1. Publication of microarray results

   • Ulrich Müller
   • Manuel B. Graeber
   • James R. Lupski

   Editorial 26 April 2003 Pages: 155 - 155

2. Dementia with Lewy bodies: disease concept and genetics

   • Manuel B. Graeber
   • Ulrich Müller

   Review Article 26 July 2003 Pages: 157 - 162

   

3. Gene expression profiling of Duchenne muscular dystrophy skeletal muscle

   • Judith N. Haslett
   • Despina Sanoudou
   • Louis M. Kunkel

   Original Article 16 April 2003 Pages: 163 - 171

4. Refined mapping of the Welander distal myopathy region on chromosome 2p13 positions the new candidate region telomeric of the DYSF locus

   • Désirée von Tell
   • Carl E. G. Bruder
   • Gabrielle Åhlberg

   Original Article 27 June 2003 Pages: 173 - 177

   

5. Refined localization of dominant intermediate Charcot-Marie-Tooth neuropathy and exclusion of seven known candidate genes in the region

   • Danqing Zhu
   • Marina Kennerson
   • Garth Nicholson

   Original Article 22 May 2003 Pages: 179 - 183

   

6. Haplotype analysis of the ETM2 locus in familial essential tremor

   • Joseph J. Higgins
   • Joseph Jankovic
   • Melanie U. Ruszczyk

   Original Article 22 May 2003 Pages: 185 - 189

   

7. Charcot-Marie-Tooth disease: a novel Tyr145Ser mutation in the myelin protein zero (MPZ, P0) gene causes different phenotypes in homozygous and heterozygous carriers within one family

   • Alejandro Leal
   • Corinna Berghoff
   • Dieter Heuss

   Original Article 05 July 2003 Pages: 191 - 197

   

8. A heteroplasmic mitochondrial complex I gene mutation in adult-onset dystonia

   • David K. Simon
   • Jennifer Friedman
   • Mark A. Tarnopolsky

   Original Article 17 May 2003 Pages: 199 - 205

   

9. Association of dopamine D4 receptor (DRD4) exon III repeat polymorphism with temperament in 3-year-old infants

   • Alessandro De Luca
   • Mario Rizzardi
   • Bruno Dallapiccola

   Original Article 27 March 2003 Pages: 207 - 212

10. Association of late-onset Alzheimer disease with a genotype of PLAU, the gene encoding urokinase-type plasminogen activator on chromosome 10q22.2

    • U. Finckh
    • K. van Hadeln
    • A. Gal

    Original Article 24 July 2003 Pages: 213 - 217

    

11. Point mutations in exon 1 of the NR4A2 gene are not a major cause of familial Parkinson′s disease

    • Alexander Zimprich
    • Friedrich Asmus
    • Thomas Gasser

    Letter to the Editors 25 June 2003 Pages: 219 - 220

12. Variants in the ALS2 gene are not associated with sporadic amyotrophic lateral sclerosis

    • Ammar Al-Chalabi
    • Valerie K. Hansen
    • Robert H. Brown Jr

    Letter to the Editor 27 May 2003 Pages: 221 - 222