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/vufind/Search/Results?lookfor=%22Kotim%C3%A4ki%2C+Jouko%22&type=Person&sort=year
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PubPharm (20)
1
New Genetic Variants in CYP2B6 and SLC6A Support the Role of Oxidative Stress in Familial Ménière's Disease
enthalten in:
Genes
| 2022
von
Skarp, S.
|
Korvala, J.
|
Kotimäki, J.
| +3
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2
Autosomal recessive nonsyndromic hearing impairment in two Finnish families due to the population enriched CABP2 c.637+1G>T variant
enthalten in:
Molecular genetics & genomic medicine
| 2022
von
Bharadwaj, T.
|
Schrauwen, I.
|
Acharya, A.
| +7
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3
Autosomal recessive nonsyndromic hearing impairment in two Finnish families due to the population enriched CABP2 c.637+1G>T variant
enthalten in:
Molecular Genetics & Genomic Medicine
| 2022
von
Bharadwaj, T.
|
Schrauwen, I.
|
Acharya, A.
| +7
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4
Whole-exome sequencing suggests multiallelic inheritance for childhood-onset Ménière's disease
enthalten in:
Annals of human genetics
| 2019
von
Skarp, S.
|
Kanervo, L.
|
Kotimäki, J.
| +3
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5
Whole‐exome sequencing suggests multiallelic inheritance for childhood‐onset Ménière's disease
enthalten in:
Annals of Human Genetics
| 2019
von
Skarp, S.
|
Kanervo, L.
|
Kotimäki, J.
| +3
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6
Concomitant diseases and their effect on disease prognosis in Meniere's disease : diabetes mellitus identified as a negative prognostic factor
enthalten in:
Acta oto-laryngologica
| 2018
von
Pieskä, T.
|
Kotimäki, J.
|
Männikkö, M.
| +2
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7
Higher prevalence of autoimmune diseases and longer spells of vertigo in patients affected with familial Ménière's disease : A clinical comparison of familial and sporadic Ménière's disease
enthalten in:
American journal of audiology
| 2014
von
Hietikko, E.
|
Sorri, M.
|
Männikkö, M.
| +1
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8
Kikuchi disease in a young Finnish man
enthalten in:
Duodecim; laaketieteellinen aikakauskirja
| 2014
von
Kotimäki, J.
|
Koukkari, O.
|
Syväniemi, E.
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9
High incidence of Meniere-like symptoms in relatives of Meniere patients in the areas of Oulu University Hospital and Kainuu Central Hospital in Finland
enthalten in:
European journal of medical genetics
| 2013
von
Hietikko, E.
|
Kotimäki, J.
|
Sorri, M.
| +1
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10
High incidence of Meniere-like symptoms in relatives of Meniere patients in the areas of Oulu University Hospital and Kainuu Central Hospital in Finland
enthalten in:
European journal of medical genetics
| 2013
von
Hietikko, E.
|
Kotimäki, J.
|
Sorri, M.
| +1
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Duodecim; laaketieteellinen aikakauskirja
2
European journal of medical genetics
1
Acta oto-laryngologica
1
American journal of audiology
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Genetics in medicine : official journal of the ...
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International journal of circumpolar health
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EC 1.14.14.1
1
EC 3.4.24.69
1
Extracellular Matrix Proteins
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GABA Plasma Membrane Transport Proteins
1
HCFC1 protein, human
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