Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Pedro Valencia-Mayoral"'
Autor:
Uriel Gomez-Ramirez, Carolina G. Nolasco-Romero, Araceli Contreras-Rodríguez, Gerardo Zuñiga, Sandra Mendoza-Elizalde, Francisco-Javier Prado-Galbarro, Fernando Pérez Aguilar, Jonatan Elihu Pedraza Tinoco, Pedro Valencia-Mayoral, Norma Velázquez-Guadarrama
Publikováno v:
Microorganisms, Vol 11, Iss 11, p 2748 (2023)
Dysbiosis plays an important role in the development of bacterial infections in the gastric mucosa, particularly Helicobacter pylori. The international guidelines for the treatment of H. pylori infections suggest standard triple therapy (STT). Nevert
Externí odkaz:
https://doaj.org/article/877c357d057548afae842fd330841142
Autor:
Magdalena Cerón‐Rodríguez, Daniela Castillo‐García, Carlos‐Patricio Acosta‐Rodríguez‐Bueno, Jesús Aguirre‐Hernández, Juan‐Rafael Murillo‐Eliosa, Pedro Valencia‐Mayoral, Argelia Escobar‐Sánchez, Juan‐Luis Salgado‐Loza
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 7, Pp n/a-n/a (2022)
Abstract Pompe disease (PD) is an autosomal recessive disorder by a deficiency of acid α‐glucosidase (GAA) with intralysosomal glycogen accumulation in multiple tissues. We present the case of a 5‐month‐old male with hypertrophic cardiomyopath
Externí odkaz:
https://doaj.org/article/1d4d719b65a24738b6cb1df1be263651
Autor:
Alan I. Vicenteño-León, Zindy J. Durán-Reyes, Alfredo Domínguez-Muñoz, Emilio J. Fernández-Portilla, Pedro Valencia-Mayoral
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 79, Iss 6 (2022)
Introducción: Los ganglioneuromas son neoplasias histológicamente benignas derivadas del sistema nervioso simpático, cuya ocurrencia en el tubo digestivo es rara y comúnmente sindromática. De acuerdo con el patrón de la lesión y la extensión
Externí odkaz:
https://doaj.org/article/383f0499b5294438bccf11ddb267bc2e
Autor:
Rodrigo Ortegón-Gallareta, Rodrigo Vázquez-Frías, Gerardo Blanco-Rodriguez, Alejandra Consuelo-Sánchez, Claudia Jimena Ortiz-Rivera, Juan Rafael Murillo-Eliosa, Alan I. Vicenteño-León, Pedro Valencia-Mayoral
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 79, Iss 6 (2022)
Background: Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant inherited disease characterized by the development of polyps in the gastrointestinal tract, mucocutaneous pigmentation, and the risk of developing malignant neoplasms. This study a
Externí odkaz:
https://doaj.org/article/c09a29521b7540c5969fa47b04e6e39f
Autor:
Sandra Mendoza-Elizalde, Ana Caren Cortés-Márquez, Gerardo Zuñiga, René Cerritos, Pedro Valencia-Mayoral, Alejandra Consuelo Sánchez, Hector Olivares-Clavijo, Norma Velázquez-Guadarrama
Publikováno v:
BMC Microbiology, Vol 19, Iss 1, Pp 1-15 (2019)
Abstract Background Helicobacter pylori recurrence after successful eradication is an important problem. Children are particularly vulnerable to reinfection, by intrafamilial transmission which facilitates the acquisition or recombination of new gene
Externí odkaz:
https://doaj.org/article/f5197db50a8a49c3a1d4906a467bcaea
Autor:
Magdalena Cerón-Rodríguez, Edgar Ricardo Vázquez-Martínez, Constanza García-Delgado, Alberto Ortega-Vázquez, Pedro Valencia-Mayoral, Lyuva Ramírez-Devars, Christian Arias-Villegas, Irma Eloísa Monroy-Muñoz, Marisol López, Alicia Cervantes, Marco Cerbón, Verónica Fabiola Morán-Barroso
