Pineda M - Search Results

1

[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: pineda m. Rev Neurol. 1999 Jul 1-15;29(1):59-63. Rev Neurol. 1999. PMID: 10528314 Review. 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: pineda m. Rev Neurol. 1998 Jan;26(149):38-42. Rev Neurol. 1998. PMID: 9533203 Spanish.

3

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

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

4

[Risk factors in cerebrovascular disease in childhood].

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

5

[Aspects of neuropathy in mitochondrial diseases].

Colomer J, Iturriaga C, Bestué M, Artuch R, Briones P, Montoya J, Vilaseca MA, Pineda M. Colomer J, et al. Among authors: pineda m. Rev Neurol. 2000 Jun 16-30;30(12):1117-21. Rev Neurol. 2000. PMID: 10935234 Spanish.

6

[Mitochondrial encephalomyelitis, lactic acidosis and cerebrovascular accidents (MELAS) in pediatric age with the A3243G mutation in the tRNALeu(UUR) gene of mitochondrial DNA].

Coelho-Miranda L, Playan A, Artuch R, Vilaseca MA, Colomer J, Briones P, Coll-Cantí J, Conill J, Sans A, López de Munain A, Solano A, Alcaine MJ, Montoya J, Pineda M. Coelho-Miranda L, et al. Among authors: pineda m. Rev Neurol. 2000 Nov 1-15;31(9):804-11. Rev Neurol. 2000. PMID: 11127079 Spanish.

7

[Familiar chronic progressive external ophthalmoplegia of mitochondrial origin].

Pineda M, Playán-Ariso A, Alcaine-Villarroya MJ, Vernet AM, Serra-Castanera A, Solano A, Vilaseca MA, Artuch R, López-Pérez M, Briones-Godino MP, Andreu A, Montoya J. Pineda M, et al. Rev Neurol. 2004 Jun 1-15;38(11):1023-7. Rev Neurol. 2004. PMID: 15202078 Free article. Spanish.

8

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

9

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: pineda m. Clin Chim Acta. 1997 Jul 25;263(2):147-55. doi: 10.1016/s0009-8981(97)00061-2. Clin Chim Acta. 1997. PMID: 9246419

10

[Rett's syndrome in the Spanish population].

Pineda M, Aracil A, Vernet A, Espada M, Cobo E, Arteaga R, Artigas J, Barrionuevo C, Bautista-González L, Berenguer-Molla R, Caballero J, Cabrera J, Campistol J, Campos J, Casas-Fernández C, Castelló M, Castro-Gago M, Castroviejo P, Colomer J, Delgado P, Domingo R, Domínguez-Jiménez A, Fernández-Alvarez E, García-Aymerich J, Vidal R, et al. Pineda M, et al. Rev Neurol. 1999 Jan 1-15;28(1):105-9. Rev Neurol. 1999. PMID: 10101777 Review. Spanish.

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