Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Angélica López Hernández"'
Publikováno v:
Globalization and Health, Vol 20, Iss 1, Pp 1-16 (2024)
Abstract Background Traffic-related crashes are a leading cause of premature death and disability. The safe systems approach is an evidence-informed set of innovations to reduce traffic-related injuries and deaths. First developed in Sweden, global h
Externí odkaz:
https://doaj.org/article/e292e8d6871a491b8594e285883f2481
Autor:
Angélica, López-Hernández, Carlos, Castillo-Salgado, Julia Berenice, Ramírez-González, Silvia, Martínez Valverde, Ramon, Durazo-Arvizu, Luis, Duran-Arenas, Reyna Lizette, Pacheco-Domínguez
Publikováno v:
In Vaccine: X December 2023 15
Autor:
Laura Sánchez-Chapul, Rosa Elena Escobar-Cedillo, Luz Berenice López-Hernández, Andrea Suarez-Ocón, Alexandra Luna-Angulo, María Dolores Curiel-Leal, Julia Angélica López-Hernández, Antonio Miranda-Duarte, Guillermina Avila-Ramirez, Benjamín Gómez-Díaz
Publikováno v:
Folia Neuropathologica, Vol 59, Iss 3, Pp 276-283 (2021)
Muscular dystrophies are a group of well-defined genetic disorders characterized by the variable distribution of muscle wasting and progressive weakness. The diagnosis and treatment of these diseases remain challenging due to genetic heterogeneity an
Autor:
Julia Berenice Ramírez-González, Angélica López-Hernández, Malaquías López-Cervantes, Ramon Durazo-Arvizu, Jesica Figueroa-Padilla, Reyna Lizette Pacheco-Domínguez
Publikováno v:
Epidemiology and Infection
Data regarding humoral immunity against HPV infection are scarce. Most analyses focus on the identification of viruses on mucous membranes and primarily refer to women of reproductive age. The aim of this work was to estimate the seroprevalence of an
Autor:
Julia Angélica López-Hernández, Bladimir Roque-Ramírez, Alexandra Luna-Angulo, David J. Bunyan, Héctor Rangel-Villalobos, Benjamín Gómez-Díaz, Luis Ruano-Calderón, Mónica Alejandra Anaya-Segura, Ramón Mauricio Coral-Vázquez, Luz Berenice López-Hernández, Rosa Elena Escobar-Cedillo, Carolina Zúñiga-Guzman, Francisco Javier Estrada-Mena, Silvia García
Publikováno v:
International Journal of Molecular Sciences, Vol 16, Iss 3, Pp 5334-5346 (2015)
International Journal of Molecular Sciences
Volume 16
Issue 3
Pages 5334-5346
International Journal of Molecular Sciences
Volume 16
Issue 3
Pages 5334-5346
Novel therapeutic approaches are emerging to restore dystrophin function in Duchenne Muscular Dystrophy (DMD), a severe neuromuscular disease characterized by progressive muscle wasting and weakness. Some of the molecular therapies, such as exon skip
Autor:
Jana Sachwitz, Julia Angélica López-Hernández, Karen Grønskov, Lene Bjerring Gede, Irène Netchine, Zeynep Tümer, Miriam Elbracht, Thomas Eggermann, Johan T. den Dunnen
Publikováno v:
Human mutation. 39(3)
Silver-Russell syndrome (SRS) is a clinically and molecularly heterogeneous disorder involving prenatal and postnatal growth retardation, and the term SRS-like is broadly used to describe individuals with clinical features resembling SRS. The main mo
Autor:
Angelica Lopez Hernandez, Jennifer L. Weinberg, Amena El-Harakeh, Lola Adeyemi, Neelima Potharaj, Nandini Oomman, Anna Kalbarczyk
Publikováno v:
Annals of Global Health, Vol 88, Iss 1 (2022)
Background: Global health networks serve to bring members together towards a specific objective. However, for myriad reasons, women often lack access to networks that facilitate leadership and career development. In 2020, the Johns Hopkins Center for
Externí odkaz:
https://doaj.org/article/2101dd29bf5549c2adf73d2de32dfb9c
Autor:
Rosa Elena Escobar-Cedillo, Luz López-Hernández, Antonio Miranda-Duarte, María Dolores Curiel-Leal, Andrea Suarez-Ocón, Laura Sánchez-Chapul, Alexandra Berenice Luna-Angulo, Guillermina Ávila-Ramírez, Julia Angélica López-Hernández, Benjamín Gómez-Díaz
Publikováno v:
Folia Neuropathologica, Vol 59, Iss 3, Pp 276-283 (2021)
Muscular dystrophies are a group of well-defined genetic disorders characterized by the variable distribution of muscle wasting and progressive weakness. The diagnosis and treatment of these diseases remain challenging due to genetic heterogeneity an
Externí odkaz:
https://doaj.org/article/603df209725b4742932efdc90362ee5b