Genetic Ancestry, Race, and Severity of Acutely Decompensated Cirrhosis in Latin America

Autor: Ferreira, Caroline Marcondes, Benedita Terrabuio, Debora R., Fernandes da Costa, Roberto M., Signorelli, Izabelle Venturini, Pinto, Caroline A., Estanes-Hernández, Alma, Manriquez, Jesús Ruiz, Gutierrez-Acevedo, María N., Martinez-Garmendia, Agustina M., Ligia Aparecida, M., Macêdo, Everton, Mantovani, Augusto, Longo, Larisse, Vilela, Eduardo Garcia, Valderrama, María G., Santos-Rondon, Michelle V.S., Cardenas, Bertha, Rentería, Jorge Garavito, Torres-Made, Lilian Montserrat, Tenorio Castillo, Laura C., Aquino Ramos, José M., de Fátima Higuera de la Tijera, María, Aires, Rodrigo S., Salinas-Gómez, Diana C., Allendes, Francisca, Schacher, Fernando C., Neto, Guilherme John, Valdivia, Raúl Castro, Pagés, Josefina, Roblero, Juan P., Fainboim, Hugo, Souza, Fernanda Fernandes, Colombato, Luis, de Mello Peres, Renata, Miranda, Larissa O., Oliveira, Jade C., Ortiz, Leyla Nazal, Simian, Daniela, Puentes, Gabriel Mezzano, de Cássia Martins Alves da Silva, Rita, Gordon, Iaarah Montalvo, Chi Cervera, Luis A., Girala Salomón, Marcos A., Cuevas, María T., Montes, Pedro, Cattaneo Buteler, Máximo J., Farias, Alberto Queiroz, Curto Vilalta, Anna, Momoyo Zitelli, Patricia, Pereira, Gustavo, Goncalves, Luciana L., Torre, Aldo, Diaz, Juan Manuel, Gadano, Adrian C., Mattos, Angelo Z., Mendes, Liliana S.C., Alvares-da-Silva, Mario R., Bittencourt, Paulo L., Benitez, Carlos, Couto, Claudia Alves, Mendizabal, Manuel, Toledo, Claudio L., Mazo, Daniel F.C., Castillo Barradas, Mauricio, Uson Raposo, Eva M., Padilla-Machaca, P. Martín, Zarela Lozano Miranda, Adelina, Malé-Velázquez, René, Castro Lyra, André, Dávalos-Moscol, Milagros B., Pérez Hernández, José L., Ximenes, Rafael O., Faria Silva, Giovanni, Beltrán-Galvis, Oscar A., González Huezo, María S., Bessone, Fernando, Rocha, Tarciso D.S., Fassio, Eduardo, Terra, Carlos, Marín, Juan I., Sierra Casas, Patricia, de la Peña-Ramirez, Carlos, Aguilar Parera, Ferran, Fernandes, Flavia, da Penha Zago-Gomes, Maria, Méndez-Guerrero, Osvely, Marciano, Sebastián, Mattos, Angelo A., Oliveira, Joao C., Guerreiro, Gabriel T.S., Codes, Liana, Arrese, Marco, Nardelli, Mateus J., Silva, Marcelo O., Palma-Fernandez, Renato, Alcantara, Camila, Sánchez Garrido, Cristina, Trebicka, Jonel, Gustot, Thierry, Fernández, Javier, Clària, Joan, Jalan, Rajiv, Angeli, Paolo, Arroyo, Vicente, Moreau, Richard, Carrilho, Flair J.

Publikováno v: In Gastroenterology September 2023 165(3):696-716

Clinical and microbiological characteristics of bacterial infections in patients with cirrhosis. A prospective cohort study from Argentina and Uruguay

Autor: Carolina Vazquez, María Nelly Gutierrez-Acevedo, Sabrina Barbero, Lorena del Carmen Notari, Marina Agozino, José Luis Fernandez, María Margarita Anders, Nadia Lorena Grigera, Florencia Antinucci, Orlando Nicolas Federico Orozco-Ganem, María Dolores Murga, María Daniela Perez, Ana Gracia Palazzo, Liria Martinez Rejtman, Ivonne Giselle Duarte, Julio Daniel Vorobioff, Victoria Trevizan, Sofía Bulaty, Fernando Bessone, Marcelo Valverde, Martín Elizondo, Silvia Mabel Borzi, Teodoro Eduardo Stieben, Adriano Carlos Masola, Sebastian Eduardo Ferretti, Diego Arufe, Ezequiel Demirdjian, María Pia Raffa, Mirta Peralta, Hugo Alberto Fainboim, Cintia Elizabet Vazquez, Pablo Marcelo Ruiz, José Emanuel Martínez, Leandro Alfredo Heffner, Andrea Odzak, Melisa Dirchwolf, Astrid Smud, Manuel Mendizabal, Pablo Anibal Calzetta, Ana Martinez, Jesica Tomatis, Andres Bruno, Agñel Ramos, Josefina Pages, Silvina Tevez, Adrian Carlos Gadano, Diego Hernan Giunta, Sebastián Marciano

Publikováno v: Annals of Hepatology, Vol 28, Iss 4, Pp 101097- (2023)

Introduction and Objectives: there is insufficient data regarding bacterial infections in patients with cirrhosis to support recommendations for empiric antibiotic treatments, particularly in Latin America. This study aimed to evaluate bacterial infe

Externí odkaz: https://doaj.org/article/d55fc3436c1343a7897ad8c3ddbc2561

Enzyme replacement therapy interruption in mucopolysaccharidosis type IVA patients and its impact in different clinical outcomes

Autor: Juan Politei, Gloria Liliana Porras‐Hurtado, Norberto Guelbert, Alejandro Fainboim, Dafne Dain Gandelman Horovitz, José María Satizábal

Publikováno v: JIMD Reports, Vol 58, Iss 1, Pp 104-113 (2021)

Abstract Mucopolysaccharidosis type IVA (MPS IVA) is an autosomal recessive lysosomal storage disorder caused by mutations in the GALNS gene, which leads to deficient activity of N‐acetylglucosamine‐6‐sulfate sulfatase. MPS IVA patients usually

Externí odkaz: https://doaj.org/article/f0fb260f41ed4795bd194a39e13c55a0

Autoimmune and non-autoimmune thyroid dysfunction in HCV infected and HCV–HIV co-infected patients before and after interferon alpha therapy: A prospective study

Autor: Lowenstein, Alicia, Fainboim, Hugo, Reyes, Adriana, Lutzky, Cynthia, Ameigeiras, Beatriz, Schroder, Teresa, Eugenio Russmann, Maria Laura

Publikováno v: In Endocrinología, Diabetes y Nutrición April 2020 67(4):263-271

Low-dose agalsidase beta treatment in male pediatric patients with Fabry disease: A 5-year randomized controlled trial

Autor: Ramaswami, Uma, Bichet, Daniel G., Clarke, Lorne A., Dostalova, Gabriela, Fainboim, Alejandro, Fellgiebel, Andreas, Forcelini, Cassiano M., An Haack, Kristina, Hopkin, Robert J., Mauer, Michael, Najafian, Behzad, Scott, C. Ronald, Shankar, Suma P., Thurberg, Beth L., Tøndel, Camilla, Tylki-Szymanska, Anna, Bénichou, Bernard, Wijburg, Frits A.

Publikováno v: In Molecular Genetics and Metabolism May 2019 127(1):86-94