Progressive supranuclear palsy phenotypic presentation associated with anti MA2 antibody
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s13760-023-02358-z.pdf
Reference10 articles.
1. Dalmau J, Graus F, Villarejo A et al (2004) Clinical analysis of antiMa2-associated encephalitis. Brain 127:1831–1844
2. H€oglinger GU, Respondek G, Stamelou M. (2017) Clinical diagnosis of progressive supranuclear palsy: the movement disorder society criteria. Mov Disord 32(6):853–864
3. Morris HR, Osaki Y, Holton J, Lees AJ et al (2003) Tau exon 10 +16 mutation FTDP-17 presenting clinically as sporadic young onset PSP. Neurology 61(1):102–104
4. Jabbari E, Woodside J, Tan MMX et al. (2019) The genetic and clinicopathological profile of early-onset progressive supranuclear palsy. Mov Disord. 34(9):1307–1314.
5. Sankhla CS, Patil KB, Sawant N, Gupta S (2016) Diagnostic accuracy of Magnetic Resonance Parkinsonism Index in differentiating progressive supranuclear palsy from Parkinson’s disease and controls in Indian patients. Neurol India 64(2):239–245
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