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Kotimäki, Jouko
17
results:
Search for persons
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Format
Online (17)
Mediatypes
Articles (Online) (6)
OpenAccess-fulltext (11)
Languages
english (15)
finnish (1)
Sorted by: Relevance
Sorted by: Year
?
1
New Genetic Variants in CYP2B6 and SLC6A Support the Role o..:
Skarp, Sini
;
Korvala, Johanna
;
Kotimäki, Jouko
...
Genes. 13 (2022) 6 - p. 998 , 2022
Link:
https://doi.org/10.3390/..
?
2
Autosomal recessive nonsyndromic hearing impairment in two ..:
Bharadwaj, Thashi
;
Schrauwen, Isabelle
;
Acharya, Anushree
...
Molecular Genetics & Genomic Medicine. 10 (2022) 3 - p. , 2022
Link:
https://doi.org/10.1002/..
?
3
Whole‐exome sequencing suggests multiallelic inheritance fo..:
Skarp, Sini
;
Kanervo, Laura
;
Kotimäki, Jouko
...
Annals of Human Genetics. 83 (2019) 6 - p. 389-396 , 2019
Link:
https://doi.org/10.1111/..
?
4
High incidence of Meniere-like symptoms in relatives of Men..:
Hietikko, Elina
;
Kotimäki, Jouko
;
Sorri, Martti
.
European Journal of Medical Genetics. 56 (2013) 6 - p. 279-285 , 2013
Link:
https://doi.org/10.1016/..
?
5
Finnish familial Meniere disease is not linked to chromosom..:
Hietikko, Elina
;
Kotimäki, Jouko
;
Kentala, Erna
...
Genetics in Medicine. 13 (2011) 5 - p. 415-420 , 2011
Link:
https://doi.org/10.1097/..
?
6
Prevalence of meniere disease in finland:
Kotimäki, Jouko
;
Sorri, Martti
;
Aantaa, Eero
.
The Laryngoscope. 109 (1999) 5 - p. 748-753 , 1999
Link:
https://doi.org/10.1097/..
?
7
Meniérèn tauti pysyy hoidollisena haasteena:
Karvonen, Joel
;
Kotimäki, Jouko
;
Löppönen, Heikki
Duodecim. , 2024
Link:
https://erepo.uef.fi/han..
?
8
Autosomal recessive nonsyndromic hearing impairment in two ..:
Bharadwaj, Thashi
;
Schrauwen, Isabelle
;
Acharya, Anushree
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8922966/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
9
New genetic variants in CYP2B6 and SLC6A support the role o..:
Skarp, S. (Sini)
;
Korvala, J. (Johanna)
;
Kotimäki, J. (Jouko)
... , 2022
Link:
http://urn.fi/urn:nbn:fi..
?
10
Autosomal recessive nonsyndromic hearing impairment in two ..:
Bharadwaj, Thashi
;
Schrauwen, Isabelle
;
Acharya, Anushree
...
10.1002/mgg3.1866. , 2022
Link:
http://hdl.handle.net/10..
?
11
Autosomal recessive nonsyndromic hearing impairment in two ..:
Bharadwaj, T. (Thashi)
;
Schrauwen, I. (Isabelle)
;
Acharya, A. (Anushree)
... , 2022
Link:
http://urn.fi/urn:nbn:fi..
?
12
New Genetic Variants in CYP2B6 and SLC6A Support the Role o..:
Skarp, Sini
;
Korvala, Johanna
;
Kotimäki, Jouko
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9222295/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
13
Meniere's disease in Finland:an epidemiological and clinica..:
Kotimäki, J. (Jouko)
info:eu-repo/semantics/altIdentifier/pissn/0355-3221. , 2003
Link:
http://urn.fi/urn:isbn:9..
?
14
Autosomal recessive nonsyndromic hearing impairment in two ..:
Thashi Bharadwaj
;
Isabelle Schrauwen
;
Anushree Acharya
...
https://doi.org/10.1002/mgg3.1866. , 2022
Link:
https://doi.org/10.1002/..
?
15
New Genetic Variants in CYP2B6 and SLC6A Support the Role o..:
Sini Skarp
;
Johanna Korvala
;
Jouko Kotimäki
...
https://www.mdpi.com/2073-4425/13/6/998. , 2022
Link:
https://doi.org/10.3390/..
1-15