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Revista De Neurologia|June 18, 2004
[Smith-Magenis syndrome: a report of two new cases and an approximation to their characteristic behavioural phenotype]O Blanco-Barca, M Gallego-Blanco, C Ruiz-Ponte, et al.
Revista De Neurologia|April 25, 2007
[Reversible posterior leukoencephalopathy syndrome: an infrequent complication in the course of haemolytic-uremic syndrome]C Gómez-Lado, F Martinón-Torres, A Alvarez-Moreno, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|June 1, 1996
Cerebrospinal fluid purine metabolites after complex febrile convulsionsM Castro-Gago, S Rodríguez-Segade, F Camiña Darriba, et al.
Journal of Neurosurgical Sciences|April 23, 2008
Therapeutic criteria in communicating childhood hydrocephalusA Rodríguez-Nuñez, M Somoza-Martín, C Gómez-Lado, et al.
Epilepsia|December 28, 1999
Long-term treatment of children with epilepsy with valproate or carbamazepine may cause subclinical hypothyroidismJ Eirís-Puñal, M Del Río-Garma, M C Del Río-Garma, et al.
Revista De Neurologia|October 29, 2003
[Phenotypic variability of deletion 22q11.2. An analysis of 16 observations with special emphasis on the neurological manifestations]J Eirís-Puñal, J M Iglesias-Meleiro, M O Blanco-Barca, et al.
Revista De Neurologia|October 31, 2000
[Hereditary neuropathy with liability to pressure palsies (tomaculous neuropathy). Clinical, electrophysical and molecular study of two affected families]J Eirís-Punal, M Vidal-Lijó, F Barros-Angueira, et al.
Journal of Child Neurology|March 12, 1999
Congenital hydranencephalic-hydrocephalic syndrome associated with mitochondrial dysfunctionM Castro-Gago, A Alonso, E Pintos-Martínez, et al.
Revista De Neurologia|December 11, 2019
[De novo heterozygous mutation in the MBD5 gene associated with bilateral band heterotopia and polymicrogyria]M Castro-Gago, C Gómez-Lado, F Barros-Angueira, et al.
Revista De Neurologia|September 8, 2020
Clinical and neurophysiological response to ephedrine in a patient affected with slow-channel congenital myasthenic syndromeJ Eirís-Puñal, P Fuentes-Pita, C Gómez-Lado, et al.
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