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NDUFA1 p.Gly32Arg variant in early-onset dementia.
Huttula S, Väyrynen H, Helisalmi S, Kytövuori L, Luukkainen L, Hiltunen M, Remes AM, Krüger J. Huttula S, et al. Among authors: hiltunen m. Neurobiol Aging. 2022 Jun;114:113-116. doi: 10.1016/j.neurobiolaging.2021.09.026. Epub 2022 Jan 21. Neurobiol Aging. 2022. PMID: 35131137 Free article.
Identification of a novel 4.6-kb genomic deletion in presenilin-1 gene which results in exclusion of exon 9 in a Finnish early onset Alzheimer's disease family: an Alu core sequence-stimulated recombination?
Hiltunen M, Helisalmi S, Mannermaa A, Alafuzoff I, Koivisto AM, Lehtovirta M, Pirskanen M, Sulkava R, Verkkoniemi A, Soininen H. Hiltunen M, et al. Eur J Hum Genet. 2000 Apr;8(4):259-66. doi: 10.1038/sj.ejhg.5200423. Eur J Hum Genet. 2000. PMID: 10854108
Apolipoprotein E alleles in women with pre-eclampsia.
Makkonen N, Heinonen S, Hiltunen M, Helisalmi S, Mannermaa A, Kirkinen P. Makkonen N, et al. Among authors: hiltunen m. J Clin Pathol. 2001 Aug;54(8):652-4. doi: 10.1136/jcp.54.8.652. J Clin Pathol. 2001. PMID: 11477126 Free PMC article.
389 results