Search Results - "Angeles‐López, Quetzalli Denisse"

Mast cells and histamine are involved in the neuronal damage observed in a quinolinic acid‐induced model of Huntington's disease by Martínez‐Gopar, Pablo Eliasib, Pérez‐Rodríguez, Marian Jesabel, Rodríguez‐Manzo, Gabriela, Garduño‐Gutierrez, René, Tristán‐López, Luis, Angeles‐López, Quetzalli Denisse, González‐Espinosa, Claudia, Pérez‐Severiano, Francisca

“…Huntington´s disease (HD) is a pathological condition that can be studied in mice by the administration of quinolinic acid (QUIN), an agonist of the…”
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I20 The combined therapy with laquinimod and an essential fatty acid-rich diet has a neuroprotective effect in an acute mice model of Huntington disease by Angeles-López, Quetzalli Denisse, Morales-Martínez, Adriana, Sánchez-Chinchillas, Argelia, Hernández-Cerón, Miguel, Pérez-Severiano, Francisca, Segovia-Vila, José

“…Huntington’s disease (HD) is a progressive neurodegenerative disorder clinically characterized by involuntary movements and psychiatric and behavioral…”
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Association of variants in the ABCB1, CYP2C19 and CYP2C9 genes for Juvenile Myoclonic Epilepsy by Jara-Prado, Aurelio, Guerrero-Camacho, Jorge Luis, Ángeles-López, Quetzalli Denisse, Ochoa-Morales, Adriana, Dávila-Ortiz de Montellano, David José, Ramírez-García, Miguel Ángel, Breda-Yepes, Michelle, Durón, Reyna M., Delgado-Escueta, Antonio V., Barrios-González, Diego A., Martínez-Juárez, Iris E.

“…Juvenile myoclonic epilepsy (JME) is the most common of the generalized genetic epilepsies, with multiple causal and susceptibility genes; however, its…”
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