Rubio JC - Search Results

1

Early-onset multisystem mitochondrial disorder caused by a nonsense mutation in the mitochondrial DNA cytochrome C oxidase II gene.

Campos Y, García-Redondo A, Fernández-Moreno MA, Martínez-Pardo M, Goda G, Rubio JC, Martín MA, del Hoyo P, Cabello A, Bornstein B, Garesse R, Arenas J. Campos Y, et al. Among authors: rubio jc. Ann Neurol. 2001 Sep;50(3):409-13. doi: 10.1002/ana.1141. Ann Neurol. 2001. PMID: 11558799

2

Multiple deletions of mitochondrial DNA in muscle from a patient with benign progressive external ophthalmoplegia.

Campos Y, Martín MA, Rubio JC, Ricard C, Cabello A, Arenas J. Campos Y, et al. Among authors: rubio jc. J Inherit Metab Dis. 1996;19(3):366-7. doi: 10.1007/BF01799268. J Inherit Metab Dis. 1996. PMID: 8803781 No abstract available.

3

Cerebrospinal fluid carnitine levels in patients with Parkinson's disease.

Jiménez-Jiménez FJ, Rubio JC, Molina JA, Martín MA, Campos Y, Benito-León J, Ortí-Pareja M, Gasalla T, Arenas J. Jiménez-Jiménez FJ, et al. Among authors: rubio jc. J Neurol Sci. 1997 Feb 12;145(2):183-5. doi: 10.1016/s0022-510x(96)00259-6. J Neurol Sci. 1997. PMID: 9094047 Clinical Trial.

4

Leigh syndrome associated with the T9176C mutation in the ATPase 6 gene of mitochondrial DNA.

Campos Y, Martín MA, Rubio JC, Solana LG, García-Benayas C, Terradas JL, Arenas J. Campos Y, et al. Among authors: rubio jc. Neurology. 1997 Aug;49(2):595-7. doi: 10.1212/wnl.49.2.595. Neurology. 1997. PMID: 9270604

5

Bilateral striatal necrosis and MELAS associated with a new T3308C mutation in the mitochondrial ND1 gene.

Campos Y, Martín MA, Rubio JC, Gutiérrez del Olmo MC, Cabello A, Arenas J. Campos Y, et al. Among authors: rubio jc. Biochem Biophys Res Commun. 1997 Sep 18;238(2):323-5. doi: 10.1006/bbrc.1997.7166. Biochem Biophys Res Commun. 1997. PMID: 9299504

6

Association of genetically proven deficiencies of myophosphorylase and AMP deaminase: a second case of 'double trouble'.

Rubio JC, Martín MA, Bautista J, Campos Y, Segura D, Arenas J. Rubio JC, et al. Neuromuscul Disord. 1997 Sep;7(6-7):387-9. doi: 10.1016/s0960-8966(97)00095-3. Neuromuscul Disord. 1997. PMID: 9327403

7

Complex I defect in muscle from patients with Huntington's disease.

Arenas J, Campos Y, Ribacoba R, Martín MA, Rubio JC, Ablanedo P, Cabello A. Arenas J, et al. Among authors: rubio jc. Ann Neurol. 1998 Mar;43(3):397-400. doi: 10.1002/ana.410430321. Ann Neurol. 1998. PMID: 9506560

8

Cerebrospinal fluid carnitine levels in patients with Alzheimer's disease.

Rubio JC, de Bustos F, Molina JA, Jiménez-Jiménez FJ, Benito-León J, Martín MA, Campos Y, Ortí-Pareja M, Cabrera-Valdivia F, Arenas J. Rubio JC, et al. J Neurol Sci. 1998 Mar 5;155(2):192-5. doi: 10.1016/s0022-510x(97)00314-6. J Neurol Sci. 1998. PMID: 9562266 Clinical Trial.

9

[Enzyme complex defects of the mitochondrial respiratory chain].

Rubio JC, Martín MA, del Hoyo P, de Bustos F, Campos Y, Arenas J. Rubio JC, et al. Rev Neurol. 1998 Apr;26 Suppl 1:S15-20. Rev Neurol. 1998. PMID: 9810586 Review. Spanish.

10

[Molecular genetics of alterations in the mitochondrial respiratory chain].

Martín MA, Campos Y, de Bustos F, del Hoyo P, Rubio JC, Arenas J. Martín MA, et al. Among authors: rubio jc. Rev Neurol. 1998 Apr;26 Suppl 1:S27-35. Rev Neurol. 1998. PMID: 9810588 Review. Spanish.

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