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Kytövuori, L. (Laura)
58
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Format
Online (58)
Mediatypes
Articles (Online) (23)
OpenAccess-fulltext (35)
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?
1
Clinical spectrum and genotype-phenotype associations in Fi..:
Sipilä, Jussi O.T.
;
Kytövuori, Laura
;
Kaasinen, Valtteri
Journal of the Neurological Sciences. 448 (2023) - p. 120620 , 2023
Link:
https://doi.org/10.1016/..
?
2
A severe neurodegenerative disease with Lewy bodies and a m..:
Sipilä, Jussi O. T.
;
Kytövuori, Laura
;
Rauramaa, Tuomas
...
npj Parkinson's Disease. 9 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1038/..
?
3
Association of biallelic RFC1 expansion with early‐onset Pa..:
Ylikotila, Pauli
;
Sipilä, Jussi
;
Alapirtti, Tiina
...
European Journal of Neurology. 30 (2023) 5 - p. 1256-1261 , 2023
Link:
https://doi.org/10.1111/..
?
4
Biallelic expansion in RFC1 as a rare cause of Parkinson's ..:
Kytövuori, Laura
;
Sipilä, Jussi
;
Doi, Hiroshi
...
npj Parkinson's Disease. 8 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1038/..
?
5
Association between mitochondrial DNA haplogroups J and K, ..:
Kiiskilä, Jukka M.
;
Hassinen, Ilmo E.
;
Kettunen, Johannes
...
BMC Sports Science, Medicine and Rehabilitation. 14 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1186/..
?
6
NDUFA1 p.Gly32Arg variant in early-onset dementia:
Huttula, Samuli
;
Väyrynen, Henri
;
Helisalmi, Seppo
...
Neurobiology of Aging. 114 (2022) - p. 113-116 , 2022
Link:
https://doi.org/10.1016/..
?
7
Cognitive impairment is not uncommon in patients with biall..:
Korpioja, Anita
;
Krüger, Johanna
;
Hurme-Niiranen, Anri
...
Parkinsonism & Related Disorders. 103 (2022) - p. 98-101 , 2022
Link:
https://doi.org/10.1016/..
?
8
Association of mitochondrial DNA haplogroups J and K with l..:
Kiiskilä, Jukka
;
Jokelainen, Jari
;
Kytövuori, Laura
...
BMC Genomics. 22 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1186/..
?
9
Molecular epidemiology of hereditary ataxia in Finland:
Lipponen, Joonas
;
Helisalmi, Seppo
;
Raivo, Joose
...
BMC Neurology. 21 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1186/..
?
10
Mitochondrial DNA Variation in Sudden Cardiac Death: A Popu..:
Kytövuori, Laura
;
Junttila, Juhani
;
Huikuri, Heikki
...
Neurology. 94 (2020) 15_supplement - p. , 2020
Link:
https://doi.org/10.1212/..
?
11
Analysis of functional variants in mitochondrial DNA of Fin..:
Kiiskilä, Jukka
;
Moilanen, Jukka S.
;
Kytövuori, Laura
..
BMC Genomics. 20 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1186/..
?
12
Mitochondrial DNA variation in sudden cardiac death: a popu..:
Kytövuori, Laura
;
Junttila, Juhani
;
Huikuri, Heikki
...
International Journal of Legal Medicine. 134 (2019) 1 - p. 39-44 , 2019
Link:
https://doi.org/10.1007/..
?
13
Finnish Parkinson's disease study integrating protein-prote..:
Siitonen, Ari
;
Kytövuori, Laura
;
Nalls, Mike A.
...
Scientific Reports. 9 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1038/..
?
14
Mutation m.15923A>G in the MT-TT gene causes mild myopathy ..:
Kärppä, Mikko
;
Kytövuori, Laura
;
Saari, Markku
.
BMC Neurology. 18 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1186/..
?
15
Case report: a novel frameshift mutation in the mitochondri..:
Kytövuori, Laura
;
Kärppä, Mikko
;
Tuominen, Hannu
...
BMC Neurology. 17 (2017) 1 - p. , 2017
Link:
https://doi.org/10.1186/..
1-15