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Brain & Development|February 2, 2010
Rett syndrome with and without detected MECP2 mutations: an attempt to redefine phenotypesTeresa Temudo, Mónica Santos, Elisabete Ramos, et al.
Human Mutation|July 29, 2018
LAMA2 gene mutation update: Toward a more comprehensive picture of the laminin-α2 variome and its related phenotypesJorge Oliveira, Angela Gruber, Márcio Cardoso, et al.
Plos One|June 23, 2021
Inflammasome genes polymorphisms may influence the development of hepatitis C in the Amazonas, BrazilDiana Mota Toro, Rajendranath Ramasawmy, Pedro Vieira Silva Neto, et al.
Einstein (Sao Paulo, Brazil)|October 19, 2013
Coronary computed tomography angiography with 320-row detector and using the AIDR-3D: initial experienceRoberto Sasdelli Neto, Cesar Higa Nomura, Ana Carolina Sandoval Macedo, et al.
Diseases of the Esophagus : Official Journal of the International Society for Diseases of the Esophagus|April 26, 2024
Western European Variation in the Organization of Esophageal Cancer Surgical CareMaurits R Visser, Daan M Voeten, Suzanne S Gisbertz, et al.
JMIR Research Protocols|July 13, 2026
AI-Assisted Chest X-Ray Interpretation in Resource-Limited Settings: LuAna Stepped-Wedge Trial ProtocolMaria Carolina Bueno da Silva, Paula Bresciani M de Andrade, Henrique Min Ho Lee, et al.
Frontiers in Artificial Intelligence|February 24, 2025
Clinical validation of an artificial intelligence algorithm for classifying tuberculosis and pulmonary findings in chest radiographsThiago Fellipe Ortiz de Camargo, Guilherme Alberto Sousa Ribeiro, Maria Carolina Bueno da Silva, et al.
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