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Page 1
ATP8A2-related disorders as recessive cerebellar ataxia.
J Neurol. 2020 Jan;267(1):203-213. doi: 10.1007/s00415-019-09579-4. Epub 2019 Oct 14.
J Neurol. 2020.
PMID: 31612321
Free article.
A novel missense variant in ATP11C is associated with reduced red blood cell phosphatidylserine flippase activity and mild hereditary hemolytic anemia.
van Dijk MJ, van Oirschot BA, Harrison AN, Recktenwald SM, Qiao M, Stommen A, Cloos AS, Vanderroost J, Terrasi R, Dey K, Bos J, Rab MAE, Bogdanova A, Minetti G, Muccioli GG, Tyteca D, Egée S, Kaestner L, Molday RS, van Beers EJ, van Wijk R.
van Dijk MJ, et al. Among authors: harrison an.
Am J Hematol. 2023 Dec;98(12):1877-1887. doi: 10.1002/ajh.27088. Epub 2023 Sep 6.
Am J Hematol. 2023.
PMID: 37671681
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Novel variants in critical domains of ATP8A2 and expansion of clinical spectrum.
Heidari E, Harrison AN, Jafarinia E, Tavasoli AR, Almadani N, Molday RS, Garshasbi M.
Heidari E, et al. Among authors: harrison an.
Hum Mutat. 2021 May;42(5):491-497. doi: 10.1002/humu.24180. Epub 2021 Mar 14.
Hum Mutat. 2021.
PMID: 33565221
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The Combination of IFN β and TNF Induces an Antiviral and Immunoregulatory Program via Non-Canonical Pathways Involving STAT2 and IRF9.
Mariani MK, Dasmeh P, Fortin A, Caron E, Kalamujic M, Harrison AN, Hotea DI, Kasumba DM, Cervantes-Ortiz SL, Mukawera E, Serohijos AWR, Grandvaux N.
Mariani MK, et al. Among authors: harrison an.
Cells. 2019 Aug 17;8(8):919. doi: 10.3390/cells8080919.
Cells. 2019.
PMID: 31426476
Free PMC article.
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