Artuch R - Search Results

1

The Genetic Landscape of Mitochondrial Diseases in Spain: A Nationwide Call.

Bellusci M, Paredes-Fuentes AJ, Ruiz-Pesini E, Gómez B; MITOSPAIN Working Group; Martín MA, Montoya J, Artuch R. Bellusci M, et al. Among authors: artuch r. Genes (Basel). 2021 Oct 9;12(10):1590. doi: 10.3390/genes12101590. Genes (Basel). 2021. PMID: 34680984 Free PMC article.

2

Increased urine methylmalonic acid excretion in infants with apnoeas.

Artuch R, Calvo M, Ribes A, Camarasa F, Vilaseca MA. Artuch R, et al. J Inherit Metab Dis. 1998 Feb;21(1):86-7. doi: 10.1023/a:1005383919335. J Inherit Metab Dis. 1998. PMID: 9501280 No abstract available.

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

4

Multiple endocrine involvement in two pediatric patients with Kearns-Sayre syndrome.

Artuch R, Pavía C, Playán A, Vilaseca MA, Colomer J, Valls C, Rissech M, González MA, Pou A, Briones P, Montoya J, Pineda M. Artuch R, et al. Horm Res. 1998;50(2):99-104. doi: 10.1159/000023243. Horm Res. 1998. PMID: 9701704

5

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

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

6

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

7

[Risk factors in cerebrovascular disease in childhood].

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

8

[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: artuch r. Rev Neurol. 2000 Jun 16-30;30(12):1117-21. Rev Neurol. 2000. PMID: 10935234 Spanish.

9

Oxygen consumption measurement in lymphocytes for the diagnosis of pediatric patients with oxidative phosphorylation diseases.

Artuch R, Colomé C, Playán A, Alcaine MJ, Briones P, Montoya J, Vilaseca MA, Pineda M. Artuch R, et al. Clin Biochem. 2000 Aug;33(6):481-5. doi: 10.1016/s0009-9120(00)00137-5. Clin Biochem. 2000. PMID: 11074240

10

[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: artuch r. Rev Neurol. 2000 Nov 1-15;31(9):804-11. Rev Neurol. 2000. PMID: 11127079 Spanish.

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