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Page 1
Phenotyping and treatment of phenylketonuria.
Porta F, Mussa A, Garelli D, Spada M. Porta F, et al. Among authors: spada m. Lancet. 2011 Feb 5;377(9764):465; author reply 466. doi: 10.1016/S0140-6736(11)60157-8. Lancet. 2011. PMID: 21296231 No abstract available.
Lysosomal enzyme activities in phenylketonuria.
Porta F, Pagliardini S, Pagliardini V, Dotta A, Mussa A, Spada M. Porta F, et al. Among authors: spada m. Mol Genet Metab. 2011 Apr;102(4):508. doi: 10.1016/j.ymgme.2011.01.014. Epub 2011 Feb 2. Mol Genet Metab. 2011. PMID: 21316999 No abstract available.
Tetrahydrobiopterin and phenylketonuria.
Porta F, Spada M, Garelli D, Mussa A, Ponzone A. Porta F, et al. Among authors: spada m. J Pediatr. 2011 May;158(5):864; author reply 864-5. doi: 10.1016/j.jpeds.2010.12.002. Epub 2011 Feb 15. J Pediatr. 2011. PMID: 21324389 No abstract available.
Dopamine agonists in dihydropteridine reductase deficiency.
Porta F, Mussa A, Concolino D, Spada M, Ponzone A. Porta F, et al. Among authors: spada m. Mol Genet Metab. 2012 Apr;105(4):582-4. doi: 10.1016/j.ymgme.2012.01.013. Epub 2012 Jan 25. Mol Genet Metab. 2012. PMID: 22325981
778 results