@article{Herrera Morban_2017, place={Quartu Sant’Elena (CA, Italy)}, title={Phenylketonuria: central nervous system and microbiome interaction}, volume={6}, url={https://jpnim.com/index.php/jpnim/article/view/060207}, DOI={10.7363/060207}, abstractNote={Phenylketonuria (PKU) is an autosomal recessive inborn error of metabolism characterized by increased phenylalanine (Phe) levels causing an inadequate neurodevelopment; the treatment of PKU is a Phe-restricting diet, and as such it can modulate the intestinal microbiome of the individual, generating central nervous system secondary disturbances that, added to the baseline disturbance, can influence the outcome of the disease.}, number={2}, journal={Journal of Pediatric and Neonatal Individualized Medicine (JPNIM)}, author={Herrera Morban, Demian Arturo}, year={2017}, month={Jun.}, pages={e060207} }