Cerone R - Search Results

1

Long-term follow-up of a patient with mild tetrahydrobiopterin-responsive phenylketonuria.

Cerone R, Schiaffino MC, Fantasia AR, Perfumo M, Birk Moller L, Blau N. Cerone R, et al. Mol Genet Metab. 2004 Feb;81(2):137-9. doi: 10.1016/j.ymgme.2003.11.008. Mol Genet Metab. 2004. PMID: 14741196

2

Phenylketonuria: diet for life or not?

Cerone R, Schiaffino MC, Di Stefano S, Veneselli E. Cerone R, et al. Acta Paediatr. 1999 Jun;88(6):664-6. doi: 10.1080/08035259950169350. Acta Paediatr. 1999. PMID: 10419254

3

[Evaluation of a new amino acid mixture for the treatment of phenylketonuria].

Cerone R, Barella C, Fantasia AR, Schiaffino MC. Cerone R, et al. Minerva Pediatr. 1999 Nov-Dec;51(11-12):403-6. Minerva Pediatr. 1999. PMID: 10768006 Italian.

4

Isolated sulphite oxidase deficiency: clinical and biochemical features in an Italian patient.

Schiaffino MC, Fantasia AR, Minniti G, Caruso U, Carnevale F, Cerone R. Schiaffino MC, et al. Among authors: cerone r. J Inherit Metab Dis. 2004;27(1):101-2. doi: 10.1023/b:boli.0000016674.61073.e4. J Inherit Metab Dis. 2004. PMID: 15065571

5

Plasma amino acids during the first 24 hours of life: feasibility of early diagnosis in the newborn at risk of amino acid disorders.

Caruso U, Cerone R, Fantasia AR, Schiaffino MC, Zignego G, Romano C. Caruso U, et al. Among authors: cerone r. J Inherit Metab Dis. 1989;12 Suppl 2:311-4. doi: 10.1007/BF03335408. J Inherit Metab Dis. 1989. PMID: 2512432 No abstract available.

6

Tyrosinemia type III: diagnosis and ten-year follow-up.

Cerone R, Holme E, Schiaffino MC, Caruso U, Maritano L, Romano C. Cerone R, et al. Acta Paediatr. 1997 Sep;86(9):1013-5. doi: 10.1111/j.1651-2227.1997.tb15192.x. Acta Paediatr. 1997. PMID: 9343288

7

Pregnancy and tyrosinaemia type II.

Cerone R, Fantasia AR, Castellano E, Moresco L, Schiaffino MC, Gatti R. Cerone R, et al. J Inherit Metab Dis. 2002 Aug;25(4):317-8. doi: 10.1023/a:1016558510123. J Inherit Metab Dis. 2002. PMID: 12227462

8

Long-term follow-up and outcome of phenylketonuria patients on sapropterin: a retrospective study.

Keil S, Anjema K, van Spronsen FJ, Lambruschini N, Burlina A, Bélanger-Quintana A, Couce ML, Feillet F, Cerone R, Lotz-Havla AS, Muntau AC, Bosch AM, Meli CA, Billette de Villemeur T, Kern I, Riva E, Giovannini M, Damaj L, Leuzzi V, Blau N. Keil S, et al. Among authors: cerone r. Pediatrics. 2013 Jun;131(6):e1881-8. doi: 10.1542/peds.2012-3291. Epub 2013 May 20. Pediatrics. 2013. PMID: 23690520

9

Minor facial anomalies in combined methylmalonic aciduria and homocystinuria due to a defect in cobalamin metabolism.

Cerone R, Schiaffino MC, Caruso U, Lupino S, Gatti R. Cerone R, et al. J Inherit Metab Dis. 1999 May;22(3):247-50. doi: 10.1023/a:1005521702298. J Inherit Metab Dis. 1999. PMID: 10384379 No abstract available.

10

Cobalamin (Cbl) C/D deficiency: clinical, neurophysiological and neuroradiologic findings in 14 cases.

Biancheri R, Cerone R, Schiaffino MC, Caruso U, Veneselli E, Perrone MV, Rossi A, Gatti R. Biancheri R, et al. Among authors: cerone r. Neuropediatrics. 2001 Feb;32(1):14-22. doi: 10.1055/s-2001-12217. Neuropediatrics. 2001. PMID: 11315197

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