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Striatal DAT SPECT: Caveat Emptor!
Perlmutter JS, Stoessl AJ. Perlmutter JS, et al. Among authors: stoessl aj. Mov Disord. 2019 Oct;34(10):1430-1432. doi: 10.1002/mds.27811. Mov Disord. 2019. PMID: 31769089 No abstract available.
Cerebral metabolism of glucose in benign hereditary chorea.
Suchowersky O, Hayden MR, Martin WR, Stoessl AJ, Hildebrand AM, Pate BD. Suchowersky O, et al. Among authors: stoessl aj. Mov Disord. 1986;1(1):33-44. doi: 10.1002/mds.870010105. Mov Disord. 1986. PMID: 2973557
In vivo dopaminergic and serotonergic dysfunction in DCTN1 gene mutation carriers.
Felicio AC, Dinelle K, Agarwal PA, McKenzie J, Heffernan N, Road JD, Appel-Cresswell S, Wszolek ZK, Farrer MJ, Schulzer M, Sossi V, Stoessl AJ. Felicio AC, et al. Among authors: stoessl aj. Mov Disord. 2014 Aug;29(9):1197-201. doi: 10.1002/mds.25893. Epub 2014 May 5. Mov Disord. 2014. PMID: 24797316 Free PMC article.
DAT-SPECT diagnoses dopamine depletion, but not PD.
Stoessl AJ, Halliday GM. Stoessl AJ, et al. Mov Disord. 2014 Dec;29(14):1705-6. doi: 10.1002/mds.26000. Epub 2014 Aug 22. Mov Disord. 2014. PMID: 25154601 No abstract available.
DNAJC13 genetic variants in parkinsonism.
Gustavsson EK, Trinh J, Guella I, Vilariño-Güell C, Appel-Cresswell S, Stoessl AJ, Tsui JK, McKeown M, Rajput A, Rajput AH, Aasly JO, Farrer MJ. Gustavsson EK, et al. Among authors: stoessl aj. Mov Disord. 2015 Feb;30(2):273-8. doi: 10.1002/mds.26064. Epub 2014 Nov 12. Mov Disord. 2015. PMID: 25393719
289 results