戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 can be construed as a novel endophenotype of juvenile myoclonic epilepsy.
2 ings, and so constitutes an endophenotype of juvenile myoclonic epilepsy.
3 human homologues are related to the cause of juvenile myoclonic epilepsy.
4  abnormalities in the medial frontal lobe in juvenile myoclonic epilepsy.
5 ognitive effort can cause myoclonic jerks in juvenile myoclonic epilepsy.
6 tment of idiopathic generalized epilepsy and juvenile myoclonic epilepsy.
7 ized epilepsy with febrile seizures plus and juvenile myoclonic epilepsy.
8 ation R482X was identified in a patient with juvenile myoclonic epilepsy.
9 D) subunits, which causes autosomal dominant juvenile myoclonic epilepsy.
10 e trafficking, leading to autosomal dominant juvenile myoclonic epilepsy.
11                         Twenty patients with juvenile myoclonic epilepsy, 10 patients each with child
12 l structure and function in 37 patients with juvenile myoclonic epilepsy, 16 unaffected siblings and
13  types of epilepsy, 226 patients with either juvenile myoclonic epilepsy, absence epilepsy, or febril
14 D (AD), causes an autosomal dominant form of juvenile myoclonic epilepsy (ADJME).
15 between cortical regions in 30 patients with juvenile myoclonic epilepsy and 26 healthy controls.
16 imaging, in a cohort of 28 participants with juvenile myoclonic epilepsy and detected changes in an a
17 absence epilepsy, juvenile absence epilepsy, juvenile myoclonic epilepsy and epilepsy with generalize
18                                              Juvenile myoclonic epilepsy and the EEG trait segregated
19 provide evidence that a gene responsible for juvenile myoclonic epilepsy and the subclinical, 3.5- to
20 lume, shape and positioning in patients with juvenile myoclonic epilepsy and their siblings, which ar
21 functions has been reported in patients with juvenile myoclonic epilepsy and their unaffected sibling
22          Individuals with autosomal dominant juvenile myoclonic epilepsy are heterozygous for a GABA(
23 uch as benign familial neonatal convulsions, juvenile myoclonic epilepsy, as well as benign epilepsy
24 s-sectional data collected by The Biology of Juvenile Myoclonic Epilepsy (BIOJUME) consortium.
25 main protein Jerky, previously implicated in juvenile myoclonic epilepsy development.
26 l, neuropsychological and imaging studies in juvenile myoclonic epilepsy have consistently pointed to
27 controversial, and functional MRI studies in juvenile myoclonic epilepsy have not tested hippocampal
28 rmined homogenous patient populations (PAX6, juvenile myoclonic epilepsy) have strengthened the link
29                                              Juvenile myoclonic epilepsy is a common type of idiopath
30                                              Juvenile myoclonic epilepsy is a heritable idiopathic ge
31                 A form of autosomal dominant juvenile myoclonic epilepsy is caused by a nonconservati
32                                              Juvenile myoclonic epilepsy is the most common genetic g
33                                              Juvenile myoclonic epilepsy is the most common idiopathi
34                                              Juvenile myoclonic epilepsy is the most frequent idiopat
35 agnetoencephalography (MEG) from people with juvenile myoclonic epilepsy (JME) and healthy controls.
36                      The implication is that juvenile myoclonic epilepsy (JME) does not exist as the
37                                  Adults with juvenile myoclonic epilepsy (JME) have subtle brain stru
38                                              Juvenile myoclonic epilepsy (JME) is a common form of ge
39                                              Juvenile myoclonic epilepsy (JME) is a common idiopathic
40                                              Juvenile myoclonic epilepsy (JME) is a distinctive and c
41                                              Juvenile myoclonic epilepsy (JME) is associated with cor
42     Further, 40% of individual patients with juvenile myoclonic epilepsy (JME), a syndrome of IGE in
43            The IGEs that we studied included juvenile myoclonic epilepsy (JME), epilepsy with only ge
44                            The IGEs included juvenile myoclonic epilepsy (JME), juvenile absence epil
45 t two loci were segregating in subjects with juvenile myoclonic epilepsy (JME), one predisposing to g
46  including childhood absence epilepsy (CAE), juvenile myoclonic epilepsy (JME), pure febrile seizures
47 common form of inherited epilepsy in humans, juvenile myoclonic epilepsy (JME).
48 3) progressive myoclonic epilepsy (PME) from juvenile myoclonic epilepsy (JME).
49 gen (HLA) markers were genetically linked to juvenile myoclonic epilepsy (JME); this was confirmed in
50 iracetam was confirmed only in patients with juvenile myoclonic epilepsy (JME; IPTW-adjusted HR, 0.47
51 dy subjects with two forms of IGE, including juvenile myoclonic epilepsy (n = 93) and absence epileps
52  were found in eight out of 20 patients with juvenile myoclonic epilepsy, one out of 10 patients with
53 rs, 10 of whom were clinically affected with juvenile myoclonic epilepsy or presented with subclinica
54 ctivation along the hippocampal long axis in juvenile myoclonic epilepsy patients with and without ma
55                                Patients with juvenile myoclonic epilepsy showed increased functional
56 ars, median 40) of 11 of those patients with juvenile myoclonic epilepsy (six female; age range 22-54