Recent progress in the genetics of human epilepsies Pierre SzepetowskiA. P. Monaco Review article Pages: 153 - 163
Clinical and molecular genetics of primary dystonias U. MüllerDaniela SteinbergerAndrea H. Németh Review article Pages: 165 - 177
No genetic association between the LRP receptor and sporadic or late-onset familial Alzheimer disease William K. ScottLarry H. YamaokaMargaret A. Pericak-Vance Original article Pages: 179 - 183
Identification of two mutations and a polymorphism in the chloride channel CLCN-1 in patients with Becker's generalized myotonia Jesus EstebanA. M. NeumeyerR. H. Brown Original article Pages: 185 - 188
Genetic fine mapping of the Miyoshi myopathy locus and exclusion of eight candidate genes K. BejaouiJ. LiuR. H. Brown Original article Pages: 189 - 196
Novel mutations of mitochondrial complex I in pathologically proven Parkinson disease Siegfried KöselE. M. Grasbon-FrodlManuel B. Graeber Original article Pages: 197 - 204
Adult-onset glycogen storage disease type II: phenotypic and allelic heterogeneity in German patients M. VorgerdBarbara BurwinkelManfred W. Kilimann Original article Pages: 205 - 211
Lack of association between apolipoprotein E genotype and sporadic amyotrophic lateral sclerosis Teepu SiddiqueM. A. Pericak-VanceRobert H. Brown Original article Pages: 213 - 216
Chromosomal localization of two genes underlying late-infantile neuronal ceroid lipofuscinosis J. L. HainesRose-Mary N. BoustanyT. J. Lerner Original article Pages: 217 - 222
Histopathology and APOE genotype of the first Alzheimer disease patient, Auguste D. M. B. GraeberS. KöselP. Mehraein Original article Pages: 223 - 228