Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Andrea R. Cajal"'
Autor:
Carlos A. Vaccaro, Silvina Mariel Richard, Walter Hernán Pavicic, Andrea Constanza Mayordomo, Andrea R. Cajal, Tamara Alejandra Piñero, Claudio M. Bravi, Federico Jauk, Julieta Natalia Soarez, Hernán García-Rivello, Anaclara Sanchez Dova, María Belén Cerliani, Josefina Fuhr Etcheverry
Publikováno v:
Personalized medicine. 18(3)
Aim: We investigated the role of maternal ancestry in neoplastic hematological malignancies (HMs) risk in a population from Central Argentina. Materials & methods: We analyzed 125 cases with HMs and 310 controls from a public hospital, and a set of 2
Autor:
Mev Dominguez-Valentin, Andrea R. Cajal, Ines Sammartino, Maria Alicia Verzura, Natalia Causada-Calo, Walter Hernán Pavicic, Fabiana Alejandra Ferro, Juan Pablo Santino, Tamara Alejandra Piñero, Carlos A. Vaccaro, Pablo Kalfayan, María Laura Gonzalez
Publikováno v:
Familial Cancer. 17:395-402
Microsatellite instability (MSI) is a hallmark tool for Lynch syndrome (LS) screening and a prognostic marker for sporadic colorectal cancer (CRC). In regions with limited resources and scarce CRC molecular characterization as South America, the impl
Autor:
Lucas Costa, Carla Sesarini, Roberto C. Pallia, Pablo Argibay, Miguel Garcia Coto, Muriel Naymark, Andrea R. Cajal, Nora Grañana
Publikováno v:
Autism Research. 7:162-166
Autism spectrum disorders (ASD) can be conceptualized as a genetic dysfunction that disrupts development and function of brain circuits mediating social cognition and language. At least some forms of ASD may be associated with high level of excitatio
Autor:
Natalia Causada Calo, Ines Sammartino, María Laura Gonzalez, Andrea R. Cajal, Tamara Alejandra Piñero, Mev Dominguez-Valentin, Carlos A. Vaccaro, Pablo Kalfayan, Alejandra Ferro, Patrik Wernhoff
Publikováno v:
Frontiers in Oncology, Vol 6 (2016)
Frontiers in Oncology
Frontiers in Oncology
Heredity is a major risk factor for colorectal cancer (CRC). Identification of individuals and families at increased risk allows for targeted surveillance, which has been shown to reduce morbidity and mortality from CRC (1, 2). Lynch syndrome is a mu
Autor:
Andrea R, Cajal, Tamara A, Piñero, Alicia, Verzura, Juan Pablo, Santino, Angela R, Solano, Pablo G, Kalfayan, Alejandra, Ferro, Carlos, Vaccaro
Publikováno v:
Medicina. 76(3)
Lynch syndrome is the most frequent syndrome in hereditary colorectal cancer, a family-specific deleterious mutations in genes encoding DNA reparation proteins: MLH1 (mutL homolog 1), MSH2, MSH6 (mutS homolog 2 y 6, respectively), PMS2 (PMS1 homolog
Autor:
Carla V, Sesarini, Lucas, Costa, Muriel, Naymark, Nora, Grañana, Andrea R, Cajal, Miguel, García Coto, Roberto C, Pallia, Pablo F, Argibay
Publikováno v:
Autism research : official journal of the International Society for Autism Research. 7(1)
Autism spectrum disorders (ASD) can be conceptualized as a genetic dysfunction that disrupts development and function of brain circuits mediating social cognition and language. At least some forms of ASD may be associated with high level of excitatio
Autor:
Maria Ana Redal, Andrea R. Cajal, Carlos Finkelsztein, Laura A. Lesik, Pablo Argibay, José Faccioli, Lucas Costa
Publikováno v:
Psychiatric Genetics. 22:103-104