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1.
Minimal prevalence of Huntington's disease in the South of Brazil and instability of the expanded CAG tract during intergenerational transmissions.
Genet Mol Biol
; 42(2): 329-336, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-31259362
2.
Neuropsychiatric Symptoms in Patients with Dementia Associated with Increased Psychological Distress in Caregivers During the COVID-19 Pandemic.
J Alzheimers Dis
; 80(4): 1705-1712, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-33646168
3.
Free carnitine and branched chain amino acids are not good biomarkers in Huntington's disease.
Arq Neuropsiquiatr
; 78(2): 81-87, 2020 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-32159721
4.
The progression rate of spinocerebellar ataxia type 2 changes with stage of disease.
Orphanet J Rare Dis
; 13(1): 20, 2018 01 25.
Artículo
en Inglés
| MEDLINE | ID: mdl-29370806
5.
Neurological phenotypes in spinocerebellar ataxia type 2: Role of mitochondrial polymorphism A10398G and other risk factors.
Parkinsonism Relat Disord
; 42: 54-60, 2017 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-28648514
6.
Free carnitine and branched chain amino acids are not good biomarkers in Huntington's disease / Carnitina livre e aminoácidos de cadeia ramificada não são bons biomarcadores na doença de Huntington
Arq. neuropsiquiatr
; 78(2): 81-87, Feb. 2020. tab, graf
Artículo
en Inglés
| LILACS | ID: biblio-1089002
7.
8.
Minimal prevalence of Huntington's disease in the South of Brazil and instability of the expanded CAG tract during intergenerational transmissions
Artículo
en Inglés
| ARCA | ID: arc-36719
9.
The progression rate of spinocerebellar ataxia type 2 changes with stage of disease
Artículo
en Inglés
| ARCA | ID: arc-29451
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