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K Majamaa

Showing results (61-70 of 67) with videos related to

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Journal of Internal Medicine|September 16, 2004
Improved adherence to practice guidelines yields better outcome in high-risk patients with acute coronary syndrome without ST elevation: findings from nationwide FINACS studiesS Vikman, K E J Airaksinen, I Tierala, et al.
European Journal of Neurology|September 11, 2002
Molecular genetic analysis of the alpha-synuclein and the parkin gene in Parkinson's disease in FinlandJ M Autere, M J Hiltunen, A J Mannermaa, et al.
Human Molecular Genetics|November 25, 2000
Human mtDNA sublimons resemble rearranged mitochondrial genoms found in pathological statesO A Kajander, A T Rovio, K Majamaa, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 5, 2001
Modifier locus for mitochondrial DNA disease: linkage and linkage disequilibrium mapping of a nuclear modifier gene for maternally inherited deafnessY Bykhovskaya, H Yang, K Taylor, et al.
Neurology|May 24, 2006
A 3-year clinical follow-up of adult patients with 3243A>G in mitochondrial DNAK A M Majamaa-Voltti, S Winqvist, A M Remes, et al.
Neurology|December 1, 1993
Exclusion of mutations in the gene for type III collagen (COL3A1) as a common cause of intracranial aneurysms or cervical artery dissections: results from sequence analysis of the coding sequences of type III collagen from 55 unrelated patientsH Kuivaniemi, D J Prockop, Y Wu, et al.
American Journal of Human Genetics|July 31, 1998
Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult populationK Majamaa, J S Moilanen, S Uimonen, et al.
Pageof 7

Showing results (61-70 of 67) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 67 results.
Journal of Internal Medicine|September 16, 2004
Improved adherence to practice guidelines yields better outcome in high-risk patients with acute coronary syndrome without ST elevation: findings from nationwide FINACS studiesS Vikman, K E J Airaksinen, I Tierala, et al.
European Journal of Neurology|September 11, 2002
Molecular genetic analysis of the alpha-synuclein and the parkin gene in Parkinson's disease in FinlandJ M Autere, M J Hiltunen, A J Mannermaa, et al.
Human Molecular Genetics|November 25, 2000
Human mtDNA sublimons resemble rearranged mitochondrial genoms found in pathological statesO A Kajander, A T Rovio, K Majamaa, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 5, 2001
Modifier locus for mitochondrial DNA disease: linkage and linkage disequilibrium mapping of a nuclear modifier gene for maternally inherited deafnessY Bykhovskaya, H Yang, K Taylor, et al.
Neurology|May 24, 2006
A 3-year clinical follow-up of adult patients with 3243A>G in mitochondrial DNAK A M Majamaa-Voltti, S Winqvist, A M Remes, et al.
Neurology|December 1, 1993
Exclusion of mutations in the gene for type III collagen (COL3A1) as a common cause of intracranial aneurysms or cervical artery dissections: results from sequence analysis of the coding sequences of type III collagen from 55 unrelated patientsH Kuivaniemi, D J Prockop, Y Wu, et al.
American Journal of Human Genetics|July 31, 1998
Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult populationK Majamaa, J S Moilanen, S Uimonen, et al.
Pageof 7