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1 re shocked whenever the nuchal muscle became atonic.
3 range of seizure types, including myoclonic-atonic, atonic, myoclonic, absence, and generalised toni
4 in the late onset group, including myoclonic-atonic epilepsy (two patients), Lennox-Gastaut not emerg
5 ophila will help solve undiagnosed myoclonic atonic epilepsy or developmental and epileptic encephalo
6 nd the disease phenotypes, such as myoclonic atonic epilepsy versus developmental delay, in this stud
7 developmental disorders, including myoclonic atonic epilepsy, childhood absence epilepsy, autism, and
9 s (visual agnosia, sensory hypersensitivity, atonic episodes, restricted mobility) to social isolatio
11 defined as hemiclonic, tonic, clonic, tonic-atonic, generalised tonic-clonic, and focal with clearly
12 f seizure types, including myoclonic-atonic, atonic, myoclonic, absence, and generalised tonic-clonic
14 generalised tonic-clonic, bilateral clonic, atonic, or focal to bilateral tonic-clonic) per 28 days
16 ts experiencing daily absence, myoclonic, or atonic seizures became seizure-free (except some remaini
19 distinct features of epilepsy with myoclonic-atonic seizures, combined with advances in molecular gen
24 tonic-clonic, generalized tonic, generalized atonic, simple partial, and partial complex seizure type
25 es (primarily generalized, tonic-clonic, and atonic) that began on average at 6.8 months of age (rang