Publikováno v:
Annals of Hepatology, Vol 18, Iss 4, Pp 613-619 (2019)
Introduction and Objectives: Niemann-Pick disease type A (NPD-A) and B (NPD-B) are lysosomal storage diseases with a birth prevalence of 0.4–0.6/100,000. They are caused by a deficiency in acid sphingomyelinase, an enzyme encoded by SMPD1. We analy
Externí odkaz:
https://doaj.org/article/2860933d119f4801b5f959487eaff78c
Autor:
Ana Caren Cortés-Márquez, Sandra Mendoza-Elizalde, Francisco Arenas-Huertero, Jimena Trillo-Tinoco, Pedro Valencia-Mayoral, Alejandra Consuelo-Sánchez, Jonathan Zarate-Franco, Ada Ruth Dionicio-Avendaño, José de Jesús Herrera-Esquivel, Elio Germán Recinos-Carrera, Christian Colín-Valverde, Sandra Rivera-Gutiérrez, Alfonso Reyes-López, Juan Carlos Vigueras-Galindo, Norma Velázquez-Guadarrama
Publikováno v:
BMC Infectious Diseases, Vol 18, Iss 1, Pp 1-9 (2018)
Abstract Background Helicobacter pylori is a major aetiologic agent associated with gastritis. H. pylori infections increase the expression of the Toll-like receptor (TLR), which in turn modulates the expression of microRNA (miRNA)-146a and miRNA-155
Externí odkaz:
https://doaj.org/article/9cfccec695424c8794d4a24c73ed5585
Autor:
Uriel Gomez-Ramirez, Pedro Valencia-Mayoral, Sandra Mendoza-Elizalde, Juan Rafael Murillo-Eliosa, Fortino Solórzano Santos, Araceli Contreras-Rodríguez, Gerardo Zúñiga, Pamela Aguilar-Rodea, Verónica Leticia Jiménez-Rojas, Juan Carlos Vigueras Galindo, Marcela Salazar-García, Norma Velázquez-Guadarrama
Publikováno v:
Pathogens, Vol 10, Iss 9, p 1203 (2021)
Microbiomes are defined as complex microbial communities, which are mainly composed of bacteria, fungi, and viruses residing in diverse regions of the human body. The human stomach consists of a unique and heterogeneous habitat of microbial communiti
Externí odkaz:
https://doaj.org/article/0e65e5dfddc649a5983756ea71772a06
Autor:
Víctor M. Luna-Pineda, Leticia Moreno-Fierros, Vicenta Cázares-Domínguez, Damaris Ilhuicatzi-Alvarado, Sara A. Ochoa, Ariadnna Cruz-Córdova, Pedro Valencia-Mayoral, Alejandra Rodríguez-Leviz, Juan Xicohtencatl-Cortes
Publikováno v:
Frontiers in Microbiology, Vol 10 (2019)
Curli, a type of fimbriae widely distributed in uropathogenic Escherichia coli (UPEC), are involved in adhesion to human bladder cell surfaces and biofilm development. The role of UPEC curli was evaluated in a murine model of urinary tract infection.
Externí odkaz:
https://doaj.org/article/90a451bc67564e87afd14dd771845990
Autor:
Alejandra del Pilar Reyes-de la Rosa, Gustavo Varela-Fascinetto, Constanza García-Delgado, Edgar Ricardo Vázquez-Martínez, Pedro Valencia-Mayoral, Marco Cerbón, Verónica Fabiola Morán-Barroso
Publikováno v:
Case Reports in Genetics, Vol 2018 (2018)
Alagille syndrome (MIM 118450) is an autosomal dominant disorder characterized by paucity of intrahepatic bile ducts, chronic cholestasis, pulmonary stenosis, butterfly-like vertebrae, posterior embryotoxon, and dysmorphic facial features. Most cases
Externí odkaz:
https://doaj.org/article/5bf0d92095aa4c68aec77ae380922796