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Neuronal ceroid lipofuscinoses (NCLs) are a group of autosomal-recessive hereditary lysosomal storage diseases caused by mutations in at least 8 genes (CLN1-CLN8) [115]

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Fitsiou, E., Pulido, T., Campisi, J., Alimirah, F

Materials and methods Animals Wild-type (C57BL/6J) mice obtained from the Jackson Laboratory [24], were used in this study

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Evaluation of Neuroprtective Effects of L-Carnitine and Fat Emulsion in the CVA Patients: A Prospective, Randomized, Double Blind, Clinical Trial