Familial cortical tremor and epilepsy: A well-defined syndrome with genetic heterogeneity waiting for nosological placement in the ILAE classification
Author:
Publisher
Elsevier BV
Subject
Behavioral Neuroscience,Neurology (clinical),Neurology
Reference5 articles.
1. Familial cortical myoclonic tremor with epilepsy: the third locus (FCMTE3) maps to 5p;Depienne;Neurology,2010
2. Autosomal dominant cortical tremor, myoclonus and epilepsy: many syndromes, one phenotype;Striano;Acta Neurol Scand,2005
3. Life-threatening status epilepticus following gabapentin administration in a patient with benign adult familial myoclonic epilepsy;Striano;Epilepsia,2007
4. 1H MR spectroscopy indicates prominent cerebellar dysfunction in benign adult familial myoclonic epilepsy;Striano;Epilepsia,2009
5. Familial cortical tremor with epilepsy and cerebellar pathological findings;Van Rootselaar;Mov Disord,2004
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Familial cortical myoclonic tremor and epilepsy: Description of a new South African pedigree with 30 year follow up;Parkinsonism & Related Disorders;2017-05
2. Benign adult familial myoclonus epilepsy is a progressive disorder: no longer idiopathic generalized epilepsy;Epileptic Disorders;2016-03
3. Rational search for genes in familial cortical myoclonic tremor with epilepsy, clues from recent advances;Seizure;2016-01
4. Reply: Autosomal recessive epilepsy associated with contactin 2 mutation is different from familial cortical tremor, myoclonus and epilepsy;Brain;2013-06-25
5. Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2;Brain;2013-03-21
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