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Kari Majamaa

Showing results (1-10 of 141) with videos related to

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European Journal of Human Genetics : EJHG|August 27, 2003
Lack of a modulative factor in locus 8p23 in a Finnish family with nonsyndromic sensorineural hearing loss associated with the 1555A>G mitochondrial DNA mutationSaara Finnilä, Kari Majamaa
Molecular Biology and Evolution|June 5, 2003
Phylogenetic network and physicochemical properties of nonsynonymous mutations in the protein-coding genes of human mitochondrial DNAJukka S Moilanen, Kari Majamaa
BMJ Neurology Open|February 16, 2024
Incidence and prevalence of mtDNA-related adult mitochondrial disease in Southwest Finland, 2009-2022: an observational, population-based studyMika H Martikainen, Kari Majamaa
European Journal of Human Genetics : EJHG|May 12, 2005
Mitochondrial DNA and ACTN3 genotypes in Finnish elite endurance and sprint athletesAnna-Kaisa Niemi, Kari Majamaa
Journal of Neurology|September 5, 2009
Epidemiology and characteristics of occipital brain infarcts in young adults in southwestern FinlandMika H Martikainen, Kari Majamaa
Neuromuscular Disorders : NMD|July 11, 2013
Novel GJB1 mutation causing adult-onset Charcot-Marie-Tooth disease in a female patientMika H Martikainen, Kari Majamaa
Clinical Parkinsonism & Related Disorders|May 8, 2023
Stable low prevalence of Huntington's disease in FinlandJussi O T Sipilä, Kari Majamaa
Neuromuscular Disorders : NMD|February 18, 2014
Novel mitofusin 2 splice-site mutation causes Charcot-Marie-Tooth disease type 2 with prominent sensory dysfunctionMika H Martikainen, Laura Kytövuori, Kari Majamaa
Journal of Neurology|February 18, 2009
Procollagen propeptides in chronic subdural hematoma reveal sustained dural collagen synthesis after head injuryAnna-Leena Heula, Juha Sajanti, Kari Majamaa
BMC Neurology|December 15, 2022
Magnetic resonance imaging negative myelopathy in Leber's hereditary optic neuropathy: a case reportMika H Martikainen, Miika Suomela, Kari Majamaa
Pageof 15

Showing results (1-10 of 141) with videos related to

Sort By:
Pageof 15
European Journal of Human Genetics : EJHG|August 27, 2003
Lack of a modulative factor in locus 8p23 in a Finnish family with nonsyndromic sensorineural hearing loss associated with the 1555A>G mitochondrial DNA mutationSaara Finnilä, Kari Majamaa
Molecular Biology and Evolution|June 5, 2003
Phylogenetic network and physicochemical properties of nonsynonymous mutations in the protein-coding genes of human mitochondrial DNAJukka S Moilanen, Kari Majamaa
BMJ Neurology Open|February 16, 2024
Incidence and prevalence of mtDNA-related adult mitochondrial disease in Southwest Finland, 2009-2022: an observational, population-based studyMika H Martikainen, Kari Majamaa
European Journal of Human Genetics : EJHG|May 12, 2005
Mitochondrial DNA and ACTN3 genotypes in Finnish elite endurance and sprint athletesAnna-Kaisa Niemi, Kari Majamaa
Journal of Neurology|September 5, 2009
Epidemiology and characteristics of occipital brain infarcts in young adults in southwestern FinlandMika H Martikainen, Kari Majamaa
Neuromuscular Disorders : NMD|July 11, 2013
Novel GJB1 mutation causing adult-onset Charcot-Marie-Tooth disease in a female patientMika H Martikainen, Kari Majamaa
Clinical Parkinsonism & Related Disorders|May 8, 2023
Stable low prevalence of Huntington's disease in FinlandJussi O T Sipilä, Kari Majamaa
Neuromuscular Disorders : NMD|February 18, 2014
Novel mitofusin 2 splice-site mutation causes Charcot-Marie-Tooth disease type 2 with prominent sensory dysfunctionMika H Martikainen, Laura Kytövuori, Kari Majamaa
Journal of Neurology|February 18, 2009
Procollagen propeptides in chronic subdural hematoma reveal sustained dural collagen synthesis after head injuryAnna-Leena Heula, Juha Sajanti, Kari Majamaa
BMC Neurology|December 15, 2022
Magnetic resonance imaging negative myelopathy in Leber's hereditary optic neuropathy: a case reportMika H Martikainen, Miika Suomela, Kari Majamaa
Pageof 15