Pompucci G - Search Results

1

Paolacci S, Pompucci G, Paolini B, Del Ciondolo I, Miggiano GAD, Aquilanti B, Scaramuzza A, Velluti V, Matera G, Gagliardi L, Bertelli M. Paolacci S, et al. Among authors: pompucci g. Acta Biomed. 2019 Sep 30;90(10-S):87-89. doi: 10.23750/abm.v90i10-S.8766. Acta Biomed. 2019. PMID: 31577261 Free PMC article. Review.

2

Prevalence of mutations in LEP, LEPR, and MC4R genes in individuals with severe obesity.

Paolini B, Maltese PE, Del Ciondolo I, Tavian D, Missaglia S, Ciuoli C, Zuntini M, Cecchin S, Bertelli M, Pompucci G. Paolini B, et al. Among authors: pompucci g. Genet Mol Res. 2016 Aug 19;15(3). doi: 10.4238/gmr.15038718. Genet Mol Res. 2016. PMID: 27706562 Free article.

3

Genetic background, nutrition and obesity: a review.

Vettori A, Pompucci G, Paolini B, Del Ciondolo I, Bressan S, Dundar M, Kenanoğlu S, Unfer V, Bertelli M; Geneob Project. Vettori A, et al. Among authors: pompucci g. Eur Rev Med Pharmacol Sci. 2019 Feb;23(4):1751-1761. doi: 10.26355/eurrev_201902_17137. Eur Rev Med Pharmacol Sci. 2019. PMID: 30840300 Free article. Review.

4

Neurological disorders of purine and pyrimidine metabolism.

Micheli V, Camici M, Tozzi MG, Ipata PL, Sestini S, Bertelli M, Pompucci G. Micheli V, et al. Among authors: pompucci g. Curr Top Med Chem. 2011;11(8):923-47. doi: 10.2174/156802611795347645. Curr Top Med Chem. 2011. PMID: 21401501 Review.

5

NAD metabolism in HPRT-deficient mice.

Micheli V, Jacomelli G, Di Marcello F, Notarantonio L, Sestini S, Cerboni B, Bertelli M, Pompucci G, Jinnah HA. Micheli V, et al. Among authors: pompucci g. Metab Brain Dis. 2009 Jun;24(2):311-9. doi: 10.1007/s11011-009-9134-9. Epub 2009 Mar 25. Metab Brain Dis. 2009. PMID: 19319672 Free PMC article.

6

Biochemical and molecular study of mentally retarded patient with partial deficiency of hypoxanthine-guanine phosphoribosyltransferase.

Micheli V, Gathof BS, Rocchigiani M, Jacomelli G, Sestini S, Peruzzi L, Notarantonio L, Cerboni B, Hayek G, Pompucci G. Micheli V, et al. Among authors: pompucci g. Biochim Biophys Acta. 2002 May 21;1587(1):45-52. doi: 10.1016/s0925-4439(02)00053-4. Biochim Biophys Acta. 2002. PMID: 12009423 Free article.

7

Enzyme activities leading to NAD synthesis in the erythrocytes of HPRT deficient subjects.

Sestini S, Micheli V, Rocchigiani M, Jacomelli G, Manzoni F, Gathof B, Hayek G, Cardona F, Zammarchi E, Pompucci G. Sestini S, et al. Among authors: pompucci g. Adv Exp Med Biol. 1998;431:181-4. doi: 10.1007/978-1-4615-5381-6_35. Adv Exp Med Biol. 1998. PMID: 9598055 No abstract available.

8

Are allopurinol and metabolites found in HPRT deficient erythrocytes responsible for increased NAD synthesis?

Micheli V, Jacomelli G, Sestini S, Notarantonio L, Cerboni B, Peruzzi L, Pompucci G. Micheli V, et al. Among authors: pompucci g. Nucleosides Nucleotides Nucleic Acids. 2004 Oct;23(8-9):1189-91. doi: 10.1081/NCN-200027454. Nucleosides Nucleotides Nucleic Acids. 2004. PMID: 15571228

9

Simple non-radiochemical HPLC-linked method for screening for purine metabolism disorders using dried blood spot.

Jacomelli G, Micheli V, Peruzzi L, Notarantonio L, Cerboni B, Sestini S, Pompucci G. Jacomelli G, et al. Among authors: pompucci g. Clin Chim Acta. 2002 Oct;324(1-2):135-9. doi: 10.1016/s0009-8981(02)00243-7. Clin Chim Acta. 2002. PMID: 12204435

10

HPRTSardinia: a new point mutation causing HPRT deficiency without Lesch-Nyhan disease.

Cossu A, Orrù S, Jacomelli G, Carcassi C, Contu L, Sestini S, Corradi MR, Pompucci G, Carcassi A, Micheli V. Cossu A, et al. Among authors: pompucci g. Biochim Biophys Acta. 2006 Jan;1762(1):29-33. doi: 10.1016/j.bbadis.2005.03.012. Epub 2005 Apr 13. Biochim Biophys Acta. 2006. PMID: 16216473 Free article.

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