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PedAM

Pediatric Disease Annotations & Medicines




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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