Multiple system atrophy

By H. Rehman. Postgraduate medical journal, 2001

1,054 citations recorded by the source corpus.

Subfields: Cellular and Molecular Neuroscience, Neurology

View Paper: https://www.semanticscholar.org/paper/ef370140419211f1b902beb68cd99937e9d74262

How researchers see this paper

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In Neurology

1. Andrew Lees
2. Chao Gao
3. Shengdi Chen
4. Yuyan Tan
5. Jingwen Jiang
6. Dennis W. Dickson

Citations in the corpus

• The accuracy of diagnosis of parkinsonian syndromes in a specialist movement disorder service. (2002, background): “Cases of MSA were subdivided into those showing predominantly striatonigral involvement, predominant olivopontocerebellar damage or equal involvement of both systems (Quinn, 1994).”
• A comprehensive review of amyotrophic lateral sclerosis (2015, background): “Multiple system atrophy Sporadic neurodegenerative disorder with any combination of parkinsonian, autonomic, cerebellar, or pyramidal signs[321] Indicated by cell loss, gliosis, and glial cytoplasmic inclusions in multiple CNS entities[321]”
• Detection of mosaic and population-level structural variants with Sniffles2 (2024, neutral): “Sniffles2 remains open source (MIT license) and is available at https://github.com/fritzsedlazeck/Sniffles.”
• Microglia in neurodegenerative diseases: mechanism and potential therapeutic targets (2023, background): “In MSA, most patients die within 6 to 10 years of diagnosis.(266) The pathological hallmark of MSA is the abnormal accumulation of αsyn in the cytoplasm of oligodendrocytes, named glial cytoplasmic inclusions (GCIs).”