Machado–Joseph disease (MJD), also known as Machado–Joseph Azorean disease, Machado's disease, Joseph's disease or spinocerebellar ataxia type 3 (SCA3)...
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Rheobase (section Machado–Joseph disease)
neurological pathologies, including diabetic neuropathy, CIDP, Machado–Joseph disease, and ALS. The strength-duration time constant (chronaxie) and rheobase...
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Groote Eylandt (section Machado-Joseph Disease (MJD))
Coolsteerdt. However, the relative prevalence of the hereditary Machado-Joseph Disease (MJD) in the Groote Eylandt community (a condition otherwise mainly...
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Spinocerebellar ataxia (category Rare diseases)
GeneTests sca3 at NIH/UW GeneTests Spinocerebellar Ataxias including Machado-Joseph Disease at NINDS sca6 at NIH/UW GeneTests sca7 at NIH/UW GeneTests sca8...
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MJD may refer to: Modified Julian Date, see Julian day § Variants Machado–Joseph disease Maurice Jones-Drew, former NFL running back Mizo Janata Dal, an...
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Ataxin-3 is a protein that in humans is encoded by the ATXN3 gene. Machado–Joseph disease, also known as spinocerebellar ataxia-3, is an autosomal dominant...
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R S T U V W X Y Z This list contains acronyms and initials related to diseases (infectious or non-infectious) and medical disorders. Acronyms in healthcare...
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ataxia (such as the hereditary spinocerebellar ataxia known as Machado–Joseph disease) and multiple system atrophy (MSA), with which it is primarily associated...
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Chromosome 14 (section Diseases and disorders)
AHNAK2: encoding protein Ahnak nucleoprotein 2 ATXN3: Ataxin-3 (Machado-Joseph disease) BCL2L2: encoding the anti-apoptotic protein Bcl-w of the Bcl-2...
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disease is named after a patient, examples being Lou Gehrig disease, Hartnup disease, and Mortimer disease. In one instance, Machado–Joseph disease,...
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viral cerebellar ataxia Gerstmann–Sträussler–Scheinker syndrome Machado–Joseph disease Microcephaly N-acetylaspartate deficiency Neuhauser–Eichner–Opitz...
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across Australia from Sydney Cove. The prevalence of the hereditary Machado–Joseph disease in the Groote Eylandt community has been attributed to outside contact...
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spinocerebellar ataxia type 1 ( trinucleotide expansion in the SCA1gene), Machado-Joseph disease ( trinucleotide expansion in the SCA3 gene), myotonic dystrophy...
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spinal stenosis Lupus erythematosus – neurological sequelae Lyme disease Machado–Joseph disease Macrencephaly Macrocephalia Macropsia Mal de debarquement Megalencephalic...
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Cerebellum (redirect from Cerebellar diseases)
cerebellum may be absent. The inherited neurological disorders Machado–Joseph disease, ataxia telangiectasia, and Friedreich's ataxia cause progressive...
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multi-ubiquitin binding subunit of the 26S proteasome. Vertebrate Machado-Joseph disease protein 1 (Ataxin-3), which acts as a histone-binding protein that...
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2015), amyloid lateral sclerosis (ALS) (Schwarz et al. 2006), and Machado–Joseph disease (Alves et al. 2008). Their therapeutic potential has also been assessed...
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The genetic presence of Machado–Joseph disease in 4 families is thought to derive from a Makassar ancestor who carried the disease. Several Macassan words...
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Trinucleotide repeat disorder (redirect from Polyglutamine disease)
trinucleotide repeat disorders, a subset of microsatellite expansion diseases (also known as repeat expansion disorders), are a set of over 30 genetic...
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PMID 26613986. Schmidt J, Schmidt T (2018). "Animal Models of Machado-Joseph Disease". Polyglutamine Disorders. Advances in Experimental Medicine and...
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combinatorial approach to identify calpain cleavage sites in the Machado-Joseph disease protein ataxin-3". Brain. 140 (5): 1280–1299. doi:10.1093/brain/awx039...
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Guilherme Karan (category Deaths from neurodegenerative disease)
since the time of the assault Karam began to manifest symptoms of Machado-Joseph disease, a degenerative syndrome, also known as spinocerebellar ataxia type...
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dehydrogenase deficiency and Gilbert's Syndrome Glycogen storage disease type III Machado-Joseph disease 1906 – Henri Moissan, Chemistry 1911 - Tobias Asser, Peace...
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at the University of the Azores, where she conducted her PhD on "Machado-Joseph disease: from genetic variability to clinical heterogeneity". She then trained...
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cause SCA2 with polyglutamine expansion. Ataxin 3, coded by ATXN3. Machado-Joseph disease is caused by polyglutamine expansions in ataxin 3. Ataxin 7, coded...
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with SCA3 being the most common subtype of all of Type 1. SCA3, Machado-Joseph disease, is the most common because the mutation repeats more than 56 times...
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Genetically modified animal (section Disease control)
PMID 26613986. Schmidt J, Schmidt T (2018). "Animal Models of Machado-Joseph Disease". Polyglutamine Disorders. Advances in Experimental Medicine and...
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spinocerebellar ataxia in South Brazil - 66 new cases with Machado-Joseph disease, SCA7, SCA8, or unidentified disease-causing mutations". Journal of Neurology. 248...
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worm model of spinocerebellar ataxia type 3 (also known as SCA3 or Machado-Joseph disease), an orphan disorder. Befiradol also reversed depression-like behavior...
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associated with specific neurodegenerative disorders such as ataxin-3 in Machado–Joseph disease or mSOD1 in amyotrophic lateral sclerosis likely supporting mitochondrial...
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