Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Raúl, Aguilera Rodríguez"'
Autor:
Kenia Hechevarría Bárzaga, Raúl Aguilera Rodríguez, Dennis Almaguer Gotay, Amarilis Álvarez Sosa, Luis Enrique Almaguer Mederos
Publikováno v:
Revista Habanera de Ciencias Médicas, Vol 18, Iss 5, Pp 704-716 (2019)
Introduction: Several proteinopathies of the nervous system are associated with disturbances in components of the hypothalamic–pituitary–gonadal axis.Objective: To assess the relevance of components of the hypothalamic–pituitary–gonadal axis
Externí odkaz:
https://doaj.org/article/34702fef36d34e7f8a0e050b2365c6c0
Publikováno v:
Revista Habanera de Ciencias Médicas, Vol 19, Iss 0, Pp e3389-e3389 (2020)
Introduction: The recent emergence of COVID-19 has become a serious global health problem. The identification of comorbidities associated with the clinical severity in COVID-19 patients is of paramount significance for the appropriate therapeutic app
Externí odkaz:
https://doaj.org/article/be9ce370f5d64c4f816b4f7ad9a21034
Autor:
Luis Enrique Almaguer Mederos, Dany Cuello Almarales, Dennis Almaguer Gotay, Raúl Aguilera Rodríguez
Publikováno v:
Revista Cubana de Investigaciones Biomédicas, Vol 37, Iss 4 (2019)
Se realizó una revisión de la literatura especializada con el objetivo de evaluar el estado del arte en cuanto a la aplicación de terapias de reemplazo celular en enfermedades poliglutamínicas. Se consultaron las bases de datos HighWire y PubMed,
Externí odkaz:
https://doaj.org/article/3bb9fe8a3a254748b33ec09a5b05468d
Autor:
Georg Auburger, Luis E. Almaguer-Mederos, Maria Velázquez-Garcés, Ilbedis Pérez-Ávila, Ricardo Hechavarría-Pupo, Dennis Almaguer-Gotay, Annelié Rodríguez-Estupiñán, Raúl Aguilera-Rodríguez
Publikováno v:
Movement Disorders. 36:1372-1380
Background Spinocerebellar ataxia type 2 is a progressive neurodegenerative disorder due to an unstable expansion of a CAG repeat in the ATXN2 gene. Although weight loss has been associated with disease progression in several neurodegenerative condit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80a3b0cbd5af82901f6ae224a613891a
https://doi.org/10.1002/mds.28498
https://doi.org/10.1002/mds.28498
Autor:
Kenia Hechavarría-Barzaga, Yanelis Silva-Ricardo, Dennis Almaguer-Gotay, Dany Cuello-Almarales, Amarilis Álvarez-Sosa, Yanetza González-Zaldivar, Annelié Rodríguez-Estupiñán, Raúl Aguilera-Rodríguez, Yaimé Vázquez-Mojena, Yamilé Chapman-Rodríguez, Luis E. Almaguer-Mederos
Publikováno v:
The Cerebellum. 19:597-604
Spinocerebellar ataxia type 2 (SCA2) is a progressive neurodegenerative disorder due to an unstable expansion of a CAG repeat in the ATXN2 gene. Despite clinical and experimental evidence indicating the relevance of the gonadotropic axis to the progn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fef81bd8340ecdeb2bd908edf130a583
https://doi.org/10.1007/s12311-020-01134-6
https://doi.org/10.1007/s12311-020-01134-6
Autor:
Jandy Campins Alí, Osiel Gámez Rodríguez, María B Ramírez Bautista, Yanetza González-Zaldivar, Yaimeé Vázquez-Mojena, Frank J Carrillo Rodes, Nayime Y Navas Napóles, Jacqueline Medrano-Montero, Luis Velázquez-Pérez, Aldo A Sigler Villanueva, Noharis Y Cordero Navarro, Leonardo A Guerra Rondón, Roberto Rodríguez-Labrada, Luis Enrique Almaguer Mederos, Nalia Canales-Ochoa, Tania Rodríguez Graña, María O. Hernández Oliver, Annelié Estupiñán Rodríguez, Yennis Domínguez Barrios, Orlando R Serrano Barrera, Lissi Flores Angulo, Javier García Zacarías, Raúl Aguilera Rodríguez, Reydenis Torres Vega, Ilya Sagaró Zambrano, Alejandro Leyva-Mérida
