Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Amanda Chirino"'
Autor:
C. Alejandra Morato Torres, Faria Zafar, Yu-Chih Tsai, Jocelyn Palafox Vazquez, Michael D. Gallagher, Ian McLaughlin, Karl Hong, Jill Lai, Joyce Lee, Amanda Chirino-Perez, Angel Omar Romero-Molina, Francisco Torres, Juan Fernandez-Ruiz, Tetsuo Ashizawa, Janet Ziegle, Francisco Javier Jiménez Gil, Birgitt Schüle
Publikováno v:
HGG Advances, Vol 3, Iss 4, Pp 100137- (2022)
Summary: Spinocerebellar ataxia type 10 (SCA10) is an autosomal-dominant disorder caused by an expanded pentanucleotide repeat in the ATXN10 gene. This repeat expansion, when fully penetrant, has a size of 850–4,500 repeats. It has been shown that
Externí odkaz:
https://doaj.org/article/d277d02bf6d7434f953472087dacb93d
Autor:
Miguel García-Grimshaw, Amanda Chirino-Pérez, Fernando Daniel Flores-Silva, Sergio Iván Valdés-Ferrer, María de los Ángeles Vargas-Martínez, Ana Itiel Jiménez-Ávila, Oswaldo Alan Chávez-Martínez, Enrique Manuel Ramos-Galicia, Osvaldo Alexis Marché-Fernández, Martha Fernanda Ramírez-Carrillo, Samara Lissete Grajeda-González, Marco Eduardo Ramírez-Jiménez, Emma Adriana Chávez-Manzanera, María Teresa Tusié-Luna, Ana Ochoa-Guzmán, Carlos Cantú-Brito, Juan Fernandez-Ruiz, Erwin Chiquete
Publikováno v:
Neurological Sciences. 43:2217-2229
A high proportion of coronavirus disease 2019 (COVID-19) survivors may develop long-term cognitive impairment. We aimed to develop a multivariate causal model exposing the links between COVID-19-associated biomarkers, illness-related variables, and t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c903c51bcc1e725ebfac5eb77ea19969
https://doi.org/10.1007/s10072-021-05798-8
https://doi.org/10.1007/s10072-021-05798-8
Autor:
Gustavo Padron-Rivera, Angel Omar Romero-Molina, Rosalinda Diaz, Israel Vaca-Palomares, Adriana Ochoa-Morales, César Romero-Rebollar, Amanda Chirino-Pérez, Juan Fernandez-Ruiz
Publikováno v:
Neurodegenerative Diseases. 22:24-28
Background: Recent resting-state functional magnetic resonance imaging studies have reported abnormal functional connectivity (FC) in the prefrontal cortex (PFC)-striatum circuit in patients with premanifest Huntington’s disease (HD). However, ther
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6732cf0910f79e865bc99bf7ff54957
https://doi.org/10.1159/000526778
https://doi.org/10.1159/000526778
Autor:
Juan Fernandez-Ruiz, Carlos R. Hernandez-Castillo, Gabriel Ramirez-Garcia, Amanda Chirino-Pérez, Diana L. Torres, Rosalinda Diaz, Israel Vaca-Palomares
Publikováno v:
Movement Disorders. 36:2910-2921
Background Spinocerebellar ataxia type 10 is a neurodegenerative disorder caused by the expansion of an ATTCT pentanucleotide repeat. Its clinical features include ataxia and, in some cases, epileptic seizures. There is, however, a dearth of informat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87c1d363c63a488ab95b16363f3ca3b1
https://doi.org/10.1002/mds.28728
https://doi.org/10.1002/mds.28728
Autor:
José Ignacio Muñoz-López, Juan Fernandez-Ruiz, Lilia Nuñez-Orozco, Gabriel Ramirez-Garcia, Rosalinda Diaz, Óscar Marrufo-Meléndez, Amanda Chirino-Pérez, Carlos R. Hernandez-Castillo
Publikováno v:
The Cerebellum. 21:208-218
The cerebellar cognitive affective syndrome (CCAS) has been consistently described in patients with acute/subacute cerebellar injuries. However, studies with chronic patients have had controversial findings that have not been explored with new cerebe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fbab1977d4b68a62302d6e657bcc9600
