Montoya J - Search Results

1

Mitochondrial diseases associated with cerebral folate deficiency.

Garcia-Cazorla A, Quadros EV, Nascimento A, Garcia-Silva MT, Briones P, Montoya J, Ormazábal A, Artuch R, Sequeira JM, Blau N, Arenas J, Pineda M, Ramaekers VT. Garcia-Cazorla A, et al. Among authors: montoya j. Neurology. 2008 Apr 15;70(16):1360-2. doi: 10.1212/01.wnl.0000309223.98616.e4. Neurology. 2008. PMID: 18413591 No abstract available.

2

[Mitochondrial respiratory chain deficiency may present as multiple sclerosis].

Iñiguez C, Arenas J, Montoya J, Mostacero E, López del Val J, Morales F. Iñiguez C, et al. Among authors: montoya j. Neurologia. 1998 Apr;13(4):199-203. Neurologia. 1998. PMID: 9608760 Spanish.

3

Familial multiple symmetric lipomatosis associated with the A8344G mutation of mitochondrial DNA.

Gámez J, Playán A, Andreu AL, Bruno C, Navarro C, Cervera C, Arbós MA, Schwartz S, Enriquez JA, Montoya J. Gámez J, et al. Among authors: montoya j. Neurology. 1998 Jul;51(1):258-60. doi: 10.1212/wnl.51.1.258. Neurology. 1998. PMID: 9674814

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. Among authors: montoya j. Horm Res. 1998;50(2):99-104. doi: 10.1159/000023243. Horm Res. 1998. PMID: 9701704

5

Correlation of sperm motility with mitochondrial enzymatic activities.

Ruiz-Pesini E, Diez C, Lapeña AC, Pérez-Martos A, Montoya J, Alvarez E, Arenas J, López-Pérez MJ. Ruiz-Pesini E, et al. Among authors: montoya j. Clin Chem. 1998 Aug;44(8 Pt 1):1616-20. Clin Chem. 1998. PMID: 9702947

6

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

7

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. Among authors: montoya j. Clin Biochem. 2000 Aug;33(6):481-5. doi: 10.1016/s0009-9120(00)00137-5. Clin Biochem. 2000. PMID: 11074240

8

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

9

Exercise intolerance resulting from a muscle-restricted mutation in the mitochondrial tRNA(Leu (CUN)) gene.

Vives-Bauza C, Gamez J, Roig M, Briones P, Cervera C, Solano A, Montoya J, Andreu AL. Vives-Bauza C, et al. Among authors: montoya j. Ann Med. 2001 Oct;33(7):493-6. doi: 10.3109/07853890109002099. Ann Med. 2001. PMID: 11680798 Free article.

10

Characterisation of repeat and palindrome elements in patients harbouring single deletions of mitochondrial DNA.

Solano A, Gámez J, Carod FJ, Pineda M, Playán A, López-Gallardo E, Andreu AL, Montoya J. Solano A, et al. Among authors: montoya j. J Med Genet. 2003 Jul;40(7):e86. doi: 10.1136/jmg.40.7.e86. J Med Genet. 2003. PMID: 12843335 Free PMC article. No abstract available.

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