Although ataxia is the most distressing manifestation of Machado-Joseph disease (MJD), little is known about its natural history. Therefore, we prospectively followed a cohort of patients with MJD for 13 months to characterize the progression of ataxia and identify its contributory factors. The international cooperative ataxia rating scale (ICARS) was used to estimate severity of ataxia at baseline and at follow-up. Thirty-four patients were enrolled in the study, 22 of whom were men. Mean age at onset of the disease was 34.7 years and length of expanded CAG repeat was 66. Mean ICARS scores at baseline was 37.6 and at follow-up was 42.7 (P < 0.001). Multivariate analysis did not find significant association of progression of disease and age...
Trabalho Final do Mestrado Integrado em Medicina apresentado à Faculdade de MedicinaSpinocerebellar ...
Previous imaging studies in the Machado-Joseph disease (MJD/SCA3) have mostly concentrated on the ce...
Machado-Joseph disease (MJD) is an autosomal dominant hereditary ataxia reported in the Portuguese d...
Abstract Machado-Joseph Disease (MJD), also known as spinocerebellar ataxia type 3 (SCA3), represent...
Machado-Joseph disease, or spinocerebellar ataxia type 3(MJD/SCA3), is the most frequent late onset ...
Machado-Joseph disease or spinocerebellar ataxia 3 (MJD/SCA3) is a clinically heterogeneous, neurode...
Objective: In spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD), the expanded cytosine...
Machado-Joseph disease (MJD)/spinocerebellar ataxia type 3 (SCA3) is the most common autosomal domin...
Machado-Joseph disease (MJD/SCA3) is the most common form of dominantly inherited ataxia worldwide. ...
Recent advances in molecular genetics has clarified the disease locus in the chromosomal mapping, in...
Background: Machado-Joseph disease (MJD) is one of the most common forms of neurodegenerative ataxia...
Spinocerebellar ataxia type 3 or Machado-Joseph disease is the most common spinocerebellar ataxia. i...
OBJECTIVES: To perform a systematic review and meta-analysis of genetic risk factors for age at onse...
Background: Machado-Joseph disease (MJD SCA3), a spinocerebellar ataxia related to expansion of a CA...
Machado-Joseph disease (SCA3/MJD) is the most common spinocerebellar ataxia worldwide, and particula...
Trabalho Final do Mestrado Integrado em Medicina apresentado à Faculdade de MedicinaSpinocerebellar ...
Previous imaging studies in the Machado-Joseph disease (MJD/SCA3) have mostly concentrated on the ce...
Machado-Joseph disease (MJD) is an autosomal dominant hereditary ataxia reported in the Portuguese d...
Abstract Machado-Joseph Disease (MJD), also known as spinocerebellar ataxia type 3 (SCA3), represent...
Machado-Joseph disease, or spinocerebellar ataxia type 3(MJD/SCA3), is the most frequent late onset ...
Machado-Joseph disease or spinocerebellar ataxia 3 (MJD/SCA3) is a clinically heterogeneous, neurode...
Objective: In spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD), the expanded cytosine...
Machado-Joseph disease (MJD)/spinocerebellar ataxia type 3 (SCA3) is the most common autosomal domin...
Machado-Joseph disease (MJD/SCA3) is the most common form of dominantly inherited ataxia worldwide. ...
Recent advances in molecular genetics has clarified the disease locus in the chromosomal mapping, in...
Background: Machado-Joseph disease (MJD) is one of the most common forms of neurodegenerative ataxia...
Spinocerebellar ataxia type 3 or Machado-Joseph disease is the most common spinocerebellar ataxia. i...
OBJECTIVES: To perform a systematic review and meta-analysis of genetic risk factors for age at onse...
Background: Machado-Joseph disease (MJD SCA3), a spinocerebellar ataxia related to expansion of a CA...
Machado-Joseph disease (SCA3/MJD) is the most common spinocerebellar ataxia worldwide, and particula...
Trabalho Final do Mestrado Integrado em Medicina apresentado à Faculdade de MedicinaSpinocerebellar ...
Previous imaging studies in the Machado-Joseph disease (MJD/SCA3) have mostly concentrated on the ce...
Machado-Joseph disease (MJD) is an autosomal dominant hereditary ataxia reported in the Portuguese d...