Vilaseca MA - Search Results

1

Campistol J, Chávez B, Vilaseca MA, Artuch R. Campistol J, et al. Among authors: vilaseca ma. Rev Neurol. 2000 Jun;30 Suppl 1:S105-9. Rev Neurol. 2000. PMID: 10904975 Spanish.

2

[Respiratory chain and pyruvate metabolism deficiencies in pediatric patients: evaluation of biochemical tests for selective screening].

Artuch R, Pineda M, Vilaseca MA, Briones P, Ribes A, Colomer J, Vernet A, Campistol J. Artuch R, et al. Among authors: vilaseca ma. Rev Neurol. 1998 Jan;26(149):38-42. Rev Neurol. 1998. PMID: 9533203 Spanish.

3

[Ubiquinone: metabolism and functions. Ubiquinone deficiency and its implication in mitochondrial encephalopathies. Treatment with ubiquinone].

Artuch R, Colomé C, Vilaseca MA, Pineda M, Campistol J. Artuch R, et al. Among authors: vilaseca ma. Rev Neurol. 1999 Jul 1-15;29(1):59-63. Rev Neurol. 1999. PMID: 10528314 Review. Spanish.

4

[Pathogenetic mechanisms in phenylketonuria: disorders affecting the metabolism of neurotransmitters and the antioxidant system].

Ormazábal A, Artuch R, Vilaseca MA, García-Cazorla A, Campistol J. Ormazábal A, et al. Among authors: vilaseca ma. Rev Neurol. 2004 Nov 16-30;39(10):956-61. Rev Neurol. 2004. PMID: 15573314 Free article. Review. Spanish.

5

[Cerebral creatine transporter deficiency: an infradiagnosed neurometabolic disease].

Campistol J, Arias-Dimas A, Poo P, Pineda M, Hoffman M, Vilaseca MA, Artuch R, Ribes A. Campistol J, et al. Among authors: vilaseca ma. Rev Neurol. 2007 Mar 16-31;44(6):343-7. Rev Neurol. 2007. PMID: 17385170 Free article. Spanish.

6

[Neurological, neuropsychological, and ophthalmological evolution after one year of docosahexaenoic acid supplementation in phenylketonuric patients].

Gutiérrez-Mata AP, Vilaseca MA, Capdevila-Cirera A, Vidal-Oller M, Alonso-Colmenero I, Colomé R, López-Sala A, Lambruschini-Ferri N, Gutiérrez A, Gassió R, Artuch R, Campistol J. Gutiérrez-Mata AP, et al. Among authors: vilaseca ma. Rev Neurol. 2012 Aug 16;55(4):200-6. Rev Neurol. 2012. PMID: 22829083 Free article. Clinical Trial. Spanish.

7

Controlled diet in phenylketonuria may cause serum carnitine deficiency.

Vilaseca MA, Briones P, Ferrer I, Campistol J, Riverola A, Castillo P, Ramon F. Vilaseca MA, et al. J Inherit Metab Dis. 1993;16(1):101-4. doi: 10.1007/BF00711322. J Inherit Metab Dis. 1993. PMID: 8487489

8

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

9

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

10

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

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