Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Magdalena Ceron"'
Autor:
Karla Cifuentes-Uribe, Alejandra Reyes-De La Rosa, Rodrigo Moreno-Salgado, America Villasenor-Dominguez, Magdalena Ceron-Rodriguez, Romina Viveros-Rodriguez, Vianney Cortes-Gonzalez, Gilda Garza-Mayén
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101312- (2024)
Externí odkaz:
https://doaj.org/article/f218e05bdcd5431aa0c8f53d7cd2dd5e
Publikováno v:
In Molecular Genetics and Metabolism February 2024 141(2)
Autor:
Eva María Santos López, Iraís Sánchez Ortega, Israel Samuel Ibarra Ortega, Magdalena Ceron, Esmeralda Rangel Vargas, José Antonio Rodríguez Ávila
Publikováno v:
Pädi Boletín Científico de Ciencias Básicas e Ingenierías del ICBI. 7:47-51
Actualmente el consumo de productos cárnicos se ha relacionado con el riesgo de aparición de enfermedades crónicas, tales como enfermedades cardiovasculares, cáncer, hipertensión, diabetes y obesidad. Esto debido al alto contenido de grasa, nula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88bcd67ab623ca8a748a504bd9483972
https://doi.org/10.29057/icbi.v7i14.4973
https://doi.org/10.29057/icbi.v7i14.4973
Autor:
Richard Baquero Rodriguez, Ana Katherina Serrano Gayubo, Juan Carlos Prieto Rivera, Juan Guillermo Cardenas Aguilera, Carmen Inés Rodríguez Cuéllar, Maria Fernanda Reina Ávila, Mayra Alexandra Estévez Capacho, Heidy Mateus, Maylin Valencia González, Kelly Rocío Chacón Acevedo, Maria Paula Gutiérrez Sepúlveda, Dominique P Germain, Juan Politei, Alejandro Fabian Fainboim, Magdalena Cerón Rodríguez, Gustavo Cabrera, Edicson Rodríguez Ibarra, Martha Isabel Carrascal Guzmán, Lida Esperanza Martínez Cáceres, Sandra Yaneth Ospina Lagos, Hernán Trimarchi, Miguel Liern
Publikováno v:
Revista Ciencias de la Salud, Vol 21, Iss 3 (2023)
Antecedentes: La enfermedad de Fabry (EF) es una enfermedad rara ligada a X secundaria al depósito lisosomal de glicoesfingolípidos debido a la deficiencia de la enzima alfa galactosidasa A (α-Gal A). A pesar de su baja frecuencia, es una condici
Externí odkaz:
https://doaj.org/article/af4409f518254bde91f5bf4071f9aac5
Publikováno v:
Molecular Genetics and Metabolism. 114:S86-S87
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d7489dc156da8e06f60a0b52515cf30
https://doi.org/10.1016/j.ymgme.2014.12.191
https://doi.org/10.1016/j.ymgme.2014.12.191
Autor:
Magdalena Ceron
Publikováno v:
Molecular Genetics and Metabolism. 117:S33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd9d7c64dc131791c251d31aba3424ba
https://doi.org/10.1016/j.ymgme.2015.12.217
https://doi.org/10.1016/j.ymgme.2015.12.217
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
Osteomyelitis in a breastfed child with Gaucher disease type I with an indistinguishable bone crisis
Autor:
Magdalena Ceron, Edgar Barajas
Publikováno v:
Molecular Genetics and Metabolism. 114:S18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90f7d2b7bfa20d4b0711cfb69415723e
https://doi.org/10.1016/j.ymgme.2014.12.022
https://doi.org/10.1016/j.ymgme.2014.12.022
Autor:
Diana A. Guerrero-Reséndiz, María T. Gómez Chavarría, Víctor Olivar-López, Magdalena Cerón-Rodríguez, Mónica Villa-Guillén, Horacio Márquez-González
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 79, Iss 2 (2022)
Background: Child abuse is one of the leading causes of morbidity and mortality worldwide. This study aimed to identify whether the approach to the diagnosis of child abuse was comprehensive in a tertiary care hospital. Methods: We conducted a retros
Externí odkaz:
https://doaj.org/article/3195a5faf68b434e9cf8f60e3d6f0ffa
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