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Cytosolic Accumulation of L-Proline Disrupts GABA-Ergic Transmission through GAD BlockadeNeonatal seizures: advances in mechanisms and managementSevere infantile epileptic encephalopathy due to mutations in PLCB1: expansion of the genotypic and phenotypic disease spectrumA preterm neonate with seizures unresponsive to conventional treatment.Epileptic Encephalopathy in Childhood: A Stepwise Approach for Identification of Underlying Genetic Causes.Advances in clinical determinants and neurological manifestations of B vitamin deficiency in adults.Diagnosis of glycine encephalopathy in a pediatric patient by detection of a GLDC mutation during initial next generation DNA sequencing.Inborn Errors of Metabolism and Epilepsy: Current Understanding, Diagnosis, and Treatment Approaches.[Epilepsy-new diagnostic tools, old drugs? : Therapeutic consequences of epilepsy genetics].Metabolic etiologies in West syndrome.
P2860
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P2860
description
article científic
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article scientifique
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articol științific
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articolo scientifico
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artigo científico
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artigo científico
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artigo científico
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artikel ilmiah
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artikull shkencor
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artículo científico
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name
Inborn errors of metabolism causing epilepsy.
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type
label
Inborn errors of metabolism causing epilepsy.
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prefLabel
Inborn errors of metabolism causing epilepsy.
@en
P2093
P2860
P1476
Inborn errors of metabolism causing epilepsy.
@en
P2093
Emma J Footitt
Peter T Clayton
Shamima Rahman
Sophia Varadkar
P2860
P356
10.1111/J.1469-8749.2012.04406.X
P577
2012-09-24T00:00:00Z