1. Paradoxical worsening of seizure activity with pregabalin in an adult with isodicentric 15 (IDIC-15) syndrome involving duplications of the GABRB3, GABRA5 and GABRG3 genes Di Rocco, Alessandro; Loggini, Andrea; Di Rocco, Maja; Di Rocco, Pietro; Rossi, Roger; Gimelli, Giorgio; Bazil, Carl W. 2013 Articles ConvulsionsPregabalinGABA--ReceptorsDevelopmental disabilitiesDevelopmental disabilities--Genetic aspectsAbnormalities, Human--Genetic aspectsGeneticsMedicineNeurosciences
2. Comprehensive Analysis of the 16p11.2 Deletion and Null Cntnap2 Mouse Models of Autism Spectrum Disorder Brunner, Daniela; Kabitzke, Patricia; He, Dansha; Cox, Kimberly; Thiede, Lucinda; Hanania, Taleen; Sabath, Emily; Alexandrov, Vadim; Saxe, Michael; Peles, Elior; Mills, Alea; Spooren, Will; Ghosh, Anirvan; Feliciano, Pamela; Benedetti, Marta; Clayton, Alice Luo; Biemans, Barbara 2015 Articles Mice as laboratory animalsNeurosciences--ResearchAutismMedicineGeneticsNeurosciences
3. Intermediate Phenotypes of ATP1A3 Mutations: Phenotype–Genotype Correlations Termsarasab, Pichet; Yang, Amy C.; Frucht, Steven J. 2015 Articles NeurosciencesMedicineMedical sciencesGenetics
4. Neuroferritinopathy: Pathophysiology, Presentation, Differential Diagnoses and Management Kumar, Niraj; Rizek, Philippe; Jog, Mandar 2016 Articles Medical geneticsGenetic disordersPhysiology, PathologicalIron--Metabolism--DisordersNervous system--DegenerationMovement disordersMedicineNeurosciencesGenetics