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Kari Majamaa

Showing results (11-20 of 141) with videos related to

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BMJ Case Reports|July 11, 2012
Novel POLG1 mutations in a patient with adult-onset progressive external ophthalmoplegia and encephalopathyMika H Martikainen, Reetta Hinttala, Kari Majamaa
Journal of Neurology|May 9, 2013
Impaired information-processing speed and working memory in leukoencephalopathy with brainstem and spinal cord involvement and elevated lactate (LBSL) and DARS2 mutations: a report of three adult patientsMika H Martikainen, Ulla Ellfolk, Kari Majamaa
Molecular Biology and Evolution|September 2, 2003
Lineage-specific selection in human mtDNA: lack of polymorphisms in a segment of MTND5 gene in haplogroup JJukka S Moilanen, Saara Finnila, Kari Majamaa
Acta Diabetologica|April 12, 2012
Prevalence of mitochondrial diabetes in southwestern Finland: a molecular epidemiological studyMika H Martikainen, Tapani Rönnemaa, Kari Majamaa
Mitochondrion|February 12, 2013
Juvenile parkinsonism, hypogonadism and Leigh-like MRI changes in a patient with m.4296G>A mutation in mitochondrial DNAMika H Martikainen, Laura Kytövuori, Kari Majamaa
BMJ Neurology Open|September 26, 2024
Neurological manifestations in adult patients with the m.3243A>G variant in mitochondrial DNAKari Majamaa, Mikko Kärppä, Jukka S Moilanen
Diabetes & Vascular Disease Research|April 30, 2015
Association of mitochondrial DNA haplogroups and vascular complications of diabetes mellitus: A population-based studyMika H Martikainen, Tapani Rönnemaa, Kari Majamaa
Acta Neurochirurgica|October 2, 2015
Glycosaminoglycans in subdural fluid and CSF after meningeal injuryAnna-Leena Heula, Juha Sajanti, Kari Majamaa
Journal of Neurology|February 8, 2003
Peripheral neuropathy in patients with the 3243A>G mutation in mitochondrial DNAMikko Kärppä, Pirjo Syrjälä, Uolevi Tolonen, et al.
Human Genetics|June 13, 2003
Increased variation in mtDNA in patients with familial sensorineural hearing impairmentMervi S Lehtonen, Jukka S Moilanen, Kari Majamaa
Pageof 15

Showing results (11-20 of 141) with videos related to

Sort By:
Pageof 15
BMJ Case Reports|July 11, 2012
Novel POLG1 mutations in a patient with adult-onset progressive external ophthalmoplegia and encephalopathyMika H Martikainen, Reetta Hinttala, Kari Majamaa
Journal of Neurology|May 9, 2013
Impaired information-processing speed and working memory in leukoencephalopathy with brainstem and spinal cord involvement and elevated lactate (LBSL) and DARS2 mutations: a report of three adult patientsMika H Martikainen, Ulla Ellfolk, Kari Majamaa
Molecular Biology and Evolution|September 2, 2003
Lineage-specific selection in human mtDNA: lack of polymorphisms in a segment of MTND5 gene in haplogroup JJukka S Moilanen, Saara Finnila, Kari Majamaa
Acta Diabetologica|April 12, 2012
Prevalence of mitochondrial diabetes in southwestern Finland: a molecular epidemiological studyMika H Martikainen, Tapani Rönnemaa, Kari Majamaa
Mitochondrion|February 12, 2013
Juvenile parkinsonism, hypogonadism and Leigh-like MRI changes in a patient with m.4296G>A mutation in mitochondrial DNAMika H Martikainen, Laura Kytövuori, Kari Majamaa
BMJ Neurology Open|September 26, 2024
Neurological manifestations in adult patients with the m.3243A>G variant in mitochondrial DNAKari Majamaa, Mikko Kärppä, Jukka S Moilanen
Diabetes & Vascular Disease Research|April 30, 2015
Association of mitochondrial DNA haplogroups and vascular complications of diabetes mellitus: A population-based studyMika H Martikainen, Tapani Rönnemaa, Kari Majamaa
Acta Neurochirurgica|October 2, 2015
Glycosaminoglycans in subdural fluid and CSF after meningeal injuryAnna-Leena Heula, Juha Sajanti, Kari Majamaa
Journal of Neurology|February 8, 2003
Peripheral neuropathy in patients with the 3243A>G mutation in mitochondrial DNAMikko Kärppä, Pirjo Syrjälä, Uolevi Tolonen, et al.
Human Genetics|June 13, 2003
Increased variation in mtDNA in patients with familial sensorineural hearing impairmentMervi S Lehtonen, Jukka S Moilanen, Kari Majamaa
Pageof 15