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1 ocal epilepsy and 8 patients with idiopathic generalized epilepsy.
2 substrate for seizures in some patients with generalized epilepsy.
3 N1A is not a major contributor to idiopathic generalized epilepsy.
4  convulsions, a dominantly inherited form of generalized epilepsy.
5 ither channel can cause a form of idiopathic generalized epilepsy.
6 rgency epilepsy visits and focal rather than generalized epilepsy.
7 tients with neurodevelopmental disorders and generalized epilepsy.
8 cal epilepsy and 9 have similar efficacy for generalized epilepsy.
9  from a cohort of 107 people with idiopathic generalized epilepsy.
10 ated with all epilepsies and 39 with genetic generalized epilepsy.
11  the most effective treatment for idiopathic generalized epilepsy.
12 ary treatment, its application is limited in generalized epilepsy.
13 lepsy compared to controls-in particular for generalized epilepsy.
14 morphism A867D is associated with idiopathic generalized epilepsy.
15 mmon susceptibility variants associated with generalized epilepsy.
16 m of human AE3 is associated with idiopathic generalized epilepsy.
17 m of human AE3 is associated with idiopathic generalized epilepsy.
18  muscular dystrophy, brain abnormalities and generalized epilepsy.
19 GMA) is a well-defined subtype of idiopathic generalized epilepsy.
20 association with various forms of idiopathic generalized epilepsy.
21 tin (SST)(+) interneurons, results in severe generalized epilepsy.
22 ion and how this contributes to the onset of generalized epilepsy.
23 spike-and-wave episodes in a rodent model of generalized epilepsy.
24 ay give rise to hyperexcitability underlying generalized epilepsy.
25 al retardation, and most recently idiopathic generalized epilepsy.
26 mily having both FHM and a high incidence of generalized epilepsy.
27 tical network lie at the heart of idiopathic generalized epilepsy.
28 pilepsy, extratemporal epilepsy, and genetic generalized epilepsy.
29 sy (typical and atypical), and myoclonic and generalized epilepsies.
30                                   Idiopathic generalized epilepsies account for about 40% of epilepsy
31  epilepsy (CAE), a common form of idiopathic generalized epilepsy, accounts for 5%-15% of childhood e
32 epresents the strongest risk CNV for genetic generalized epilepsy across the whole genome.
33  association of neurodevelopmental disorder, generalized epilepsy, action myoclonus/cortical tremor a
34 t of 35 adults with heterogeneous idiopathic generalized epilepsies and 40 healthy adult controls.
35 8.3 (95% confidence interval 2.93-15.31) for generalized epilepsy and 2.5 (95% confidence interval 0.
36  1.0 (95% confidence interval 0.00-2.19) for generalized epilepsy and 2.6 (95% confidence interval 1.
37 oss-trait genetic enrichment between genetic generalized epilepsy and all psychiatric disorders and b
38         We studied a patient with idiopathic generalized epilepsy and frequent absences, using electr
39                   Frings mice are a model of generalized epilepsy and have seizures in response to lo
40 ffective drug in the treatment of idiopathic generalized epilepsy and juvenile myoclonic epilepsy.
41                     We observed that genetic generalized epilepsy and non-acquired focal epilepsy for
42 on (D434G) associated with human syndrome of generalized epilepsy and paroxysmal dyskinesia (GEPD), w
43 e results identify a gene that is mutated in generalized epilepsy and paroxysmal dyskinesia and have
44 arization of action potentials, resulting in generalized epilepsy and paroxysmal dyskinesia by allowi
45 sociated with a human syndrome of coexistent generalized epilepsy and paroxysmal dyskinesia on chromo
46 have been associated with a dominant form of generalized epilepsy and paroxysmal dyskinesia.
47 to human neurological diseases of coexistent generalized epilepsy and paroxysmal dyskinesia.
