1. Nervous NDRGs: the N-myc downstream–regulated gene family in the central and peripheral nervous system

   • Simone L. Schonkeren
   • Maartje Massen
   • Veerle Melotte

   Review Article Open access 04 September 2019 Pages: 173 - 186

   

2. VPS53 gene is associated with a new phenotype of complicated hereditary spastic paraparesis

   • Moran Hausman-Kedem
   • Shay Ben-Shachar
   • Aviva Fattal-Valevski

   Original Article 16 August 2019 Pages: 187 - 195

   

3. Identification and characterization of novel and rare susceptible variants in Indian amyotrophic lateral sclerosis patients

   • Priyam Narain
   • Aditya K. Padhi
   • James Gomes

   Original Article 20 August 2019 Pages: 197 - 208

   

4. Homozygous frameshift variant in NTNG2, encoding a synaptic cell adhesion molecule, in individuals with developmental delay, hypotonia, and autistic features

   • Bassam Abu-Libdeh
   • Motee Ashhab
   • Tamar Harel

   Original Article 02 August 2019 Pages: 209 - 213

   

5. Frequency of the LRRK2 G2019S mutation in South African patients with Parkinson’s disease

   • Nicola du Toit
   • Riaan van Coller
   • Soraya Bardien

   Short Communication 06 September 2019 Pages: 215 - 218

6. Extensive clinical and genetic workup is worthwhile in patients with Leigh-like syndrome due to the TSFM variant c.547G>A

   • Josef Finsterer

   Letter to Editor 03 August 2019 Pages: 219 - 220

7. Acknowledgement to referees 2018/2019

   ACKNOWLEDGEMENT TO REFEREE 03 September 2019 Pages: 221 - 221