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1 nlesional focal epilepsy and 8 patients with idiopathic generalized epilepsy.
2 n found in association with various forms of idiopathic generalized epilepsy.
3 an AE3 polymorphism A867D is associated with idiopathic generalized epilepsy.
4 renia, mental retardation, and most recently idiopathic generalized epilepsy.
5 thalamocortical network lie at the heart of idiopathic generalized epilepsy.
6 polymorphism of human AE3 is associated with idiopathic generalized epilepsy.
7 sts that SCN1A is not a major contributor to idiopathic generalized epilepsy.
8 polymorphism of human AE3 is associated with idiopathic generalized epilepsy.
9 ations in either channel can cause a form of idiopathic generalized epilepsy.
10 recordings from a cohort of 107 people with idiopathic generalized epilepsy.
11 alproate is the most effective treatment for idiopathic generalized epilepsy.
12 wakening (EGMA) is a well-defined subtype of idiopathic generalized epilepsy.
14 ood absence epilepsy (CAE), a common form of idiopathic generalized epilepsy, accounts for 5%-15% of
15 of a cohort of 35 adults with heterogeneous idiopathic generalized epilepsies and 40 healthy adult c
17 the most effective drug in the treatment of idiopathic generalized epilepsy and juvenile myoclonic e
18 absence seizures, which characterize various idiopathic generalized epilepsies, are not fully underst
19 (A) receptor genes have been associated with idiopathic generalized epilepsies, but the cellular cons
20 enile myoclonic epilepsy is a common type of idiopathic generalized epilepsy characterized by myoclon
21 we identify two subtypes common to focal and idiopathic generalized epilepsies, characterized by prog
22 venile myoclonic epilepsy is the most common idiopathic generalized epilepsy, characterized by freque
23 idiopathic generalized epilepsies) with the idiopathic generalized epilepsies group showing a more d
24 onic seizures only under the sole heading of idiopathic generalized epilepsies (IGE) with variable ph
25 es (EMA, Jeavons syndrome), 14 patients with idiopathic generalized epilepsies (IGE) without ECS, and
26 ent patterns of domino-like seizure onset in Idiopathic Generalized Epilepsy (IGE) and present a nove
36 emporal lobe epilepsy (TLE), 288 adults with idiopathic generalized epilepsy (IGE), and 1328 healthy
37 investigated families with adolescent-onset idiopathic generalized epilepsy (IGE), for linkage to ma
45 fect of PRS(GGE) was significantly larger on idiopathic generalized epilepsies, in females and for ea
46 ciated with a considerably increased risk of idiopathic generalized epilepsy, intellectual disability
48 ance, similar to that widely accepted in the idiopathic generalized epilepsies, is the usual mode of
49 lial neonatal convulsions (BFNC), a class of idiopathic generalized epilepsy, is an autosomal dominan
50 localization-related epilepsies (n = 24) and idiopathic generalized epilepsies (n = 20) compared to h
51 reatest extent in relatives of probands with idiopathic generalized epilepsies (standardized incidenc
52 Juvenile myoclonic epilepsy is a heritable idiopathic generalized epilepsy syndrome, characterized
56 e channel activity have been associated with idiopathic generalized epilepsies, whereas mutations tha
57 ndromes (localization-related epilepsies and idiopathic generalized epilepsies) with the idiopathic g