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Phenotypes, genotypes, and the management of paroxysmal movement disorders.
Silveira-Moriyama L, Kovac S, Kurian MA, Houlden H, Lees AJ, Walker MC, Roze E, Paciorkowski AR, Mink JW, Warner TT. Silveira-Moriyama L, et al. Dev Med Child Neurol. 2018 Jun;60(6):559-565. doi: 10.1111/dmcn.13744. Epub 2018 Mar 30. Dev Med Child Neurol. 2018. PMID: 29600549 Free article. Review.
Routine gene testing is not necessary to guide treatment for typical forms of paroxysmal kinesigenic dyskinesia (PKD), paroxysmal nonkinesigenic dyskinesia (PNKD), and episodic ataxia type 1 or 2. It can, however, be helpful in the management of atypic …
Routine gene testing is not necessary to guide treatment for typical forms of paroxysmal kinesigenic dyskinesia (PKD), paroxysmal nonkinesig …
Diagnosis and management of acute movement disorders.
Dressler D, Benecke R. Dressler D, et al. J Neurol. 2005 Nov;252(11):1299-306. doi: 10.1007/s00415-005-0006-x. Epub 2005 Oct 10. J Neurol. 2005. PMID: 16208529 Review.
Other paroxysmal dyskinesias include hypnogenic paroxysmal dyskinesias, paroxysmal exertional dyskinesia, infantile paroxysmal dystonias, Sandifer's syndrome and symptomatic paroxysmal dyskinesias. In Hereditary Episodic Ataxia Type 1 attacks of ata
Other paroxysmal dyskinesias include hypnogenic paroxysmal dyskinesias, paroxysmal exertional dyskinesia, infantile paroxysmal dystonias, Sa …
Idiopathic megalencephaly-possible cause and treatment opportunities: from patient to lab.
Almgren M, Schalling M, Lavebratt C. Almgren M, et al. Eur J Paediatr Neurol. 2008 Nov;12(6):438-45. doi: 10.1016/j.ejpn.2007.11.008. Epub 2008 Jan 31. Eur J Paediatr Neurol. 2008. PMID: 18242108 Review.
Findings propose that potassium ion channelopathy may underlie disease for a group of infants or young children displaying idiopathic megalencephaly and early onset epilepsy or episodic ataxia type 1. Carbamazepine's remarkable protective effects on th …
Findings propose that potassium ion channelopathy may underlie disease for a group of infants or young children displaying idiopathic megale …