Giovannini M - Search Results

1

Double blind placebo control trial of large neutral amino acids in treatment of PKU: effect on blood phenylalanine.

Matalon R, Michals-Matalon K, Bhatia G, Burlina AB, Burlina AP, Braga C, Fiori L, Giovannini M, Grechanina E, Novikov P, Grady J, Tyring SK, Guttler F. Matalon R, et al. Among authors: giovannini m. J Inherit Metab Dis. 2007 Apr;30(2):153-8. doi: 10.1007/s10545-007-0556-4. Epub 2007 Feb 27. J Inherit Metab Dis. 2007. PMID: 17334706 Clinical Trial.

2

Phenylketonuria: dietary and therapeutic challenges.

Giovannini M, Verduci E, Salvatici E, Fiori L, Riva E. Giovannini M, et al. J Inherit Metab Dis. 2007 Apr;30(2):145-52. doi: 10.1007/s10545-007-0552-8. Epub 2007 Mar 8. J Inherit Metab Dis. 2007. PMID: 17347911 Review.

3

Pharmacokinetics of orally administered tetrahydrobiopterin in patients with phenylalanine hydroxylase deficiency.

Zurflüh MR, Fiori L, Fiege B, Ozen I, Demirkol M, Gärtner KH, Thöny B, Giovannini M, Blau N. Zurflüh MR, et al. Among authors: giovannini m. J Inherit Metab Dis. 2006 Dec;29(6):725-31. doi: 10.1007/s10545-006-0425-6. Epub 2006 Nov 7. J Inherit Metab Dis. 2006. PMID: 17091341 Free article.

4

Long term effects of long chain polyunsaturated fats in hyperphenylalaninemic children.

Agostoni C, Verduci E, Massetto N, Fiori L, Radaelli G, Riva E, Giovannini M. Agostoni C, et al. Among authors: giovannini m. Arch Dis Child. 2003 Jul;88(7):582-3. doi: 10.1136/adc.88.7.582. Arch Dis Child. 2003. PMID: 12818902 Free PMC article. Clinical Trial.

5

Incidence of BH4-responsiveness in phenylalanine-hydroxylase-deficient Italian patients.

Fiori L, Fiege B, Riva E, Giovannini M. Fiori L, et al. Among authors: giovannini m. Mol Genet Metab. 2005 Dec;86 Suppl 1:S67-74. doi: 10.1016/j.ymgme.2005.06.017. Epub 2005 Sep 28. Mol Genet Metab. 2005. PMID: 16198137

6

Phenylalanine hydroxylase mutations and phenylalanine-tyrosine metabolism in heterozygotes for phenylalanine hydroxylase deficiency.

Verduci E, Riva E, Agostoni C, Leviti S, Fiori L, Lammardo AM, Biondi ML, Giovannini M. Verduci E, et al. Among authors: giovannini m. Acta Paediatr. 2002;91(7):805-10. doi: 10.1080/08035250213217. Acta Paediatr. 2002. PMID: 12200907

7

Testing for tetrahydrobiopterin responsiveness in patients with hyperphenylalaninemia due to phenylalanine hydroxylase deficiency.

Cerone R, Andria G, Giovannini M, Leuzzi V, Riva E, Burlina A. Cerone R, et al. Among authors: giovannini m. Adv Ther. 2013 Mar;30(3):212-28. doi: 10.1007/s12325-013-0011-x. Epub 2013 Feb 20. Adv Ther. 2013. PMID: 23436109 Review.

8

PAH deficiency in Italy: correlation of genotype with phenotype in the Sicilian population.

Romano V, Guldberg P, Güttler F, Meli C, Mollica F, Pavone L, Giovannini M, Riva E, Biasucci G, Luotti D, Palillo L, Calí F, Ceratto N, Anello G, Bosco P. Romano V, et al. Among authors: giovannini m. J Inherit Metab Dis. 1996;19(1):15-24. doi: 10.1007/BF01799343. J Inherit Metab Dis. 1996. PMID: 8830172

9

Treating phenylketonuria: a single centre experience.

Giovannini M, Riva E, Salvatici E, Fiori L, Paci S, Verduci E, Agostoni C. Giovannini M, et al. J Int Med Res. 2007 Nov-Dec;35(6):742-52. doi: 10.1177/147323000703500602. J Int Med Res. 2007. PMID: 18034987 Free article.

10

Nutrition in children affected by inherited metabolic diseases.

Giovannini M, Biasucci G, Luotti D, Fiori L, Riva E. Giovannini M, et al. Ann Ist Super Sanita. 1995;31(4):489-502. Ann Ist Super Sanita. 1995. PMID: 8851705 Review.

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