Detalhe da pesquisa
1.
Unraveling the role of relative telomere length and CAG expansion on initial symptoms of juvenile Huntington disease.
Eur J Neurol
; 30(3): 612-621, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36421025
2.
Clinical and Molecular Findings of Intermediate Allele Carriers in the HTT Gene from the Mexican Mestizo Population.
Neurodegener Dis
; 22(1): 34-42, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35926480
3.
Founder effect and ancestral origin of the spinocerebellar ataxia type 7 (SCA7) mutation in Mexican families.
Neurogenetics
; 15(1): 13-7, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24374739
4.
Telomere length analysis on leukocytes derived from patients with Huntington Disease.
Mech Ageing Dev
; 185: 111189, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31759995
5.
Implicit learning impairment identified via predictive saccades in Huntington's disease correlates with extended cortico-striatal atrophy.
Cortex
; 121: 89-103, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31550618
6.
Homocysteine-induced brain lipid peroxidation: effects of NMDA receptor blockade, antioxidant treatment, and nitric oxide synthase inhibition.
Neurotox Res
; 5(4): 237-43, 2003.
Artigo
em Inglês
| MEDLINE | ID: mdl-12835115
7.
Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican population.
Mov Disord
; 22(7): 1050-3, 2007 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17427938