Show
Sort by
-
Mutations in SACS cause atypical and late-onset forms of ARSACS
-
Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations
-
Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T > C
-
Opinion of Belgian neurologists on antiepileptic drug treatment in 2006: Belgian study on epilepsy treatment (BESET-2)
-
Opinion of belgian neurologists on antiepileptic drugs: Belgian study on epilepsy treatment (BESET)
-
Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathy
-
MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2
-
Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy
-
Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy
-
Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia