Warning: The NCBI web site requires JavaScript to function. more...
Generate a file for use with external citation management software.
Epilepsy in Wolf-Hirschhorn syndrome (4p-).
Kagitani-Shimono K, Imai K, Otani K, Kamio N, Okinaga T, Toribe Y, Suzuki Y, Ozono K.
Epilepsia. 2005 Jan;46(1):150-5.
Related citations
Lamotrigine adjunctive therapy among children and adolescents with primary generalized tonic-clonic seizures.
Trevathan E, Kerls SP, Hammer AE, Vuong A, Messenheimer JA.
Pediatrics. 2006 Aug;118(2):e371-8. Epub 2006 Jul 17.
Point mutation tRNA(Ser(UCN)) in a child with hearing loss and myoclonus epilepsy.
Ramelli GP, Gallati S, Weis J, Krähenbühl S, Burgunder JM.
J Child Neurol. 2006 Mar;21(3):253-5.
Neuronal Ceroid-Lipofuscinoses.
Mole SE, Williams RE.
In: Pagon RA, Bird TD, Dolan CR, Stephens K, Adam MP, editors. GeneReviews™ [Internet]. Seattle (WA): University of Washington, Seattle; 1993-.2001 Oct 10 [updated 2010 Mar 02].
Infant-onset progressive myoclonus epilepsy.
Harbord MG, Hwang PA, Robinson BH, Becker LE, Hunjan A, Murphy EG.
J Child Neurol. 1991 Apr;6(2):134-42.
Seizures in myoclonic epilepsy with ragged-red fibers detected by DNA analysis: a case report.
Sitburana O, Witoonpanich R, Phudhichareonrat S, Lertrit P, Supavilai R.
J Med Assoc Thai. 2001 Jul;84(7):1051-5.
Prolonged postictal stupor: nonconvulsive status epilepticus, medication effect, or postictal state?
Langheinrich TC, Chattopadhyay A, Kuc S, Reuber M.
Epilepsy Behav. 2005 Nov;7(3):548-51. Epub 2005 Sep 27.
Neonatal seizures and limb malformations associated with liver-specific complex IV respiratory chain deficiency.
Kurian MA, O'Mahoney ES, Rustin P, Brown G, Treacy EP, King MD.
Eur J Paediatr Neurol. 2004;8(1):55-9.
Generalized tonic-clonic seizures in patients with complex-partial seizures: natural history and prognostic relevance.
Schmidt D, Tsai JJ, Janz D.
Epilepsia. 1983 Feb;24(1):43-8.
Phenytoin versus valproate monotherapy for partial onset seizures and generalized onset tonic-clonic seizures.
Tudur Smith C, Marson AG, Williamson PR.
Cochrane Database Syst Rev. 2001;(4):CD001769. Review.
A double mutation (A8296G and G8363A) in the mitochondrial DNA tRNA (Lys) gene associated with myoclonus epilepsy with ragged-red fibers.
Arenas J, Campos Y, Bornstein B, Ribacoba R, Martín MA, Rubio JC, Santorelli FM, Zeviani M, DiMauro S, Garesse R.
Neurology. 1999 Jan 15;52(2):377-82.
G8363A mutation in the mitochondrial DNA transfer ribonucleic acidLys gene: another cause of Leigh syndrome.
Shtilbans A, Shanske S, Goodman S, Sue CM, Bruno C, Johnson TL, Lava NS, Waheed N, DiMauro S.
J Child Neurol. 2000 Nov;15(11):759-61.
Generalized nonconvulsive status epilepticus in symptomatic partial epilepsy.
Miyama S.
Pediatr Neurol. 2007 Mar;36(3):195-8.
[Nonconvulsive status epilepticus of frontal origin. A case report].
Fernández-Torre JL, González C, Sánchez JM.
Rev Neurol. 2000 Jun 1-15;30(11):1040-3. Spanish.
Severe epilepsy as the major symptom of new mutations in the mitochondrial tRNA(Phe) gene.
Zsurka G, Hampel KG, Nelson I, Jardel C, Mirandola SR, Sassen R, Kornblum C, Marcorelles P, Lavoué S, Lombès A, Kunz WS.
Neurology. 2010 Feb 9;74(6):507-12.
[Therapy of generalized tonic-clonic status epilepticus in adulthood].
Beyenburg S, Bauer J, Elger CE.
Nervenarzt. 2000 Feb;71(2):65-77. Review. German.
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.
Treatment of pediatric epilepsy: European expert opinion, 2007.
Wheless JW, Clarke DF, Arzimanoglou A, Carpenter D.
Epileptic Disord. 2007 Dec;9(4):353-412. Review.
[Electroencephalography in status epilepticus in sleep (ESES) in various clinical pictures].
Popović Miocinović L, Durrigl V, Kapitanović Vidak H, Grubesić Z, Sremić S.
Acta Med Croatica. 2005;59(1):69-74. Croatian.
[Progressive myoclonic epilepsy as a sign of a late form of Alpers syndrome].
Galván-Manso M, Tabuenca Y, Medrano P, Ruiz-Escusol S, Giménez-Mas JA, López-Pisón J.
Rev Neurol. 2000 Dec 1-15;31(11):1036-9. Spanish.
Filters: Manage Filters
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on