Two siblings with early infantile myoclonic encephalopathy due to mutation in the gene encoding mitochondrial glutamate/H+ symporter SLC25A22.

[1]  S. Khan,et al.  Epileptic Encephalopathies: An Overview , 2012, Epilepsy research and treatment.

[2]  A. Polizzi,et al.  Ohtahara syndrome with emphasis on recent genetic discovery , 2012, Brain and Development.

[3]  M. Mastrangelo,et al.  A diagnostic algorithm for the evaluation of early onset genetic-metabolic epileptic encephalopathies. , 2012, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

[4]  F. Molinari.  Mitochondria and neonatal epileptic encephalopathies with suppression burst , 2010, Journal of bioenergetics and biomembranes.

[5]  A. Munnich,et al.  Mutations in the mitochondrial glutamate carrier SLC25A22 in neonatal epileptic encephalopathy with suppression bursts , 2009, Clinical genetics.

[6]  A. Sweatt,et al.  Mitochondrial transport proteins of the brain , 2007, Journal of Neuroscience Research.

[7]  S. Moshé,et al.  Are early myoclonic encephalopathy (EME) and the Ohtahara syndrome (EIEE) independent of each other? , 2006, Epilepsy Research.

[8]  Y. Ben-Ari,et al.  Opposing role of synaptic and extrasynaptic NMDA receptors in regulation of the extracellular signal‐regulated kinases (ERK) activity in cultured rat hippocampal neurons , 2006, The Journal of physiology.

[9]  A. Munnich,et al.  Impaired mitochondrial glutamate transport in autosomal recessive neonatal myoclonic epilepsy. , 2005, American journal of human genetics.

[10]  Shunsuke Ohtahara,et al.  Epileptic Encephalopathies in Early Infancy With Suppression-Burst , 2003, Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society.

[11]  H. Bading,et al.  Extrasynaptic NMDARs oppose synaptic NMDARs by triggering CREB shut-off and cell death pathways , 2002, Nature Neuroscience.

[12]  Y. Ohtsuka,et al.  Early Infantile Epileptic Syndromes with Suppression‐Bursts: Early Myoclonic Encephalopathy vs. Ohtahara Syndrome , 1993, The Japanese journal of psychiatry and neurology.