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 y epilepsy' and 324 (95% UI 249 to 404) for 'idiopathic epilepsy').
2 y epilepsy' and 433 (95% CI 428 to 438) for 'idiopathic epilepsy').
3 in SCN1A and SCN2A cause several subtypes of idiopathic epilepsy.
4 ptors and, therefore, a potential remedy for idiopathic epilepsy.
5 EJM1, the first gene identified for a common idiopathic epilepsy.
6 than recurrent seizures reminiscent of human idiopathic epilepsy.
7 ly identified in a rare Mendelian variety of idiopathic epilepsy.
8 nderlie the functional abnormalities in this idiopathic epilepsy.
9 mon neuronal excitability disorder, sporadic idiopathic epilepsy.
10 at position 43 (R43Q), is linked to familial idiopathic epilepsies.
11 ues for research on pathogenic mechanisms of idiopathic epilepsies.
12 ve children (age 8-18) with new/recent onset idiopathic epilepsy and 62 healthy controls underwent st
13  logistic regression analysis identified non-idiopathic epilepsy and abnormal motor-sensory (neurolog
14 te to common paroxysmal disorders, including idiopathic epilepsy and migraine, that share features wi
15   Prevalence estimates of 'total epilepsy', 'idiopathic epilepsy' and 'secondary epilepsy' in Denmark
16 se the largest subset of monogenic causes of idiopathic epilepsy, and pathogenic variants contribute
17  neural development may be a cause of common idiopathic epilepsy, and the findings have implications
18                                  A number of idiopathic epilepsies are dominantly inherited, such as
19                                              Idiopathic epilepsies are now being correlated with spec
20 ADHD is a prevalent comorbidity of new onset idiopathic epilepsy associated with a diversity of salie
21  We generated a digenic mouse model of human idiopathic epilepsy by combining two epilepsy-associated
22 d SCN2A are responsible for several dominant idiopathic epilepsy disorders, including generalized epi
23                                Patients with idiopathic epilepsy exhibit cognitive dysfunction and ac
24                      Recently, some forms of idiopathic epilepsy have been causally related to geneti
25                                              Idiopathic epilepsy (IE) is the most common chronic neur
26 udy (GBD) produces prevalence estimates for 'idiopathic epilepsy' (ie, of unknown aetiology) and 'sec
27                                Some forms of idiopathic epilepsy in animals and humans are associated
28 he molecular genetic basis of these familial idiopathic epilepsies is entirely unknown, but a mutatio
29 ociated with hip dysplasia, elbow dysplasia, idiopathic epilepsy, lymphoma, mast cell tumour and gran
30 Children (age: 8-18 years) with recent-onset idiopathic epilepsy (n = 53) and healthy controls (n = 5
31 To date 5% of the imaged cohort or 8% of non-idiopathic epilepsy patients have undergone surgical pro
32                                              Idiopathic epilepsy (Rem1: rate ratio [RR], 3.64, p < 0.
33                        The remainder had non-idiopathic epilepsy syndromes of which 22% had positive
34                                              Idiopathic epilepsy syndromes were identified in 162 (31
35                         Male characters with idiopathic epilepsy tend to be mad, bad, and commonly da
36 ollies and Greater Swiss Mountain Dogs) with idiopathic epilepsy was compared to 20 healthy control d