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Relationship of neutrophil-to-lymphocyte and platelet-to-lymphocyte ratio with visual acuity after surgical repair of open globe injury

Background: Male EBP disorder with neurologic defects (MEND) syndrome is an　X‐linked disease caused by hypomorphic mutations in the EBP (emopamil‐binding　protein) gene. Modifier genes may explain the clinical variability among individuals　who share a primary mutation. Methods: We studied four males...

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Detalles Bibliográficos
Autores principales:	Mohamed Noriega, Karim, Treviño Herrera, Alan Bる, Mohamed Noriega, Jibran, Velasco Sepúlveda, Braulio H., Martínez Pacheco, Víctor Alejandro, Guevara Villarreal, Dante A., Rodríguez Medellín, Delia L., Sepúlveda Salinas, Anna G., Villarreal Mendez, Gerardo, González Cortés, Jesús H., Elizondo Omaña, Rodrigo Enrique, Guzmán López, Santos, Mohamed Hamsho, Jesús
Formato:	Artículo
Lenguaje:	inglés
Publicado:	Frontiers Media 2021
Acceso en línea:	http://eprints.uanl.mx/29897/1/29897.pdf

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