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Depression and Anxiety|April 1, 2015
DETECTION OF ANXIETY DISORDERS IN PRIMARY CARE: A META-ANALYSIS OF ASSISTED AND UNASSISTED DIAGNOSESElena Olariu, Carlos G Forero, Jose Ignacio Castro-Rodriguez, et al.
Revista Espanola De Patologia : Publicacion Oficial De La Sociedad Espanola De Anatomia Patologica Y De La Sociedad Espanola De Citologia|February 26, 2026
SEAP-GETNE consensus on prognostic and predictive molecular biomarkers in thyroid cancerIgnacio Ruz-Caracuel, Teresa Alonso-Gordoa, Susana Hernández, et al.
Transplantation Proceedings|January 3, 2025
Hemophagocytic Lymphohistiocytosis in a Kidney Transplant Recipient: Case ReportMaría Araceli Povedano Medina, Álvaro Arnau Prieto, Aitor Parra Zurutuza, et al.
Cancers|June 26, 2025
Validation of the Updated Porto Proposal in Papillary Thyroid Microtumors: Analysis of Cases at a University Hospital in Catalonia, SpainKarmele Saez de Gordoa, Elias Tasso, Alexandre Rei, et al.
European Journal of Medical Genetics|June 12, 2013
New case of mitochondrial HMG-CoA synthase deficiency. Functional analysis of eight mutationsMónica Ramos, Sebastián Menao, María Arnedo, et al.
International Journal of Molecular Sciences|July 2, 2021
Molecular Landscape of Vulvar Squamous Cell CarcinomaNuria Carreras-Dieguez, José Guerrero, Maria Teresa Rodrigo-Calvo, et al.
Molecular Biology Reports|September 29, 2011
Characterization of splice variants of the genes encoding human mitochondrial HMG-CoA lyase and HMG-CoA synthase, the main enzymes of the ketogenesis pathwayBeatriz Puisac, Mónica Ramos, María Arnedo, et al.
Clinical Genetics|May 21, 2013
Could a patient with SMC1A duplication be classified as a human cohesinopathy?C Baquero-Montoya, M C Gil-Rodríguez, M E Teresa-Rodrigo, et al.
Archivos De Bronconeumologia|November 30, 2019
Evaluation of the Integrated Tuberculosis Research Program Sponsored by the Spanish Society of Pulmonology and Thoracic Surgery: 11 Years onTeresa Rodrigo, José-María García-García, José A Caminero, et al.
Biomed Research International|March 1, 2016
Identification and Functional Characterization of Two Intronic NIPBL Mutations in Two Patients with Cornelia de Lange SyndromeMaría E Teresa-Rodrigo, Juliane Eckhold, Beatriz Puisac, et al.
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