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W Wittig, J Frenzel, G Zwacka, D Boda
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Case report of Lafora disease: a rare genetic disorder manifesting as progressive myoclonic epilepsy. [PDF]
Naderian R+3 more
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A Review of Neonatal Selective Serotonin Reuptake Inhibitor Withdrawal Syndrome. [PDF]
Mamillapalli L+9 more
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A case of early epileptic encephalopathy caused by new mutation at W218C in <i>KCNQ2</i> and review literature. [PDF]
Yang J+7 more
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Excretion of organic acids associated with biotin deficiency in chronic anticonvulsant therapy [PDF]
Berlit, Peter+3 more
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Cytochrome P-450 purified to apparent homogeneity from phenobarbital-induced rabbit liver microsomes: Catalytic activity and other properties [PDF]
Theodore A. van der Hoeven+2 more
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