Familial cortical myoclonic tremor with epilepsy: A single syndromic classification for a group of pedigrees bearing common features
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Absence of linkage to 8q24 in a European family with familial adult myoclonic epilepsy (FAME)
Laubage P, Amer LO, Simonetta-Moreau M, et al. Absence of linkage to 8q24 in a European family with familial adult myoclonic epilepsy (FAME). Neurology 2002;58:941-4.
Benign adult familial myoclonic epilepsy. Genetic heterogeneity and allelism with ADCME
de Falco FA, Striano P, de Falco A, et al. Benign adult familial myoclonic epilepsy. Genetic heterogeneity and allelism with ADCME. Neurology 2003;60:1381-85.
Autosomal dominant cortical myoclonus and epilepsy (ADCME) with complex partial seizures and generalized seizures. A newly recognized epilepsy syndrome with linkage to chromosome 2p11.1-q12.2
Guerrini R, Bonanni P, Patrignani A, et al. Autosomal dominant cortical myoclonus and epilepsy (ADCME) with complex partial seizures and generalized seizures. A newly recognized epilepsy syndrome with linkage to chromosome 2p11.1-q12.2. Brain 2001;124:2459-75.
Pathogenesis of giant somatosensory evoked potentials in progressive myoclonic epilepsy
Shibasaki H, Yamashita Y, Neshige R, et al. Pathogenesis of giant somatosensory evoked potentials in progressive myoclonic epilepsy. Brain 1985;108:225-40.
Autosomal dominant cortical tremor, myoclonus and epilepsy: Many syndromes, one phenotype
(Review)
Striano P, Zara F, Striano S. Autosomal dominant cortical tremor, myoclonus and epilepsy: many syndromes, one phenotype (Review). Acta Neurol Scand 2005;111:211-7.
