Zobrazeno 1 - 8
of 8
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:
Adriana PerezGrovas‐Saltijeral, Adriana Ochoa‐Morales, Aurelio Jara‐Prado, Rafael Velázquez‐Cruz, Berenice Rivera‐Paredez, David Dávila‐OrtizdeMontellano, Edmar O. Benítez‐Alonso, Mónica Santamaría‐Olmedo, Rosalba Sevilla‐Montoya, Ernesto Marfil‐Marín, Margarita Valdés‐Flores, Leticia Martínez‐Ruano, Alejandra Camacho‐Molina, Alberto Hidalgo‐Bravo
Publikováno v:
European Journal of Neurology. 30:612-621
Juvenile-onset Huntington disease (JHD) is defined when symptoms initiate before 20 years of age. Mechanisms explaining differences between juvenile and adult onset are not fully understood. Our aim was to analyze the distribution of initial symptoms
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)
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
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
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
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
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