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26. Myoclonus epilepsy and ataxia due to potassium channel mutation (MEAK): a cause of progressive myoclonic epilepsy. Mahale RR; Tiwari R; Arunachal G; Padmanabha H; Mailankody P Acta Neurol Belg; 2022 Jun; 122(3):801-803. PubMed ID: 33725338 [No Abstract] [Full Text] [Related]
27. [Diagnostic focus on the child with myoclonic seizures in isolation or associated with other types of seizures]. Herranz JL; de las Cuevas I Rev Neurol; 1998 Feb; 26(150):301-7. PubMed ID: 9563099 [TBL] [Abstract][Full Text] [Related]
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36. Clinical and neurophysiologic features of progressive myoclonus epilepsy without renal failure caused by SCARB2 mutations. Rubboli G; Franceschetti S; Berkovic SF; Canafoglia L; Gambardella A; Dibbens LM; Riguzzi P; Campieri C; Magaudda A; Tassinari CA; Michelucci R Epilepsia; 2011 Dec; 52(12):2356-63. PubMed ID: 22050460 [TBL] [Abstract][Full Text] [Related]
37. Occipital epilepsy versus progressive myoclonic epilepsy in a patient with continuous occipital spikes and photosensitivity in electroencephalogram: A case report. Lv Y; Zhang N; Liu C; Shi M; Sun L Medicine (Baltimore); 2018 Apr; 97(15):e0299. PubMed ID: 29642155 [TBL] [Abstract][Full Text] [Related]
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