Zobrazeno 1 - 10
of 10
pro vyhledávání: '"María Teresa Sans"'
Autor:
Alejandro Rodríguez, Frederic Gómez, Carolina Sarvisé, Cristina Gutiérrez, Montserrat Galofre Giralt, María Dolores Guerrero-Torres, Sergio Pardo-Granell, Ester Picó-Plana, Clara Benavent-Bofill, Sandra Trefler, Julen Berrueta, Laura Canadell, Laura Claverias, Erika Esteve Pitarch, Montserrat Olona, Graciano García Pardo, Xavier Teixidó, Laura Bordonado, María Teresa Sans, María Bodí
Publikováno v:
Biomedicines, Vol 11, Iss 12, p 3330 (2023)
Background: Data on the benefits of rapid microbiological testing on antimicrobial consumption (AC) and antimicrobial resistance patterns (ARPs) are scarce. We evaluated the impact of a protocol based on rapid techniques on AC and ARP in intensive ca
Externí odkaz:
https://doaj.org/article/78f372f6ac084b29af1daa57e5c6fc88
Autor:
Maria Eduarda Gomes, Fernanda Kehdy, Fernanda Saloum de Neves-Manta, Dafne Dain Gandelman Horovitz, Maria Teresa Sanseverino, Gabriela Ferraz Leal, Têmis Maria Felix, Denise Pontes Cavalcanti, Juan Clinton Llerena, Sayonara Gonzalez
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-7 (2024)
Abstract Cartilage-hair hypoplasia syndrome (CHH) is an autosomal recessive disorder frequently linked to n.72A>G (previously known as n.70A>G and n.71A>G), the most common RMRP variant worldwide. More than 130 pathogenic variants in this gene have a
Externí odkaz:
https://doaj.org/article/34039a6314534692b817227cc3c278af
Autor:
María Teresa Sans Mateu, Silvia Montolio Breva, Cristina Gutiérrez Fornes, Rafael Sánchez Parrilla
Publikováno v:
Revista de Medicina de Laboratorio.
Autor:
Francyne Kubaski, Zackary M. Herbst, Maira Graeff Burin, Kristiane Michelin‐Tirelli, Franciele B. Trapp, Rejane Gus, Alice B. O. Netto, Ana Carolina Brusius‐Facchin, Sandra Leistner‐Segal, Maria Teresa Sanseverino, Carolina Moura Fischinger de Souza, Matheus V. M. B. Wilke, Thiago Oliveira, Jose A. A. Magalhães, Roberto Giugliani
Publikováno v:
JIMD Reports, Vol 63, Iss 2, Pp 162-167 (2022)
Abstract Metachromatic leukodystrophy (MLD) is an autosomal recessive lysosomal disorder caused by deficiency of arylsulfatase A (ARSA), leading to an accumulation of sulfatides. Sulfatides have been quantified in urine, dried blood spots (DBS), and
Externí odkaz:
https://doaj.org/article/cb2cd21c4abc442088c12a59965a6411
Publikováno v:
CLIL Journal of Innovation and Research in Plurilingual and Pluricultural Education, Vol 4, Iss 2 (2021)
En els últims anys, el feedback correctiu ha despertat molt interès i s’han dut a terme un nombre considerable de recerques en aquest àmbit, especialment en la didàctica de l’anglès com a llengua segona o estrangera. El present article se ce
Externí odkaz:
https://doaj.org/article/e29e69eeb35a499da00c45d19612d1a6
Autor:
María Teresa Sanséau, Mónica Cohendoz
Publikováno v:
Intersecciones en Comunicación, Vol 1, Iss 14 (2021)
El 13 de junio de 2020 nos llegó la triste noticia del fallecimiento de Rosa María Brenca. Ella fue una de las fundadoras, y coordinadora en el inicio, de la carrera de Comunicación Social de nuestra Facultad de Ciencias Sociales, UNCPBA, sede Ola
Externí odkaz:
https://doaj.org/article/3e2046d88d194423abe380192e0bdc25
Autor:
Maria Teresa Sans Bertran
Publikováno v:
Bellaterra Journal of Teaching & Learning Language & Literature, Vol 13, Iss 1 (2020)
Externí odkaz:
https://doaj.org/article/1b4b25927e2b43e8808ac4531b46f055
Autor:
Maria Teresa Sans Bertran
Publikováno v:
Bellaterra Journal of Teaching & Learning Language & Literature, Vol 11, Iss 3 (2018)
La investigació que es presenta és l’estudi de cas d’un alumne intern d’origen marroquí d’un centre penitenciari de l’àrea metropolitana de Barcelona en el marc del projecte europeu KA2 StrategicPartnershipRiUscire. Els primers resultat
Externí odkaz:
https://doaj.org/article/5495263315df46aba552fcc6ea91ef9e
Autor:
Sandra Leistner-Segal, Ana Carolina Brusius-Facchin, Rejane Gus, Maira Burin, Maria Teresa Sanseverino, José Antônio Magalhães, Roberto Giugliani
Publikováno v:
Clinical and Biomedical Research, Vol 34, Iss 4 (2014)
Introduction: Mucopolysaccharidosis type II (MPSII) is an X-linked lysosomal disorder caused by deficiency of iduronate-2-sulfatase (IDS). In this study, we proposed a new protocol for prenatal diagnosis, using DNA obtained from amniotic fluid cells
Externí odkaz:
https://doaj.org/article/338d7fcfbc6542e59e99b67e4181bc90
Autor:
Moacir Wajner, Alethéa G. Barschak, Ana Paula Luft, Ricardo Pires, Eugênio Grillo, Alfredo Lohr, Carolina Funayama, Maria Teresa Sanseverino, Roberto Giugliani, Carmen R. Vargas
Publikováno v:
Jornal de Pediatria, Vol 77, Iss 5, Pp 401-406 (2001)
OBJETIVO: o objetivo deste trabalho foi o de verificar a prevalência das acidúrias orgânicas em pacientes brasileiros de alto risco. MÉTODOS: técnicas laboratoriais para a detecção e quantificação de ácidos orgânicos por cromatografia gaso
Externí odkaz:
https://doaj.org/article/bc29f859de1c4b288aa19a3b853c9cd7