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Page 1
LGI2 truncation causes a remitting focal epilepsy in dogs.
Seppälä EH, Jokinen TS, Fukata M, Fukata Y, Webster MT, Karlsson EK, Kilpinen SK, Steffen F, Dietschi E, Leeb T, Eklund R, Zhao X, Rilstone JJ, Lindblad-Toh K, Minassian BA, Lohi H. Seppälä EH, et al. Among authors: jokinen ts. PLoS Genet. 2011 Jul;7(7):e1002194. doi: 10.1371/journal.pgen.1002194. Epub 2011 Jul 28. PLoS Genet. 2011. PMID: 21829378 Free PMC article.
Magnetic resonance imaging findings in Finnish Spitz dogs with focal epilepsy.
Viitmaa R, Cizinauskas S, Bergamasco LA, Kuusela E, Pascoe P, Teppo AM, Jokinen TS, Kivisaari L, Snellman M. Viitmaa R, et al. Among authors: jokinen ts. J Vet Intern Med. 2006 Mar-Apr;20(2):305-10. doi: 10.1892/0891-6640(2006)20[305:mrifif]2.0.co;2. J Vet Intern Med. 2006. PMID: 16594587 Free article.
Cerebellar cortical abiotrophy in Lagotto Romagnolo dogs.
Jokinen TS, Rusbridge C, Steffen F, Viitmaa R, Syrjä P, De Lahunta A, Snellman M, Cizinauskas S. Jokinen TS, et al. J Small Anim Pract. 2007 Aug;48(8):470-3. doi: 10.1111/j.1748-5827.2006.00298.x. J Small Anim Pract. 2007. PMID: 17490444
Benign familial juvenile epilepsy in Lagotto Romagnolo dogs.
Jokinen TS, Metsähonkala L, Bergamasco L, Viitmaa R, Syrjä P, Lohi H, Snellman M, Jeserevics J, Cizinauskas S. Jokinen TS, et al. J Vet Intern Med. 2007 May-Jun;21(3):464-71. doi: 10.1892/0891-6640(2007)21[464:bfjeil]2.0.co;2. J Vet Intern Med. 2007. PMID: 17552452 Free article.
A missense change in the ATG4D gene links aberrant autophagy to a neurodegenerative vacuolar storage disease.
Kyöstilä K, Syrjä P, Jagannathan V, Chandrasekar G, Jokinen TS, Seppälä EH, Becker D, Drögemüller M, Dietschi E, Drögemüller C, Lang J, Steffen F, Rohdin C, Jäderlund KH, Lappalainen AK, Hahn K, Wohlsein P, Baumgärtner W, Henke D, Oevermann A, Kere J, Lohi H, Leeb T. Kyöstilä K, et al. Among authors: jokinen ts. PLoS Genet. 2015 Apr 15;11(4):e1005169. doi: 10.1371/journal.pgen.1005169. eCollection 2015 Apr. PLoS Genet. 2015. PMID: 25875846 Free PMC article.
Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes.
Hytönen MK, Arumilli M, Lappalainen AK, Owczarek-Lipska M, Jagannathan V, Hundi S, Salmela E, Venta P, Sarkiala E, Jokinen T, Gorgas D, Kere J, Nieminen P, Drögemüller C, Lohi H. Hytönen MK, et al. PLoS Genet. 2016 May 17;12(5):e1006037. doi: 10.1371/journal.pgen.1006037. eCollection 2016 May. PLoS Genet. 2016. PMID: 27187611 Free PMC article.
ADAM23 is a common risk gene for canine idiopathic epilepsy.
Koskinen LL, Seppälä EH, Weissl J, Jokinen TS, Viitmaa R, Hänninen RL, Quignon P, Fischer A, André C, Lohi H. Koskinen LL, et al. Among authors: jokinen ts. BMC Genet. 2017 Jan 31;18(1):8. doi: 10.1186/s12863-017-0478-6. BMC Genet. 2017. PMID: 28143391 Free PMC article.
Basal Autophagy Is Altered in Lagotto Romagnolo Dogs with an ATG4D Mutation.
Syrjä P, Anwar T, Jokinen T, Kyöstilä K, Jäderlund KH, Cozzi F, Rohdin C, Hahn K, Wohlsein P, Baumgärtner W, Henke D, Oevermann A, Sukura A, Leeb T, Lohi H, Eskelinen EL. Syrjä P, et al. Vet Pathol. 2017 Nov;54(6):953-963. doi: 10.1177/0300985817712793. Epub 2017 Jun 6. Vet Pathol. 2017. PMID: 28583040
45 results