| Hartman AL
Does the effectiveness of the ketogenic diet in different epilepsies yield insights into its mechanisms? [Journal Article]
Epilepsia 2008 Nov.:53-6.
Abstract | Full Citation | | Bassuk AG, Wallace RH, Buhr A, et al.
A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome. [Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't]
Am J Hum Genet 2008 Nov; 83(5):572-81.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Temucin CM, Buyukserbetci G, Ozdamar SE, et al.
A rare phenotype: progresive myoclonic epilepsy with lower motor neuron involvement. [Letter]
Epilepsia 2008 Oct; 49(10):1809-12.
Full Citation | Publisher Full Text | Find Related Articles | | Bruton J, Crowe S
Combined general and regional anesthesia in a child with Ohtahara syndrome. [Letter]
Paediatr Anaesth 2008 Nov; 18(11):1111-2.
Full Citation | Find Related Articles | | Nakken KO, Johannessen SI
[Seizure exacerbation caused by antiepileptic drugs.] [English Abstract, Journal Article]
Tidsskr Nor Laegeforen 2008 Sep 25; 128(18):2052-5.
Abstract | Full Citation | | Posner E, Panayiotopoulos C
The significance of specific diagnosis in the treatment of epilepsies. [JOURNAL ARTICLE]
Dev Med Child Neurol 2008 Sep 20.
Full Citation | Publisher Full Text | Find Related Articles | | Bour LJ, van Rootselaar AF, Koelman JH, et al.
Oculomotor abnormalities in myoclonic tremor: a comparison with spinocerebellar ataxia type 6. [Journal Article]
Brain 2008 Sep; 131(Pt 9):2295-303.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Auvin S
Treatment of Juvenile Myoclonic Epilepsy. [JOURNAL ARTICLE]
CNS Neurosci Ther 2008 Jul 30.
Abstract | Full Citation | | McArdle EJ, Kunic JD, George AL
Novel SCN1A frameshift mutation with absence of truncated Na(V)1.1 protein in severe myoclonic epilepsy of infancy. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Aug 4.
Full Citation | | Wiedemann FR, Bartels C, Kirches E, et al.
Unusual presentations of patients with the mitochondrial MERRF mutation A8344G. [JOURNAL ARTICLE]
Clin Neurol Neurosurg 2008 Jul 24.
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