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Malignant lymphoma presenting as bilateral sensorineural hearing loss-A case report

Referentgranskad
Öppen tillgång
DOI
10.1002/ccr3.6711
Raunio, Frida; Kelppe, Jetta; Hafren, Lena
Clinical case reports2022Publicationer information ikon

Auditory pathway plasticity in adult humans after unilateral idiopathic sudden sensorineural hearing loss

Referentgranskad
Vasama, J.
Hearing Research1995Publicationer information ikon

Effects of social distancing on the incidence of Bell's palsy and sudden sensorineural hearing loss

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DOI
10.1080/00016489.2021.2025425
Hafren, Lena; Saarinen, Riitta; Lundberg, Marie
Acta oto-laryngologica2022Publicationer information ikon

Clinical and genetic characterisation of childhood-onset sensorineural hearing loss reveal associated phenotypes and enrichment of pathogenic founder mutations in the Finnish population

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DOI
10.1080/14992027.2024.2402840
Kraatari-Tiri, Minna; Pykälainen, Tyrni; Pohjola, Pia; Häkli, Sanna; Rahikkala, Elisa
International journal of audiology2024Publicationer information ikon

Association of multiple sclerosis and sudden sensorineural hearing loss

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Öppen tillgång
DOI
10.1177/2055217316652155
Atula, S.; Sinkkonen, S. T.; Saat, R.; Sairanen, T.; Atula, T.
Multiple sclerosis2016Publicationer information ikon

Quality of Life and Hearing Eight Years After Sudden Sensorineural Hearing Loss

Referentgranskad
DOI
10.1002/lary.26133
Härkönen, Kati;Härkönen, Kati;Kivekäs, Ilkka;Kivekäs, Ilkka;Rautiainen, Markus;Rautiainen, Markus;Ko...
laryngoscope2017Publicationer information ikon

Mitochondrial DNA sequence variation in patients with sensorineural hearing impairment and in the Finnish population

Lehtonen, Mervi
Acta Universitatis Ouluensis. Series D, Medica2002Publicationer information ikon

WFS1 variants in Finnish patients with diabetes mellitus, sensorineural hearing impairment or optic atrophy, and in suicide victims

Referentgranskad
DOI
10.1038/jhg.2013.29
Kytövuori, Laura; Seppänen, Allan; Martikainen, Mika H; Moilanen, Jukka S; Kamppari, Seija; Särkioja...
Journal of human genetics2013Publicationer information ikon

WFS1 variants in Finnish patients with diabetes mellitus, sensorineural hearing impairment or optic atrophy, and in suicide victims

Referentgranskad
DOI
10.1038/jhg.2013.29
Kytövuori, Laura; Seppänen, Allan; Martikainen, Mika H; Moilanen, Jukka S; Kamppari, Seija; Särkioja...
Journal of human genetics2013Publicationer information ikon

Homozygous M34T mutation of the GJB2 gene associates with an autosomal recessive nonsyndromic sensorineural hearing impairment in Finnish families

Referentgranskad
Öppen tillgång
DOI
10.3109/00016489.2012.669498
Lopponen, Tuija; Dietz, Aarno; Vaisanen, Marja-Leena; Valtonen, Hannu; Kosunen, Ari; Hyvarinen, Antt...
Acta oto-laryngologica2012

Malignant lymphoma presenting as bilateral sensorineural hearing loss-A case report

Referentgranskad
Öppen tillgång
DOI
10.1002/ccr3.6711
2022

Auditory pathway plasticity in adult humans after unilateral idiopathic sudden sensorineural hearing loss

Referentgranskad
1995

Effects of social distancing on the incidence of Bell's palsy and sudden sensorineural hearing loss

Referentgranskad
Öppen tillgång
DOI
10.1080/00016489.2021.2025425
2022

Clinical and genetic characterisation of childhood-onset sensorineural hearing loss reveal associated phenotypes and enrichment of pathogenic founder mutations in the Finnish population

Referentgranskad
Öppen tillgång
DOI
10.1080/14992027.2024.2402840
2024

Association of multiple sclerosis and sudden sensorineural hearing loss

Referentgranskad
Öppen tillgång
DOI
10.1177/2055217316652155
2016

Quality of Life and Hearing Eight Years After Sudden Sensorineural Hearing Loss

Referentgranskad
DOI
10.1002/lary.26133
2017

Mitochondrial DNA sequence variation in patients with sensorineural hearing impairment and in the Finnish population

2002

WFS1 variants in Finnish patients with diabetes mellitus, sensorineural hearing impairment or optic atrophy, and in suicide victims

Referentgranskad
DOI
10.1038/jhg.2013.29
2013

WFS1 variants in Finnish patients with diabetes mellitus, sensorineural hearing impairment or optic atrophy, and in suicide victims

Referentgranskad
DOI
10.1038/jhg.2013.29
2013

Homozygous M34T mutation of the GJB2 gene associates with an autosomal recessive nonsyndromic sensorineural hearing impairment in Finnish families

Referentgranskad
Öppen tillgång
DOI
10.3109/00016489.2012.669498
2012