Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Nury Tatiana Rincón Cuenca"'
Autor:
Andrés Felipe Herrera Ortiz, Nury Tatiana Rincón Cuenca, Valeria del Castillo Herazo, Diana Marcela Oliveros Jiménez, Laura García Maestre, Mary Eugenia Posada, Luz Angela Moreno
Publikováno v:
Radiology Case Reports, Vol 20, Iss 3, Pp 1294-1297 (2025)
The coexistence of fibrous dysplasia and aneurysmal bone cyst in the craniofacial region is extremely rare. This article presents a unique case involving the skull base, diagnosed using computed tomography and magnetic resonance. Imaging revealed a c
Externí odkaz:
https://doaj.org/article/8c608cd8f670411fac7ef69189ad7192
Autor:
Andrés Felipe Herrera Ortiz, MD, Santiago Aristizabal, MD, Juan Guillermo Arámbula, MD, Valeria del Castillo, MD, Juan Calderon, MD, Nury Tatiana Rincón Cuenca, MD, María José Abuchar, MD, María Mónica Yepes, MD, Angela Guarnizo, MD
Publikováno v:
Radiology Case Reports, Vol 18, Iss 2, Pp 515-518 (2023)
Multiple sclerosis is a frequent condition where the diagnosis relies on clinical presentation, neurologic examination, cerebro spinal fluid markers, and diagnostic imaging tests; however, atypical variants of the disease can lead to misdiagnosis in
Externí odkaz:
https://doaj.org/article/1fcbd89da63741f496215424ec113fd5
Autor:
Nury Tatiana Rincón Cuenca, MD, María Fernanda Castro Peñaranda, MD, Camilo Andres Calderón Valderrama, MD, Santiago Aristizábal Ortiz, MD, Andrés Felipe Herrera Ortiz, MD
Publikováno v:
Radiology Case Reports, Vol 17, Iss 9, Pp 3035-3039 (2022)
Aicardi syndrome is an X-linked-dominant genetic condition that is present almost exclusively in females. To diagnose Aicardi syndrome, the classic triad of agenesis of the corpus callosum, infantile spasms, and chorioretinal lacunae must be present.
Externí odkaz:
https://doaj.org/article/518b9ec61aec4e24b4e3878b6ce08ef2
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
Publikováno v:
Revista Cuarzo, Vol 27, Iss 1 (2021)
Introduction: Child maltreatment is a worldwide problem; not only for its repercussions at the time of the act but also for its possible sequelae, therefore, it is important to know and characterize the changes found in magnetic resonance, to correla
Externí odkaz:
https://doaj.org/article/8b891388cda4426ab90c65d3e136d11a
Autor:
Andrés Felipe Herrera Ortiz, Eduard Cadavid Camacho, Julián Cubillos Rojas, Tatiana Cadavid Camacho, Stephani Zoe Guevara, Nury Tatiana Rincón Cuenca, Andrés Vásquez Perdomo, Valeria Del Castillo Herazo, Rubén Giraldo Malo
Publikováno v:
Principles and Practice of Clinical Research Journal. 7:47-57
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dca53b3dffb51419bb235164be671999
https://doi.org/10.21801/ppcrj.2021.74.6
https://doi.org/10.21801/ppcrj.2021.74.6
Publikováno v:
Revista Cuarzo. 27:27-33
Introduction: Child maltreatment is a global problem, not only for its repercussions at the time of the act but also for its possible sequelae; therefore, it is crucial to characterize the changes found in magnetic resonance, to correlate the structu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::533c41d9e3477ed93947125e7dbae541
https://doi.org/10.26752/cuarzo.v27.n1.522
https://doi.org/10.26752/cuarzo.v27.n1.522