Methods of treating certain neurological diseases using exogenous uridine or a uridine source alone as a precursor of endogenous cytidine, particularly in the human brain, are disclosed. Methods are also disclosed wherein exogenous uridine or a uridine source is combined either with drugs increasing uridine availability or with compounds that serve as a source of choline in phospholipid synthesis.

 
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> Hemiasterlin derivatives and uses thereof

> Lactam-containing compounds and derivatives thereof as factor Xa inhibitors

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