AINHOA GARCIA RIBES-rekin lankidetzan egindako argitalpenak (11)
2022
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Mutations, Genes, and Phenotypes Related to Movement Disorders and Ataxias
International Journal of Molecular Sciences, Vol. 23, Núm. 19
2013
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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
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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
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Suspected Herpes Encephalitis and Opercular Syndrome in Childhood
Pediatric Neurology, Vol. 36, Núm. 3, pp. 202-206
2006
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Acute onset ataxia in infancy: Its aetiology, treatment and follow-up
Revista de Neurologia, Vol. 42, Núm. 6, pp. 321-324
2005
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Apraxia of gait: An acquired sequela with a poor prognosis
Revista de Neurologia, Vol. 40, Núm. 5, pp. 279-281
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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
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Idiopathic catastrophic epileptic encephalopathy: An untreatable convulsive malady in infancy
Revista de Neurologia, Vol. 38, Núm. 10, pp. 931-934
2003
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Amnesia global transitoria: Una enfermedad del adulto presente en la infancia
Anales de Pediatria
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Disturbances of neuroblast migration and amniocentesis. An under-diagnosed problem?
Revista de Neurologia, Vol. 36, Núm. 1, pp. 33-36
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Factors related to the short-term remission of tics in children with Tourette syndrome
Revista de Neurologia, Vol. 37, Núm. 10, pp. 901-903