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Year | Number of Results |
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2003 | 1 |
2012 | 1 |
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2020 | 1 |
2024 | 1 |
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Page 1
Natural History of Vanishing White Matter.
Ann Neurol. 2018 Aug;84(2):274-288. doi: 10.1002/ana.25287. Epub 2018 Sep 6.
Ann Neurol. 2018.
PMID: 30014503
Free PMC article.
Epilepsy in Duchenne and Becker muscular dystrophies.
Armijo Gómez JA, Fernandez-Garcia MA, Camacho A, Liz M, Ortez C, Lafuente-Hidalgo M, Toledo Bravo-de Laguna L, Estévez-Arias B, Carrera-García L, Expósito-Escudero J, Domínguez-Carral J, Nascimento A, Natera-de Benito D.
Armijo Gómez JA, et al. Among authors: toledo bravo de laguna l.
Ann Clin Transl Neurol. 2024 May 1. doi: 10.1002/acn3.52058. Online ahead of print.
Ann Clin Transl Neurol. 2024.
PMID: 38693632
Free article.
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[Paroxysmal stereotypy-tic-dystonia syndrome].
Cabrera-López JC, Martí-Herrero M, Fernández-Burriel M, Toledo-Bravo de Laguna L, Domínguez-Ramírez S, Fortea-Sevilla S.
Cabrera-López JC, et al. Among authors: toledo bravo de laguna l.
Rev Neurol. 2003 Apr 16-30;36(8):729-34.
Rev Neurol. 2003.
PMID: 12717651
Free article.
Spanish.
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[Three cases of Pallister-Killian syndrome].
Toledo-Bravo de Laguna L, del Campo-Casanelles M, Santana-Rodriguez A, Santana-Artiles A, Sebastian-Garcia I, Cabrera-Lopez JC.
Toledo-Bravo de Laguna L, et al.
Rev Neurol. 2014 Jan 16;58(2):63-8.
Rev Neurol. 2014.
PMID: 24399622
Free article.
Spanish.
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Associations of paediatric demyelinating and encephalitic syndromes with myelin oligodendrocyte glycoprotein antibodies: a multicentre observational study.
Armangue T, Olivé-Cirera G, Martínez-Hernandez E, Sepulveda M, Ruiz-Garcia R, Muñoz-Batista M, Ariño H, González-Álvarez V, Felipe-Rucián A, Jesús Martínez-González M, Cantarín-Extremera V, Concepción Miranda-Herrero M, Monge-Galindo L, Tomás-Vila M, Miravet E, Málaga I, Arrambide G, Auger C, Tintoré M, Montalban X, Vanderver A, Graus F, Saiz A, Dalmau J; Spanish Pediatric anti-MOG Study Group.
Armangue T, et al.
Lancet Neurol. 2020 Mar;19(3):234-246. doi: 10.1016/S1474-4422(19)30488-0. Epub 2020 Feb 10.
Lancet Neurol. 2020.
PMID: 32057303
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[Aicardi-Goutieres syndrome due to mutation of the IFIH1 gene with pontine involvement. A case report].
Florido-Rodriguez A, Eiris-Punal J, Barros-Angueira F, Toledo-Bravo de Laguna L, Santana-Artiles A, Sebastian-Garcia I, Santana-Rodriguez A, Cabrera-Lopez JC.
Florido-Rodriguez A, et al. Among authors: toledo bravo de laguna l.
Rev Neurol. 2016 Oct 1;63(7):309-14.
Rev Neurol. 2016.
PMID: 27658362
Free article.
Spanish.
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[X-linked hereditary spastic paraplegia due to mutation in the L1CAM gene: three cases reports of CRASH syndrome].
Muñoz A, Cabrera-López JC, Santana-Rodríguez A, Toledo-Bravo de Laguna L, Santana-Artiles A, Sebastián-García I.
Muñoz A, et al. Among authors: toledo bravo de laguna l.
Rev Neurol. 2016 Mar 1;62(5):218-22.
Rev Neurol. 2016.
PMID: 26916325
Free article.
Spanish.
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[Familial hemiplegic migraine type 2: two paediatric case reports].
Toledo-Bravo de Laguna L, Santana-Rodríguez A, Cabrera-López JC, Santana-Artiles A, Sebastián-García I.
Toledo-Bravo de Laguna L, et al.
Rev Neurol. 2012 Feb 16;54(4):222-6.
Rev Neurol. 2012.
PMID: 22314763
Free article.
Spanish.
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