48  was identified both in a German family with generalized epilepsy and praxis-induced seizures and in
49 variants in 238 exomes from familial genetic generalized epilepsies, and in other public exome data s
50 psy Rats from Strasbourg, a model of genetic generalized epilepsy, and inbred non-epileptic control r
51 e identified loci, 32 were novel for genetic generalized epilepsy, and two were novel for all epileps
52 ave historically been thought of as 'primary generalized' epilepsies, appear to originate in local mi
53                                    Focal and generalized epilepsy are the 2 most frequent types of ep
54 zures, which characterize various idiopathic generalized epilepsies, are not fully understood, but im
55 n the molecular pathogenic basis for genetic generalized epilepsies associated with mutations in the
56 ) is characterized by moderate to severe ID, generalized epilepsy, autism spectrum disorder, sensory
57 r genes have been associated with idiopathic generalized epilepsies, but the cellular consequences of
58 onic epilepsy is a common type of idiopathic generalized epilepsy characterized by myoclonic, general
59  two subtypes common to focal and idiopathic generalized epilepsies, characterized by progression of
60 lonic epilepsy is the most common idiopathic generalized epilepsy, characterized by frequent myocloni
61 d and a 4.5-fold enrichment of patients with generalized epilepsy compared to controls in the top 0.5
62 ncrease in the risk of having a diagnosis of generalized epilepsy, compared with individuals without
63                                Patients with generalized epilepsy exhibit cerebral cortical disinhibi
64 ified common genetic burden in patients with generalized epilepsy (GE-PRS) or focal epilepsy (FE-PRS)
65 sy PRS (PRS(GGE)) increased risk for genetic generalized epilepsy (GGE) (hazard ratio [HR] 1.73 per P
66                                      Genetic generalized epilepsy (GGE) syndromes start during childh
67 rom 38 people with epilepsy (17 with genetic generalized epilepsy (GGE), 21 with mesial temporal lobe
68 t groups of epilepsies: severe DEEs, genetic generalized epilepsy (GGE), and non-acquired focal epile
69  generalized epilepsies) with the idiopathic generalized epilepsies group showing a more disrupted pa
70 es only under the sole heading of idiopathic generalized epilepsies (IGE) with variable phenotype'.
71 avons syndrome), 14 patients with idiopathic generalized epilepsies (IGE) without ECS, and 16 healthy
72 s of domino-like seizure onset in Idiopathic Generalized Epilepsy (IGE) and present a novel approach
73        MRI scans of patients with idiopathic generalized epilepsy (IGE) are normal on visual assessme
74                        Women with idiopathic generalized epilepsy (IGE) face challenges in treatment
75                                   Idiopathic generalized epilepsy (IGE) is a brain network disease, b
76                                   Idiopathic generalized epilepsy (IGE) is a class of genetically det
77                                   Idiopathic generalized epilepsy (IGE) is a common, complex disease
78                                   Idiopathic generalized epilepsy (IGE) is a complex disease with hig
79                                   Idiopathic generalized epilepsy (IGE) is a complex epilepsy syndrom
80 e cerebral haemodynamic status of idiopathic generalized epilepsy (IGE) is a very complicated process
81 ural hyperexcitability underlying idiopathic generalized epilepsy (IGE) is not known.
82 e epilepsy (TLE), 288 adults with idiopathic generalized epilepsy (IGE), and 1328 healthy controls fr
83 ed families with adolescent-onset idiopathic generalized epilepsy (IGE), for linkage to markers spann
84                  In patients with idiopathic generalized epilepsy (IGE), visual inspection of routine
85 patients of reproductive age with idiopathic generalized epilepsy (IGE).
86 ilepsy (LRE, n = 59) or idiopathic (primary) generalized epilepsy (IGE, n = 35) receiving either a cy
87                                   Idiopathic generalized epilepsies (IGEs) account for approximately
88                        Most human idiopathic generalized epilepsies (IGEs) are polygenic, but virtual
89 e worldwide, and 40% of these are idiopathic generalized epilepsies (IGEs).
