Publicaciones en las que colabora con AINHOA GARCIA RIBES (11)

2022

  1. Mutations, Genes, and Phenotypes Related to Movement Disorders and Ataxias

    International Journal of Molecular Sciences, Vol. 23, Núm. 19

2013

  1. MECP2 gene study in a large cohort: Testing of 240 female patients and 861 healthy controls (519 females and 342 males)

    Journal of Molecular Diagnostics, Vol. 15, Núm. 5, pp. 723-729

2012

  1. CDKL5 gene status in female patients with epilepsy and Rett-like features: two new mutations in the catalytic domain

    BMC Medical Genetics, Vol. 13

2007

  1. Suspected Herpes Encephalitis and Opercular Syndrome in Childhood

    Pediatric Neurology, Vol. 36, Núm. 3, pp. 202-206

2006

  1. Acute onset ataxia in infancy: Its aetiology, treatment and follow-up

    Revista de Neurologia, Vol. 42, Núm. 6, pp. 321-324

2005

  1. Apraxia of gait: An acquired sequela with a poor prognosis

    Revista de Neurologia, Vol. 40, Núm. 5, pp. 279-281

  2. Callosal agenesis, chorioretinal lacunae, absence of infantile spasms, and normal development: Aicardi syndrome without epilepsy?

    Developmental Medicine and Child Neurology, Vol. 47, Núm. 6, pp. 419-420

2004

  1. Idiopathic catastrophic epileptic encephalopathy: An untreatable convulsive malady in infancy

    Revista de Neurologia, Vol. 38, Núm. 10, pp. 931-934

2003

  1. Amnesia global transitoria: Una enfermedad del adulto presente en la infancia

    Anales de Pediatria

  2. Disturbances of neuroblast migration and amniocentesis. An under-diagnosed problem?

    Revista de Neurologia, Vol. 36, Núm. 1, pp. 33-36

  3. Factors related to the short-term remission of tics in children with Tourette syndrome

    Revista de Neurologia, Vol. 37, Núm. 10, pp. 901-903