Riudor E - Search Results

1

Safety of ornithine phenylacetate in cirrhotic decompensated patients: an open-label, dose-escalating, single-cohort study.

Ventura-Cots M, Arranz JA, Simón-Talero M, Torrens M, Blanco A, Riudor E, Fuentes I, Suñé P, Soriano G, Córdoba J. Ventura-Cots M, et al. Among authors: riudor e. J Clin Gastroenterol. 2013 Nov-Dec;47(10):881-7. doi: 10.1097/MCG.0b013e318299c789. J Clin Gastroenterol. 2013. PMID: 23751856

2

Ornithine phenylacetate prevents disturbances of motor-evoked potentials induced by intestinal blood in rats with portacaval anastomosis.

Oria M, Romero-Giménez J, Arranz JA, Riudor E, Raguer N, Córdoba J. Oria M, et al. Among authors: riudor e. J Hepatol. 2012 Jan;56(1):109-14. doi: 10.1016/j.jhep.2011.06.026. Epub 2011 Aug 9. J Hepatol. 2012. PMID: 21835138

3

Optimization of allopurinol challenge: sample purification, protein intake control, and the use of orotidine response as a discriminative variable improve performance of the test for diagnosing ornithine carbamoyltransferase deficiency.

Arranz JA, Riudor E, Rodés M, Roig M, Climent C, Rubio V, Sentís M, Burlina A. Arranz JA, et al. Among authors: riudor e. Clin Chem. 1999 Jul;45(7):995-1001. Clin Chem. 1999. PMID: 10388475 Clinical Trial.

4

Influence of dose and age on the response of the allopurinol test for ornithine carbamoyltransferase deficiency in control infants.

Riudor E, Arranz JA, Rodés M, Rubio V, Sentís M, Burlina AB. Riudor E, et al. J Inherit Metab Dis. 2000 Nov;23(7):662-8. doi: 10.1023/a:1005610325170. J Inherit Metab Dis. 2000. PMID: 11117427

5

Estimation of the total number of disease-causing mutations in ornithine transcarbamylase (OTC) deficiency. Value of the OTC structure in predicting a mutation pathogenic potential.

Arranz JA, Riudor E, Marco-Marín C, Rubio V. Arranz JA, et al. Among authors: riudor e. J Inherit Metab Dis. 2007 Apr;30(2):217-26. doi: 10.1007/s10545-007-0429-x. Epub 2007 Mar 1. J Inherit Metab Dis. 2007. PMID: 17334707

6

Proteomic analysis in cerebrospinal fluid of patients with atypical nonketotic hyperglycinemia and pulmonary hypertension - A pilot study.

Rodríguez CE, Arranz JA, Colomé N, Bech-Serra JJ, Canals F, Del Toro M, Riudor E. Rodríguez CE, et al. Among authors: riudor e. Proteomics Clin Appl. 2009 Dec;3(12):1430-9. doi: 10.1002/prca.200800251. Epub 2009 Oct 7. Proteomics Clin Appl. 2009. PMID: 21136962

7

Complete deletion of ornithine transcarbamylase gene confirmed by CGH array of X chromosome.

Arranz JA, Madrigal I, Riudor E, Armengol L, Milà M. Arranz JA, et al. Among authors: riudor e. J Inherit Metab Dis. 2007 Oct;30(5):813. doi: 10.1007/s10545-007-0578-y. Epub 2007 Jun 14. J Inherit Metab Dis. 2007. PMID: 17570074

8

Hyperlactatemia and in utero exposure to antiretrovirals: is the control group the clue?

Soler-Palacín P, Martín-Nalda A, Martínez-Gómez X, Melendo S, Riudor E, Arranz JA, Espiau M, Figueras C. Soler-Palacín P, et al. Among authors: riudor e. AIDS Res Hum Retroviruses. 2012 Aug;28(8):752-8. doi: 10.1089/AID.2011.0198. Epub 2011 Nov 16. AIDS Res Hum Retroviruses. 2012. PMID: 22010980

9

Partial ornithine transcarbamylase deficiency.

Riudor E, Arranz JA, Rodés M. Riudor E, et al. Pediatrics. 2003 May;111(5 Pt 1):1123-4; author reply 1123-4. doi: 10.1542/peds.111.5.1123-a. Pediatrics. 2003. PMID: 12728104 No abstract available.

10

Glycogen storage disease type III with hypoketosis.

Clemente M, Gussinyer M, Arranz JA, Riudor E, Yeste D, Albisu M, Carrascosa A. Clemente M, et al. Among authors: riudor e. J Pediatr Endocrinol Metab. 2010 Aug;23(8):833-6. doi: 10.1515/jpem.2010.134. J Pediatr Endocrinol Metab. 2010. PMID: 21073127

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