Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Rosalinda Diaz"'
Autor:
Gabriel Ramirez-Garcia, Victor Galvez, Rosalinda Diaz, Aurelio Campos-Romo, Juan Fernandez-Ruiz
Publikováno v:
PeerJ, Vol 10, p e12917 (2022)
Huntington’s Disease (HD) is an autosomal neurodegenerative disease characterized by motor, cognitive, and psychiatric symptoms. Cognitive impairment develops gradually in HD patients, progressing later into a severe cognitive dysfunction. The Mont
Externí odkaz:
https://doaj.org/article/f669d0ed3be54e76ac6e1776d83dbc2f
Publikováno v:
Behavioural Neurology, Vol 2015 (2015)
Objective. To evaluate the effect of age-related cognitive changes in a visuomotor learning task that depends on strategic control and contrast it with the effect in a task principally depending on visuomotor recalibration. Methods. Participants perf
Externí odkaz:
https://doaj.org/article/b3dc7487e7e7466d9574ee714a980fb9
Autor:
Carlos R Hernandez-Castillo, Victor Galvez, Roberto Mercadillo, Rosalinda Diaz, Aurelio Campos-Romo, Juan Fernandez-Ruiz
Publikováno v:
PLoS ONE, Vol 10, Iss 8, p e0135449 (2015)
Previous studies of SCA2 have revealed significant degeneration of white matter tracts in cerebellar and cerebral regions. The motor deficit in these patients may be attributable to the degradation of projection fibers associated with the underlying
Externí odkaz:
https://doaj.org/article/313485b32fc143798bf51aaa940a16cf
Publikováno v:
The Scientific World Journal, Vol 2, Pp 1070-1078 (2002)
This study sought to examine whether the administration of quinfamide at 3- or 6-month intervals diminished the frequency of Entamoeba histolytica cysts in stool samples compared to controls. The prospective, longitudinal, randomized, single-blind st
Externí odkaz:
https://doaj.org/article/afb9a60228c14771865fa8f0097eba2c
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:
Rosalinda Diaz, T.J.R. Rezende, C.R. Hernandez-Castillo, Fanny Mochel, Juan Fernandez-Ruiz, Ian H. Harding, I. Adanyeguh
Publikováno v:
AJNR Am J Neuroradiol
BACKGROUND AND PURPOSE: Spinocerebellar ataxia type 7 is an autosomal dominant neurodegenerative disease caused by a cytosine-adenine-guanine (CAG) repeat expansion. Clinically, spinocerebellar ataxia type 7 is characterized by progressive cerebellar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d2200925c20461e6b0969e3b658c398
https://doi.org/10.3174/ajnr.a7202
https://doi.org/10.3174/ajnr.a7202
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:
Israel Vaca-Palomares, Juan Fernandez-Ruiz, Carlos R. Hernandez-Castillo, Rosalinda Diaz, Adriana Ochoa, Gustavo Padron-Rivera
Publikováno v:
The Cerebellum. 20:942-945
Recent findings suggest a significant effect of the cerebellar circuit deterioration on the clinical manifestation of Huntington's disease, calling for a better understanding of the cerebellar degeneration in this disorder. Recent brain imaging analy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25f64301a277de4fa8e2efa36cdeb740
https://doi.org/10.1007/s12311-021-01256-5
https://doi.org/10.1007/s12311-021-01256-5
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