90  (GLUT1) deficiency causes common idiopathic generalized epilepsies (IGEs).
91  absence epilepsy (CAE) and other idiopathic generalized epilepsies (IGEs).
92 hared loci between schizophrenia and genetic generalized epilepsy implicated biological processes rel
93 iduals with neurodevelopmental disorders and generalized epilepsy in a cohort of 2,310 individuals wh
94 nes for hippocampal sclerosis in TLE and for generalized epilepsy in IGE.
95 (GGE) was significantly larger on idiopathic generalized epilepsies, in females and for earlier epile
96      In contrast, all three variants causing generalized epilepsy induced a loss-of-function (reduced
97  a considerably increased risk of idiopathic generalized epilepsy, intellectual disability, and schiz
98 de novo variants in FZR1 had childhood-onset generalized epilepsy, intellectual disability, mild atax
99                      Overlap with idiopathic generalized epilepsies is limited and of uncertain genet
100 ar to that widely accepted in the idiopathic generalized epilepsies, is the usual mode of inheritance
101 al convulsions (BFNC), a class of idiopathic generalized epilepsy, is an autosomal dominantly inherit
102                        Patients with genetic generalized epilepsy, lesional focal epilepsy, non-acqui
103 temporal lobe epilepsy (n = 330) and genetic generalized epilepsies (n = 1408), suggesting a selectiv
104 n-related epilepsies (n = 24) and idiopathic generalized epilepsies (n = 20) compared to healthy cont
105  epilepsy with normal MRI (n = 275), genetic generalized epilepsy (n = 182) and non-lesional extratem
106 lity, majority pharmaco-resistant); Group 4, generalized epilepsy (n = 20, mild to moderate intellect
107 ata for all epilepsies (n = 44 889), genetic generalized epilepsy (n = 33 446), focal epilepsy (n = 3
108  review (odds ratio 3.8, 95% CI 2.4-6.1) and generalized epilepsy (odds ratio 1.9, 95% CI 1.2-3.0).
109 significantly higher GE-PRS in patients with generalized epilepsy of European-ancestry compared to pa
110 vulsions (BFNC) is a rare autosomal dominant generalized epilepsy of the newborn infant.
111 ble for the susceptibility locus for genetic generalized epilepsy on 17q21.32 (close to rs72823592).
112 uropean ancestry-derived PRS did not predict generalized epilepsy or focal epilepsy in Japanese-ances
113                                      Genetic generalized epilepsy patients have the highest CNV burde
114 ronized firing behavior and produce a stable generalized epilepsy phenotype.
115                 We found that a high genetic generalized epilepsy PRS (PRS(GGE)) increased risk for g
116                                For focal and generalized epilepsy, selection of ASDs should consider
117 eutic benefit for controlling other types of generalized epilepsies should be evaluated.
118 ent in relatives of probands with idiopathic generalized epilepsies (standardized incidence ratio 6.0
119                In relatives of probands with generalized epilepsy, standardized incidence ratios were
120 yoclonic epilepsy is the most common genetic generalized epilepsy syndrome, characterized by a comple
121 myoclonic epilepsy is a heritable idiopathic generalized epilepsy syndrome, characterized by myocloni
122 the molecular etiology of a human idiopathic generalized epilepsy syndrome.
123 candidate gene for this inherited idiopathic generalized epilepsy syndrome.
124 nic epilepsy is the most frequent idiopathic generalized epilepsy syndrome.
125  stages were noted with focal more than with generalized epilepsy syndromes (P < 0.01).
126 n channels, GABAA receptors (GABAARs), cause generalized epilepsy syndromes in humans.
127 tic predisposition is common for many of the generalized epilepsy syndromes, and mutations in genes e
128 s benzodiazepine modulation in families with generalized epilepsy syndromes.
129 ls or networks involved in the physiology of generalized epilepsy syndromes.
