Playán A - Search Results

1

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

2

[Diseases of mitochondrial DNA].

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

3

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: playan a. 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.

4

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. Among authors: playan a. Ann Neurol. 2003 Oct;54(4):527-30. doi: 10.1002/ana.10682. Ann Neurol. 2003. PMID: 14520668

5

Peripheral neuropathy with ataxia in childhood as a result of the G8363A mutation in mitochondrial DNA.

Pineda M, Solano A, Artuch R, Andreu AL, Playan A, Vilaseca MA, Colomer J, Briones P, Casademont J, Montoya J. Pineda M, et al. Among authors: playan a. Pediatr Res. 2004 Jul;56(1):55-9. doi: 10.1203/01.PDR.0000130475.20571.98. Epub 2004 May 5. Pediatr Res. 2004. PMID: 15128915

6

[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. Among authors: playan a. Rev Neurol. 2000 Feb 16-29;30(4):330-2. Rev Neurol. 2000. PMID: 10789142 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: playan a. Salud Publica Mex. 2001 Mar-Apr;43(2):151-61. Salud Publica Mex. 2001. PMID: 11381844 Review. Spanish.

8

[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.

9

[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: playan a. Rev Neurol. 1998 Dec;27(160):1005-7. Rev Neurol. 1998. PMID: 9951025 Spanish.

10

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: playan a. Neurology. 1998 Jul;51(1):258-60. doi: 10.1212/wnl.51.1.258. Neurology. 1998. PMID: 9674814

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