Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Nieves Santos Falcón"'
Autor:
Miguel G. Rojas, Zachary M. Zigmond, Simone Pereira-Simon, Nieves Santos Falcon, Maya Suresh Kumar, Filipe F. Stoyell-Conti, Christina Kosanovic, Anthony J. Griswold, Alghidak Salama, Xiaofeng Yang, Marwan Tabbara, Roberto I. Vazquez-Padron, Laisel Martinez
Publikováno v:
PLoS ONE, Vol 19, Iss 1 (2024)
Externí odkaz:
https://doaj.org/article/ff87a5c7f0a74beab6887cb1d7d5c447
Autor:
D Cuello-Almarales, Luis Velázquez-Pérez, R Aguilera-Rodríguez, D Almaguer-Gotay, Nieves Santos Falcón, Georg Auburger, L E Almaguer-Mederos, Yanetza González-Zaldivar, J M L Mesa, Susana Gispert
Publikováno v:
Clinical genetics. 94(3-4)
Spinocerebellar ataxia type 2 (SCA2) is a neurodegenerative disorder caused by the unstable expansion of a cytosine-adenine-guanine (CAG)/cytosine-adenine-adenine (CAA) repeat in the ATXN2 gene, which normally encodes 22 glutamines (Q22). A large stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::188b67533ba128d97c4039d5bfa19373
https://pubmed.ncbi.nlm.nih.gov/29756284
https://pubmed.ncbi.nlm.nih.gov/29756284
Autor:
Miguel G. Rojas, Simone Pereira-Simon, Zachary M. Zigmond, Javier Varona Santos, Mikael Perla, Nieves Santos Falcon, Filipe F. Stoyell-Conti, Alghidak Salama, Xiaofeng Yang, Xiaochun Long, Juan C. Duque, Loay H. Salman, Marwan Tabbara, Laisel Martinez, Roberto I. Vazquez-Padron
Publikováno v:
Cells, Vol 13, Iss 10, p 793 (2024)
Arteries and veins develop different types of occlusive diseases and respond differently to injury. The biological reasons for this discrepancy are not well understood, which is a limiting factor for the development of vein-targeted therapies. This s
Externí odkaz:
https://doaj.org/article/a69769cc73884282a9e2c00bf25cb441
Autor:
Luis E, Almaguer-Mederos, Raúl, Aguilera-Rodríguez, Dany, Cuello-Almarales, Dennis, Almaguer-Gotay, Yanetza, González-Zaldívar, Yaimé, Vázquez-Mojena, Nieves, Santos-Falcón, Gilberto, Sánchez-Cruz, Luis, Velázquez-Pérez
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 32(9)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fe70236dbd8f74e526d0c4f8d31e2bb4
https://pubmed.ncbi.nlm.nih.gov/28620961
https://pubmed.ncbi.nlm.nih.gov/28620961
Autor:
José Miguel Laffita-Mesa, Yanetza González Zaldívar, RR Armiñán, TM Cyuz, Suzana Gispert, MV Manresa, V Chang, Y R Almira, MP Herrera, Gilberto Sánchez Cruz, Georg Auburger, Luis E. Almaguer-Mederos, E M Góngora, D C Almarales, Luis Velázquez Pérez, KE Batallán, Nieves Santos Falcón
Publikováno v:
Clinical Genetics. 78:169-174
Previous studies have investigated the close association that exists between CAG repeat number and the age at onset in SCA2 = spinocerebellar ataxia type 2. These studies have focused on affected individuals. To further characterize this association
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e08d4012360dad56751e6e78fae27b30
https://doi.org/10.1111/j.1399-0004.2009.01358.x
https://doi.org/10.1111/j.1399-0004.2009.01358.x
Autor:
Raúl Aguilera Rodríguez, Dany Coello Almarales, José M. Laffita Mesa, Julio César Rodríguez Díaz, Luis Enrique Almaguer Mederos, Yanetza González Zaldívar, Roberto Rodríguez Labrada, Gilberto Sánchez Cruz, Humberto Jorge Cedeño, Nieves Santos Falcón, Karel Escalona Batallan, Luis Velázquez Pérez, Milena Paneque Herrera, Dennis Almaguer Gotay
Publikováno v:
Neuroscience Letters. 454:157-160
The objective of this study was to determine the prevalence of hereditary ataxias in Cuba, with a special focus on the clinical and molecular features of SCA2. Clinical assessments were performed by neurological examinations and application of the SA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::989f0e7e886ffcee045a13d90dcde5e1
https://doi.org/10.1016/j.neulet.2009.03.015
https://doi.org/10.1016/j.neulet.2009.03.015
Autor:
Luis Enrique Almaguer Mederos, Roberto Rodríguez Labrada, Luis Velázquez-Pérez, Nieves Santos Falcón, Yanetza González Zaldívar, Yaimeé Vázquez Mojena, Tania Cruz-Mariño, José Miguel Laffita-Mesa, Dennis Almaguer-Gotay
Publikováno v:
European journal of human genetics : EJHG. 20(1)
The role of short, large or intermediate normal alleles (ANs) of the ataxin-2 gene in generating expanded alleles (EAs) causing spinocerebellar ataxia type 2 (SCA2) is poorly understood. It has been postulated that SCA2 prevalence is related to the f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ade0f364ac4dd2bdcce327e705197ef6
https://pubmed.ncbi.nlm.nih.gov/21934711
https://pubmed.ncbi.nlm.nih.gov/21934711
Autor:
Luis, Velázquez-Pérez, Carola, Seifried, Nieves, Santos-Falcón, Michael, Abele, Ulf, Ziemann, Luis Enrique, Almaguer, Edilberto, Martínez-Góngora, Gilberto, Sánchez-Cruz, Nalia, Canales, Ruth, Pérez-González, Mercedes, Velázquez-Manresa, Bettina, Viebahn, Sebastian, von Stuckrad-Barre, Michael, Fetter, Thomas, Klockgether, Georg, Auburger
Publikováno v:
Annals of neurology. 56(3)
We assessed maximal saccade velocity (MSV) in 82 spinocerebellar ataxia type 2 (SCA2) patients and 80 controls, correlating it to disease duration, polyglutamine expansion size, age at onset, ataxia score, age, and sex. Little overlap with normal val
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::761ce9b93c307020a0af82c1b3361c37
https://pubmed.ncbi.nlm.nih.gov/15349876
https://pubmed.ncbi.nlm.nih.gov/15349876
Autor:
G. Sánchez, J. Laffita, Yanetza González Zaldívar, George Auburger, Y R Almira, Susana Gispert, Dany Coello Almarales, Nieves Santos Falcón, L.E. Almaguer Mederos, D. Almaguer, Luis Velázquez
Publikováno v:
Clinical Neurophysiology. 119:S173
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e12de928bf0633aebf3cc557999fbbb3
https://doi.org/10.1016/s1388-2457(08)60647-1
https://doi.org/10.1016/s1388-2457(08)60647-1
Autor:
Raquel Rojas Bruzón, Guillermo Martínez Valdez, Nieves Santos Falcon, Luis Mederos Almaguer, Víctor Tamayo Chang, Juana Álvarez Ocampo
Publikováno v:
Correo Científico Médico, Vol 21, Iss 3 (2017)
Introducción: el acné es una de las afecciones dermatológicas más frecuentes en la práctica médica, de ellas, el acné conglobata se caracteriza por ser poco común. La génesis del acné conglobata es compleja y depende de la interacción de v
Externí odkaz:
https://doaj.org/article/ba8dcdbc30484e67a5acd1a166e9dd27