Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Narlly Ruiz-Quintero"'
Autor:
Gabriela Hernández-Molina, Narlly Ruiz-Quintero, Guadalupe Lima, Diego Hernández-Ramírez, Amaya Llorente-Chávez, Vanessa Saavedra-González, Rodolfo Jiménez-Soto, Luis Llorente
Publikováno v:
International Ophthalmology. 42:2355-2361
Autor:
Gabriela, Hernández-Molina, Narlly, Ruiz-Quintero, Guadalupe, Lima, Diego, Hernández-Ramírez, Amaya, Llorente-Chávez, Vanessa, Saavedra-González, Rodolfo, Jiménez-Soto, Luis, Llorente
Publikováno v:
International ophthalmology. 42(8)
To evaluate CCL2, CXCL8, and CXCL10 in the tears of patients with Primary Sjögren's syndrome (PSS) and correlate them with ocular symptoms/discomfort and objective ocular tests.We studied 21 patients with PSS. A single ophthalmologist, expert in dry
Autor:
Carlos Y, Castrejón-Morales, Omar, Granados-Portillo, Ivette, Cruz-Bautista, Narlly, Ruiz-Quintero, Iliana, Manjarrez, Guadalupe, Lima, Diego F, Hernández-Ramírez, Miguel, Astudillo-Angel, Luis, Llorente, Gabriela, Hernández-Molina
Publikováno v:
Clinical and experimental rheumatology. 38(4)
Lipid mediators derived from polyunsaturated fatty acids (FA), have been related to inflammation and immune response regulation. Herein we evaluated the intake and serum levels of ω-3 and ω-6 FA among patients with primary Sjögren's syndrome (pSS)
Autor:
Amaya Llorente-Chavez, Guadalupe Lima, Vanessa Saavedra-González, Rodolfo Jimenez-Soto, Diego F. Hernández-Ramírez, Narlly Ruiz-Quintero, Gabriela Hernández-Molina, Luis Llorente
Publikováno v:
Poster Presentations.
Background: Previous studies have linked the participation of multiple chemokines and cytokines in the physiopathology of primary Sjogren’s syndrome (PSS), however data regarding their presence in tears is scarce Objectives: To evaluate a panel of
Autor:
Diego F. Hernández-Ramírez, Miguel Astudillo-Angel, Luis Llorente, Carlos Y Castrejón-Morales, Iliana Manjarrez, Omar Granados-Portillo, Guadalupe Lima, Ivette Cruz-Bautista, Gabriela Hernández-Molina, Narlly Ruiz-Quintero
Publikováno v:
Poster Presentations.
Autor:
Vianney Cortés-González, Narlly Ruiz-Quintero, Dalia Guadarrama-Vallejo, Cristina Villanueva-Mendoza, Juan Carlos Zenteno, Martin Guzman-Sanchez, Verónica Giordano-Herrera
Publikováno v:
American Journal of Medical Genetics Part A. 170:3294-3297
Tietz syndrome and Waardenburg syndrome type 2A are allelic conditions caused by MITF mutations. Tietz syndrome is inherited in an autosomal dominant pattern and is characterized by congenital deafness and generalized skin, hair, and eye hypopigmenta