Disease | cerebellar ataxia |
Phenotype | C0393571|multiple system atrophy |
Sentences | 7 |
PubMedID- 24868404 | multiple system atrophy with predominant cerebellar ataxia (msa-c) is an adult-onset, sporadic, progressive neurodegenerative disease characterized by prominent cerebellar ataxia with varying severity of autonomic failure, urogenital dysfunction, parkinsonian features and corticospinal disorders.1 msa can reduce perceived quality of life,2 but no cure or protection is currently available. |
PubMedID- 22209432 | Objective: to investigate whether proton density-weighted imaging can detect the "hot cross bun" sign in the pons in multiple system atrophy with predominant cerebellar ataxia significantly better than t2-weighted imaging at 3t. |
PubMedID- 26350408 | Is multiple system atrophy with cerebellar ataxia (msa-c) like spinocerebellar ataxia and multiple system atrophy with parkinsonism (msa-p) like parkinson's disease. |
PubMedID- 24868383 | Preserved glucose metabolism of deep cerebellar nuclei in a case of multiple system atrophy with predominant cerebellar ataxia: f-18 fluorodeoxyglucose positron emission tomography study. |
PubMedID- 26477028 | Characteristic diffusion tensor tractography in multiple system atrophy with predominant cerebellar ataxia and cortical cerebellar atrophy. |
PubMedID- 25785588 | Msa-c = multiple system atrophy with predominant cerebellar ataxia. |
PubMedID- 22073234 | A, b, c, aa, bb, cc, amyotrophic lateral sclerosis; d, e, f, dd, ee, ff, pantothenate kinase-associated neurodegeneration; g, h, i, gg, hh, ii, multiple system atrophy with cerebellar ataxia; j, k, l, jj, kk, ll, progressive supranuclear palsy; m, n, o, mm, nn, oo, parkinson disease with dementia. |
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