DOI: 10.1055/s-00029025

Journal of Pediatric Epilepsy

Issue 03 · Volume 01 · September 2012 DOI: 10.1055/s-005-29708 Genetic Testing in Clinical Practice

Foreword

  • 133
    Porter, Brenda E.:

    Foreword

    • Review Article

  • 135
    Sheidley, Beth Rosen; Poduri, Annapurna:

    Genetics in clinical epilepsy: Issues in genetic testing and counseling

  • 143
    Wusthoff, Courtney J.:

    Benign familial neonatal epilepsy

  • 151
    Olson, Heather E.; Poduri, Annapurna:

    CDKL5 mutations in early onset epilepsy: Case report and review of the literature

  • 161
    Jähn, Johanna A.; Helbig, Ingo:

    Structural genomic variants in pediatric seizure disorders

  • 171
    Paciorkowski, Alex R.; Porter, Brenda E.:

    MEF2C haploinsufficiency syndrome: A severe neurodevelopmental disorder with variable epilepsy

  • 179
    Singhal, Nilika S.; Sullivan, Joseph E.:

    PCDH19-related epilepsy

    • Letter to the Editor

  • 185
    Ho, Gladys; Gold, Wendy; Williamson, Sarah L.; Christodoulou, John:

    Pathogenicity of C-terminal mutations in CDKL5