Publicaciones destacadas

  • Vestibulo-ocular reflex dynamics with head-impulses discriminates spinocerebellar ataxias types 1, 2 and 3 and Friedreich ataxia

    Autores: Luis L, Costa J, Muñoz E, de Carvalho M, Carmona S, Schneider E, Gordon CR, Valls-Solé J. .
    Referencia: J Vestib Res 2016.
  • Subclinical nigrostriatal dopaminergic denervation in the cerebellar subtype of multiple system atrophy (MSA-C).

    Autores: Muñoz E, Iranzo A, Rauek S, Lomeña F, Gallego J, Ros D, Santamaría J, Tolosa E.
    Referencia: Journal Of Neurology 2011.
  • Abnormal corticospinal tract modulation of the soleus H reflex in patients with pure spastic paraparesis

    Autores: Serranová T, Valls-Solé J, Muñoz E, Genís D, Jech R, Seeman P..
    Referencia: Neuroscience Letters 2008.
  • Association of the ARLTS1 Cys148Arg variant with sporadic and familial colorectal cancer

    Autores: Castellvi-Bel, Sergi; Castells, Antoni; de Cid, Rafael; Munoz, Jenifer; Balaguer, Francesc; Gonzalo, Victoria; Andreu, Montserrat; Llor, Xavier; Jover, Rodrigo; Bessa, Xavier; Xicola, Rosa M; Pons, Elisenda; Alenda, Cristina; Paya, Artemio; Carracedo, Angel; Pique, Josep M.
    Referencia: Carcinogenesis 2007.
  • Decreased frontal choline and neuropsychological performance in preclinical Huntington’s disease

    Autores: Gómez-Ansón B, Alegret M, Muñoz E, Sainz A, Tolosa A.
    Referencia: Neurology 2007.
  • Severe cerebral white matter involvement in an autopsied case of dentatorubropallidoluysian atrophy

    Autores: E. Muñoz, J. Campdelacreu, I. Ferrer , M.J. Rey, A. Cardozo, B. Gómez, E. Tolosa.
    Referencia: 2004.
  • Abnormalities of prepulse inhibition do not depend on blink reflex excitability: a study in Parkinson's disease and Huntington's disease

    Autores: Valls-Sole, J; Munoz, JE; Valldeoriola, F.
    Referencia: Clinical Neurophysiology 2004.
  • Relative high frequency of the c.255delA parkin gene mutation in Spanish patients with autosomal recessive parkinsonism

    Autores: E. Muñoz, E. Tolosa, P. Pastor, MJ. Martí, F. Valldeoriola, J. Campdelacreu, R. Oliva.
    Referencia: J Neurol Neurosurg Psychiatry 2002.
  • Intranuclear inclusions, neuronal loss and CAG mosaicism in two patients with Machado-Joseph disease

    Autores: 2. E.Muñoz, M.J. Rey, M. Milà, A. Cardozo, T. Ribalta, E.Tolosa, I. Ferrer. .
    Referencia: J Neurol Sci 2002.
  • Dentatorubral pallidoluyisian atrophy in a Spanish family: a clinical, radiological, pathological and genetic study

    Autores: E. Muñoz, M. Milá, A. Sánchez, P. Latorre, A. Ariza, M. Codina, F. Ballesta, E. Tolosa.
    Referencia: J Neurol Neurosurg Psychiatry 1999.

Proyectos destacados

  • Catalan Network of Multiple System Atrophy: Biomarkers and Pathophysiology

    Duración: 01/01/2015 - 30/12/2017
  • Desenvolupament de estrategies neuroprotectores amb BDNF per la malaltia de Huntington

    Duración: 01/01/2007 - 30/12/2009
  • Factors genètics i ambientals que influencien l´ expressió fenotípica de la malaltia de Parkinson causada per mutacions en el gen LRR. Estudis clínics i d´ imatge en persones sense parkinsonisme i portadores de la mutació

    Duración: 01/01/2007 - 30/12/2009