Add to ORKGBenign adult familial myoclonic epilepsy (BAFME) has been mapped to chromosome 8q24; however, genetic heterogeneity has been recently suggested. The authors report a clinical and electrophysiologic study of two Italian BAFME families showing linkage to chromosome 2p11.1-q12.2. Their report supports the evidence of non-Japanese families with BAFME and suggests a possible allelism with the recently described autosomal dominant cortical myoclonus and epilepsy syndrome
A clinical, neurophysiological and genetic study of a familial form of myoclonic epilepsy b
Autosomal dominant familial cortical myoclonic tremor and epilepsy (FCMTE) is characterized by dista...
SummaryObjectiveMyoclonic epilepsy is a common epileptic syndrome with high genetic contribution. We...
Benign adult familial myoclonic epilepsy (BAFME) has been mapped to chromosome 8q24; however, geneti...
Benign adult familial myoclonic epilepsy (BAFME) is an autosomal dominant condition characterized by...
Benign adult familial myoclonic epilepsy (BAFME) is an autosomal dominant condition characterized by...
Benign adult familial myoclonic epilepsy (BAFME or FAME) is an autosomal dominant condition, charact...
Benign Adult Familial Myoclonic Epilepsy is an AD syndrome characterized from a non progressive cort...
Familial essential myoclonus and epilepsy (FEME) is hereditary epileptic disorder characterized by a...
SummaryBenign adult familial myoclonic epilepsy is an autosomal dominant idiopathic epileptic syndro...
Depienne and colleagues recently mapped to 5p15.31–p15 a French family with cortical tremor, myoclon...
In 1997, a locus for benign familial infantile convulsions (BFIC) was mapped to chromosome 19q. Furt...
Fourteen of the 26 members of two families with hereditary myoclonic epilepsy were studied, and the ...
Familial adult myoclonus epilepsy (FAME) is a rare autosomal dominant disorder characterized by adul...
Familial adult myoclonus epilepsy (FAME) is a rare autosomal dominant disorder characterized by adul...
A clinical, neurophysiological and genetic study of a familial form of myoclonic epilepsy b
Autosomal dominant familial cortical myoclonic tremor and epilepsy (FCMTE) is characterized by dista...
SummaryObjectiveMyoclonic epilepsy is a common epileptic syndrome with high genetic contribution. We...
Benign adult familial myoclonic epilepsy (BAFME) has been mapped to chromosome 8q24; however, geneti...
Benign adult familial myoclonic epilepsy (BAFME) is an autosomal dominant condition characterized by...
Benign adult familial myoclonic epilepsy (BAFME) is an autosomal dominant condition characterized by...
Benign adult familial myoclonic epilepsy (BAFME or FAME) is an autosomal dominant condition, charact...
Benign Adult Familial Myoclonic Epilepsy is an AD syndrome characterized from a non progressive cort...
Familial essential myoclonus and epilepsy (FEME) is hereditary epileptic disorder characterized by a...
SummaryBenign adult familial myoclonic epilepsy is an autosomal dominant idiopathic epileptic syndro...
Depienne and colleagues recently mapped to 5p15.31–p15 a French family with cortical tremor, myoclon...
In 1997, a locus for benign familial infantile convulsions (BFIC) was mapped to chromosome 19q. Furt...
Fourteen of the 26 members of two families with hereditary myoclonic epilepsy were studied, and the ...
Familial adult myoclonus epilepsy (FAME) is a rare autosomal dominant disorder characterized by adul...
Familial adult myoclonus epilepsy (FAME) is a rare autosomal dominant disorder characterized by adul...
A clinical, neurophysiological and genetic study of a familial form of myoclonic epilepsy b
Autosomal dominant familial cortical myoclonic tremor and epilepsy (FCMTE) is characterized by dista...
SummaryObjectiveMyoclonic epilepsy is a common epileptic syndrome with high genetic contribution. We...