Click the Why column to see why an item matched the search.
| Match | Type | Why |
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| Spinocerebellar ataxia type 8: molecular genetic comparisons and haplotype analysis of 37 families with ataxia. | Academic Article |
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| Sensory ataxia and cardiac hypertrophy caused by neurovascular oxidative stress in chemogenetic transgenic mouse lines. | Academic Article |
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| Psychosis in Spinocerebellar Ataxias: a Case Series and Study of Tyrosine Hydroxylase in Substantia Nigra. | Academic Article |
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| Knee Stability and Movement Coordination Impairments: Knee Ligament Sprain Revision 2017. | Academic Article |
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| Protein kinase C gamma, a protein causative for dominant ataxia, negatively regulates nuclear import of recessive-ataxia-related aprataxin. | Academic Article |
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| A novel AFG3L2 mutation in a Somalian patient with spinocerebellar ataxia type 28. | Academic Article |
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| Fragile X carrier screening and spinocerebellar ataxia in older males. | Academic Article |
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| Acute Ataxia in Children: A Review of the Differential Diagnosis and Evaluation in the Emergency Department. | Academic Article |
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| Multi-omic profiling reveals the ataxia protein sacsin is required for integrin trafficking and synaptic organization. | Academic Article |
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| Treatment with a catalytic antioxidant corrects the neurobehavioral defect in ataxia-telangiectasia mice. | Academic Article |
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| Abnormal processing of transfected plasmid DNA in cells from patients with ataxia telangiectasia. | Academic Article |
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| Ataxia after pontine stroke: insights from pontocerebellar fibers in monkey. | Academic Article |
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| Ataxia and vision loss: flow cytometric diagnosis of primary central nervous system lymphoma. | Academic Article |
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| Ataxia without telangiectasia. | Academic Article |
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| Ataxia, dementia, and hypogonadotropism caused by disordered ubiquitination. | Academic Article |
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