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Page 1
Reply to: "Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion".
De la Casa-Fages B, Fernández-Eulate G, Gamez J, Barahona-Hernando R, Morís G, García-Barcina M, Infante J, Zulaica M, Fernández-Pelayo U, Muñoz-Oreja M, Urtasun M, Olaskoaga A, Zelaya V, Jericó I, Saez-Villaverde R, Catalina I, Sola E, Martínez-Sáez E, Pujol A, Ruiz M, Schlüter A, Spinazzola A, Muñoz-Blanco JL, Grandas F, Holt I, Álvarez V, López de Munaín A. De la Casa-Fages B, et al. Among authors: grandas f. Mov Disord. 2019 Dec;34(12):1932-1933. doi: 10.1002/mds.27899. Mov Disord. 2019. PMID: 31845766 No abstract available.
Parkinsonism and spastic paraplegia type 7: Expanding the spectrum of mitochondrial Parkinsonism.
De la Casa-Fages B, Fernández-Eulate G, Gamez J, Barahona-Hernando R, Morís G, García-Barcina M, Infante J, Zulaica M, Fernández-Pelayo U, Muñoz-Oreja M, Urtasun M, Olaskoaga A, Zelaya V, Jericó I, Saez-Villaverde R, Catalina I, Sola E, Martínez-Sáez E, Pujol A, Ruiz M, Schlüter A, Spinazzola A, Muñoz-Blanco JL, Grandas F, Holt I, Álvarez V, López de Munaín A. De la Casa-Fages B, et al. Among authors: grandas f. Mov Disord. 2019 Oct;34(10):1547-1561. doi: 10.1002/mds.27812. Epub 2019 Aug 21. Mov Disord. 2019. PMID: 31433872
Paroxysmal Kinesigenic Dystonia in a Lesch-Nyhan Disease Variant.
De La Casa-Fages B, Pérez-Sánchez JR, Grandas F. De La Casa-Fages B, et al. Among authors: grandas f. Mov Disord Clin Pract. 2014 May 23;1(2):123-124. doi: 10.1002/mdc3.12034. eCollection 2014 Jun. Mov Disord Clin Pract. 2014. PMID: 30363892 Free PMC article. No abstract available.
Stiff-man syndrome in a child.
Garzo C, Pérez-Sotelo M, Traba A, Esteban A, Grandas F, Muñoz-Blanco JL. Garzo C, et al. Among authors: grandas f. Mov Disord. 1998 Mar;13(2):365-8. doi: 10.1002/mds.870130233. Mov Disord. 1998. PMID: 9580310 No abstract available.
Treatment of stiff-person syndrome with chronic plasmapheresis.
De la Casa-Fages B, Anaya F, Gabriel-Ortemberg M, Grandas F. De la Casa-Fages B, et al. Among authors: grandas f. Mov Disord. 2013 Mar;28(3):396-7. doi: 10.1002/mds.25167. Epub 2012 Dec 12. Mov Disord. 2013. PMID: 23239368 No abstract available.
Thalamic atrophy in patients with pure hereditary spastic paraplegia type 4.
Navas-Sánchez FJ, Fernández-Pena A, Martín de Blas D, Alemán-Gómez Y, Marcos-Vidal L, Guzmán-de-Villoria JA, Fernández-García P, Romero J, Catalina I, Lillo L, Muñoz-Blanco JL, Ordoñez-Ugalde A, Quintáns B, Pardo J, Sobrido MJ, Carmona S, Grandas F, Desco M. Navas-Sánchez FJ, et al. Among authors: grandas f. J Neurol. 2021 Jul;268(7):2429-2440. doi: 10.1007/s00415-020-10387-4. Epub 2021 Jan 28. J Neurol. 2021. PMID: 33507371
122 results