Yaimee Vazquez-Mojena
Yaimee Vazquez-Mojena
Center for Research and Rehabilitation of Hereditary Ataxias
Nenhum email confirmado
Título
Citado por
Citado por
Ano
Comprehensive study of early features in spinocerebellar ataxia 2: delineating the prodromal stage of the disease
L Velázquez-Pérez, R Rodríguez-Labrada, EM Cruz-Rivas, ...
The Cerebellum 13 (5), 568-579, 2014
622014
Estimation of the age at onset in spinocerebellar ataxia type 2 Cuban patients by survival analysis
LE Almaguer‐Mederos, NS Falcón, YR Almira, YG Zaldivar, ...
Clinical genetics 78 (2), 169-174, 2010
612010
Unexpanded and intermediate CAG polymorphisms at the SCA2 locus (ATXN2) in the Cuban population: evidence about the origin of expanded SCA2 alleles
JM Laffita-Mesa, LC Velázquez-Pérez, NS Falcón, T Cruz-Marino, ...
European Journal of Human Genetics 20 (1), 41-49, 2012
582012
Sleep disorders in spinocerebellar ataxia type 2 patients
L Velázquez-Pérez, U Voss, R Rodríguez-Labrada, G Auburger, ...
Neurodegenerative Diseases 8 (6), 447-454, 2011
562011
Subtle rapid eye movement sleep abnormalities in presymptomatic spinocerebellar ataxia type 2 gene carriers
R Rodríguez‐Labrada, L Velázquez‐Perez, NC Ochoa, LG Polo, ...
Movement disorders 26 (2), 347-350, 2011
522011
Oral zinc sulphate supplementation for six months in SCA2 patients: a randomized, double-blind, placebo-controlled trial
L Velázquez-Pérez, J Rodríguez-Chanfrau, JC García-Rodríguez, ...
Neurochemical research 36 (10), 1793-1800, 2011
412011
Saccadic latency is prolonged in Spinocerebellar Ataxia type 2 and correlates with the frontal-executive dysfunctions
R Rodríguez-Labrada, L Velázquez-Pérez, C Seigfried, N Canales-Ochoa, ...
Journal of the neurological sciences 306 (1-2), 103-107, 2011
362011
De Novo Mutations in Ataxin-2 Gene and ALS Risk
JM Laffita-Mesa, JM Rodríguez Pupo, R Moreno Sera, Y Vázquez Mojena, ...
PLoS One 8 (8), e70560, 2013
282013
The Cuban program for predictive testing of SCA2: 11 years and 768 individuals to learn from
T Cruz‐Mariño, L Velázquez‐Pérez, Y González‐Zaldivar, ...
Clinical genetics 83 (6), 518-524, 2013
242013
Transmisión asintomática y presintomática del SARS-CoV-2: la cara oculta de la COVID-19
RR Labrada, YV Mojena, LCV Pérez
Anales de la Academia de Ciencias de Cuba 10 (2), 770, 2020
222020
Spinocerebellar ataxia type 2 neurodegeneration differentially affects error-based and strategic-based visuomotor learning
I Vaca-Palomares, R Díaz, R Rodríguez-Labrada, J Medrano-Montero, ...
The Cerebellum 12 (6), 848-855, 2013
212013
Estimation of survival in spinocerebellar ataxia type 2 Cuban patients
LE Almaguer-Mederos, RA Rodríguez, YG Zaldivar, DA Gotay, ...
Clinical genetics 83 (3), 293-294, 2013
212013
P rodromal spinocerebellar ataxia type 2: Prospects for early interventions and ethical challenges
L Velázquez‐Pérez, R Rodríguez‐Labrada, JM Laffita‐Mesa
Movement Disorders 32 (5), 708-718, 2017
192017
Association of glutathione S-transferase omega polymorphism and spinocerebellar ataxia type 2
LE Almaguer-Mederos, D Almaguer-Gotay, R Aguilera-Rodríguez, ...
Journal of the neurological sciences 372, 324-328, 2017
152017
Role of glutathione S-transferases in the spinocerebellar ataxia type 2 clinical phenotype
D Almaguer-Gotay, LE Almaguer-Mederos, R Aguilera-Rodríguez, ...
Journal of the neurological sciences 341 (1-2), 41-45, 2014
152014
Buccal cell micronucleus frequency is significantly elevated in patients with spinocerebellar ataxia type 2
DA Cuello-Almarales, LE Almaguer-Mederos, Y Vázquez-Mojena, ...
Archives of medical research 48 (3), 297-302, 2017
142017
Genetic features of Huntington disease in Cuban population: implications for phenotype, epidemiology and predictive testing
Y Vázquez-Mojena, L Laguna-Salvia, JM Laffita-Mesa, ...
Journal of the neurological sciences 335 (1-2), 101-104, 2013
132013
Ethical dilemmas in genetic testing: examples from the Cuban program for predictive diagnosis of hereditary ataxias
TC Mariño, RR Armiñán, HJ Cedeño, JML Mesa, YG Zaldivar, ...
Journal of genetic counseling 20 (3), 241-248, 2011
132011
Epidemiological, clinical, and molecular characterization of Cuban families with spinocerebellar ataxia type 3/Machado-Joseph disease
Y González-Zaldívar, Y Vázquez-Mojena, JM Laffita-Mesa, ...
Cerebellum & ataxias 2 (1), 1-6, 2015
122015
Uncommon features in Cuban families affected with Friedreich ataxia
T Cruz-Mariño, Y González-Zaldivar, JM Laffita-Mesa, ...
Neuroscience letters 472 (2), 85-89, 2010
112010
O sistema não pode efectuar a operação agora. Tente novamente mais tarde.
Artigos 1–20