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Phibbs, Fenna; Fang, John Y; Cooper, Michael K et al. (2009) Prevalence of unilateral tremor in autosomal dominant essential tremor. Mov Disord 24:108-11
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Sharkey, Lisa M; Jones, Julie M; Hedera, Peter et al. (2009) Evaluation of SCN8A as a candidate gene for autosomal dominant essential tremor. Parkinsonism Relat Disord 15:321-3
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Blair, Marcia A; Ma, Shaochun; Phibbs, Fenna et al. (2008) Reappraisal of the role of the DRD3 gene in essential tremor. Parkinsonism Relat Disord 14:471-5
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Zhao, Jiali; Matthies, Dawn S; Botzolakis, Emmanuel J et al. (2008) Hereditary spastic paraplegia-associated mutations in the NIPA1 gene and its Caenorhabditis elegans homolog trigger neural degeneration in vitro and in vivo through a gain-of-function mechanism. J Neurosci 28:13938-51
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Blair, Marcia A; Riddle, Megan E; Wells, Jennifer F et al. (2007) Infantile onset of hereditary spastic paraplegia poorly predicts the genotype. Pediatr Neurol 36:382-6
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Blair, M A; Ma, S; Abou-Khalil, B et al. (2007) Genetic variants in the IMPA2 gene do not confer increased risk of febrile seizures in Caucasian patients. Eur J Neurol 14:424-7
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Hedera, P; Blair, M A; Andermann, E et al. (2007) Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3. Neurology 68:2107-12
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Hedera, Peter; Ma, Shaochun; Blair, Marcia A et al. (2006) Identification of a novel locus for febrile seizures and epilepsy on chromosome 21q22. Epilepsia 47:1622-8
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Ma, Shaochun; Blair, Marcia A; Abou-Khalil, Bassel et al. (2006) Mutations in the GABRA1 and EFHC1 genes are rare in familial juvenile myoclonic epilepsy. Epilepsy Res 71:129-34
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Blair, Marcia A; Ma, Shaochun; Hedera, Peter (2006) Mutation in KIF5A can also cause adult-onset hereditary spastic paraplegia. Neurogenetics 7:47-50
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Showing the most recent 10 out of 22 publications
