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M A Kaunisto

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Diabetologia|October 31, 2007
Association analysis of podocyte slit diaphragm genes as candidates for diabetic nephropathyP Ihalmo, M Wessman, M A Kaunisto, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 21, 2007
No association of migraine to the GABA-A receptor complex on chromosome 15G Oswell, M A Kaunisto, M Kallela, et al.
Neurology|February 9, 2005
Decreased cerebellar total creatine in episodic ataxia type 2: a 1H MRS studyH Harno, S Heikkinen, M A Kaunisto, et al.
Neurology|December 25, 2003
Subclinical vestibulocerebellar dysfunction in migraine with and without auraH Harno, T Hirvonen, M A Kaunisto, et al.
Cephalalgia : an International Journal of Headache|June 30, 2009
Genetic association study of endothelin-1 and its receptors EDNRA and EDNRB in migraine with auraP Tikka-Kleemola, M A Kaunisto, E Hämäläinen, et al.
Neurogenetics|October 8, 2003
Novel splice site CACNA1A mutation causing episodic ataxia type 2M A Kaunisto, H Harno, M Kallela, et al.
American Journal of Human Genetics|June 15, 2006
Trait components provide tools to dissect the genetic susceptibility of migraineV Anttila, M Kallela, G Oswell, et al.
Neurology|April 14, 2010
A visual migraine aura locus maps to 9q21-q22P Tikka-Kleemola, V Artto, S Vepsäläinen, et al.
Cephalalgia : an International Journal of Headache|November 23, 2006
Testing of variants of the MTHFR and ESR1 genes in 1798 Finnish individuals fails to confirm the association with migraine with auraM A Kaunisto, M Kallela, E Hämäläinen, et al.
Neurogenetics|May 11, 2004
A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2M A Kaunisto, H Harno, K R J Vanmolkot, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Diabetologia|October 31, 2007
Association analysis of podocyte slit diaphragm genes as candidates for diabetic nephropathyP Ihalmo, M Wessman, M A Kaunisto, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 21, 2007
No association of migraine to the GABA-A receptor complex on chromosome 15G Oswell, M A Kaunisto, M Kallela, et al.
Neurology|February 9, 2005
Decreased cerebellar total creatine in episodic ataxia type 2: a 1H MRS studyH Harno, S Heikkinen, M A Kaunisto, et al.
Neurology|December 25, 2003
Subclinical vestibulocerebellar dysfunction in migraine with and without auraH Harno, T Hirvonen, M A Kaunisto, et al.
Cephalalgia : an International Journal of Headache|June 30, 2009
Genetic association study of endothelin-1 and its receptors EDNRA and EDNRB in migraine with auraP Tikka-Kleemola, M A Kaunisto, E Hämäläinen, et al.
Neurogenetics|October 8, 2003
Novel splice site CACNA1A mutation causing episodic ataxia type 2M A Kaunisto, H Harno, M Kallela, et al.
American Journal of Human Genetics|June 15, 2006
Trait components provide tools to dissect the genetic susceptibility of migraineV Anttila, M Kallela, G Oswell, et al.
Neurology|April 14, 2010
A visual migraine aura locus maps to 9q21-q22P Tikka-Kleemola, V Artto, S Vepsäläinen, et al.
Cephalalgia : an International Journal of Headache|November 23, 2006
Testing of variants of the MTHFR and ESR1 genes in 1798 Finnish individuals fails to confirm the association with migraine with auraM A Kaunisto, M Kallela, E Hämäläinen, et al.
Neurogenetics|May 11, 2004
A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2M A Kaunisto, H Harno, K R J Vanmolkot, et al.
Pageof 1