Montoya J - Search Results

1

[Acute presentation of leukodystrophy due to mitochondrial cytopathology and multiple deletions of mitochondrial DNA].

Rábano JA, Playan A, Guirado F, Montoya J, Baldellou A, López-Pisón J. Rábano JA, et al. Among authors: montoya j. Rev Neurol. 1998 Dec;27(160):1005-7. Rev Neurol. 1998. PMID: 9951025 Spanish.

2

[Diseases of mitochondrial DNA].

Montoya J, Playán A, Solano A, Alcaine MJ, López-Pérez MJ, Pérez-Martos A. Montoya J, et al. Rev Neurol. 2000 Aug 16-31;31(4):324-33. Rev Neurol. 2000. PMID: 11008288 Review. Spanish.

3

[Leigh syndrome resulting from a de novo mitochondrial DNA mutation (T8993G)].

Playán A, Solano-Palacios A, González de la Rosa JB, Merino-Arribas JM, Andreu AL, López-Pérez M, Montoya J. Playán A, et al. Among authors: montoya j. Rev Neurol. 2002 Jun 16-30;34(12):1124-6. Rev Neurol. 2002. PMID: 12134275 Free article. Spanish.

4

De Toni-Debré-Fanconi syndrome due to a palindrome-flanked deletion in mitochondrial DNA.

Solano A, Russo G, Playán A, Parisi M, DiPietro M, Scuderi A, Palumbo M, Renis M, López-Pérez MJ, Andreu AL, Montoya J. Solano A, et al. Among authors: montoya j. Pediatr Nephrol. 2004 Jul;19(7):790-3. doi: 10.1007/s00467-004-1473-5. Epub 2004 May 7. Pediatr Nephrol. 2004. PMID: 15133725

5

[Recent advances in genetics of epilepsy. Genetic of mitochondrial epilepsy].

Montoya J, Playán A, Alcaine MJ, Solano A, Fernández-Silva P, Enríquez JA. Montoya J, et al. Rev Neurol. 2000 Feb 16-29;30(4):330-2. Rev Neurol. 2000. PMID: 10789142 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: montoya j. Rev Neurol. 2000 Nov 1-15;31(9):804-11. Rev Neurol. 2000. PMID: 11127079 Spanish.

7

[Genetic diseases of the mitochondrial DNA in humans].

Solano A, Playán A, López-Pérez MJ, Montoya J. Solano A, et al. Among authors: montoya j. Salud Publica Mex. 2001 Mar-Apr;43(2):151-61. Salud Publica Mex. 2001. PMID: 11381844 Review. Spanish.

8

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.

9

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

10

[Human mitochondrial genetic system].

Enríquez JA, Martínez-Azorín F, Garesse R, López-Pérez MJ, Pérez-Martos A, Bornstein B, Montoya J. Enríquez JA, et al. Among authors: montoya j. Rev Neurol. 1998 Apr;26 Suppl 1:S21-6. Rev Neurol. 1998. PMID: 9810587 Review. Spanish.

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