López-Marín L - Search Results

1

[MCT8-specific thyroid hormone cell transporter deficiency: a case report and review of the literature].

López-Marín L, Martín-Belinchón M, Gutiérrez-Solana LG, Morte-Molina B, Duat-Rodríguez A, Bernal J. López-Marín L, et al. Rev Neurol. 2013 Jun 16;56(12):615-22. Rev Neurol. 2013. PMID: 23744248 Free article. Review. Spanish.

2

[Clinical, electroencephalographic and genomic characteristics of patients with epilepsy with febrile seizures plus].

Cantarín-Extremera V, García-Peñas JJ, Gutiérrez-Solana LG, García-Fernández M, Ruiz-Falcó ML, Duat-Rodríguez A, López-Marín L. Cantarín-Extremera V, et al. Rev Neurol. 2011 Apr 1;52(7):404-11. Rev Neurol. 2011. PMID: 21425109 Free article. Spanish.

3

[Characteristics and evolution of patients with Alice in Wonderland syndrome].

Losada-Del Pozo R, Cantarín-Extremera V, García-Peñas JJ, Duat-Rodríguez A, López-Marín L, Gutiérrez-Solana LG, Ruiz-Falcó ML. Losada-Del Pozo R, et al. Rev Neurol. 2011 Dec 1;53(11):641-8. Rev Neurol. 2011. PMID: 22086425 Free article. Spanish.

4

[Para-infectious seizures in children: a retrospective study of 34 cases].

Lara-Herguedas J, García-Peñas JJ, Ruiz-Falcó ML, Gutiérrez-Solana LG, Duat-Rodríguez A, Arrabal-Fernández ML, López-Marín L. Lara-Herguedas J, et al. Rev Neurol. 2008 Mar 16-31;46(6):321-5. Rev Neurol. 2008. PMID: 18368673 Free article. Spanish.

5

[Analysis of a series of cases with an initial diagnosis of acute disseminated encephalomyelitis over the period 2000-2010].

Rodríguez-Fernández C, López-Marín L, López-Pino MÁ, Gutiérrez-Solana LG, Soto-Insuga V, Conejo-Moreno D. Rodríguez-Fernández C, et al. Rev Neurol. 2013 Oct 1;57(7):297-305. Rev Neurol. 2013. PMID: 24052440 Free article. Spanish.

6

Neuroimaging findings in patient series with mucopolysaccharidosis.

Calleja Gero ML, González Gutiérrez-Solana L, López Marín L, López Pino MA, Fournier Del Castillo C, Duat Rodríguez A. Calleja Gero ML, et al. Neurologia. 2012 Sep;27(7):407-13. doi: 10.1016/j.nrl.2011.10.007. Epub 2011 Dec 15. Neurologia. 2012. PMID: 22178048 Free article. English, Spanish.

7

[Dravet syndrome and mitochondrial disease, are they comorbid pathologies?].

Cantarin-Extremera V, Ruiz-Falco Rojas ML, Garcia-Fernandez M, Duat-Rodriguez A, Lopez-Marin L, Calleja-Gero ML. Cantarin-Extremera V, et al. Rev Neurol. 2014 Nov 1;59(9):429-31. Rev Neurol. 2014. PMID: 25342058 Free article. Spanish. No abstract available.

8

[Two new cases of Leigh syndrome caused by mutation m.13513G> A in the MTND5 gene].

Jimenez-Legido M, Bernardino-Cuesta B, Lopez-Marin L, Cantarin-Extremera V, Blazquez-Encinar A, Martin-Casanueva MA, Gutierrez-Solana LG. Jimenez-Legido M, et al. Rev Neurol. 2019 Apr 1;68(7):312-314. doi: 10.33588/rn.6807.2018393. Rev Neurol. 2019. PMID: 30906981 Free article. Spanish.

9

[Anti-NMDA receptor encephalitis with unilateral hemispheric affectation].

Jimenez-Legido M, Cantarin-Extremera V, Bernardino-Cuesta B, Garcia-Fernandez M, Lopez-Marin L, Duat-Rodriguez A, Ruiz-Falco Rojas ML, Gutierrez-Solana LG. Jimenez-Legido M, et al. Rev Neurol. 2019 Jun 16;68(12):533-534. doi: 10.33588/rn.6812.2018440. Rev Neurol. 2019. PMID: 31173335 Free article. Spanish.

10

Immune-mediated mechanisms in the pathogenesis of Hopkins syndrome.

Cantarín-Extremera V, González-Gutiérrez-Solana L, Ramírez-Orellana M, López-Marín L, Duat-Rodríguez A, Ruíz-Falcó-Rojas ML. Cantarín-Extremera V, et al. Pediatr Neurol. 2012 Nov;47(5):373-4. doi: 10.1016/j.pediatrneurol.2012.08.006. Pediatr Neurol. 2012. PMID: 23044022

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