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Laura kytövuori

WebAU - Kytövuori, Laura. N1 - Funding Information: This study was funded in part by grants from the Sigrid Jusélius Foundation, the Terttu Foundation, the Yrjö Jahnsson Foundation and the Finnish Parkinson Foundation and from the Japan Agency for Medical Research and Development (AMED) (grant numbers JP22ek0109486, JP22ek0109549, … Web29 Oct 2024 · We have previously reported on paucity of mitochondrial DNA (mtDNA) haplogroups J and K among Finnish endurance athletes. Here we aimed to further …

A Systems-Level Investigation of the Genetic and Phenotypic ...

Web11 Dec 2024 · Laura Kytövuori 1Research Unit of Clinical Neuroscience, University of Oulu, Oulu, Finland 2Department of Neurology and Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland Find … Web10 Jan 2024 · Laura Kytövuori Medicine, Biology BMC Neurology 2024 TLDR Results suggest that analysis of RFC1 should be included in the routine diagnostics of idiopathic … raw denim stan smith https://ardingassociates.com

Finnish Parkinson’s disease study integrating protein …

Web1 Dec 2024 · In 2016, Laura Kytövuori et al. described a novel heteroplasmic mutation m.8561C>G in the overlapping region of MT-ATP6 and MT-ATP8 in two adults siblings presenting with cerebellar ataxia, peripheral neuropathy, diabetes mellitus and hypergonadotropic hypogonadism . Here, we report a novel C>T substitution at the same … Web10 Jan 2024 · Published: 10 January 2024 Biallelic expansion in RFC1 as a rare cause of Parkinson’s disease Laura Kytövuori, Jussi Sipilä, Hiroshi Doi, Anri Hurme-Niiranen, Ari … Web2 Oct 2024 · 4 Department of Neurology and Stroke Medicine, Yokohama City University Graduate School of Medicine, Yokohama, Japan. 5 Research Unit of Clinical Neuroscience, Medical Research Center Oulu, Oulu University Hospital and University of Oulu, P.O. Box 5000, 90014, Oulu, Finland. [email protected]. simple contact information form

Biallelic expansion in RFC1 as a rare cause of …

Category:Mitochondrial DNA variation in sudden cardiac death: a ... - Springer

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Laura kytövuori

JNS Vol 448 May 2024

Web25 Aug 2024 · Väittelijä Filosofian maisteri Laura Kytövuori Tiedekunta ja yksikkö Oulun yliopiston tutkijakoulu, Lääketieteellinen tiedekunta, Neurotieteen tutkimusyksikkö … Web31 May 2024 · Europe PMC is an archive of life sciences journal literature.

Laura kytövuori

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Web1 Jun 2024 · Sources of financial support related to the manuscript being submitted: Samuli Huttula: The University of Oulu Scholarship Foundation and Orion Research Foundation; Seppo Helisalmi: Academy of Finland, grant number 325022; Laura Kytövuori: Sigrid Jusélius Foundation and Medical Research Center Oulu; Laura Luukkainen: The … WebLaura Kytövuori, Research Unit of Clinical Medicine, University of Oulu, P.O. Box 5000, Oulu 90014, Finland. Email: [email protected] Funding information Sigrid Jusélius …

WebGenetic causes and risk factors associated with phenotypes occurring in mitochondrial disorders by: Kytövuori, L. (Laura) Published: (2024) Identification of Mutations That … Web19 Nov 2024 · Laura Kytövuori Research Unit of Clinical Neuroscience University of Oulu Oulu Finland. Author profile Search articles by ORCID 0000-0003-2790-5646 Kytövuori L1, Maria Gardberg Department of Pathology University of Turku and Turku University Hospital Turku Finland. Search articles by 'Maria Gardberg' Gardberg M2,

WebKytövuori, Laura, Geneettiset syyt ja riskitekijät mitokondriotaudeissa yleisesti esiintyvien oireiden taustalla. Oulun yliopiston tutkijakoulu; Oulun yliopisto, Lääketieteellinen … WebResults. A genetic cause of ataxia was found in 33 patients (34.4%). Seven patients had a dominantly inherited repeat expansion in ATXN8/OS.Ten patients had mitochondrial ataxia resulting from mutations in nuclear mitochondrial genes POLG or RARS2, or from a point mutation m.8561C > G or a single deletion in mtDNA.Interestingly, five patients were …

WebTiedustelut Kliinisen tutkimuksen keskus, Neurologia, p. 050-3502485. Asiantuntijat geneetikko Laura Kytövuori: laura.kytovuori oulu.fi / 0404145083 ja neurologian professori Kari Majamaa: kari.majamaa oulu.fi / 08 3154519. Näyteastia Kierrekorkillinen putki. Näyte NÄYTE: Peini lihasbiopsia otetaan tyhjään putkeen ja jäädytetään mahdollisimman …

Web27 Jan 2024 · Background and Purpose. The biallelic repeat expansion (AAGGG) exp in the replication factor C subunit 1 gene (RFC1) is a frequent cause of cerebellar ataxia, … simple contact form templateWebLaura Kytövuori; M. Juhani Junttila; Heikki V. Huikuri; Sirkka Keinänen-Kiukaanniemi; Kari Majamaa; Mika H. Martikainen; International Journal of Legal Medicine. Published on 01 Jan 2024. 0 views XX downloads; XX citations; Home Monitoring of Heart Rate as a Predictor of Imminent Cardiovascular Events. raw denim stretch calvesWebLaura Kytovuori Introduction The biallelic repeat expansion (AAGGG)exp in RFC1 causes cerebellar ataxia, neuropathy, and vestibular areflexia syndrome (CANVAS). Recently, cognitive impairment has... raw denim unwashed pimpleshttp://oyslab.saitti.net/ohjekirja/11416.html simple contemporary dining table setsWeb2 Oct 2024 · Correspondence to Laura Kytövuori. Ethics declarations. Ethics approval and consent to participate. The study protocol was approved by the Oulu University Hospital … raw denim with sneakersWebAnita Korpioja, Johanna Krüger, Anri Hurme-Niiranen, Eino Solje, Kasper Katisko, Joonas Lipponen, Maria Lehtilahti, Anne M. Remes, Kari Majamaa, Laura Kytövuori Research … simple contemporary bedroomWeb5 Nov 2024 · Opettaja Niko Ruuskanen opastaa Haukiputaan lukion oppilaita kemian harjoitustyössä. Kuva: Marko Väänänen / Yle. Niko Ruuskanen ideoi Haukiputaan lukion … simple contemporary bathroom