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Kotimäki, Jouko
17  results:
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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7

Meniérèn tauti pysyy hoidollisena haasteena:

Karvonen, Joel ; Kotimäki, Jouko ; Löppönen, Heikki
Duodecim.  , 2024
Link: https://erepo.uef.fi/han..
 
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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...
 
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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..
 
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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..
 
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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..
 
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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...
 
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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..
 
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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/..
 
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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/..
 
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