Artuch R - Search Results

1

Molecular diagnosis of coenzyme Q₁₀ deficiency: an update.

Yubero D, Montero R, Santos-Ocaña C, Salviati L, Navas P, Artuch R. Yubero D, et al. Among authors: artuch r. Expert Rev Mol Diagn. 2018 Jun;18(6):491-498. doi: 10.1080/14737159.2018.1478290. Epub 2018 May 30. Expert Rev Mol Diagn. 2018. PMID: 29781757 Review.

2

Cerebellar ataxia with coenzyme Q10 deficiency: diagnosis and follow-up after coenzyme Q10 supplementation.

Artuch R, Brea-Calvo G, Briones P, Aracil A, Galván M, Espinós C, Corral J, Volpini V, Ribes A, Andreu AL, Palau F, Sánchez-Alcázar JA, Navas P, Pineda M. Artuch R, et al. J Neurol Sci. 2006 Jul 15;246(1-2):153-8. doi: 10.1016/j.jns.2006.01.021. Epub 2006 May 3. J Neurol Sci. 2006. PMID: 16677673

3

Muscle coenzyme Q10 concentrations in patients with probable and definite diagnosis of respiratory chain disorders.

Montero R, Artuch R, Briones P, Nascimento A, García-Cazorla A, Vilaseca MA, Sánchez-Alcázar JA, Navas P, Montoya J, Pineda M. Montero R, et al. Among authors: artuch r. Biofactors. 2005;25(1-4):109-15. doi: 10.1002/biof.5520250112. Biofactors. 2005. PMID: 16873935

4

Secondary alteration of the transferrin isoelectric focusing pattern in a case of bacterial meningitis.

Quintana E, Gala S, García-Cazorla A, Montero R, Muñoz-Almagro C, Vilaseca MA, Briones P, Artuch R. Quintana E, et al. Among authors: artuch r. J Inherit Metab Dis. 2007 Apr;30(2):267. doi: 10.1007/s10545-007-0530-1. Epub 2007 Feb 15. J Inherit Metab Dis. 2007. PMID: 17372855

5

Clinical, biochemical and molecular aspects of cerebellar ataxia and Coenzyme Q10 deficiency.

Montero R, Pineda M, Aracil A, Vilaseca MA, Briones P, Sánchez-Alcázar JA, Navas P, Artuch R. Montero R, et al. Among authors: artuch r. Cerebellum. 2007;6(2):118-22. doi: 10.1080/14734220601021700. Cerebellum. 2007. PMID: 17510911 Review.

6

Idebenone treatment in paediatric and adult patients with Friedreich ataxia: long-term follow-up.

Pineda M, Arpa J, Montero R, Aracil A, Domínguez F, Galván M, Mas A, Martorell L, Sierra C, Brandi N, García-Arumí E, Rissech M, Velasco D, Costa JA, Artuch R. Pineda M, et al. Among authors: artuch r. Eur J Paediatr Neurol. 2008 Nov;12(6):470-5. doi: 10.1016/j.ejpn.2007.11.006. Epub 2008 Jan 30. Eur J Paediatr Neurol. 2008. PMID: 18234531

7

Analysis of coenzyme Q10 in muscle and fibroblasts for the diagnosis of CoQ10 deficiency syndromes.

Montero R, Sánchez-Alcázar JA, Briones P, Hernández AR, Cordero MD, Trevisson E, Salviati L, Pineda M, García-Cazorla A, Navas P, Artuch R. Montero R, et al. Among authors: artuch r. Clin Biochem. 2008 Jun;41(9):697-700. doi: 10.1016/j.clinbiochem.2008.03.007. Epub 2008 Mar 20. Clin Biochem. 2008. PMID: 18387363

8

Functional characterization of human COQ4, a gene required for Coenzyme Q10 biosynthesis.

Casarin A, Jimenez-Ortega JC, Trevisson E, Pertegato V, Doimo M, Ferrero-Gomez ML, Abbadi S, Artuch R, Quinzii C, Hirano M, Basso G, Ocaña CS, Navas P, Salviati L. Casarin A, et al. Among authors: artuch r. Biochem Biophys Res Commun. 2008 Jul 18;372(1):35-9. doi: 10.1016/j.bbrc.2008.04.172. Epub 2008 May 12. Biochem Biophys Res Commun. 2008. PMID: 18474229 Free PMC article.

9

Coenzyme Q10 deficiency associated with a mitochondrial DNA depletion syndrome: a case report.

Montero R, Sánchez-Alcázar JA, Briones P, Navarro-Sastre A, Gallardo E, Bornstein B, Herrero-Martín D, Rivera H, Martin MA, Marti R, García-Cazorla A, Montoya J, Navas P, Artuch R. Montero R, et al. Among authors: artuch r. Clin Biochem. 2009 May;42(7-8):742-5. doi: 10.1016/j.clinbiochem.2008.10.027. Epub 2008 Dec 3. Clin Biochem. 2009. PMID: 19094978

10

Coenzyme Q deficiency triggers mitochondria degradation by mitophagy.

Rodríguez-Hernández A, Cordero MD, Salviati L, Artuch R, Pineda M, Briones P, Gómez Izquierdo L, Cotán D, Navas P, Sánchez-Alcázar JA. Rodríguez-Hernández A, et al. Among authors: artuch r. Autophagy. 2009 Jan;5(1):19-32. doi: 10.4161/auto.5.1.7174. Autophagy. 2009. PMID: 19115482 Free article.

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