Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Elina Hietikko"'
Autor:
Sini, Skarp, Johanna, Korvala, Jouko, Kotimäki, Martti, Sorri, Minna, Männikkö, Elina, Hietikko
Publikováno v:
Genes. 13(6)
The objective was to study the genetic etiology of Ménière's disease (MD) using next-generation sequencing in three families with three cases of MD. Whole exome sequencing was used to identify rare genetic variants co-segregating with MD in Finnish
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f32f59e0ec96e6f5b2e58c2fe179aa81
https://pubmed.ncbi.nlm.nih.gov/35741759
https://pubmed.ncbi.nlm.nih.gov/35741759
The objective was to study the genetic etiology of Ménière’s disease (MD) using next-generation sequencing in three families with three cases of MD. Whole exome sequencing was used to identify rare genetic variants co-segregating with MD in Finni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aabce3ca7825dcc4a92b66fb5e0e4417
http://urn.fi/urn:nbn:fi-fe2023020826354
http://urn.fi/urn:nbn:fi-fe2023020826354
Publikováno v:
Annals of Human Genetics. 83:389-396
The genetic background of Ménière's disease (MD) was studied in one patient with childhood-onset MD and his grandfather affected with middle age-onset MD. Whole-exome sequencing was performed and the data were compared to 76 exomes from unrelated s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc7a6100512c53d52d0cc01f6043f5f1
https://doi.org/10.1111/ahg.12327
https://doi.org/10.1111/ahg.12327
Autor:
Ruth Peters, Elina Hietikko, Minna Koivukangas, Timo E. Strandberg, Riitta Leskinen, Sirkka Keinänen-Kiukaanniemi, Riitta Antikainen
Publikováno v:
The journal of nutrition, healthaging. 25(5)
To study the prevalence of frailty and its relationship to mortality in cohorts born before and after the Second World War using three different frailty measures. Cross-sectional data from two cohorts born in 1935 (n=593) and 1945 (n=714) were studie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f551e2ad14d9d97fbfd5acbc287c8ecc
https://pubmed.ncbi.nlm.nih.gov/33949627
https://pubmed.ncbi.nlm.nih.gov/33949627
Autor:
Hilkka Soininen, Laura Kolehmainen, Satu Havulinna, Riitta Antikainen, Elina Hietikko, Timo E. Strandberg, Jenni Lehtisalo, Jaakko Tuomilehto, Miia Kivipelto, Rainer Rauramaa, Esko Levälahti, Tiia Ngandu, Markku Peltonen, Jenni Kulmala, Auli Polonen, Tiina Laatikainen
Background frailty syndrome is common amongst older people. Low physical activity is part of frailty, but long-term prospective studies investigating leisure-time physical activity (LTPA) during the life course as a predictor of frailty are still war
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38ee1a28d6e5048401e997dd85ad2b42
http://hdl.handle.net/10138/344243
http://hdl.handle.net/10138/344243
Autor:
Eerik Kangasniemi, Elina Hietikko
Publikováno v:
Auris Nasus Larynx. 45:399-406
The role of immunological factors in the pathophysiology of Meniere's disease (MD) has been hypothesized. In order to evaluate the current level of evidence on autoimmunity in MD, original articles relevant to the matter (1970-2016) were reviewed. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b14db3a5df0970d2986f73e526adc5d6
https://doi.org/10.1016/j.anl.2017.07.008
https://doi.org/10.1016/j.anl.2017.07.008
Objective: To study comorbidities and their effect on the disease progression in Meniere’s disease (MD). Methods: Retrospective study on 350 definite MD patients diagnosed according to AAO-HNS 1995 criteria using hospital records and postal questio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3673b3d3001b51eff8e8dc05bd2e830b
Publikováno v:
International Journal of Audiology. 51:841-845
Multiple candidate genes have been presented for Ménière's disease (MD), but to date no positive replications have been reported. We review here all the previously proposed candidate genes for MD and report our results on the analysis of six such g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2306b01daec3f364fe094942873508b
https://doi.org/10.3109/14992027.2012.705900
https://doi.org/10.3109/14992027.2012.705900
Publikováno v:
Genetics in Medicine. 13:415-420
Purpose: To study the inheritance and characteristics of familial Meniere disease in Finland and genetic linkage to the previously proposed locus on chromosome 12p12.3. Methods: Sixteen Meniere families recruited from Kainuu Central Hospital and Hels
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f201dd937ac3ecbd72adc5d334d0bc17
https://doi.org/10.1097/gim.0b013e3182091a41
https://doi.org/10.1097/gim.0b013e3182091a41
Publikováno v:
American journal of audiology. 23(2)
Purpose This study compared clinical features, predisposing factors, and concomitant diseases between sporadic and familial Ménière's disease (MD). Method Retrospective chart review and postal questionnaire were used. Participants were 250 definite
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43a312dc1fc055c966c6d52451718109
https://pubmed.ncbi.nlm.nih.gov/24686733
https://pubmed.ncbi.nlm.nih.gov/24686733