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Pediatric Surgery International|September 22, 2023
Flow cytometric characterization of cecal appendix lymphocyte subpopulations in children: a pilot studyJavier Arredondo Montero, Andrea Torres López, Guillermina Hurtado Ilzarbe, et al.
Human Mutation|July 4, 2012
Revisiting genotype-phenotype overlap in neurogenetics: triplet-repeat expansions mimicking spastic paraplegiasConceição Bettencourt, Beatriz Quintáns, Raquel Ros, et al.
Archives of Neurology|September 15, 2005
A new mutation of the tau gene, G303V, in early-onset familial progressive supranuclear palsyRaquel Ros, Stéphane Thobois, Nathalie Streichenberger, et al.
Archives of Neurology|December 12, 2007
Variability of age at onset in siblings with familial Alzheimer diseaseEstrella Gómez-Tortosa, M Sagrario Barquero, Manuel Barón, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2002
Steele-Richardson-Olszewski syndrome in a patient with a single C212Y mutation in the parkin proteinBlas Morales, Armando Martínez, Isabel Gonzalo, et al.
World Journal of Pediatrics : WJP|September 16, 2022
Discriminatory capacity of serum interleukin-6 between complicated and uncomplicated acute appendicitis in children: a prospective validation studyJavier Arredondo Montero, Giuseppa Antona, Adriana Rivero Marcotegui, et al.
Pediatric Surgery International|August 16, 2022
Serum neutrophil gelatinase-associated lipocalin (NGAL) as a diagnostic tool in pediatric acute appendicitis: a prospective validation studyJavier Arredondo Montero, Giuseppa Antona, Carlos Bardají Pascual, et al.
Pediatric Surgery International|December 1, 2022
Diagnostic performance of serum pentraxin-3 in pediatric acute appendicitis: a prospective diagnostic validation studyJavier Arredondo Montero, Giuseppa Antona, Mónica Bronte Anaut, et al.
Annals of Neurology|February 3, 2004
The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementiaJuan J Zarranz, Javier Alegre, Juan C Gómez-Esteban, et al.
Annals of Neurology|April 27, 2005
Genetic linkage of autosomal dominant progressive supranuclear palsy to 1q31.1Raquel Ros, Pilar Gómez Garre, Michio Hirano, et al.
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