1. Recent progress in the genetics of human epilepsies

   • Pierre Szepetowski
   • A. P. Monaco

   Review article Pages: 153 - 163

2. Clinical and molecular genetics of primary dystonias

   • U. Müller
   • Daniela Steinberger
   • Andrea H. Németh

   Review article Pages: 165 - 177

3. No genetic association between the LRP receptor and sporadic or late-onset familial Alzheimer disease

   • William K. Scott
   • Larry H. Yamaoka
   • Margaret A. Pericak-Vance

   Original article Pages: 179 - 183

4. Identification of two mutations and a polymorphism in the chloride channel CLCN-1 in patients with Becker's generalized myotonia

   • Jesus Esteban
   • A. M. Neumeyer
   • R. H. Brown

   Original article Pages: 185 - 188

5. Genetic fine mapping of the Miyoshi myopathy locus and exclusion of eight candidate genes

   • K. Bejaoui
   • J. Liu
   • R. H. Brown

   Original article Pages: 189 - 196

6. Novel mutations of mitochondrial complex I in pathologically proven Parkinson disease

   • Siegfried Kösel
   • E. M. Grasbon-Frodl
   • Manuel B. Graeber

   Original article Pages: 197 - 204

7. Adult-onset glycogen storage disease type II: phenotypic and allelic heterogeneity in German patients

   • M. Vorgerd
   • Barbara Burwinkel
   • Manfred W. Kilimann

   Original article Pages: 205 - 211

8. Lack of association between apolipoprotein E genotype and sporadic amyotrophic lateral sclerosis

   • Teepu Siddique
   • M. A. Pericak-Vance
   • Robert H. Brown

   Original article Pages: 213 - 216

9. Chromosomal localization of two genes underlying late-infantile neuronal ceroid lipofuscinosis

   • J. L. Haines
   • Rose-Mary N. Boustany
   • T. J. Lerner

   Original article Pages: 217 - 222

10. Histopathology and APOE genotype of the first Alzheimer disease patient, Auguste D.

    • M. B. Graeber
    • S. Kösel
    • P. Mehraein

    Original article Pages: 223 - 228