PedAM
Pediatric Disease Annotations & Medicines
| Disease | multiple system atrophy |
| Phenotype | C0007758|cerebellar ataxia |
| Sentences | 7 |
| 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. |
| PubMedID- 22209432 | Conclusions: the "hot cross bun" sign considered diagnostic for multiple system atrophy with predominant cerebellar ataxia is significantly better visualised on proton density-weighted imaging than on t2-weighted imaging at 3t. |
| PubMedID- 26477028 | Characteristic diffusion tensor tractography in multiple system atrophy with predominant cerebellar ataxia and cortical cerebellar atrophy. |
| 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 | The cerebellar glucose metabolism of multiple system atrophy with predominant cerebellar ataxia (msa-c) is known to be decreased but is not defined among areas of cerebellum. |
| PubMedID- 24868404 | Background and purpose: multiple system atrophy with predominant cerebellar ataxia is a disabling neurologic disease. |
| PubMedID- 25785588 | Msa-c = multiple system atrophy with predominant cerebellar ataxia. |
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