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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.
13                                              Idiopathic generalized epilepsies account for about 40%
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
16                    We studied a patient with idiopathic generalized epilepsy and frequent absences, u
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
27                   MRI scans of patients with idiopathic generalized epilepsy (IGE) are normal on visu
28                                   Women with idiopathic generalized epilepsy (IGE) face challenges in
29                                              Idiopathic generalized epilepsy (IGE) is a brain network
30                                              Idiopathic generalized epilepsy (IGE) is a class of gene
31                                              Idiopathic generalized epilepsy (IGE) is a common, compl
32                                              Idiopathic generalized epilepsy (IGE) is a complex disea
33                                              Idiopathic generalized epilepsy (IGE) is a complex epile
34          The cerebral haemodynamic status of idiopathic generalized epilepsy (IGE) is a very complica
35 rigin of neural hyperexcitability underlying idiopathic generalized epilepsy (IGE) is not known.
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
38                             In patients with idiopathic generalized epilepsy (IGE), visual inspection
39  of female patients of reproductive age with idiopathic generalized epilepsy (IGE).
40                                              Idiopathic generalized epilepsies (IGEs) account for app
41                                   Most human idiopathic generalized epilepsies (IGEs) are polygenic,
42 ansporter 1 (GLUT1) deficiency causes common idiopathic generalized epilepsies (IGEs).
43 o childhood absence epilepsy (CAE) and other idiopathic generalized epilepsies (IGEs).
44 llion people worldwide, and 40% of these are idiopathic generalized epilepsies (IGEs).
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
47                                 Overlap with idiopathic generalized epilepsies is limited and of unce
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
53 nile myoclonic epilepsy is the most frequent idiopathic generalized epilepsy syndrome.
54 sight into the molecular etiology of a human idiopathic generalized epilepsy syndrome.
55  is also a candidate gene for this inherited idiopathic generalized epilepsy syndrome.
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