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Items: 1 to 20 of 143

1.

Hearing impairment is common among Saami adults in Northern Finland.

Lohi V, Ohtonen P, Aikio P, Sorri M, Mäki-Torkko E, Hannula S.

Int J Circumpolar Health. 2017;76(1):1398004. doi: 10.1080/22423982.2017.1398004.

2.

A nonsynonymous mutation in the WFS1 gene in a Finnish family with age-related hearing impairment.

Kytövuori L, Hannula S, Mäki-Torkko E, Sorri M, Majamaa K.

Hear Res. 2017 Nov;355:97-101. doi: 10.1016/j.heares.2017.09.013. Epub 2017 Sep 28.

PMID:
28974383
3.

Concomitant diseases and their effect on disease prognosis in Meniere's disease: diabetes mellitus identified as a negative prognostic factor.

Pieskä T, Kotimäki J, Männikkö M, Sorri M, Hietikko E.

Acta Otolaryngol. 2018 Jan;138(1):36-40. doi: 10.1080/00016489.2017.1373850. Epub 2017 Sep 15.

PMID:
28914106
4.

Use of real patients in teaching ENT diseases to undergraduate students and its effects on patient satisfaction: cross-sectional survey.

Löfgren E, Alikoski S, Hannula S, Sorri M, Alho OP.

J Laryngol Otol. 2015 Jul;129(7):666-9. doi: 10.1017/S0022215115001048. Epub 2015 Jun 5.

PMID:
26044154
5.

Mutations in the two ribosomal RNA genes in mitochondrial DNA among Finnish children with hearing impairment.

Häkli S, Luotonen M, Sorri M, Majamaa K.

BMC Med Genet. 2015 Feb 4;16:3. doi: 10.1186/s12881-015-0145-6.

6.

Hearing impairment among adults: the impact of cardiovascular diseases and cardiovascular risk factors.

Lohi V, Hannula S, Ohtonen P, Sorri M, Mäki-Torkko E.

Int J Audiol. 2015 Apr;54(4):265-73. doi: 10.3109/14992027.2014.974112. Epub 2014 Dec 30.

PMID:
25547009
7.

Childhood hearing impairment in northern Finland, etiology and additional disabilities.

Häkli S, Luotonen M, Bloigu R, Majamaa K, Sorri M.

Int J Pediatr Otorhinolaryngol. 2014 Nov;78(11):1852-6. doi: 10.1016/j.ijporl.2014.08.007. Epub 2014 Aug 17.

PMID:
25193587
8.

Response to Dobie.

Hannula S, Bloigu R, Majamaa K, Sorri M, Mäki-Torkko E.

J Am Acad Audiol. 2014 Apr;25(4):415. No abstract available.

PMID:
25126689
9.

WFS1 mutations in hearing-impaired children.

Häkli S, Kytövuori L, Luotonen M, Sorri M, Majamaa K.

Int J Audiol. 2014 Jul;53(7):446-51. doi: 10.3109/14992027.2014.887230. Epub 2014 Mar 10.

PMID:
24909696
10.
11.

Familial aggregation of pure tone hearing thresholds in an aging European population.

Hendrickx JJ, Huyghe JR, Topsakal V, Demeester K, Wienker TF, Laer LV, Eyken EV, Fransen E, Mäki-Torkko E, Hannula S, Parving A, Jensen M, Tropitzsch A, Bonaconsa A, Mazzoli M, Espeso A, Verbruggen K, Huyghe J, Huygen PL, Kremer H, Kunst SJ, Diaz-Lacava AN, Steffens M, Pyykkö I, Dhooge I, Stephens D, Orzan E, Pfister MH, Bille M, Sorri M, Cremers CW, Camp GV, de Heyning PV.

Otol Neurotol. 2013 Jul;34(5):838-44. doi: 10.1097/MAO.0b013e318288646a.

PMID:
23739559
12.

High incidence of Meniere-like symptoms in relatives of Meniere patients in the areas of Oulu University Hospital and Kainuu Central Hospital in Finland.

Hietikko E, Kotimäki J, Sorri M, Männikkö M.

Eur J Med Genet. 2013 Jun;56(6):279-85. doi: 10.1016/j.ejmg.2013.03.010. Epub 2013 Mar 29.

PMID:
23542667
13.

Audiological follow-up of children with the m.1555A>G mutation in mitochondrial DNA.

Häkli S, Luotonen M, Sorri M, Majamaa K.

Audiol Neurootol. 2013;18(1):23-30. doi: 10.1159/000342905. Epub 2012 Oct 10.

PMID:
23052064
14.

A replication study on proposed candidate genes in Ménière's disease, and a review of the current status of genetic studies.

Hietikko E, Kotimäki J, Okuloff A, Sorri M, Männikkö M.

Int J Audiol. 2012 Nov;51(11):841-5. doi: 10.3109/14992027.2012.705900. Epub 2012 Aug 30. Review.

PMID:
22934933
15.

Ear diseases and other risk factors for hearing impairment among adults: an epidemiological study.

Hannula S, Bloigu R, Majamaa K, Sorri M, Mäki-Torkko E.

Int J Audiol. 2012 Nov;51(11):833-40. doi: 10.3109/14992027.2012.707334. Epub 2012 Aug 30.

PMID:
22934931
16.

Self-reported hearing problems among older adults: prevalence and comparison to measured hearing impairment.

Hannula S, Bloigu R, Majamaa K, Sorri M, Mäki-Torkko E.

J Am Acad Audiol. 2011 Sep;22(8):550-9. doi: 10.3766/jaaa.22.8.7.

PMID:
22031679
17.

Audiogram configurations among older adults: prevalence and relation to self-reported hearing problems.

Hannula S, Bloigu R, Majamaa K, Sorri M, Mäki-Torkko E.

Int J Audiol. 2011 Nov;50(11):793-801. doi: 10.3109/14992027.2011.593562. Epub 2011 Sep 15.

PMID:
21916791
18.

Finnish familial Meniere disease is not linked to chromosome 12p12.3, and anticipation and cosegregation with migraine are not common findings.

Hietikko E, Kotimäki J, Kentala E, Klockars T, Sorri M, Männikkö M.

Genet Med. 2011 May;13(5):415-20. doi: 10.1097/GIM.0b013e3182091a41.

PMID:
21346584
19.

A genome-wide analysis of population structure in the Finnish Saami with implications for genetic association studies.

Huyghe JR, Fransen E, Hannula S, Van Laer L, Van Eyken E, Mäki-Torkko E, Aikio P, Sorri M, Huentelman MJ, Van Camp G.

Eur J Hum Genet. 2011 Mar;19(3):347-52. doi: 10.1038/ejhg.2010.179. Epub 2010 Dec 8.

20.

Hearing in a 54- to 66-year-old population in northern Finland.

Hannula S, Mäki-Torkko E, Majamaa K, Sorri M.

Int J Audiol. 2010 Dec;49(12):920-7. doi: 10.3109/14992027.2010.510146. Epub 2010 Sep 14.

PMID:
20839902

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