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Brain : a Journal of Neurology|September 25, 2008
Vocal cord paresis and diaphragmatic dysfunction are severe and frequent symptoms of GDAP1-associated neuropathyTeresa Sevilla, Teresa Jaijo, Dolores Nauffal, et al.Journal of Neuro-Oncology|May 27, 2025
Clinical and radiological features of pseudoprogression in brain tumors treated with immune checkpoint inhibitorsMaria José Ibáñez-Juliá, Luis Bataller, Francisco Javier Cabello-Murgui, et al.Movement Disorders : Official Journal of the Movement Disorder Society|July 4, 2024
STUB1 Mutations as Possible Genetic Modifiers in Spinocerebellar Ataxia Type 8Raquel Baviera-Muñoz, Lidón Carretero-Vilarroig, Ana Pedro-Ibor, et al.Journal of the Peripheral Nervous System : JPNS|January 5, 2011
Phenotypical features of the p.R120W mutation in the GDAP1 gene causing autosomal dominant Charcot-Marie-Tooth diseaseRafael Sivera, Carmen Espinós, Juan J Vílchez, et al.Journal of Neuroimmunology|August 1, 2013
Longitudinally extensive transverse myelitis with AQP4 antibodies revealing ovarian teratomaMarina Frasquet, Luis Bataller, Estefanía Torres-Vega, et al.JAMA Neurology|June 18, 2014
Cerebellar ataxia and glutamic acid decarboxylase antibodies: immunologic profile and long-term effect of immunotherapyHelena Ariño, Nuria Gresa-Arribas, Yolanda Blanco, et al.Neurology|October 1, 2013
Charcot-Marie-Tooth disease: genetic and clinical spectrum in a Spanish clinical seriesRafael Sivera, Teresa Sevilla, Juan Jesús Vílchez, et al.Journal of Neurology, Neurosurgery, and Psychiatry|February 17, 2012
Contactin-associated protein-2 antibodies in non-paraneoplastic cerebellar ataxiaEsther B E Becker, Luigi Zuliani, Rosemary Pettingill, et al.Scientific Reports|May 13, 2026
Validation of circulating miR-323a-3p and miR-625-3p to classify hypertrophic cardiomyopathy in Friedreich's ataxiaJosé Santiago Ibáñez-Cabellos, Raquel Baviera-Muñoz, Berta Alemany-Perna, et al.The Lancet. Neurology|April 8, 2014
A novel non-rapid-eye movement and rapid-eye-movement parasomnia with sleep breathing disorder associated with antibodies to IgLON5: a case series, characterisation of the antigen, and post-mortem studyLidia Sabater, Carles Gaig, Ellen Gelpi, et al.Pageof 6