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Neuropediatrics|August 12, 2003
Cerebellar hypoplasia with heterotopic purkinje cells in the molecular layer and preservation of the granule layers associated with severe encephalopathy. A new entity?I Pascual-Castroviejo, S I Pascual-Pascual, M Gutierrez-Molina, et al.Neurologia (Barcelona, Spain)|May 1, 1994
Optic gliomas in neurofibromatosis type 1 (NF-1). Presentation of 31 casesI Pascual-Castroviejo, A Martínez Bermejo, V López Martín, et al.Revista De Neurologia|February 10, 1999
[Physiopathology of neurological signs of hypoxanthine-guanine phosphoribosyltransferase deficiency]R Torres-Jiménez, F Mateos-Antón, J Arcas-Martínez, et al.Revista De Neurologia|October 22, 2008
[Segmental neurofibromatosis in children. Presentation of 43 patients]I Pascual-Castroviejo, S I Pascual-Pascual, R Velázquez-Fragua, et al.Anales De Pediatria (Barcelona, Spain : 2003)|April 12, 2003
[Cutaneous hemangiomas, vascular malformations and associated disorders. A new neurocutaneous syndrome]I Pascual-Castroviejo, J C López-Gutiérrez, S I Pascual-Pascual, et al.Revista De Neurologia|May 17, 2001
[Battered baby syndrome. Report of a case with severe sequelae]I Pascual-Castroviejo, S I Pascual Pascual, F Ruza-Tarrío, et al.Brain & Development|November 1, 1992
Early infantile epileptic encephalopathy: a case associated with hemimegalencephalyA M Bermejo, V L Martin, J Arcas, et al.Acta Paediatrica Scandinavica|September 1, 1985
Maple syrup urine disease variant form: presentation with psychomotor retardation and CT scan abnormalitiesA Verdu, J Lopez-Herce, I Pascual-Castroviejo, et al.AJNR. American Journal of Neuroradiology|September 12, 2007
Facial hemangioma and hemispheric migration disorder: presentation of 5 patientsI Pascual-Castroviejo, S-I Pascual-Pascual, J-C López-Gutiérrez, et al.Pediatric Neurology|July 1, 1993
Sturge-Weber syndrome: study of 40 patientsI Pascual-Castroviejo, C Díaz-Gonzalez, R M García-Melian, et al.Pageof 28