GenIO: a phenotype-genotype analysis web server for clinical genomics of rare diseases

por Koile, Daniel, Cordoba, Marta, de Sousa Serro, Maximiliano, Kauffman, Marcelo Andres, Yankilevich, Patricio
Publicado 2018

Comparison of commercial lateral flow immunoassays and ELISA for SARS-CoV-2 antibody detection

por Serrano, Maria Martínez, Rodríguez, David Navalpotro, Palop, Nuria Tormo, Arenas, Roberto Olmos, Córdoba, Marta Moreno, Mochón, Mª Dolores Ocete, Cardona, Concepción Gimeno
Publicado 2020

Superior Neuroprotective Efficacy of LAU-0901, a Novel Platelet-Activating Factor Antagonist, in Experimental Stroke

por Belayev, Ludmila, Eady, Tiffany N., Khoutorova, Larissa, Atkins, Kristal D., Obenaus, Andre, Cordoba, Marta, Vaquero, Juan J., Alvarez-Builla, Julio, Bazan, Nicolas G.
Publicado 2011

Whole exome sequencing in neurogenetic odysseys: An effective, cost- and time-saving diagnostic approach

por Córdoba, Marta, Rodriguez-Quiroga, Sergio Alejandro, Vega, Patricia Analía, Salinas, Valeria, Perez-Maturo, Josefina, Amartino, Hernán, Vásquez-Dusefante, Cecilia, Medina, Nancy, González-Morón, Dolores, Kauffman, Marcelo Andrés
Publicado 2018

Germline and somatic mutations in cortical malformations: Molecular defects in Argentinean patients with neuronal migration disorders

por González-Morón, Dolores, Vishnopolska, Sebastián, Consalvo, Damián, Medina, Nancy, Marti, Marcelo, Córdoba, Marta, Vazquez-Dusefante, Cecilia, Claverie, Santiago, Rodríguez-Quiroga, Sergio Alejandro, Vega, Patricia, Silva, Walter, Kochen, Silvia, Kauffman, Marcelo Andrés
Publicado 2017

Whole Genome Sequencing Reveals a De Novo SHANK3 Mutation in Familial Autism Spectrum Disorder

por Nemirovsky, Sergio I., Córdoba, Marta, Zaiat, Jonathan J., Completa, Sabrina P., Vega, Patricia A., González-Morón, Dolores, Medina, Nancy M., Fabbro, Mónica, Romero, Soledad, Brun, Bianca, Revale, Santiago, Ogara, María Florencia, Pecci, Adali, Marti, Marcelo, Vazquez, Martin, Turjanski, Adrián, Kauffman, Marcelo A.
Publicado 2015

A familiar study on self-limited childhood epilepsy patients using hIPSC-derived neurons shows a bias towards immaturity at the morphological, electrophysiological and gene express...

por Casalia, Mariana L., Casabona, Juan Cruz, García, Corina, Cavaliere Candedo, Verónica, Quintá, Héctor Ramiro, Farías, María Isabel, Gonzalez, Joaquín, Gonzalez Morón, Dolores, Córdoba, Marta, Consalvo, Damian, Mostoslavsky, Gustavo, Urbano, Francisco J., Pasquini, Juana, Murer, Mario Gustavo, Rela, Lorena, Kauffman, Marcelo A., Pitossi, Fernando J.
Publicado 2021