E-LIB Suche - Ergebnisse für: Laura Kytövuori

1

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

2

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/..

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

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/..

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

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/..

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

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/..

12

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/..

13

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/..

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/..