Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Aurora Ruz"'
Autor:
Adrián Alonso-Núñez, Tania Pérez-Márquez, Marta Alves-Villar, Carlos Fernández-Pereira, Julián Fernández-Martín, Alberto Rivera-Gallego, Cristina Melcón-Crespo, Beatriz San Millán-Tejado, Aurora Ruz-Zafra, Remedios Garofano-López, Rosario Sánchez-Martínez, Elena García-Payá, Manuel López-Mendoza, Ignacio Martín-Suárez, Saida Ortolano
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 11, p 6024 (2024)
Fabry disease is an invalidating multisystemic disorder affecting α-Galactosidase, a rate-limiting hydrolase dedicated to lipid catabolism. Non-metabolized substrates, such as Globotriaosylceramide and its derivatives trigger the direct or indirect
Externí odkaz:
https://doaj.org/article/f6efd209eb834946ab0d655f087e446f
Autor:
Pedro Besada, María Gallardo-Gómez, Tania Pérez-Márquez, Lucía Patiño-Álvarez, Sergio Pantano, Carlos Silva-López, Carmen Terán, Ana Arévalo-Gómez, Aurora Ruz-Zafra, Julián Fernández-Martín, Saida Ortolano
Publikováno v:
Biomolecules, Vol 11, Iss 12, p 1856 (2021)
Fabry disease is an X-linked multisystemic disorder caused by the impairment of lysosomal α-Galactosidase A, which leads to the progressive accumulation of glycosphingolipids and to defective lysosomal metabolism. Currently, Fabry disease is treated
Externí odkaz:
https://doaj.org/article/e6705ab692ff4b0aaf5e25a9948b031d
Autor:
Galdeano, Carla Veredas, Lucena, Carlos Ruiz, Ramos, Beatriz Martín, Guerrero, Montserrat Godoy, Rol, Guadalupe Jarava, Rueda, Javier Ruiz, Zafra, Aurora Ruz, Benítez, María Ángeles González
Publikováno v:
In Revista clinica espanola November 2023 223 Supplement 2:S537-S539
Autor:
Rosario Sánchez, Tomás Ripoll-Vera, Manuel López-Mendoza, Joaquín de Juan-Ribera, Juan Ramón Gimeno, Álvaro Hermida, María Aurora Ruz-Zafra, José Vicente Torregrosa, Antonia Mora, José Manuel García-Pinilla, Elena Fortuny, Ana Aguinaga-Barrilero, Roser Torra
Publikováno v:
Orphanet Journal of Rare Diseases. 18
Background Fabry disease (FD) is an X-linked condition caused by variants in the GLA gene. Since females have two X chromosomes, they were historically thought to be carriers. Although increased knowledge has shown that females often develop the dise
Publikováno v:
Revista Española de Enfermedades Digestivas.
Angiosarcomas are rare tumors that usually entail a poor prognosis because of extensive invasiveness and high rates of distant metastasis. Gastrointestinal tract involvement is uncommon but may cause digestive bleeding. A definitive diagnosis require
Autor:
Fernando Alfonso, María Victoria Mogollón Jiménez, Carles Díez-López, Aurora Ruz, Pablo García-Pavía, Maria Eugenia Fuentes-Cañamero, Julián Palomino-Doza, Carlos Casanova Rodríguez, Vicente Climent, Aitor Hernandez-Hernandez, Coloma Tiron, Olga Azevedo
Publikováno v:
Journal of Cardiovascular Translational Research
r-ISABIAL. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica y Sanitaria de Alicante
instname
r-ISABIAL. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica y Sanitaria de Alicante
instname
Identification of Anderson-Fabry disease (AFD) in cardiac patients has been restricted so far to patients with left ventricular hypertrophy. Coronary microvascular dysfunction has been described in AFD with and without cardiac hypertrophy and may rep
Autor:
López, Clara Hidalgo, Rueda, Javier Ruiz, Lucena, Carlos Ruiz, Zafra, Aurora Ruz, Ramos, Beatriz Martín, Galdeano, Carla Veredas, Guerrero, Montserrat Godoy, Benítez, María Ángeles González
Publikováno v:
In Revista clinica espanola November 2023 223 Supplement 2:S156-S157
Autor:
Benítez, María Ángeles González, Guerrero, Montserrat Godoy, Zafra, Aurora Ruz, López, Clara Hidalgo, Lucena, Carlos Ruiz, Ramos, Beatriz Martín, Rol, Guadalupe Jarava, López, Salvador Vergara
Publikováno v:
In Revista clinica espanola November 2023 223 Supplement 2:S21-S22
Autor:
Benítez, María Ángeles González, Rol, Guadalupe Jarava, Galdeano, Carla Veredas, Rueda, Javier Ruiz, Zafra, Aurora Ruz, Guerrero, Montserrat Godoy, López, Clara Hidalgo, López, Salvador Vergara
Publikováno v:
In Revista clinica espanola November 2023 223 Supplement 2:S20-S21
Autor:
Rosario Sánchez, Joaquín de Juan-Ribera, Juan Ramón Gimeno, Tomás Ripoll-Vera, Manuel López-Mendoza, Álvaro Hermida, Roser Torra, Maria Aurora Ruz-Zafra, Vicent Torregrosa, Antonia Mora, Elena Fortuny, José Manuel García-Pinilla
Publikováno v:
Molecular Genetics and Metabolism. 135:S108