Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Jaana, Autere"'
Autor:
Lauri Tulkki, Nicolas Martinez-Majander, Petri Haapalahti, Heli Tolppanen, Juha Sinisalo, Olli Repo, Tomi Sarkanen, Heikki Numminen, Essi Ryödi, Pauli Ylikotila, Risto O. Roine, Riikka Lautamäki, Antti Saraste, Tuuli Miettinen, Jaana Autere, Pekka Jäkälä, Marja Hedman, Juha Huhtakangas, Ulla Junttola, Jukka Putaala, Jani Pirinen
Publikováno v:
Annals of Medicine, Vol 55, Iss 1 (2023)
AbstractBackground In young patients, up to 40% of ischemic strokes remain cryptogenic despite modern-day diagnostic work-up. There are limited data on blood pressure (BP) behavior in these patients. Thus, we aimed to compare ambulatory blood pressur
Externí odkaz:
https://doaj.org/article/eb6eed3159f44586b8bacc158ba79511
Autor:
Salla Ylä-Herttuala, Jaana Autere, Susanna Westeren-Punnonen, Akseli Leino, Anne-Mari Kantanen, Katja Myllymaa, Pekka Jäkälä, Anu Muraja-Murro, Timo Leppänen, Esa Mervaala, Sami Myllymaa, Juha Töyräs
Publikováno v:
Sleep & Breathing = Schlaf & Atmung
Purpose Obstructive sleep apnea (OSA) is associated with increased risk for stroke, which is known to further impair respiratory functions. However, it is unknown whether the type and severity of respiratory events are linked to stroke or transient i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ace9c42dfc14769ef41d3f09f205919e
https://doi.org/10.1007/s11325-019-02010-2
https://doi.org/10.1007/s11325-019-02010-2
Autor:
Kari Majamaa, Pauli Ylikotila, Jaana Autere, Raphael Gibbs, Hilkka Soininen, Mike A. Nalls, Ari Siitonen, Andrew B. Singleton, Pentti J. Tienari, Johanna Eerola-Rautio, Mikko Hiltunen, Susanna Ylönen
Introduction Variation contributing to the risk of Parkinson's disease (PD) has been identified in several genes and at several loci including GBA, SMPD1, LRRK2, POLG1, CHCHD10 and MAPT, but the frequencies of risk variants seem to vary according to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8aaa25c3f022cc2b458394736f2b3fca
http://hdl.handle.net/10138/298404
http://hdl.handle.net/10138/298404
Autor:
Esa Mervaala, Jaana Autere, Anu Muraja-Murro, Anne-Mari Kantanen, Susanna Westeren-Punnonen, Juha Töyräs, Katja Myllymaa, Sami Myllymaa, Pekka Jäkälä
Publikováno v:
Sleep disorders and comorbidities: cardiopulmonary diseases, weight and other.
Obstructive sleep apnea (OSA) increases the risk of TIA and ischemic stroke, and it also worsens strokes rehabilitation outcomes. However, screening of OSA is not routinely performed in TIA or acute stroke. The aims were (i) to study the prevalence a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::293295f5f38cc757c8a7976de2715384
https://doi.org/10.1183/23120541.sleepandbreathing-2017.p79
https://doi.org/10.1183/23120541.sleepandbreathing-2017.p79
Publikováno v:
Journal of Neurology. 260:3144-3149
Parkinson's disease is associated with mitochondrial dysfunction. The POLG1 gene encodes DNA-polymerase γ, which is responsible for the replication of mitochondrial DNA. Mutations in POLG1 cause neurodegenerative diseases such as progressive externa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59b73a02d043febb918ca729d295488d
https://doi.org/10.1007/s00415-013-7132-7
https://doi.org/10.1007/s00415-013-7132-7
Autor:
Eero, Pekkonen, Sari, Atula, Jaana, Autere, Johanna, Eerola-Rautio, Valtteri, Kaasinen, Mikko, Kauppinen, Kirsti, Martikainen, Hanna, Ruottinen, Meri, Viljamaa
Publikováno v:
Duodecim; laaketieteellinen aikakauskirja. 132(1)
The treatment of Parkinson's disease may be initiated with dopamine agonist or MAO-B-inhibitor for people under 60-65 years of age. For older patients, the treatment may also be started with levodopa. If there are motor complications, such as on-off-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::26651c17ea5f9eb64c1bcdb60237ee8c
https://pubmed.ncbi.nlm.nih.gov/27044185
https://pubmed.ncbi.nlm.nih.gov/27044185
Autor:
Päivi Hartikainen, Arto Mannermaa, Jaana Autere, Jukka S. Moilanen, Merja Hallikainen, Hilkka Soininen, Saara Finnilä, Kari Majamaa
Publikováno v:
Human Genetics. 115:29-35
The activity of complex I of the mitochondrial respiratory chain has been found to be decreased in patients with Parkinson’s disease (PD), but no mutations have been identified in genes encoding complex I subunits. Recent studies have suggested tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::725ead2e26097f95402ef992d4ce66f3
https://doi.org/10.1007/s00439-004-1123-9
https://doi.org/10.1007/s00439-004-1123-9
Autor:
Kari Majamaa, Irina Alafuzoff, P. H. Hartikainen, H. Soininen, Arto Mannermaa, Jaana Autere, Pekka Jäkälä, M. Hiltunen
Publikováno v:
European Journal of Neurology. 9:479-483
Two mutations in the alpha-synuclein gene and various mutations in the parkin gene are associated with familial Parkinson's disease (PD). The present study was performed to analyse if mutations in these genes could be detected in Finnish patients wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35e24a943390c527273197ba93eb7fe3
https://doi.org/10.1046/j.1468-1331.2002.00458.x
https://doi.org/10.1046/j.1468-1331.2002.00458.x
Autor:
Maarit Lehtovirta, Päivi Hartikainen, Kari Majamaa, Jaana Autere, Saara Finnilä, Hilkka Soininen, Arto Mannermaa
Publikováno v:
Journal of medical genetics. 38(6)
Editor—Selectively neutral polymorphisms in mitochondrial DNA (mtDNA) have accumulated during human evolution along mtDNA lineages that correlate with ethnic and geographical origin. By contrast, deleterious mutations have arisen repeatedly and occ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ddf80a556cd75d3090ca8e5a0ec7f98
https://pubmed.ncbi.nlm.nih.gov/11424923
https://pubmed.ncbi.nlm.nih.gov/11424923
Publikováno v:
Neurobiology of Aging. 25:S468
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47069717521b6358dce620dc86c2817c
https://doi.org/10.1016/s0197-4580(04)81545-8
https://doi.org/10.1016/s0197-4580(04)81545-8