Solano 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. 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: solano 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. 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. 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: solano 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: solano 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. Salud Publica Mex. 2001 Mar-Apr;43(2):151-61. Salud Publica Mex. 2001. PMID: 11381844 Review. Spanish.

8

[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. Among authors: solano a. Rev Neurol. 2006 Oct 1-15;43(7):416-24. Rev Neurol. 2006. PMID: 17006861 Free article. Review. Spanish.

9

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. Among authors: solano a. J Med Genet. 2009 Jan;46(1):64-7. doi: 10.1136/jmg.2008.060616. J Med Genet. 2009. PMID: 19124644

10

Cerebral folate deficiency and leukoencephalopathy caused by a mitochondrial DNA deletion.

Pineda M, Ormazabal A, López-Gallardo E, Nascimento A, Solano A, Herrero MD, Vilaseca MA, Briones P, Ibáñez L, Montoya J, Artuch R. Pineda M, et al. Among authors: solano a. Ann Neurol. 2006 Feb;59(2):394-8. doi: 10.1002/ana.20746. Ann Neurol. 2006. PMID: 16365882

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