Search Results - "Chirino, Amanda"

Reply to: “Further Perspectives on the Neural Bases of Cognitive Impairments in Spinocerebellar Ataxia Type 10” by Chirino‐Pérez, Amanda, Vaca‐Palomares, Israel, Fernandez‐Ruiz, Juan

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Cognitive Impairments in Spinocerebellar Ataxia Type 10 and Their Relation to Cortical Thickness by Chirino‐Pérez, Amanda, Vaca‐Palomares, Israel, Torres, Diana L., Hernandez‐Castillo, Carlos R., Diaz, Rosalinda, Ramirez‐Garcia, Gabriel, Fernandez‐Ruiz, Juan

“…ABSTRACT Background Spinocerebellar ataxia type 10 is a neurodegenerative disorder caused by the expansion of an ATTCT pentanucleotide repeat. Its clinical…”
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Longitudinal Analysis of the Relation Between Clinical Impairment and Gray Matter Degeneration in Spinocerebellar Ataxia Type 7 Patients by Contreras, Anabel, Ramirez-Garcia, Gabriel, Chirino, Amanda, Morgado-Valle, Consuelo, Pasaye, Erick H., Hernandez-Castillo, Carlos, Díaz, Rosalinda, Fernandez-Ruiz, Juan, Beltran-Parrazal, Luis

“…Spinocerebellar ataxia type 7 (SCA7) is a neurodegenerative disease characterized by progressive ataxia and retinal degeneration. Previous cross-sectional…”
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ATTCT and ATTCC repeat expansions in the ATXN10 gene affect disease penetrance of spinocerebellar ataxia type 10 by Morato Torres, C. Alejandra, Zafar, Faria, Tsai, Yu-Chih, Vazquez, Jocelyn Palafox, Gallagher, Michael D., McLaughlin, Ian, Hong, Karl, Lai, Jill, Lee, Joyce, Chirino-Perez, Amanda, Romero-Molina, Angel Omar, Torres, Francisco, Fernandez-Ruiz, Juan, Ashizawa, Tetsuo, Ziegle, Janet, Jiménez Gil, Francisco Javier, Schüle, Birgitt

“…Spinocerebellar ataxia type 10 (SCA10) is an autosomal-dominant disorder caused by an expanded pentanucleotide repeat in the ATXN10 gene. This repeat…”
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Mapping the Cerebellar Cognitive Affective Syndrome in Patients with Chronic Cerebellar Strokes by Chirino-Pérez, Amanda, Marrufo-Meléndez, Oscar René, Muñoz-López, José Ignacio, Hernandez-Castillo, Carlos R., Ramirez-Garcia, Gabriel, Díaz, Rosalinda, Nuñez-Orozco, Lilia, Fernandez-Ruiz, Juan

“…The cerebellar cognitive affective syndrome (CCAS) has been consistently described in patients with acute/subacute cerebellar injuries. However, studies with…”
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Critical role of acute hypoxemia on the cognitive impairment after severe COVID-19 pneumonia: a multivariate causality model analysis by García-Grimshaw, Miguel, Chirino-Pérez, Amanda, Flores-Silva, Fernando Daniel, Valdés-Ferrer, Sergio Iván, Vargas-Martínez, María de los Ángeles, Jiménez-Ávila, Ana Itiel, Chávez-Martínez, Oswaldo Alan, Ramos-Galicia, Enrique Manuel, Marché-Fernández, Osvaldo Alexis, Ramírez-Carrillo, Martha Fernanda, Grajeda-González, Samara Lissete, Ramírez-Jiménez, Marco Eduardo, Chávez-Manzanera, Emma Adriana, Tusié-Luna, María Teresa, Ochoa-Guzmán, Ana, Cantú-Brito, Carlos, Fernandez-Ruiz, Juan, Chiquete, Erwin

“…Background A high proportion of coronavirus disease 2019 (COVID-19) survivors may develop long-term cognitive impairment. We aimed to develop a multivariate…”
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Extensive cerebellar and thalamic degeneration in spinocerebellar ataxia type 10 by Hernandez-Castillo, Carlos R., Diaz, Rosalinda, Vaca-Palomares, Israel, Torres, Diana L., Chirino, Amanda, Campos-Romo, Aurelio, Ochoa, Adriana, Rasmussen, Astrid, Fernandez-Ruiz, Juan

“…Spinocerebellar ataxia type 10 (SCA10) is a hereditary neurodegenerative disorder caused by repeat expansions in the ATXN10 gene. Patients present with…”
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Motor and cognitive impairments in spinocerebellar ataxia type 7 and its correlations with cortical volumes by Chirino, Amanda, Hernandez‐Castillo, Carlos R., Galvez, Victor, Contreras, Anabel, Diaz, Rosalinda, Beltran‐Parrazal, Luis, Fernandez‐Ruiz, Juan

“…Spinocerebellar Ataxia Type 7 (SCA7) is a neurodegenerative disorder caused by cytosine‐adenine‐guanine (CAG) repeat expansion. It is clinically characterized…”
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Cognitive Decline and White Matter Integrity Degradation in Myotonic Dystrophy Type I by Lopez‐Titla, Maria Margarita, Chirino, Amanda, Cruz Solis, Sara Vanessa, Hernandez‐Castillo, Carlos R., Diaz, Rosalinda, Márquez‐Quiroz, Luz del Carmen, Magaña, Jonathan J, Beltrán‐Parrazal, Luis, Fernandez‐Ruiz, Juan

“…ABSTRACT BACKGROUND AND PURPOSE Myotonic Dystrophy Type I (DM1) is a neurodegenerative, genetic, and multisystemic disorder with a large variety of symptoms…”
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SARS-CoV-2’s brain impact: revealing cortical and cerebellar differences via cluster analysis in COVID-19 recovered patients by Romero-Molina, Angel Omar, Ramirez-Garcia, Gabriel, Chirino-Perez, Amanda, Fuentes-Zavaleta, David Alejandro, Hernandez-Castillo, Carlos Roberto, Marrufo-Melendez, Oscar, Lopez-Gonzalez, Diana, Rodriguez-Rodriguez, Mónica, Castorena-Maldonado, Armando, Rodriguez-Agudelo, Yaneth, Paz-Rodriguez, Francisco, Chavez-Oliveros, Mireya, Lozano-Tovar, Susana, Gutierrez-Romero, Alonso, Arauz-Gongora, Antonio, Garcia-Santos, Raul Anwar, Fernandez-Ruiz, Juan

“…Background COVID-19 is a disease known for its neurological involvement. SARS-CoV-2 infection triggers neuroinflammation, which could significantly contribute…”
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