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Digital Health
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October 9, 2024
A sustainable artificial-intelligence-augmented digital care pathway for epilepsy: Automating seizure tracking based on electroencephalogram data using artificial intelligence
Pantea Keikhosrokiani, Minna Isomursu, Johanna Uusimaa, et al.
Duodecim; Laaketieteellinen Aikakauskirja
|
January 26, 2010
[Current prospects of genetics in epilepsy diagnostics--when and what?]
Johanna Uusimaa, Eija Gaily, Jaakko Ignatius, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
October 29, 2009
Craniofacial morphology in children of mothers with the m.3243A>G mutation in mitochondrial DNA
Taija L Pihlajaniemi, Pertti Pirttiniemi, Johanna Uusimaa, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 25, 2021
Starting a DBS service for children: It's not the latitude but the attitude - Establishment of the paediatric DBS centre in Northern Finland
Maija Lahtinen, Heli Helander, Päivi Vieira, et al.
Plos One
|
August 24, 2018
Structural analysis of human NHLRC2, mutations of which are associated with FINCA disease
Ekaterina Biterova, Alexander Ignatyev, Johanna Uusimaa, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
April 2, 2014
SIRT5 is under the control of PGC-1α and AMPK and is involved in regulation of mitochondrial energy metabolism
Marcin Buler, Sanna-Mari Aatsinki, Valerio Izzi, et al.
Acta Ophthalmologica
|
September 14, 2012
Prevalence of the primary LHON mutations in Northern Finland associated with bilateral optic atrophy and tobacco-alcohol amblyopia
Paula Korkiamäki, Marko Kervinen, Karoliina Karjalainen, et al.
Archives of Pediatrics & Adolescent Medicine
|
September 9, 2009
Antipyretic agents for preventing recurrences of febrile seizures: randomized controlled trial
Teemu Strengell, Matti Uhari, Rita Tarkka, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
September 6, 2005
Sequence analysis of nuclear genes encoding functionally important complex I subunits in children with encephalomyopathy
Reetta Hinttala, Johanna Uusimaa, Anne M Remes, et al.
Mitochondrion
|
May 26, 2016
Evaluating clinical mitochondrial respiratory chain enzymes from biopsy specimens presenting skewed probability distribution of activity data
Milla-Riikka Hautakangas, Reetta Hinttala, Heikki Rantala, et al.
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Search research articles
Search
Showing results (1-10 of 91) with videos related to
Sort By:
Page
of 10
Digital Health
|
October 9, 2024
A sustainable artificial-intelligence-augmented digital care pathway for epilepsy: Automating seizure tracking based on electroencephalogram data using artificial intelligence
Pantea Keikhosrokiani, Minna Isomursu, Johanna Uusimaa, et al.
Duodecim; Laaketieteellinen Aikakauskirja
|
January 26, 2010
[Current prospects of genetics in epilepsy diagnostics--when and what?]
Johanna Uusimaa, Eija Gaily, Jaakko Ignatius, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
October 29, 2009
Craniofacial morphology in children of mothers with the m.3243A>G mutation in mitochondrial DNA
Taija L Pihlajaniemi, Pertti Pirttiniemi, Johanna Uusimaa, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 25, 2021
Starting a DBS service for children: It's not the latitude but the attitude - Establishment of the paediatric DBS centre in Northern Finland
Maija Lahtinen, Heli Helander, Päivi Vieira, et al.
Plos One
|
August 24, 2018
Structural analysis of human NHLRC2, mutations of which are associated with FINCA disease
Ekaterina Biterova, Alexander Ignatyev, Johanna Uusimaa, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
April 2, 2014
SIRT5 is under the control of PGC-1α and AMPK and is involved in regulation of mitochondrial energy metabolism
Marcin Buler, Sanna-Mari Aatsinki, Valerio Izzi, et al.
Acta Ophthalmologica
|
September 14, 2012
Prevalence of the primary LHON mutations in Northern Finland associated with bilateral optic atrophy and tobacco-alcohol amblyopia
Paula Korkiamäki, Marko Kervinen, Karoliina Karjalainen, et al.
Archives of Pediatrics & Adolescent Medicine
|
September 9, 2009
Antipyretic agents for preventing recurrences of febrile seizures: randomized controlled trial
Teemu Strengell, Matti Uhari, Rita Tarkka, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
September 6, 2005
Sequence analysis of nuclear genes encoding functionally important complex I subunits in children with encephalomyopathy
Reetta Hinttala, Johanna Uusimaa, Anne M Remes, et al.
Mitochondrion
|
May 26, 2016
Evaluating clinical mitochondrial respiratory chain enzymes from biopsy specimens presenting skewed probability distribution of activity data
Milla-Riikka Hautakangas, Reetta Hinttala, Heikki Rantala, et al.
Page
of 10