Porta F - Search Results

1

Target Prolactin Range in Treatment of Tetrahydrobiopterin Deficiency.

Porta F, Ponzone A, Spada M. Porta F, et al. J Pediatr. 2016 Jan;168:236-239.e1. doi: 10.1016/j.jpeds.2015.09.062. Epub 2015 Oct 27. J Pediatr. 2016. PMID: 26515614

2

Unresponsiveness to tetrahydrobiopterin of phenylalanine hydroxylase deficiency.

Ponzone A, Porta F, Mussa A, Alluto A, Ferraris S, Spada M. Ponzone A, et al. Among authors: porta f. Metabolism. 2010 May;59(5):645-52. doi: 10.1016/j.metabol.2009.09.008. Epub 2009 Nov 14. Metabolism. 2010. PMID: 19913839

3

Dopamine agonists in dihydropteridine reductase deficiency.

Porta F, Mussa A, Concolino D, Spada M, Ponzone A. Porta F, et al. 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

4

Short prolactin profile for monitoring treatment in BH4 deficiency.

Porta F, Ponzone A, Spada M. Porta F, et al. Eur J Paediatr Neurol. 2015 May;19(3):360-3. doi: 10.1016/j.ejpn.2015.01.010. Epub 2015 Feb 9. Eur J Paediatr Neurol. 2015. PMID: 25707872

5

Long-term safety and effectiveness of pramipexole in tetrahydrobiopterin deficiency.

Porta F, Ponzone A, Spada M. Porta F, et al. Eur J Paediatr Neurol. 2016 Nov;20(6):839-842. doi: 10.1016/j.ejpn.2016.08.006. Epub 2016 Aug 15. Eur J Paediatr Neurol. 2016. PMID: 27562098 Free article.

6

Early Screening for Tetrahydrobiopterin Responsiveness in Phenylketonuria.

Porta F, Spada M, Ponzone A. Porta F, et al. Pediatrics. 2017 Aug;140(2):e20161591. doi: 10.1542/peds.2016-1591. Epub 2017 Jul 5. Pediatrics. 2017. PMID: 28679641

7

Phenylalanine and tyrosine metabolism in DNAJC12 deficiency: A comparison between inherited hyperphenylalaninemias and healthy subjects.

Porta F, Ponzone A, Spada M. Porta F, et al. Eur J Paediatr Neurol. 2020 Sep;28:77-80. doi: 10.1016/j.ejpn.2020.07.011. Epub 2020 Aug 1. Eur J Paediatr Neurol. 2020. PMID: 32800687

8

Tyrosine metabolism in health and disease: slow-release amino acids therapy improves tyrosine homeostasis in phenylketonuria.

Porta F, Giorda S, Ponzone A, Spada M. Porta F, et al. J Pediatr Endocrinol Metab. 2020 Nov 19;33(12):1519-1523. doi: 10.1515/jpem-2020-0319. Print 2020 Dec 16. J Pediatr Endocrinol Metab. 2020. PMID: 33581706

9

Phalangeal quantitative ultrasound in children with phenylketonuria: a pilot study.

Porta F, Spada M, Lala R, Mussa A. Porta F, et al. Ultrasound Med Biol. 2008 Jul;34(7):1049-52. doi: 10.1016/j.ultrasmedbio.2007.12.013. Epub 2008 Mar 3. Ultrasound Med Biol. 2008. PMID: 18313203

10

Impact of neonatal protein metabolism and nutrition on screening for phenylketonuria.

Ponzone A, Spada M, Roasio L, Porta F, Mussa A, Ferraris S. Ponzone A, et al. Among authors: porta f. J Pediatr Gastroenterol Nutr. 2008 May;46(5):561-9. doi: 10.1097/MPG.0b013e31815eead6. J Pediatr Gastroenterol Nutr. 2008. PMID: 18493213

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