Campistol J - Search Results

1

[Risk factors in cerebrovascular disease in childhood].

Cardo E, Pineda M, Vilaseca MA, Artuch R, Campistol J. Cardo E, et al. Among authors: campistol j. Rev Neurol. 2000 Jan 1-15;30(1):21-7. Rev Neurol. 2000. PMID: 10742991 Spanish.

2

[The role of resistance to C active protein (R-APC) in a pediatric stroke].

Cardo E, Campistol J, Kirkham F. Cardo E, et al. Among authors: campistol j. Rev Neurol. 1997 Oct;25(146):1589-91. Rev Neurol. 1997. PMID: 9462989 Spanish.

3

[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: campistol j. Rev Neurol. 1998 Jan;26(149):38-42. Rev Neurol. 1998. PMID: 9533203 Spanish.

4

[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: campistol j. Rev Neurol. 1999 Jul 1-15;29(1):59-63. Rev Neurol. 1999. PMID: 10528314 Review. Spanish.

5

[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: campistol j. Rev Neurol. 2004 Nov 16-30;39(10):956-61. Rev Neurol. 2004. PMID: 15573314 Free article. Review. Spanish.

6

[Inborn errors of metabolism with neurological symptomathology in the neonatal period].

Campistol J, Málaga-Diéguez I, García-Cazorla A, Krauel-Vidal X, Vilaseca MA. Campistol J, et al. Rev Neurol. 2005 Mar 16-31;40(6):321-6. Rev Neurol. 2005. PMID: 15795866 Free article. Spanish.

7

[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. Rev Neurol. 2007 Mar 16-31;44(6):343-7. Rev Neurol. 2007. PMID: 17385170 Free article. Spanish.

8

[Encephalopathy with methylmalonic aciduria and homocystinuria secondary to a deficient exogenous supply of vitamin B12].

Gutiérrez-Aguilar G, Abenia-Usón P, García-Cazorla A, Vilaseca MA, Campistol J. Gutiérrez-Aguilar G, et al. Among authors: campistol j. Rev Neurol. 2005 May 16-31;40(10):605-8. Rev Neurol. 2005. PMID: 15926134 Free article. Spanish.

9

An atypical French form of pyruvate carboxylase deficiency.

Pineda M, Campistol J, Vilaseca MA, Briones P, Ribes A, Temudo T, Pons M, Cusi V, Rolland MO. Pineda M, et al. Among authors: campistol j. Brain Dev. 1995 Jul-Aug;17(4):276-9. doi: 10.1016/0387-7604(95)00057-i. Brain Dev. 1995. PMID: 7503391

10

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. Among authors: campistol j. Clin Chem. 1998 Mar;44(3):662-4. Clin Chem. 1998. PMID: 9510877 No abstract available.

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