Publicacións en colaboración con investigadores/as de Hospital Clinic Barcelona (9)

2019

  1. X chromosome inactivation does not necessarily determine the severity of the phenotype in Rett syndrome patients

    Scientific Reports, Vol. 9, Núm. 1

2017

  1. The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome

    Scientific Reports, Vol. 7, Núm. 1

2016

  1. A leaky splicing mutation in NFU1 is associated with a particular biochemical phenotype. Consequences for the diagnosis

    Mitochondrion, Vol. 26, pp. 72-80

2011

  1. Correlations between Ventricular enlargement and gray and white matter volumes of cortex, thalamus, striatum, and internal capsule in schizophrenia

    European Archives of Psychiatry and Clinical Neuroscience, Vol. 261, Núm. 7, pp. 467-476

  2. The semantic organization of the animal category: Evidence from semantic verbal fluency and network theory

    Cognitive Processing, Vol. 12, Núm. 2, pp. 183-196

2010

  1. Switcher-random-walks: A cognitive-inspired mechanism for network exploration

    International Journal of Bifurcation and Chaos

2009

  1. A preliminary study of the frequency of anti-basal ganglia antibodies and streptococcal infection in attention deficit/hyperactivity disorder

    Journal of Neurology, Vol. 256, Núm. 7, pp. 1103-1108

  2. Memantine induces reversible neurologic impairment in patients with MS

    Neurology, Vol. 72, Núm. 19, pp. 1630-1633

1982

  1. Letters to the editor

    Muscle & Nerve