Publikováno v:
The Cerebellum. 19:252-264
The prevalence estimations of hereditary ataxias are biased since most epidemiological studies are confined to isolated geographical regions and few nationwide studies are available. The study aims to assess the prevalence, distribution, and neurolog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::472ac1f3baae6097a4288353cfd0ad56
https://doi.org/10.1007/s12311-020-01107-9
https://doi.org/10.1007/s12311-020-01107-9
Autor:
Tania Cruz Mariño, José Alberto Álvarez Cuesta, Raúl Aguilera Rodríguez, Luis Velázquez Pérez
Publikováno v:
Ciencias Holguín, Vol 17, Iss 1, Pp 1-10 (2011)
La ataxia de Friedreich se caracteriza por edad de comienzo antes de los 25 años, ataxia progresiva, disartria, ausencia de reflejos tendinosos profundos y alteraciones en el sentido de vibración. La presente investigación se realizó con el objet
Externí odkaz:
https://doaj.org/article/761b9af07a034670a7b855936670204b
Autor:
Lorenzo Reynaldo Cejas, Julio Cesar Rodríguez-Díaz, Dalina Laffita Pérez, Marcos Osorio Borjas, Nalia Canales Ochoa, Roberto Rodríguez Labrada, Annelié Estupiñán Rodríguez, Raúl Aguilera Rodríguez, Luis Velázquez-Pérez, Mariela Góngora Marrero, Jacqueline Medrano Montero, Dennis Almaguer Gotay, Yanetza González Zaldívar
Publikováno v:
Movement Disorders. 33:1481-1487
Background Neurorehabilitation has become in a widely used approach in spinocerebellar ataxias, but there are scarce powerful clinical studies supporting this notion. Objective The objective of this study was to assess the efficacy of a 24-week neuro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe958689d20854f72871e7225776d90a
https://doi.org/10.1002/mds.27437
https://doi.org/10.1002/mds.27437
Autor:
Annelié Rodríguez-Estupiñán, Raúl Aguilera-Rodríguez, Luis E. Almaguer-Mederos, Dany Cuello-Almarales, Dennis Almaguer-Gotay, José Miguel Laffita-Mesa, Pedro Zayas-Feria, Yaimé Vázquez-Mojena, Yanetza González-Zaldivar, Luis Velázquez-Pérez
Publikováno v:
Archives of Medical Research. 48:297-302
Spinocerebellar ataxia type 2 (SCA2) is part of a group of at least nine dominantly inherited disorders characterized by progressive degeneration of specific neuronal populations and a shared mutational mechanism involving the expansion of a CAG repe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea7e05b9a9a65e5ce19a0477f0fb851a
https://doi.org/10.1016/j.arcmed.2017.06.008
https://doi.org/10.1016/j.arcmed.2017.06.008
Autor:
Dennis Almaguer-Gotay, Georg Auburger, Luis E. Almaguer-Mederos, Nalia Canales-Ochoa, Jorge Aguiar-Santiago, Yasnay Jorge-Sainz, Yaimé Vázquez-Mojena, Roberto Rodríguez-Labrada, Dany Cuello-Almarales, Yanetza González-Zaldivar, Luis Velázquez-Pérez, Patrick MacLeod, Raúl Aguilera-Rodríguez
Publikováno v:
Journal of the Neurological Sciences. 409:116586
Background Spinocerebellar ataxia type 2 (SCA2) is a neurodegenerative disorder due to a CAG-repeat expansion. This work is intended to identify modifiers of the clinical phenotype in SCA2, following up on recent genome-wide association analyses that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8072af7c691243bde90d83984d81f59d
https://doi.org/10.1016/j.jns.2019.116586
https://doi.org/10.1016/j.jns.2019.116586