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DNA polymerase gamma variants and hepatotoxicity during maintenance therapy of childhood acute lymphoblastic leukemia: is there a causal relationship?
Pharmacogenomics J. 2023 Sep;23(5):105-111. doi: 10.1038/s41397-023-00303-0. Epub 2023 May 3.
Pharmacogenomics J. 2023.
PMID: 37138020
Free PMC article.
Association of biallelic RFC1 expansion with early-onset Parkinson's disease.
Ylikotila P, Sipilä J, Alapirtti T, Ahmasalo R, Koshimizu E, Miyatake S, Hurme-Niiranen A, Siitonen A, Doi H, Tanaka F, Matsumoto N, Majamaa K, Kytövuori L.
Ylikotila P, et al. Among authors: hurme niiranen a.
Eur J Neurol. 2023 May;30(5):1256-1261. doi: 10.1111/ene.15717. Epub 2023 Feb 12.
Eur J Neurol. 2023.
PMID: 36705320
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Cognitive impairment is not uncommon in patients with biallelic RFC1 AAGGG repeat expansion, but the expansion is rare in patients with cognitive disease.
Korpioja A, Krüger J, Hurme-Niiranen A, Solje E, Katisko K, Lipponen J, Lehtilahti M, Remes AM, Majamaa K, Kytövuori L.
Korpioja A, et al. Among authors: hurme niiranen a.
Parkinsonism Relat Disord. 2022 Oct;103:98-101. doi: 10.1016/j.parkreldis.2022.08.034. Epub 2022 Sep 6.
Parkinsonism Relat Disord. 2022.
PMID: 36088850
Free article.
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Biallelic expansion in RFC1 as a rare cause of Parkinson's disease.
Kytövuori L, Sipilä J, Doi H, Hurme-Niiranen A, Siitonen A, Koshimizu E, Miyatake S, Matsumoto N, Tanaka F, Majamaa K.
Kytövuori L, et al. Among authors: hurme niiranen a.
NPJ Parkinsons Dis. 2022 Jan 10;8(1):6. doi: 10.1038/s41531-021-00275-7.
NPJ Parkinsons Dis. 2022.
PMID: 35013364
Free PMC article.
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Novel non-neutral mitochondrial DNA mutations found in childhood acute lymphoblastic leukemia.
Järviaho T, Hurme-Niiranen A, Soini HK, Niinimäki R, Möttönen M, Savolainen ER, Hinttala R, Harila-Saari A, Uusimaa J.
Järviaho T, et al. Among authors: hurme niiranen a.
Clin Genet. 2018 Feb;93(2):275-285. doi: 10.1111/cge.13100. Epub 2017 Dec 20.
Clin Genet. 2018.
PMID: 28708239
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