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Mostrando resultados 1 a 8 de 8
Fecha de publicaciónTítuloAutor(es)
2021Infarto talámico paramedial bilateral por oclusión de la arteria de PercherónBaltar Yanes, Federico; Turcatti, Emilio; González Rabelino, Gabriel
2022Information theory approaches to improve glioma diagnostic workflows in surgical neuropathologyCevik, Lokman; Vázquez Landrove, Marilyn; Aslan, Mehmet Tahir; Khammad, Vasilii; Garagorry Guerra, Francisco José; Cabello Izquierdo, Yolanda; Wang, Wesley; Zhao, Jing; Becker, Aline Paixao; Czeisler, Catherine; Rendeiro, Anne Costa; Véras, Lucas Luis Sousa; Zanon, Maicon Fernando; Reis, Rui Manuel; Matsushita, Marcus de Medeiros; Ozduman, Koray; Pamir, M. Necmettin; Ersen Danyeli, Ayca; Pearce, Thomas; Felicella, Michelle; Eschbacher, Jennifer; Arakaki, Naomi; Martinetto, Horacio; Parwani, Anil; Thomas, Diana L.; Otero, José Javier
2023Mayo Clinic consensus report on membranous nephropathy: proposal for a novel classificationSethi, Sanjeev M.; Beck, Laurence H.; Glassock, Richard J.; Haas, Mark; de Vriese, An Sabine P.; Caza, Tiffany N.; Hoxha, Elion; Lambeau, Gérard; Tomas, Nicola M.; Madden, Benjamin; Debiec, Hanna; D'Agati, Vivette D.; Alexander, Mariam P.; Amer, Hatem; Appel, Gerald B.; Barbour, Sean J.; Caravaca-Fontán, Fernando; Cattran, Daniel C.; Casal Moura, Marta; D’Avila, Domingos O.; Fervenza, Fernando C.; Yandian, Federico
2023Mayo Clinic consensus report on membranous nephropathy: proposal for a novel classificationSethi, Sanjeev M.; Beck, Laurence H.; Glassock, Richard J.; Haas, Mark; de Vriese, An Sabine P.; Caza, Tiffany N.; Hoxha, Elion; Lambeau, Gérard; Tomas, Nicola M.; Madden, Benjamin; Debiec, Hanna; D'Agati, Vivette D.; Alexander, Mariam P.; Amer, Hatem; Appel, Gerald B.; Barbour, Sean J.; Caravaca-Fontán, Fernando; Cattran, Daniel C.; Casal Moura, Marta; D'Avila, Domingos O.; Fervenza, Fernando C.; Yandian, Federico
2021Novel frameshift mutation in PURA gene causes severe encephalopathy of unclear causeSpangenberg, Lucía; Guecaimburú, Rosario; Tapié, Alejandra; Vivas, Susana; Rodríguez, Soledad; Graña, Martín; Naya, Hugo; Raggio, Víctor
2022STK11 and KEAP1 mutations in non-small cell lung cancer patients: Descriptive analysis and prognostic value among Hispanics (STRIKE registry-CLICaP)Cordeiro de Lima, Vladimir C.; Corassa, Marcelo; Saldanha, Erick; Freitas, Helano; Arrieta, Oscar; Raez, Luis; Samtani, Suraj; Ramos, Maritza; Rojas, Carlos; Burotto, Mauricio; Chamorro, Diego F.; Recondo, Gonzalo; Ruiz-Patiño, Alejandro; Más, Luis; Zataraín-Barrón, Zyanya Lucía; Mejía, Sergio; Minata, José Nicolás; Martín, Claudio; Blaquier, Juan Bautista; Motta Guerrero, Rodrigo; Aliaga-Macha, Carlos; Carracedo, Carlos; Ordóñez- Reyes, Camila; Garcia-Robledo, Juan Esteban; Corrales, Luis; Sotelo, Carolina; Ricaurte, Luisa; Santoyo, Nicolás; Cuello, Mauricio; Jaller, Elvira; Rodríguez, July; Archila, Pilar; Bermudez, Maritza; Gamez, Tatiana; Russo, Alessandro; Viola, Lucía; Malapelle, Umberto; de Miguel Pérez, Diego; Rolfo, Christian; Rosell, Rafael; Cardona, Andrés F.
2023The Effect of Fat Intake with Increased Omega-6-to-Omega-3 Polyunsaturated Fatty Acid Ratio in Animal Models of Early and Late Alzheimer’s Disease-like PathogenesisGaleano, Pablo; de Ceglia, Marialuisa; Mastrogiovanni, Mauricio; Campanelli, Lorenzo; Medina-Vera, Dina; Campolo, Nicolás; Novack, Gisela V.; Rosell-Valle, Cristina; Suárez, Juan; Aicardo, Adrián; Campuzano, Karen; Castaño, Eduardo M.; Do Carmo, Sonia; Cuello, A. Claudio; Bartesaghi, Silvina; Radi, Rafael; Rodríguez de Fonseca, Fernando; Morelli, Laura
2021Whole genome sequencing reveals a frameshift mutation and a large deletion in YY1AP1 in a girl with a panvascular artery diseaseRaggio, Víctor; Dell’Oca, Nicolás; Simoes, Camila; Tapié, Alejandra; Medici, Conrado; Costa, Gonzalo; Rodríguez, Soledad; Greif, Gonzalo; Garrone, Estefanía; Rovella, María Laura; González, Virginia; Halty, Margarita; González, Gabriel; Shin, Jong-Yeon; Shin, Sang-Yoon; Kim, Changhoon; Seo, Jeong-Sun; Graña, Martín; Naya, Hugo; Spangenberg, Lucía