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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Autores principales:	Mohamed　Noriega, Karim, Treviño　Herrera, Alan Bる, Mohamed　Noriega, Jibran, Velasco　Sepúlveda, Braulio H., Martínez　Pacheco, Víctor A., Guevara　Villarreal, Dante A., Rodríguez　Medellín, Delia L., Sepúlveda　Salinas, Anna G., Villarreal　Méndez, Gerardo, González　Cortés, Jesús H., Elizondo　Omaña, Rodrigo E., 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