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Year Number of Results
2000 2
2003 3
2004 2
2005 3
2006 2
2007 1
2008 1
2011 2
2012 1
2013 1
2015 1
2016 1
2017 3
2020 1
2022 1
2024 0

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24 results

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Page 1
Mutations, Genes, and Phenotypes Related to Movement Disorders and Ataxias.
Martínez-Rubio D, Hinarejos I, Sancho P, Gorría-Redondo N, Bernadó-Fonz R, Tello C, Marco-Marín C, Martí-Carrera I, Martínez-González MJ, García-Ribes A, Baviera-Muñoz R, Sastre-Bataller I, Martínez-Torres I, Duat-Rodríguez A, Janeiro P, Moreno E, Pías-Peleteiro L, Gordo MO, Ruiz-Gómez Á, Muñoz E, Martí MJ, Sánchez-Monteagudo A, Fuster C, Andrés-Bordería A, Pons RM, Jesús-Maestre S, Mir P, Lupo V, Pérez-Dueñas B, Darling A, Aguilera-Albesa S, Espinós C. Martínez-Rubio D, et al. Among authors: garcia ribes a. Int J Mol Sci. 2022 Oct 6;23(19):11847. doi: 10.3390/ijms231911847. Int J Mol Sci. 2022. PMID: 36233161 Free PMC article.
[Myths and evidence on the use of botulinum toxin: spasticity in adults and in children with cerebral palsy].
Martinez-Castrillo JC, Pena-Segura JL, Sanz-Cartagena P, Alonso-Curco X, Arbelo-Gonzalez JM, Arriola-Pereda G, Coll-Bosch MD, Conejero-Casares JA, Garcia-Ribes A, Jauma-Classen S, Pagonabarraga J, Vidal-Valls J, Garcia-Ruiz PJ. Martinez-Castrillo JC, et al. Among authors: garcia ribes a. Rev Neurol. 2017 May 16;64(10):459-470. Rev Neurol. 2017. PMID: 28497442 Free article. Review. Spanish.
[Adult-onset metabolic diseases].
García Ribes A, Martínez González M, García Cazorla A. García Ribes A, et al. An Sist Sanit Navar. 2008;31 Suppl 2:75-89. An Sist Sanit Navar. 2008. PMID: 18953373 Free article. Spanish.
Molecular characterization of congenital myasthenic syndromes in Spain.
Natera-de Benito D, Töpf A, Vilchez JJ, González-Quereda L, Domínguez-Carral J, Díaz-Manera J, Ortez C, Bestué M, Gallano P, Dusl M, Abicht A, Müller JS, Senderek J, García-Ribes A, Muelas N, Evangelista T, Azuma Y, McMacken G, Paipa Merchan A, Rodríguez Cruz PM, Camacho A, Jiménez E, Miranda-Herrero MC, Santana-Artiles A, García-Campos O, Dominguez-Rubio R, Olivé M, Colomer J, Beeson D, Lochmüller H, Nascimento A. Natera-de Benito D, et al. Among authors: garcia ribes a. Neuromuscul Disord. 2017 Dec;27(12):1087-1098. doi: 10.1016/j.nmd.2017.08.003. Epub 2017 Aug 18. Neuromuscul Disord. 2017. PMID: 29054425
Sensory-motor neuropathy in a case with SPG35: Expanding the phenotype.
Axpe IR, Blanco Martín E, Garcia Ribes A, Bermejo-Ramirez R, Arroyo Andújar D. Axpe IR, et al. Among authors: garcia ribes a. J Neurol Sci. 2017 Sep 15;380:98-100. doi: 10.1016/j.jns.2017.05.054. Epub 2017 May 30. J Neurol Sci. 2017. PMID: 28870598 No abstract available.
Long-term follow-up in patients with congenital myasthenic syndrome due to RAPSN mutations.
Natera-de Benito D, Bestué M, Vilchez JJ, Evangelista T, Töpf A, García-Ribes A, Trujillo-Tiebas MJ, García-Hoyos M, Ortez C, Camacho A, Jiménez E, Dusl M, Abicht A, Lochmüller H, Colomer J, Nascimento A. Natera-de Benito D, et al. Among authors: garcia ribes a. Neuromuscul Disord. 2016 Feb;26(2):153-9. doi: 10.1016/j.nmd.2015.10.013. Epub 2015 Nov 23. Neuromuscul Disord. 2016. PMID: 26782015
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
[Idiopathic epilepsies: some therapeutic aspects].
Campos-Castelló J, Prats Viñas JM, García-Ribes A. Campos-Castelló J, et al. Among authors: garcia ribes a. Rev Neurol. 2004 Jan 16-31;38(2):180-4. Rev Neurol. 2004. PMID: 14752722 Free article. Review. Spanish.
24 results