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Scientific Reports|May 6, 2020
Challenges to rutile-based geoscientific tools: low-temperature polymorphic TiO<sub>2</sub> transformations and corresponding reactive pathwaysAndré Jorge Pinto, Nuria Sanchez-Pastor, Ivan Callegari, et al.
Frontiers in Genetics|October 25, 2017
Whole Gene Deletion of <i>EBF3</i> Supporting Haploinsufficiency of This Gene as a Mechanism of Neurodevelopmental DiseaseFátima Lopes, Gabriela Soares, Miguel Gonçalves-Rocha, et al.
Nonlinear Dynamics, Psychology, and Life Sciences|October 2, 2024
Exploring the Efficacy of Several Physiological Synchrony Methods During Collaborative Recall of StoriesMiguel Enrique Sanchez Hechavarria, Ramon Carrazana Escalona, Jorge Pinto-Vigueras, et al.
Cancer Biomarkers : Section a of Disease Markers|March 20, 2025
DNA damage of peripheral blood lymphocytes as a dual biomarker: Diagnostic and treatment response in woman breast cancer patientsAna Rita Guedes, Jorge Pinto Soares, Renato Cunha, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 16, 2015
Charcot-Marie-Tooth 4B2 caused by a novel mutation in the MTMR13/SBF2 gene in two related Portuguese familiesLuís Negrão, Luciano Almendra, Joana Ribeiro, et al.
Cell Biochemistry and Function|January 22, 2014
Age-related increases in human lymphocyte DNA damage: is there a role of aerobic fitness?Jorge Pinto Soares, Maria Paula Mota, José Alberto Duarte, et al.
International Journal of Environmental Research and Public Health|March 11, 2023
Analysis of the Cardiorespiratory Pattern of Patients Undergoing Weaning Using Artificial IntelligenceJorge Pinto, Hernando González, Carlos Arizmendi, et al.
European Journal of Gastroenterology & Hepatology|September 5, 2009
Staging and survival of rectal cancer in Vila Nova de Gaia, PortugalMiguel Henriques Abreu, Eduarda Matos, Fernando Castro Poças, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 31, 2021
Adult polyglucosan body disease-an atypical compound heterozygous with a novel GBE1 mutationAndreia Carvalho, Joana Nunes, Ricardo Taipa, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|December 25, 2015
Elevation of gamma-glutamyl transferase in adult: Should we think about progressive familiar intrahepatic cholestasis?Hugo M Oliveira, Cláudia Pereira, Ermelinda Santos Silva, et al.
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