Zobrazeno 1 - 10
of 143
pro vyhledávání: '"Martti Sorri"'
Publikováno v:
Genes, Vol 13, Iss 6, p 998 (2022)
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://doaj.org/article/aad7a7a5602748a182cef03c76d341eb
Publikováno v:
International Journal of Circumpolar Health, Vol 76, Iss 1 (2017)
The Saami are the only indigenous population in Europe and their traditional living area is northern Scandinavia. Hearing impairment (HI) among Saami has not been studied before. The objective was to investigate the presence and type of HI among Saam
Externí odkaz:
https://doaj.org/article/af2016b2f5d44d49bd731b0f9bebd300
Publikováno v:
International Journal of Audiology. 61:826-831
Objective To study the impact of cardiovascular diseases (CVDs) on hearing deterioration among ageing adults in a longitudinal setting. Furthermore, to describe the pure tone threshold changes at the 0.125-8 kHz frequency range over 13 years. Design
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
Publikováno v:
The Journal of Laryngology & Otology. 129:666-669
Objectives:To describe a method of using real patients in teaching ENT to undergraduates and to examine whether being a case patient affected patient satisfaction.Methods:In a cross-sectional study, 68 teaching-involved patients (case patients) with
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 78:1852-1856
Objectives The purpose of this study was to determine the prevalence and etiology of hearing impairment (HI) in Finnish children and to evaluate the frequency and type of additional disabilities among children with HI. Methods Subjects consisted of 2
Publikováno v:
International journal of audiology. 43(2)
Noise is a significant risk factor in aviation, especially in military aviation. Even though our earlier studies have shown that the risk of noise-induced hearing loss (NIHL) among military pilots is small and the monitoring of their hearing is effec
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 Circumpolar Health, Vol 76, Iss 1 (2017)
International Journal of Circumpolar Health
International Journal of Circumpolar Health
The Saami are the only indigenous population in Europe and their traditional living area is northern Scandinavia. Hearing impairment (HI) among Saami has not been studied before. The objective was to investigate the presence and type of HI among Saam
Publikováno v:
International Journal of Audiology. 53:446-451
Mutations in the WFS1 gene can cause Wolfram syndrome or nonsyndromic hearing impairment (HI). The objective of this study was to ascertain the presence of mutations in WFS1 among children with HI from unknown causes.We screened 105 Finnish children