https://doi.org/10.1007/s12311-021-01290-3
https://doi.org/10.1007/s12311-021-01290-3
Autor:
Erick H. Pasaye, Gabriel Ramirez-Garcia, Consuelo Morgado-Valle, Amanda Chirino, Luis Beltran-Parrazal, Anabel Contreras, Rosalinda Diaz, Juan Fernandez-Ruiz, Carlos R. Hernandez-Castillo
Publikováno v:
The Cerebellum. 20:346-360
Spinocerebellar ataxia type 7 (SCA7) is a neurodegenerative disease characterized by progressive ataxia and retinal degeneration. Previous cross-sectional studies show a significant decrease in the gray matter of the cerebral cortex, cerebellum, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d35a4345f02066112c5bf65045d1817a
https://doi.org/10.1007/s12311-020-01205-8
https://doi.org/10.1007/s12311-020-01205-8
Autor:
Amanda, Chirino-Pérez, Oscar René, Marrufo-Meléndez, José Ignacio, Muñoz-López, Carlos R, Hernandez-Castillo, Gabriel, Ramirez-Garcia, Rosalinda, Díaz, Lilia, Nuñez-Orozco, Juan, Fernandez-Ruiz
Publikováno v:
Cerebellum (London, England). 21(2)
The cerebellar cognitive affective syndrome (CCAS) has been consistently described in patients with acute/subacute cerebellar injuries. However, studies with chronic patients have had controversial findings that have not been explored with new cerebe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::782c369550a4bec72a7b3832b99e0fee
https://pubmed.ncbi.nlm.nih.gov/34109552
https://pubmed.ncbi.nlm.nih.gov/34109552
Autor:
Diana L. Torres, Astrid Rasmussen, Rosalinda Diaz, Aurelio Campos-Romo, Israel Vaca-Palomares, Juan Fernandez-Ruiz, Amanda Chirino, Carlos R. Hernandez-Castillo, Adriana Ochoa
Publikováno v:
Parkinsonism & Related Disorders. 66:182-188
Introduction Spinocerebellar ataxia type 10 (SCA10) is a hereditary neurodegenerative disorder caused by repeat expansions in the ATXN10 gene. Patients present with cerebellar ataxia frequently accompanied by seizures. Even though loss of cerebellar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ceb33094d943055484c0e58fffb7b6b
https://doi.org/10.1016/j.parkreldis.2019.08.011
https://doi.org/10.1016/j.parkreldis.2019.08.011
Autor:
Anabel, Contreras, Gabriel, Ramirez-Garcia, Amanda, Chirino, Consuelo, Morgado-Valle, Erick H, Pasaye, Carlos, Hernandez-Castillo, Rosalinda, Díaz, Juan, Fernandez-Ruiz, Luis, Beltran-Parrazal
Publikováno v:
Cerebellum (London, England). 20(3)
Spinocerebellar ataxia type 7 (SCA7) is a neurodegenerative disease characterized by progressive ataxia and retinal degeneration. Previous cross-sectional studies show a significant decrease in the gray matter of the cerebral cortex, cerebellum, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::73e93ac595a4d3835c889e700be20698
https://pubmed.ncbi.nlm.nih.gov/33184781
https://pubmed.ncbi.nlm.nih.gov/33184781
Autor:
Amanda Chirino, Rosalinda Diaz, Jonathan J. Magaña, S. Solís, Luz Del Carmen Márquez-Quiroz, Luis Beltran-Parrazal, Maria Margarita Lopez-Titla, Juan Fernandez-Ruiz, Carlos R. Hernandez-Castillo
Publikováno v:
Journal of neuroimaging : official journal of the American Society of NeuroimagingReferences. 31(1)
Background and purpose Myotonic Dystrophy Type I (DM1) is a neurodegenerative, genetic, and multisystemic disorder with a large variety of symptoms due to a CTG trinucleotide expansion located on Dystrophia Myotonica Protein Kinase (DMPK) gene. Previ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7455e3f26431b52d7110215bbde8561
https://pubmed.ncbi.nlm.nih.gov/32936994
https://pubmed.ncbi.nlm.nih.gov/32936994