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 f unsteadiness and dizziness with persistent myokymia.
2 are associated with perioral and periorbital myokymia.
3 lone, suggesting a new phenotype of isolated myokymia.
4  cerebellar ataxia and continuous interictal myokymia.
5 taxia associated with continuous interattack myokymia.
6  containing genes associated with chorea and myokymia: 1) the Huntington disease gene on chromosome 4
7 ed to the pathophysiology of episodic ataxia/myokymia, a disease associated with missense mutations o
8 ed members in Family B (KCNA1 C731A) exhibit myokymia alone, suggesting a new phenotype of isolated m
9 ominant disorder characterized by persistent myokymia and attacks of unsteadiness, slurred speech, an
10 neurological disorders (periodic ataxia with myokymia and hypo- and hyperkalemic periodic paralysis)
11 ilepsy, multiple sclerosis, episodic ataxia, myokymia, and cardiorespiratory dysregulation.
12 ies with diminished reflexes, visible facial myokymia, and distinctive electromyographic features sug
13 A1), characterized by stress-induced ataxia, myokymia, and increased prevalence of seizures.
14 A (KCNA1 G724C) exhibit partial epilepsy and myokymia but no ataxic episodes, supporting the suggesti
15              In conclusion, superior oblique myokymia can result from neurovascular contact at the ro
16 enetic causes of episodic ataxia type 1 with myokymia caused by KCNA1 mutations and episodic ataxia t
17 he linkage of human Kv1 channel mutations to myokymia/episodic ataxia type 1 (EA1) and the Shaker mut
18 describe here familial dyskinesia and facial myokymia (FDFM), a novel autosomal dominant disorder cha
19 K+ channel KCNQ2 cause neonatal epilepsy and myokymia, indicating that KCNQ2 regulates the excitabili
20                             Superior oblique myokymia is a rare movement disorder thought to be cause
21 inicians use many terms including undulating myokymia, neuromyotonia, Isaacs' syndrome and Cramp-Fasc
22 a selected group of patients with undulating myokymia or neuromyotonia, and EMG doublet or multiplet
23 d in one patient with right superior oblique myokymia (SOM), the anatomy of the trochlear nerve was d
24                          Episodic ataxia and myokymia syndrome is an autosomal dominant disorder char
25  channels accounts for neonatal epilepsy and myokymia; the cellular locus of these effects may be axo
26 tients suffering from right superior oblique myokymia underwent detailed neuro-ophthalmological exami
27 r contacts in patients with superior oblique myokymia, using a specific magnetic resonance imaging pr
28 llar dysfunction, ataxic attacks, persistent myokymia with painful cramps in skeletal muscles, and ep