Hakutulokset - Rodriguez-Labrada, Roberto

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches Tekijä Velázquez-Pérez, Luis C., Rodríguez-Labrada, Roberto, Fernandez-Ruiz, Juan

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Heritability of saccadic eye movements in spinocerebellar ataxia type 2: insights into an endophenotype marker Tekijä Rodríguez-Labrada, Roberto, Vázquez-Mojena, Yaimeé, Canales-Ochoa, Nalia, Medrano-Montero, Jacqueline, Velázquez-Pérez, Luis

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Motor Decline in Clinically Presymptomatic Spinocerebellar Ataxia Type 2 Gene Carriers Tekijä Velázquez-Perez, Luis, Díaz, Rosalinda, Pérez-González, Ruth, Canales, Nalia, Rodríguez-Labrada, Roberto, Medrano, Jacquelín, Sánchez, Gilberto, Almaguer-Mederos, Luis, Torres, Cira, Fernandez-Ruiz, Juan

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Insights into cognitive decline in spinocerebellar Ataxia type 2: a P300 event-related brain potential study Tekijä Rodríguez-Labrada, Roberto, Velázquez-Pérez, Luis, Ortega-Sánchez, Ricardo, Peña-Acosta, Arnoy, Vázquez-Mojena, Yaimeé, Canales-Ochoa, Nalia, Medrano-Montero, Jacqueline, Torres-Vega, Reidenis, González-Zaldivar, Yanetza

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Spinocerebellar Ataxia Type 2 Is Associated with the Extracellular Loss of Superoxide Dismutase but Not Catalase Activity Tekijä Almaguer-Gotay, Dennis, Almaguer-Mederos, Luis E., Aguilera-Rodríguez, Raul, Rodríguez-Labrada, Roberto, Cuello-Almarales, Dany, Estupiñán-Domínguez, Annelié, Velázquez-Pérez, Luis C., González-Zaldívar, Yanetza, Vázquez-Mojena, Yaimé

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Unexpanded and intermediate CAG polymorphisms at the SCA2 locus (ATXN2) in the Cuban population: evidence about the origin of expanded SCA2 alleles Tekijä Laffita-Mesa, José Miguel, Velázquez-Pérez, Luis C, Santos Falcón, Nieves, Cruz-Mariño, Tania, González Zaldívar, Yanetza, Vázquez Mojena, Yaimee, Almaguer-Gotay, Dennis, Almaguer Mederos, Luis Enrique, Rodríguez Labrada, Roberto

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Brain atrophy measures in preclinical and manifest spinocerebellar ataxia type 2 Tekijä Reetz, Kathrin, Rodríguez‐Labrada, Roberto, Dogan, Imis, Mirzazade, Shahram, Romanzetti, Sandro, Schulz, Jörg B., Cruz‐Rivas, Edilia M., Alvarez‐Cuesta, Jose A., Aguilera Rodríguez, Raul, Gonzalez Zaldivar, Yanetza, Auburger, Georg, Velázquez‐Pérez, Luis

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Epidemiological, clinical, and molecular characterization of Cuban families with spinocerebellar ataxia type 3/Machado-Joseph disease Tekijä González-Zaldívar, Yanetza, Vázquez-Mojena, Yaimeé, Laffita-Mesa, José M, Almaguer-Mederos, Luis E, Rodríguez-Labrada, Roberto, Sánchez-Cruz, Gilberto, Aguilera-Rodríguez, Raúl, Cruz-Mariño, Tania, Canales-Ochoa, Nalia, MacLeod, Patrick, Velázquez-Pérez, Luis

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Familial Alzheimer’s disease–associated presenilin-1 alters cerebellar activity and calcium homeostasis Tekijä Sepulveda-Falla, Diego, Barrera-Ocampo, Alvaro, Hagel, Christian, Korwitz, Anne, Vinueza-Veloz, Maria Fernanda, Zhou, Kuikui, Schonewille, Martijn, Zhou, Haibo, Velazquez-Perez, Luis, Rodriguez-Labrada, Roberto, Villegas, Andres, Ferrer, Isidro, Lopera, Francisco, Langer, Thomas, De Zeeuw, Chris I., Glatzel, Markus

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De Novo Mutations in Ataxin-2 Gene and ALS Risk Tekijä Laffita-Mesa, José Miguel, Rodríguez Pupo, Jorge Michel, Moreno Sera, Raciel, Vázquez Mojena, Yaimee, Kourí, Vivian, Laguna-Salvia, Leonides, Martínez-Godales, Michael, Valdevila Figueira, José A., Bauer, Peter O., Rodríguez-Labrada, Roberto, Zaldívar, Yanetza González, Paucar, Martin, Svenningsson, Per, Pérez, Luís Velázquez

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Impacts of the COVID-19 Pandemic on the Mental Health and Motor Deficits in Cuban Patients with Cerebellar Ataxias Tekijä González-Garcés, Yasmany, Domínguez-Barrios, Yennis, Zayas-Hernández, Arianna, Sigler-Villanueva, Aldo A., Canales-Ochoa, Nalia, Hernández Oliver, María O., Ramírez-Bautista, María B., Caballero-Laguna, Alberto, Arrufat-Pie, Eduardo, Carrillo-Rodes, Frank J., Medrano-Montero, Jacqueline, Rodríguez-Álvarez, Yanela, Gámez-Rodríguez, Osiel, Guerra-Rondón, Leonardo A., Aguilera-Batista, Osvaldo, Vazquez-Mojena, Yaimee, Rodríguez-Labrada, Roberto, Velázquez-Pérez, Luis

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