Epilepsy and inborn errors of metabolism in children
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s10545-009-1171-3.pdf
Reference22 articles.
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2. Bahi-Buisson N, Mention K, Leger PL, et al (2006b) Neonatal epilepsy and inborn errors of metabolism. Arch Pediatr 13: 284–292. doi: 10.1016/j.arcped.2005.10.024
3. Bahi-Buisson N, El Sabbagh S, Soufflet C, et al (2008) Myoclonic absence epilepsy with photosensitivity and a gain of function mutation in glutamate dehydrogenase. Seizure 17: 658–664. doi: 10.1016/j.seizure.2008.01.005
4. de Koning TJ, Klomp LW (2004) Serine-deficiency syndromes. Curr Opin Neurol 17: 197–204. doi: 10.1097/00019052-200404000-00019
5. de Koning TJ, Klomp LW, van Oppen AC, et al (2004) Prenatal and early postnatal treatment in 3-phosphoglycerate-dehydrogenase deficiency. Lancet 364: 2221–2222. doi: 10.1016/S0140-6736(04)17596-X
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