Lopez-Perez MJ - Search Results

1

Bilateral striatal necrosis associated with a novel mutation in the mitochondrial ND6 gene.

Solano A, Roig M, Vives-Bauza C, Hernandez-Peña J, Garcia-Arumi E, Playan A, Lopez-Perez MJ, Andreu AL, Montoya J. Solano A, et al. Ann Neurol. 2003 Oct;54(4):527-30. doi: 10.1002/ana.10682. Ann Neurol. 2003. PMID: 14520668

2

[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. Rev Neurol. 2002 Jun 16-30;34(12):1124-6. Rev Neurol. 2002. PMID: 12134275 Free article. Spanish.

3

[Diseases of the human mitochondrial oxidative phosphorylation system].

Ruiz-Pesini E, López-Gallardo E, Dahmani Y, Herrero MD, Solano A, Díez-Sánchez C, López-Pérez M, Montoya J. Ruiz-Pesini E, et al. Rev Neurol. 2006 Oct 1-15;43(7):416-24. Rev Neurol. 2006. PMID: 17006861 Free article. Review. Spanish.

4

Mitochondrial DNA content of human spermatozoa.

Díez-Sánchez C, Ruiz-Pesini E, Lapeña AC, Montoya J, Pérez-Martos A, Enríquez JA, López-Pérez MJ. Díez-Sánchez C, et al. Biol Reprod. 2003 Jan;68(1):180-5. doi: 10.1095/biolreprod.102.005140. Biol Reprod. 2003. PMID: 12493711

5

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. Pediatr Nephrol. 2004 Jul;19(7):790-3. doi: 10.1007/s00467-004-1473-5. Epub 2004 May 7. Pediatr Nephrol. 2004. PMID: 15133725

6

Mitochondrial DNA transcription and diseases: past, present and future.

Montoya J, López-Pérez MJ, Ruiz-Pesini E. Montoya J, et al. Biochim Biophys Acta. 2006 Sep-Oct;1757(9-10):1179-89. doi: 10.1016/j.bbabio.2006.03.023. Epub 2006 Apr 7. Biochim Biophys Acta. 2006. PMID: 16697348 Free article. Review.

7

[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.

8

[Genetic diseases of the mitochondrial DNA in humans].

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

9

An intragenic suppressor in the cytochrome c oxidase I gene of mouse mitochondrial DNA.

Acín-Pérez R, Bayona-Bafaluy MP, Bueno M, Machicado C, Fernández-Silva P, Pérez-Martos A, Montoya J, López-Pérez MJ, Sancho J, Enríquez JA. Acín-Pérez R, et al. Hum Mol Genet. 2003 Feb 1;12(3):329-39. doi: 10.1093/hmg/ddg021. Hum Mol Genet. 2003. PMID: 12554686

10

NARP syndrome in a patient harbouring an insertion in the MT-ATP6 gene that results in a truncated protein.

López-Gallardo E, Solano A, Herrero-Martín MD, Martínez-Romero I, Castaño-Pérez MD, Andreu AL, Herrera A, López-Pérez MJ, Ruiz-Pesini E, Montoya J. López-Gallardo E, et al. J Med Genet. 2009 Jan;46(1):64-7. doi: 10.1136/jmg.2008.060616. J Med Genet. 2009. PMID: 19124644

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