Piemonte F - Search Results

1

Oxidative abnormalities in Menkes disease.

Rizzo C, Bertini E, Piemonte F, Leuzzi V, Sabetta G, Federici G, Luchetti A, Dionisi-Vici C. Rizzo C, et al. Among authors: piemonte f. J Inherit Metab Dis. 2000 Jun;23(4):349-51. doi: 10.1023/a:1005675012708. J Inherit Metab Dis. 2000. PMID: 10896291 No abstract available.

2

Investigation of the active site of human placenta glutathione transferase pi by means of a spin-labelled glutathione analogue.

Caccuri AM, Polizio F, Piemonte F, Tagliatesta P, Federici G, Desideri A. Caccuri AM, et al. Among authors: piemonte f. Biochim Biophys Acta. 1992 Aug 21;1122(3):265-8. doi: 10.1016/0167-4838(92)90402-y. Biochim Biophys Acta. 1992. PMID: 1324006

3

Colorimetric and fluorometric assays of glutathione transferase based on 7-chloro-4-nitrobenzo-2-oxa-1,3-diazole.

Ricci G, Caccuri AM, Lo Bello M, Pastore A, Piemonte F, Federici G. Ricci G, et al. Among authors: piemonte f. Anal Biochem. 1994 May 1;218(2):463-5. doi: 10.1006/abio.1994.1209. Anal Biochem. 1994. PMID: 8074309 No abstract available.

4

The effects of pregnancy steroids on adaptation of beta cells to pregnancy involve the pancreatic glucose sensor glucokinase.

Magnaterra R, Porzio O, Piemonte F, Bertoli A, Sesti G, Lauro D, Marlier LN, Federici G, Borboni P. Magnaterra R, et al. Among authors: piemonte f. J Endocrinol. 1997 Nov;155(2):247-53. doi: 10.1677/joe.0.1550247. J Endocrinol. 1997. PMID: 9415059

5

Alternative splicing of human plasma cholesteryl ester transfer protein mRNA in Caco-2 cells and its modulation by oleic acid.

Dessí M, Motti C, Cortese C, Leonardis E, Giovannini C, Federici G, Piemonte F. Dessí M, et al. Among authors: piemonte f. Mol Cell Biochem. 1997 Dec;177(1-2):107-12. doi: 10.1023/a:1006823601032. Mol Cell Biochem. 1997. PMID: 9450651

6

Novel 7-DHCR mutation in a child with Smith-Lemli-Opitz syndrome.

Patrono C, Rizzo C, Tessa A, Giannotti A, Borrelli P, Carrozzo R, Piemonte F, Bertini E, Dionisi-Vici C, Santorelli FM. Patrono C, et al. Among authors: piemonte f. Am J Med Genet. 2000 Mar 13;91(2):138-40. doi: 10.1002/(sici)1096-8628(20000313)91:2<138::aid-ajmg12>3.0.co;2-q. Am J Med Genet. 2000. PMID: 10748414

7

OXPHOS and mtDNA alterations in a family with spastic paraparesis.

Santorelli FM, Piemonte F, Carrozzo R, Tessa A, Patrono C, Tozzi G, Bertini E. Santorelli FM, et al. Among authors: piemonte f. Acta Neurol Scand. 2000 Apr;101(4):255-8. doi: 10.1034/j.1600-0404.2000.101004255.x. Acta Neurol Scand. 2000. PMID: 10770522

8

A novel SURF1 mutation results in Leigh syndrome with peripheral neuropathy caused by cytochrome c oxidase deficiency.

Santoro L, Carrozzo R, Malandrini A, Piemonte F, Patrono C, Villanova M, Tessa A, Palmeri S, Bertini E, Santorelli FM. Santoro L, et al. Among authors: piemonte f. Neuromuscul Disord. 2000 Aug;10(6):450-3. doi: 10.1016/s0960-8966(99)00122-4. Neuromuscul Disord. 2000. PMID: 10899453

9

The T9176G mtDNA mutation severely affects ATP production and results in Leigh syndrome.

Carrozzo R, Tessa A, Vázquez-Memije ME, Piemonte F, Patrono C, Malandrini A, Dionisi-Vici C, Vilarinho L, Villanova M, Schägger H, Federico A, Bertini E, Santorelli FM. Carrozzo R, et al. Among authors: piemonte f. Neurology. 2001 Mar 13;56(5):687-90. doi: 10.1212/wnl.56.5.687. Neurology. 2001. PMID: 11245730

10

Determination of blood total, reduced, and oxidized glutathione in pediatric subjects.

Pastore A, Piemonte F, Locatelli M, Lo Russo A, Gaeta LM, Tozzi G, Federici G. Pastore A, et al. Among authors: piemonte f. Clin Chem. 2001 Aug;47(8):1467-9. Clin Chem. 2001. PMID: 11468240 No abstract available.

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