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</script>The past year has seen advances in delineating the clinical features, natural history and imaging characteristics of multiple system atrophy. The initiating pathogenetic mechanisms remain unknown. However, any aetiological or pathophysiological hypothesis must consider not only neuronal loss and gliosis but also the recently described characteristic oligodendrolial cytoplasmic inclusions.
Diagnostic Imaging, Inclusion Bodies, Neurologic Examination, Brain, Shy-Drager Syndrome, Corpus Striatum, Diagnosis, Differential, Substantia Nigra, Oligodendroglia, Autonomic Nervous System Diseases, Cerebellar Diseases, Nerve Degeneration, Olivopontocerebellar Atrophies, Humans, Atrophy, Nervous System Diseases
Diagnostic Imaging, Inclusion Bodies, Neurologic Examination, Brain, Shy-Drager Syndrome, Corpus Striatum, Diagnosis, Differential, Substantia Nigra, Oligodendroglia, Autonomic Nervous System Diseases, Cerebellar Diseases, Nerve Degeneration, Olivopontocerebellar Atrophies, Humans, Atrophy, Nervous System Diseases
| citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 35 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
