Recent Publications on Machado-Joseph Disease: |  |
Analysis of segregation patterns in Machado-Joseph disease pedigrees.
Machado-Joseph disease (MJD), also known as spinocerebellar ataxia type 3...
Direct Link | 9th August, 2008
| Center of Research in Natural Resources (CIRN) and Department of Biology,
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Striatal and nigral pathology in a lentiviral rat model of Machado-Joseph disease.
Machado-Joseph disease (MJD) is a fatal, dominant neurodegenerative...
Direct Link | 8th August, 2008
| Center for Neurosciences and Cell Biology, University of Coimbra, Coimbra,
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| [The advances in research on phosphorylation of polyglutamine disease.]
| 7th August, 2008
| Department of Neurology, Xiangya Hospital, Central South University,
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| PolyQ-expanded ataxin-3 interacts with full-length ataxin-3 in a polyQ length-dependent manner.
| 1st August, 2008
| Laboratory of Molecular Neuropathology, Hefei National Laboratory for
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Polyglutamine-expanded ataxin-3 causes cerebellar dysfunction of SCA3 transgenic mice by inducing transcriptional dysregulation.
In the present study, we prepared a SCA3 animal model by generating...
Direct Link | 30th July, 2008
| Department of Anesthesiology, Chang Gung Memorial Hospital, Kwei-San,
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Movement-related cortical potentials in patients with Machado-Joseph disease.
OBJECTIVE: Movement-related cortical potentials (MRCP; nomenclature of...
Direct Link | 17th July, 2008
| Neuroscience Laboratory, Department of Neurology, China Medical University
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Homozygosity enhances severity in spinocerebellar ataxia type 3.
Spinocerebellar ataxia type 3, or Machado-Joseph disease, is an autosomal...
Direct Link | 11th July, 2008
| Genetic Unit, Sarah Network of Rehabilitation Hospitals, Brasilia, DF,
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Segregation distortion of wild-type alleles at the Machado-Joseph disease locus: a study in normal families from the Azores islands (Portugal).
Machado-Joseph disease (MJD) is caused by an expansion of a triplet repeat...
Direct Link | 18th June, 2008
| Department of Biology/CIRN, University of the Azores, Rua Mae de Deus,
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New insights into the pathoanatomy of spinocerebellar ataxia type 3 (Machado-Joseph disease).
PURPOSE OF REVIEW: This review summarizes recent neuropathological...
Direct Link | 14th June, 2008
| Institute for Clinical Neuroanatomy, J. W. Goethe-University, D-60590
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cDNA cloning and tissue expression analyses of the encoding regions for three novel porcine genes- MJD1, CDC42 and NECD.
The cDNAs for Machado-Joseph disease protein 1 homolog (MJD1), cell...
Direct Link | 13th June, 2008
| Key Laboratory of Animal Nutrition and Feed of Yunnan Province, Yunnan
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Fatigue and daytime somnolence in Machado Joseph Disease (spinocerebellar ataxia type 3).
Objective Machado-Joseph disease (MJD), also known as spinocerebellar...
Direct Link | 3rd June, 2008
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Cognitive and social cognitive functioning in spinocerebellar ataxia : a preliminary characterization.
INTRODUCTION : The spinocerebellar ataxias (SCAs), are rare...
Direct Link | 29th May, 2008
| Institute of Cognitive Neuroscience, 17 Queen Square, London, WC1N 3AR,
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Muscle excitability abnormalities in Machado-Joseph disease.
OBJECTIVES: To estimate the frequency of and to characterize muscle...
Direct Link | 22nd May, 2008
| Department of Neurology, University of Campinas, Campinas, Sao Paulo,
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Axonal Dysfunction in the Deep White Matter in Machado-Joseph Disease.
We evaluated spectroscopy findings at the deep white matter in...
Direct Link | 17th May, 2008
| Neuroimaging Laboratory, Universidade Estadual de Campinas-UNICAMP,
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A neurological examination score for the assessment of spinocerebellar ataxia 3 (SCA3).
Spinocerebellar ataxias (SCAs) are characterized by a heterogeneous set of...
Direct Link | 8th May, 2008
| Medical Genetics Service, Hospital de Clinicas de Porto Alegre, Porto
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