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Pediatric Neurology|August 10, 2005
Familial arachnoid cystsGema Arriola, Pedro de Castro, Alfonso VerdúBrain & Development|April 12, 2003
Dandy-Walker malformation in an infant with tetrasomy 9pMaría R Cazorla Calleja, Alfonso Verdú, Valentin FélixBrain & Development|September 22, 2009
Early infantile epileptic encephalopathy with unusual favourable outcomeMaría Rosario Cazorla, Alfonso Verdú, Carmen Montes, et al.Pediatric Neurology|April 18, 2007
Neuroimage findings in 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiencyMaría R Cazorla, Alfonso Verdú, Celia Pérez-Cerdá, et al.Journal of Paediatrics and Child Health|February 24, 2007
Varicella encephalopathy in immunocompetent childrenAmparo Carreño, Jesús López-Herce, Alfonso Verdú, et al.Archives of Medical Research|March 22, 2005
Association between systemic lupus erythematosus, rheumatoid arthritis, hyperprolactinemia and thyroid autoantibodiesCaroline Kaercher Kramer, Tatiana Freitas Tourinho, Waldir Pedro de Castro, et al.Journal of Child Neurology|February 20, 2015
Complexity of the Hereditary Motor and Sensory Neuropathies: Clinical and Cellular Characterization of the MPZ p.D90E MutationVincenzo Lupo, Samuel I Pascual-Pascual, Paula Sancho, et al.Anales De Pediatria|September 23, 2023
Current situation of Specialized Health Training in pediatrics and its specific areas: Challenges and needsGema Arriola Pereda, Jose I Labarta Aizpún, María Jesús Sánchez, et al.International Journal of Molecular Sciences|January 23, 2024
Proteomic Profiling Identifies Candidate Diagnostic Biomarkers of Hydrosalpinx in Endometrial Fluid: A Pilot StudyRoberto Gonzalez-Martin, Pedro de Castro, Carmen Fernandez, et al.Neuromuscular Disorders : NMD|January 24, 2009
Infantile mitochondrial encephalomyopathy with unusual phenotype caused by a novel BCS1L mutation in an isolated complex III-deficient patientAlberto Blázquez, Mari Carmen Gil-Borlado, María Morán, et al.Pageof 3