Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Leticia Martínez-Ruano"'
Autor:
Amin Cervantes-Arriaga, David J. García-Romero, Marco Muñuzuri-Camacho, Oscar Esquivel-Zapata, David Dávila-Ortiz de Montellano, Leticia Martínez-Ruano, Ana J. Hernández-Medrano, María A. Ruiz-Mafud, Gloria I. Cerda-Hernández, Arturo Abundes-Corona, Mayela Rodríguez-Violante
Publikováno v:
Revista Mexicana de Neurociencia, Vol 24, Iss 2 (2023)
Objective: This study aims to identify the possible factors that delay the time-to-diagnosis of Huntington’s disease (HD). Methods: A cross-sectional study in HD patients was carried out. Variables registered were CAG repeats, age of onset, primary
Externí odkaz:
https://doaj.org/article/3d506afd74554f03a3e49953cd5bec62
Autor:
Miguel Ángel Ramírez-García, David José Dávila-Ortiz de Montellano, Leticia Martínez-Ruano, Adriana Ochoa-Morales, Sandra Romero-Hidalgo, Juan Carlos Zenteno, Petra Yescas-Gómez
Publikováno v:
Neurodegenerative Diseases. 22:34-42
Introduction: There are reports of different clinical statuses in carriers of intermediate alleles (IAs) of CAG trinucleotide repeats in the HTT gene, from individuals affected by a clinical picture indistinguishable from Huntington’s disease (HD)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::115085237c3effc122d2ffa3f408018b
https://doi.org/10.1159/000526260
https://doi.org/10.1159/000526260
Autor:
Israel Vaca-Palomares, Leticia Martínez-Ruano, Adriana Ochoa-Morales, Juan Fernandez-Ruiz, Donald C. Brien, Douglas P. Munoz, Brian C. Coe
Publikováno v:
Cortex. 121:89-103
The ability to anticipate events and execute motor commands prior to a sensory event is an essential capability for human's everyday life. This implicitly learned anticipatory behavior depends on the past performance of repeated sensorimotor interact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::508536f7947d724ac1a5f6a3479e4382
https://doi.org/10.1016/j.cortex.2019.06.013
https://doi.org/10.1016/j.cortex.2019.06.013
Autor:
Alberto Hidalgo-Bravo, Alejandra Camacho-Molina, Antonio Miranda-Duarte, Leticia Martínez-Ruano, Adriana Ochoa-Morales, Aurelio Jara-Prado, Adriana PerezGrovas-Saltijeral
Publikováno v:
Mechanisms of Ageing and Development. 185:111189
Introduction Huntington´s disease (HD) is a neurodegenerative disorder characterized by neuropsychiatric, motor and cognitive manifestations. It is caused by expansion of the trinucleotide CAG on HTT. The molecular bases are not completely understoo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2683f8a14a022871887d904415231420
https://doi.org/10.1016/j.mad.2019.111189
https://doi.org/10.1016/j.mad.2019.111189
Autor:
Leticia Martínez-Ruano, Ulises Rodríguez-Ortiz, Adriana Ochoa, Sarait Nadja Rodríguez-Ibarra, Marie Catherine Boll-Woehrlen
Publikováno v:
Archivos de Neurociencias. 21
Las ataxias degenerativas consisten en un grupo heterogéneo de enfermedades que se dividen en una mayoría de entidades hereditarias y formas esporádicas. Con el afán de realizar un estudio exhaustivo y mejorar la calidad de atención de estos pac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d9d395e3682dcacb7c6f0e611121072
https://doi.org/10.31157/an.v21i3.122
https://doi.org/10.31157/an.v21i3.122
Autor:
Christopher Mader, Luis Ruano, Marcela Fragoso-Benítez, Adriana Ochoa, Leticia Martínez-Ruano, Petra Yescas, Misti C. White, Sanjay I. Bidichandani, Tetsuo Ashizawa, Roxana Gutiérrez, Astrid Rasmussen, Irene De Biase, Elisa Alonso
Publikováno v:
Movement Disorders. 22:1050-1053
Dominant ataxias show wide geographic variation. We analyzed 108 dominant families and 123 sporadic ataxia patients from Mexico for mutations causing SCA1-3, 6-8, 10, 12, 17 and DRPLA. Only 18.5% of dominant families remained undiagnosed; SCA2 accoun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2a1de4ab4906200512ccdc0fa06afe0
https://doi.org/10.1002/mds.21470
https://doi.org/10.1002/mds.21470
Autor:
Adriana Ochoa-Morales, Carla Marquez-Luna, M. Teresa Villarreal-Molina, Victor Acuña-Alonzo, Sandra Romero-Hidalgo, M. Elisa Alonso-Vilatela, Petra Yescas-Gómez, Leticia Martínez-Ruano, Samuel Canizales-Quinteros, Lizbeth García-Velázquez
Publikováno v:
Neurogenetics. 15(1)
Spinocerebellar ataxia type 7 (SCA7) is an autosomal dominant disease characterized by progressive cerebellar ataxia and macular degeneration causing progressive blindness. It accounts for 1 to 11.6 % of spinocerebellar ataxias (SCAs) cases worldwide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13f0d4da01e7404855b8631e0e968ff0
https://pubmed.ncbi.nlm.nih.gov/24374739
https://pubmed.ncbi.nlm.nih.gov/24374739