130     Here we demonstrate using a rat model of generalized epilepsy that diffuse optical tomography (DO
131       In addition, the mice exhibit primary, generalized epilepsy that is accompanied by remarkably l
132 myoclonic epilepsy (JME) is a common form of generalized epilepsy that starts in adolescence.
133                                          For generalized epilepsy, the selection of the ASD is based
134 road epilepsy spectrum, ranging from genetic generalized epilepsies to developmental and epileptic en
135  a range of epilepsy phenotypes from genetic generalized epilepsy to developmental and epileptic ence
136 epsy ranges broadly in severity from genetic generalized epilepsy to developmental and epileptic ence
137 omputational biomarker to classify focal and generalized epilepsy using interictal EEG.
138 ereas the onset of seizures in patients with generalized epilepsy was later (median: 42 months) with
139   With a 34-fold risk for developing genetic generalized epilepsy, we show for the first time that th
140 ctivity have been associated with idiopathic generalized epilepsies, whereas mutations that disrupt i
141  within the seizure network in two models of generalized epilepsy with absence seizures (Wag/Rij rats
142                                              Generalized epilepsy with absence seizures is the main e
143  various degrees of intellectual disability, generalized epilepsy with atypical absences and generali
144 ed with genetic forms of epilepsy, including generalized epilepsy with febrile seizures plus (GEFS+ t
145  QT syndrome type 3 or Brugada syndrome) and generalized epilepsy with febrile seizures plus (GEFS+)
146 ociated with at least two forms of epilepsy, generalized epilepsy with febrile seizures plus (GEFS+)
147                     Two mutations that cause generalized epilepsy with febrile seizures plus (GEFS+)
148 N1A, on chromosome 2q24 in two families with generalized epilepsy with febrile seizures plus (GEFS+)
149                                              Generalized epilepsy with febrile seizures plus (GEFS+)
150 ant idiopathic epilepsy disorders, including generalized epilepsy with febrile seizures plus (GEFS+)
151 ed with genetic epilepsy syndromes including generalized epilepsy with febrile seizures plus (GEFS+)
152 with a growing number of disorders including generalized epilepsy with febrile seizures plus (GEFS+),
153  epilepsy (JME), pure febrile seizures (FS), generalized epilepsy with febrile seizures plus (GEFS+),
154 ma2 subunit mutation, Q351X, associated with generalized epilepsy with febrile seizures plus (GEFS+),
155 all Italian family with dominantly inherited generalized epilepsy with febrile seizures plus (GEFS+).
156 GABRD, have been identified in families with generalized epilepsy with febrile seizures plus (GEFS+).
157  were proposed as susceptibility alleles for generalized epilepsy with febrile seizures plus and juve
158 ociated with at least two forms of epilepsy, generalized epilepsy with febrile seizures plus and seve
159 ) in an inheritable form of epilepsy (GEFS+, generalized epilepsy with febrile seizures plus) in huma
160                                           In generalized epilepsy with febrile seizures plus, an auto
161 romes, including childhood absence epilepsy, generalized epilepsy with febrile seizures plus, and Dra
162 al. as a heritable susceptibility allele for generalized epilepsy with febrile seizures plus, are als
163 ssociated with the genetic epilepsy syndrome generalized epilepsy with febrile seizures plus, which i
164 unction observed for alleles associated with generalized epilepsy with febrile seizures plus.
165 dium channel Na(V)1.1 are a primary cause of generalized epilepsy with febrile seizures plus.
166 receptor, the GABA(A) receptor, is linked to generalized epilepsy with febrile seizures.
167                                      Genetic generalized epilepsy with photosensitivity demonstrated
168 ng patient groups were included: (i) genetic generalized epilepsy with photosensitivity, 16 subjects
169 calization-related epilepsies and idiopathic generalized epilepsies) with the idiopathic generalized
170 cts (mean age 25 +/- 10 years); (ii) genetic generalized epilepsy without photosensitivity, 13 patien

 
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