  12. Acute reversible myoclonic encephalopathy associated with fluoxetine therapy. Ghika-Schmid, F., Ghika, J., Vuadens, P., Bogousslavsky, J., Regli, F., Despland, P.A. Mov. Disord. (1997) [Pubmed]
  13. Myoclonus and adult coeliac disease. Tison, F., Arne, P., Henry, P. J. Neurol. (1989) [Pubmed]
  14. Ketamine and myoclonic encephalopathy of infants (Kinsbourne syndrome). Burrows, F.A., Seeman, R.G. Anesth. Analg. (1982) [Pubmed]
  15. Myoclonus and epilepsy in childhood: a review of treatment with valproate, ethosuximide, lamotrigine and zonisamide. Wallace, S.J. Epilepsy Res. (1998) [Pubmed]
  16. Histochemical and molecular genetic study of MELAS and MERRF in Korean patients. Kim, D.S., Jung, D.S., Park, K.H., Kim, I.J., Kim, C.M., Lee, W.H., Rho, S.K. J. Korean Med. Sci. (2002) [Pubmed]
  17. Myoclonic encephalopathy in the CDKL5 gene mutation. Buoni, S., Zannolli, R., Colamaria, V., Macucci, F., di Bartolo, R.M., Corbini, L., Orsi, A., Zappella, M., Hayek, J. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. (2006) [Pubmed]
  18. Spasms in clusters in epilepsies other than typical West syndrome. Ohtsuka, Y., Kobayashi, K., Ogino, T., Oka, E. Brain Dev. (2001) [Pubmed]
  19. Myoclonic encephalopathy due to bismuth salts: treatment with dimercaprol and analysis of CSF transmitters. Molina, J.A., Calandre, L., Bermejo, F. Acta neurologica Scandinavica. (1989) [Pubmed]
  20. Steroid-dependent form of Kinsbourne syndrome: successful treatment with trazodone. Papini, M., Pasquinelli, A., Filippini, A. Italian journal of neurological sciences. (1992) [Pubmed]
WikiGenes - Universities