1. Whole genome expression analyses of single- and double-knock-out mice implicate partially overlapping functions of alpha- and gamma-synuclein

   • Melanie Kuhn
   • Karina Haebig
   • Olaf Riess

   Original Article 22 February 2007 Pages: 71 - 81

   

2. The medial and lateral substantia nigra in Parkinson’s disease: mRNA profiles associated with higher brain tissue vulnerability

   • D. C. Duke
   • L. B. Moran
   • M. B. Graeber

   Original Article 09 January 2007 Pages: 83 - 94

   

3. Leucine-rich repeat kinase 1: a paralog of LRRK2 and a candidate gene for Parkinson’s disease

   • Julie P. Taylor
   • Mary M. Hulihan
   • Matthew J. Farrer

   Original Article 16 January 2007 Pages: 95 - 102

   

4. Biological effects of the PINK1 c.1366C>T mutation: implications in Parkinson disease pathogenesis

   • Anne Grünewald
   • Guido J. Breedveld
   • Vincenzo Bonifati

   Original Article 12 January 2007 Pages: 103 - 109

   

5. A novel gene derived from a segmental duplication shows perturbed expression in Alzheimer’s disease

   • Dimitrios Avramopoulos
   • Ruihua Wang
   • Susan S. Bassett

   Original Article 16 February 2007 Pages: 111 - 120

   

6. Nf1 expression is dependent on strain background: implications for tumor suppressor haploinsufficiency studies

   • Jessica J. Hawes
   • Robert G. Tuskan
   • Karlyne M. Reilly

   Original Article 11 January 2007 Pages: 121 - 130

   

7. Functional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymia

   • Haijun Chen
   • Christian von Hehn
   • Fuki M. Hisama

   Original Article Open access 29 November 2006 Pages: 131 - 135

   

8. Mutations of the LMNA gene can mimic autosomal dominant proximal spinal muscular atrophy

   • Sabine Rudnik-Schöneborn
   • Elke Botzenhart
   • Klaus Zerres

   Original Article 29 November 2006 Pages: 137 - 142

   

9. Altered neurodevelopment associated with mutations of RSK2: a morphometric MRI study of Coffin–Lowry syndrome

   • Shelli R. Kesler
   • Richard J. Simensen
   • Allan L. Reiss

   Short Communication 22 February 2007 Pages: 143 - 147

   

10. Large germline deletions and duplication in isolated cerebral cavernous malformation patients

    • U. Felbor
    • S. Gaetzner
    • A. M. Siegel

    Short Communication 09 January 2007 Pages: 149 - 153

    

11. NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe

    • Stephan Klebe
    • Arnaud Lacour
    • Giovanni Stevanin

    Letters to the Editors 05 January 2007 Pages: 155 - 157