Vilaseca MA - Search Results

1

Children with stroke: polymorphism of the MTHFR gene, mild hyperhomocysteinemia, and vitamin status.

Cardo E, Monrós E, Colomé C, Artuch R, Campistol J, Pineda M, Vilaseca MA. Cardo E, et al. Among authors: vilaseca ma. J Child Neurol. 2000 May;15(5):295-8. doi: 10.1177/088307380001500505. J Child Neurol. 2000. PMID: 10830195

2

Evaluation of hyperhomocysteinaemia in children with stroke.

Cardo E, Vilaseca MA, Campistol J, Artuch R, Colomé C, Pineda M. Cardo E, et al. Among authors: vilaseca ma. Eur J Paediatr Neurol. 1999;3(3):113-7. doi: 10.1016/s1090-3798(99)90098-3. Eur J Paediatr Neurol. 1999. PMID: 10461566

3

Anti-epileptic drug treatment in children: hyperhomocysteinaemia, B-vitamins and the 677C-->T mutation of the methylenetetrahydrofolate reductase gene.

Vilaseca MA, Monrós E, Artuch R, Colomé C, Farré C, Valls C, Cardo E, Pineda M. Vilaseca MA, et al. Eur J Paediatr Neurol. 2000;4(6):269-77. doi: 10.1053/ejpn.2000.0379. Eur J Paediatr Neurol. 2000. PMID: 11277368

4

Plasma thiols and their determinants in phenylketonuria.

Colomé C, Artuch R, Sierra C, Brandi N, Lambruschini N, Campistol J, Vilaseca MA. Colomé C, et al. Among authors: vilaseca ma. Eur J Clin Nutr. 2003 Aug;57(8):964-8. doi: 10.1038/sj.ejcn.1601631. Eur J Clin Nutr. 2003. PMID: 12879091

5

Tocopherol in inborn errors of intermediary metabolism.

Moyano D, Vilaseca MA, Pineda M, Campistol J, Vernet A, Póo P, Artuch R, Sierra C. Moyano D, et al. Among authors: vilaseca ma. Clin Chim Acta. 1997 Jul 25;263(2):147-55. doi: 10.1016/s0009-8981(97)00061-2. Clin Chim Acta. 1997. PMID: 9246419

6

Selective screening for hyperhomocysteinemia in pediatric patients.

Vilaseca MA, Moyano D, Artuch R, Ferrer I, Pineda M, Cardo E, Campistol J, Pavia C, Camacho JA. Vilaseca MA, et al. Clin Chem. 1998 Mar;44(3):662-4. Clin Chem. 1998. PMID: 9510877 No abstract available.

7

Biochemical monitoring of the treatment in paediatric patients with mitochondrial disease.

Artuch R, Vilaseca MA, Pineda M. Artuch R, et al. Among authors: vilaseca ma. J Inherit Metab Dis. 1998 Dec;21(8):837-45. doi: 10.1023/a:1005470702369. J Inherit Metab Dis. 1998. PMID: 9870209

8

Glutaric aciduria type I with high residual glutaryl-CoA dehydrogenase activity.

Pineda M, Ribes A, Busquets C, Vilaseca MA, Aracil A, Christensen E. Pineda M, et al. Among authors: vilaseca ma. Dev Med Child Neurol. 1998 Dec;40(12):840-2. doi: 10.1111/j.1469-8749.1998.tb12362.x. Dev Med Child Neurol. 1998. PMID: 9881681 Free article.

9

Fatal haemorrhagic infarct in an infant with homocystinuria.

Cardo E, Campistol J, Caritg J, Ruiz S, Vilaseca MA, Kirkham F, Blom HJ. Cardo E, et al. Among authors: vilaseca ma. Dev Med Child Neurol. 1999 Feb;41(2):132-5. doi: 10.1017/s0012162299000250. Dev Med Child Neurol. 1999. PMID: 10075100 Free article.

10

Decreased serum ubiquinone-10 concentrations in phenylketonuria.

Artuch R, Vilaseca MA, Moreno J, Lambruschini N, Cambra FJ, Campistol J. Artuch R, et al. Among authors: vilaseca ma. Am J Clin Nutr. 1999 Nov;70(5):892-5. doi: 10.1093/ajcn/70.5.892. Am J Clin Nutr. 1999. PMID: 10539751

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