1. Heterogeneous dysregulation of microRNAs across the autism spectrum

   • Kawther Abu-Elneel
   • Tsunglin Liu
   • Kenneth S. Kosik

   Original Article 01 July 2008 Pages: 153 - 161

   

2. Differential expression of alpha-synuclein, parkin, and synphilin-1 isoforms in Lewy body disease

   • Katrin Beyer
   • Montserrat Domingo-Sàbat
   • Aurelio Ariza

   Original Article 01 July 2008 Pages: 163 - 172

   

3. Characterization of novel CAPN3 isoforms in white blood cells: an alternative approach for limb-girdle muscular dystrophy 2A diagnosis

   • L. Blázquez
   • M. Azpitarte
   • A. López de Munain

   Original Article 01 July 2008 Pages: 173 - 182

   

4. Detection of low-level somatic and germline mosaicism by denaturing high-performance liquid chromatography in a EURO-MRX family with SLC6A8 deficiency

   • Ofir T. Betsalel
   • Jiddeke M. van de Kamp
   • Gajja S. Salomons

   Original Article 01 July 2008 Pages: 183 - 190

   

5. Evidence of a founder haplotype refines the X-linked Charcot–Marie-Tooth (CMTX3) locus to a 2.5 Mb region

   • Megan Brewer
   • Febriani Changi
   • Marina Kennerson

   Original Article 01 July 2008 Pages: 191 - 195

   

6. Progranulin genetic variations in frontotemporal lobar degeneration: evidence for low mutation frequency in an Italian clinical series

   • Barbara Borroni
   • Silvana Archetti
   • Alessandro Padovani

   Original Article 08 April 2008 Pages: 197 - 205

   

7. ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia

   • Sascha Vermeer
   • Rowdy P. P. Meijer
   • Berry Kremer

   Original Article Open access 01 July 2008 Pages: 207 - 214

   

8. A family with combined mutations of the hemophilia A and X-linked adrenoleukodystrophy genes

   • Brent L. Fogel
   • Pari Young
   • Susan Perlman

   Original Article 01 July 2008 Pages: 215 - 218

   

9. Dysregulation of large-conductance Ca²⁺-activated K⁺ channel expression in nonsyndromal mental retardation due to a cereblon p.R419X mutation

   • Joseph J. Higgins
   • Jin Hao
   • Anjali M. Rajadhyaksha

   Short Communication 01 July 2008 Pages: 219 - 223

   

10. Reevaluation of a large family defines a new locus for X-linked recessive pure spastic paraplegia (SPG34) on chromosome Xq25

    • Lúcia Inês Macedo-Souza
    • Fernando Kok
    • Mayana Zatz

    Letter to the Editors 01 July 2008 Pages: 225 - 226