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1 fe, mainly consisting of epileptic spasms or myoclonic seizures.
2 tonic-clonic seizures (GTCS) and a second to myoclonic seizures.
3 or EPM1 by displaying progressive ataxia and myoclonic seizures.
4 d occasionally cognitive impairment preceded myoclonic seizures.
5 m.8344A>G mutation and epilepsy experienced myoclonic seizures.
6 behind the role of LGI1 in susceptibility to myoclonic seizures.
7 age, the homozygous mutant mice all exhibit myoclonic seizures accompanied by rapid jumping and runn
9 e found that mice lacking cystatin B develop myoclonic seizures and ataxia, similar to symptoms seen
10 -THP) had a significantly lower incidence of myoclonic seizures and less EEG activity following penty
11 ressive myoclonus epilepsy with debilitating myoclonic seizures and relatively infrequent tonic-cloni
13 By 1 year most Spnb3(-/-) animals develop a myoclonic seizure disorder with significant reductions o
14 , but nearly all P20-22 and P30-46 mSMEI had myoclonic seizures followed by generalized seizures caus
17 All but one of these patients had similar myoclonic seizures induced by linguistic activities othe
18 pilepsy (PME) is a syndrome characterized by myoclonic seizures (lightning-like jerks), generalized c