Computed tomography findings of Crouzon syndrome: A case report

Autor: Juan Guillermo Arámbula Neira, MD, Valeria del Castillo Herazo, MD, Nury Tatiana Rincón Cuenca, MD, Angélica M. Sanabria Cano, MD, Maryi Fernanda Bermudez Sarmiento, MD, María F. Castro, MD, Andrés Felipe Herrera Ortiz, MD

Publikováno v: Radiology Case Reports, Vol 17, Iss 4, Pp 1288-1292 (2022)

Crouzon syndrome is a genetic condition characterized by a premature fusion of skull sutures resulting in head and facial deformities. Crouzon syndrome is usually suspected at birth through physical examination or in the antenatal period via ultrason

Externí odkaz: https://doaj.org/article/4e8fa553f4084963aa05176564ec17d2

Clinical and CT patterns to predict EGFR mutation in patients with non-small cell lung cancer: A systematic literature review and meta-analysis

Autor: Andrés Felipe Herrera Ortiz, Tatiana Cadavid Camacho, Andrés Francisco Vásquez, Valeria del Castillo Herazo, Juan Guillermo Arámbula Neira, María Mónica Yepes, Eduard Cadavid Camacho

Publikováno v: European Journal of Radiology Open, Vol 9, Iss , Pp 100400- (2022)

Purpose: This study aims to determine if the presence of specific clinical and computed tomography (CT) patterns are associated with epidermal growth factor receptor (EGFR) mutation in patients with non-small cell lung cancer. Methods: A systematic l

Externí odkaz: https://doaj.org/article/7fcca764e67245df8f937c623d1f63cd

Popliteal artery pseudoaneurysm caused by non–penetrating trauma in a patient with hereditary multiple osteochondromatosis

Autor: Adriana Lucía López Polanco, Andrés Felipe Herrera Ortiz, Juan Guillermo Arámbula Neira, Oscar Andrés Parada Duarte, Valeria del Castillo Herazo, Andrés Felipe Durán Omaña, María Fernanda Oviedo Lara

Publikováno v: Repositorio Universidad de Santander
Universidad de Santander
instacron:Universidad de Santander
Radiology Case Reports
Radiology Case Reports, Vol 17, Iss 1, Pp 185-189 (2022)
Repositorio U. El Bosque
Universidad El Bosque
instacron:Universidad El Bosque

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Hereditary multiple osteochondromatosis is a genetic condition characterized by the appearance of numerous osteochondromas, which can cause pseudoaneurysms in rare cases. The following article describes a 15-year-old patient with a histo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d19141df53d733bcfae075857897fa9
https://repositorio.udes.edu.co/handle/001/7359