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737 results

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Heterozygous STUB1 mutation causes familial ataxia with cognitive affective syndrome (SCA48).
Genis D, Ortega-Cubero S, San Nicolás H, Corral J, Gardenyes J, de Jorge L, López E, Campos B, Lorenzo E, Tonda R, Beltran S, Negre M, Obón M, Beltran B, Fàbregas L, Alemany B, Márquez F, Ramió-Torrentà L, Gich J, Volpini V, Pastor P. Genis D, et al. Among authors: corral j. Neurology. 2018 Nov 20;91(21):e1988-e1998. doi: 10.1212/WNL.0000000000006550. Epub 2018 Oct 31. Neurology. 2018. PMID: 30381368
A kindred with cerebellar ataxia and thermoanalgesia.
Genis D, Ferrer I, Solé JV, Corral J, Volpini V, San Nicolás H, Gich J, Ramió-Torrentà L, Ferrándiz M, Puig J, Márquez F. Genis D, et al. Among authors: corral j. J Neurol Neurosurg Psychiatry. 2009 May;80(5):518-23. doi: 10.1136/jnnp.2008.151548. Epub 2008 Aug 18. J Neurol Neurosurg Psychiatry. 2009. PMID: 18710877
New subtype of spinocerebellar ataxia with altered vertical eye movements mapping to chromosome 1p32.
Serrano-Munuera C, Corral-Juan M, Stevanin G, San Nicolás H, Roig C, Corral J, Campos B, de Jorge L, Morcillo-Suárez C, Navarro A, Forlani S, Durr A, Kulisevsky J, Brice A, Sánchez I, Volpini V, Matilla-Dueñas A. Serrano-Munuera C, et al. Among authors: corral j, corral juan m. JAMA Neurol. 2013 Jun;70(6):764-71. doi: 10.1001/jamaneurol.2013.2311. JAMA Neurol. 2013. PMID: 23700170
Celiac disease and idiopathic cerebellar ataxia.
Combarros O, Infante J, López-Hoyos M, Bartolomé MJ, Berciano J, Corral J, Volpini V. Combarros O, et al. Among authors: corral j. Neurology. 2000 Jun 27;54(12):2346. doi: 10.1212/wnl.54.12.2346. Neurology. 2000. PMID: 10881272 No abstract available.
Spinocerebellar ataxia type 2 (SCA2) with white matter involvement.
Armstrong J, Bonaventura I, Rojo A, González G, Corral J, Nadal N, Volpini V, Ferrer I. Armstrong J, et al. Among authors: corral j. Neurosci Lett. 2005 Jun 24;381(3):247-51. doi: 10.1016/j.neulet.2005.02.063. Epub 2005 Mar 17. Neurosci Lett. 2005. PMID: 15896478
737 results