Cotugno G - Search Results

1

The diagnostic challenge of mild citrulline elevation at newborn screening.

Siri B, Olivieri G, Angeloni A, Cairoli S, Carducci C, Cotugno G, Di Michele S, Giovanniello T, La Marca G, Lepri FR, Novelli A, Rossi C, Semeraro M, Dionisi-Vici C. Siri B, et al. Among authors: cotugno g. Mol Genet Metab. 2022 Apr;135(4):327-332. doi: 10.1016/j.ymgme.2022.02.008. Epub 2022 Feb 20. Mol Genet Metab. 2022. PMID: 35279366

2

A Case of Suspected Hyperphenylalaninemia at Newborn Screening by Tandem Mass Spectrometry during Total Parenteral Nutrition.

Pieragostino D, Cicalini I, Di Michele S, Fusilli P, Cotugno G, Ferrante R, Bucci I, Dionisi-Vici C, Stuppia L, De Laurenzi V, Rossi C. Pieragostino D, et al. Among authors: cotugno g. Metabolites. 2020 Jan 24;10(2):44. doi: 10.3390/metabo10020044. Metabolites. 2020. PMID: 31991569 Free PMC article.

3

Chronic liver involvement in urea cycle disorders.

Ranucci G, Rigoldi M, Cotugno G, Bernabei SM, Liguori A, Gasperini S, Goffredo BM, Martinelli D, Monti L, Francalanci P, Candusso M, Parini R, Dionisi-Vici C. Ranucci G, et al. Among authors: cotugno g. J Inherit Metab Dis. 2019 Nov;42(6):1118-1127. doi: 10.1002/jimd.12144. Epub 2019 Aug 25. J Inherit Metab Dis. 2019. PMID: 31260111

4

Fruit-induced FPIES masquerading as hereditary fructose intolerance.

Fiocchi A, Dionisi-Vici C, Cotugno G, Koch P, Dahdah L. Fiocchi A, et al. Among authors: cotugno g. Pediatrics. 2014 Aug;134(2):e602-5. doi: 10.1542/peds.2013-2623. Epub 2014 Jul 7. Pediatrics. 2014. PMID: 25002667

5

Adherence to diet and quality of life in patients with phenylketonuria.

Cotugno G, Nicolò R, Cappelletti S, Goffredo BM, Dionisi Vici C, Di Ciommo V. Cotugno G, et al. Acta Paediatr. 2011 Aug;100(8):1144-9. doi: 10.1111/j.1651-2227.2011.02227.x. Epub 2011 Apr 20. Acta Paediatr. 2011. PMID: 21342250

6

Cerebro-reno-digital (Meckel-like) syndrome with Dandy-Walker malformation, cystic kidneys, hepatic fibrosis, and polydactyly.

Genuardi M, Dionisi-Vici C, Sabetta G, Mignozzi M, Rizzoni G, Cotugno G, Martini Neri ME. Genuardi M, et al. Among authors: cotugno g. Am J Med Genet. 1993 Aug 1;47(1):50-3. doi: 10.1002/ajmg.1320470111. Am J Med Genet. 1993. PMID: 8368252

7

Impaired bone metabolism in glycogen storage disease type 1 is associated with poor metabolic control in type 1a and with granulocyte colony-stimulating factor therapy in type 1b.

Melis D, Pivonello R, Cozzolino M, Della Casa R, Balivo F, Del Puente A, Dionisi-Vici C, Cotugno G, Zuppaldi C, Rigoldi M, Parini R, Colao A, Andria G, Parenti G. Melis D, et al. Among authors: cotugno g. Horm Res Paediatr. 2014;81(1):55-62. doi: 10.1159/000351022. Epub 2013 Dec 21. Horm Res Paediatr. 2014. PMID: 24401800

8

Cognitive findings and behavior in children and adolescents with phenylketonuria.

Cappelletti S, Cotugno G, Goffredo BM, Nicolò R, Bernabei SM, Caviglia S, Di Ciommo V. Cappelletti S, et al. Among authors: cotugno g. J Dev Behav Pediatr. 2013 Jul-Aug;34(6):392-8. doi: 10.1097/DBP.0b013e31829a79ef. J Dev Behav Pediatr. 2013. PMID: 23782895

9

Living with phenylketonuria from the point of view of children, adolescents, and young adults: a qualitative study.

Di Ciommo V, Forcella E, Cotugno G. Di Ciommo V, et al. Among authors: cotugno g. J Dev Behav Pediatr. 2012 Apr;33(3):229-35. doi: 10.1097/DBP.0b013e3182460d8a. J Dev Behav Pediatr. 2012. PMID: 22249384

10

Charmed baryonium.

Cotugno G, Faccini R, Polosa AD, Sabelli C. Cotugno G, et al. Phys Rev Lett. 2010 Apr 2;104(13):132005. doi: 10.1103/PhysRevLett.104.132005. Epub 2010 Apr 1. Phys Rev Lett. 2010. PMID: 20481876

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