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Anna-Elina Lehesjoki

Showing results (1-10 of 136) with videos related to

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The EMBO Journal|July 11, 2003
Molecular background of progressive myoclonus epilepsyAnna-Elina Lehesjoki
Advances in Neurology|April 24, 2002
Clinical features and genetics of Unverricht-Lundborg diseaseAnna-Elina Lehesjoki
Brain : a Journal of Neurology|January 1, 2019
Kufs or not Kufs: challenging diagnostics of a rare adult-onset neurodegenerative diseaseJaana Tyynelä, Anna-Elina Lehesjoki
Brain : a Journal of Neurology|September 14, 2017
Reply: The phenotypic and molecular spectrum of PEHO syndrome and PEHO-like disordersAnna-Kaisa Anttonen, Anna-Elina Lehesjoki
Epilepsia|November 22, 2007
Molecular background of EPM1-Unverricht-Lundborg diseaseTarja Joensuu, Anna-Elina Lehesjoki, Outi Kopra
Duodecim; Laaketieteellinen Aikakauskirja|November 20, 2010
[Finnish disease heritage]Marjo Kestilä, Elina Ikonen, Anna-Elina Lehesjoki
Biochimica Et Biophysica Acta|July 11, 2006
Molecular genetics of the NCLs -- status and perspectivesEija Siintola, Anna-Elina Lehesjoki, Sara E Mole
Advances in Experimental Medicine and Biology|January 10, 2004
Mulibrey nanism--a novel peroxisomal disorderJukka Kallijärvi, Anna-Elina Lehesjoki, Marita Lipsanen-Nyman
Human Mutation|October 13, 2011
Update of the mutation spectrum and clinical correlations of over 360 mutations in eight genes that underlie the neuronal ceroid lipofuscinosesMaria Kousi, Anna-Elina Lehesjoki, Sara E Mole
Neuroscience Letters|April 13, 2002
Cortical sensorimotor alterations in Unverricht-Lundborg disease patients without generalized seizuresTeija Silén, Tero Karjalainen, Anna-Elina Lehesjoki, et al.
Pageof 14

Showing results (1-10 of 136) with videos related to

Sort By:
Pageof 14
The EMBO Journal|July 11, 2003
Molecular background of progressive myoclonus epilepsyAnna-Elina Lehesjoki
Advances in Neurology|April 24, 2002
Clinical features and genetics of Unverricht-Lundborg diseaseAnna-Elina Lehesjoki
Brain : a Journal of Neurology|January 1, 2019
Kufs or not Kufs: challenging diagnostics of a rare adult-onset neurodegenerative diseaseJaana Tyynelä, Anna-Elina Lehesjoki
Brain : a Journal of Neurology|September 14, 2017
Reply: The phenotypic and molecular spectrum of PEHO syndrome and PEHO-like disordersAnna-Kaisa Anttonen, Anna-Elina Lehesjoki
Epilepsia|November 22, 2007
Molecular background of EPM1-Unverricht-Lundborg diseaseTarja Joensuu, Anna-Elina Lehesjoki, Outi Kopra
Duodecim; Laaketieteellinen Aikakauskirja|November 20, 2010
[Finnish disease heritage]Marjo Kestilä, Elina Ikonen, Anna-Elina Lehesjoki
Biochimica Et Biophysica Acta|July 11, 2006
Molecular genetics of the NCLs -- status and perspectivesEija Siintola, Anna-Elina Lehesjoki, Sara E Mole
Advances in Experimental Medicine and Biology|January 10, 2004
Mulibrey nanism--a novel peroxisomal disorderJukka Kallijärvi, Anna-Elina Lehesjoki, Marita Lipsanen-Nyman
Human Mutation|October 13, 2011
Update of the mutation spectrum and clinical correlations of over 360 mutations in eight genes that underlie the neuronal ceroid lipofuscinosesMaria Kousi, Anna-Elina Lehesjoki, Sara E Mole
Neuroscience Letters|April 13, 2002
Cortical sensorimotor alterations in Unverricht-Lundborg disease patients without generalized seizuresTeija Silén, Tero Karjalainen, Anna-Elina Lehesjoki, et al.
Pageof 14