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1 an AE3 polymorphism A867D is associated with idiopathic generalized epilepsy.
2 polymorphism of human AE3 is associated with idiopathic generalized epilepsy.
3 renia, mental retardation, and most recently idiopathic generalized epilepsy.
4 polymorphism of human AE3 is associated with idiopathic generalized epilepsy.
5 thalamocortical network lie at the heart of idiopathic generalized epilepsy.
6 sts that SCN1A is not a major contributor to idiopathic generalized epilepsy.
7 ations in either channel can cause a form of idiopathic generalized epilepsy.
8 wakening (EGMA) is a well-defined subtype of idiopathic generalized epilepsy.
9 n found in association with various forms of idiopathic generalized epilepsy.
11 ood absence epilepsy (CAE), a common form of idiopathic generalized epilepsy, accounts for 5%-15% of
12 of a cohort of 35 adults with heterogeneous idiopathic generalized epilepsies and 40 healthy adult c
14 the most effective drug in the treatment of idiopathic generalized epilepsy and juvenile myoclonic e
15 absence seizures, which characterize various idiopathic generalized epilepsies, are not fully underst
16 (A) receptor genes have been associated with idiopathic generalized epilepsies, but the cellular cons
17 enile myoclonic epilepsy is a common type of idiopathic generalized epilepsy characterized by myoclon
18 venile myoclonic epilepsy is the most common idiopathic generalized epilepsy, characterized by freque
19 idiopathic generalized epilepsies) with the idiopathic generalized epilepsies group showing a more d
20 onic seizures only under the sole heading of idiopathic generalized epilepsies (IGE) with variable ph
21 es (EMA, Jeavons syndrome), 14 patients with idiopathic generalized epilepsies (IGE) without ECS, and
28 investigated families with adolescent-onset idiopathic generalized epilepsy (IGE), for linkage to ma
35 ciated with a considerably increased risk of idiopathic generalized epilepsy, intellectual disability
37 ance, similar to that widely accepted in the idiopathic generalized epilepsies, is the usual mode of
38 lial neonatal convulsions (BFNC), a class of idiopathic generalized epilepsy, is an autosomal dominan
39 localization-related epilepsies (n = 24) and idiopathic generalized epilepsies (n = 20) compared to h
40 reatest extent in relatives of probands with idiopathic generalized epilepsies (standardized incidenc
41 Juvenile myoclonic epilepsy is a heritable idiopathic generalized epilepsy syndrome, characterized
45 e channel activity have been associated with idiopathic generalized epilepsies, whereas mutations tha
46 ndromes (localization-related epilepsies and idiopathic generalized epilepsies) with the idiopathic g
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