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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)
12 A (KCNA1 G724C) exhibit partial epilepsy and myokymia but no ataxic episodes, supporting the suggesti
14 enetic causes of episodic ataxia type 1 with myokymia caused by KCNA1 mutations and episodic ataxia t
15 he linkage of human Kv1 channel mutations to myokymia/episodic ataxia type 1 (EA1) and the Shaker mut
16 describe here familial dyskinesia and facial myokymia (FDFM), a novel autosomal dominant disorder cha
17 K+ channel KCNQ2 cause neonatal epilepsy and myokymia, indicating that KCNQ2 regulates the excitabili
19 inicians use many terms including undulating myokymia, neuromyotonia, Isaacs' syndrome and Cramp-Fasc
20 a selected group of patients with undulating myokymia or neuromyotonia, and EMG doublet or multiplet
21 d in one patient with right superior oblique myokymia (SOM), the anatomy of the trochlear nerve was d
23 channels accounts for neonatal epilepsy and myokymia; the cellular locus of these effects may be axo
24 tients suffering from right superior oblique myokymia underwent detailed neuro-ophthalmological exami
25 r contacts in patients with superior oblique myokymia, using a specific magnetic resonance imaging pr
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