Effect of prevention of procollagen triple-helix formation on proline 3-hydroxylation in freshly isolated chick-embryo tendon cells.

av Majamaa, K
Publicerad 1981

Labelling of prolyl hydroxylase tetrameric subunits in freshly isolated chick-embryo tendon cells and in certain chick-embryo tissues in vivo.

av Majamaa, K, Oikarinen, J
Publicerad 1982

Detection of meningeal fibrosis after subarachnoid haemorrhage by assaying procollagen propeptides in cerebrospinal fluid

av Sajanti, J., Majamaa, K.
Publicerad 1999

High concentrations of procollagen propeptides in chronic subdural haematoma and effusion

av Sajanti, J, Majamaa, K
Publicerad 2003

Prolyl 3-hydroxylase and 4-hydroxylase activities in certain rat and chick-embryo tissues and age-related changes in their activities in the rat.

av Tryggvason, K, Majamaa, K, Kivirikko, K I
Publicerad 1979

Regulation of proline 3-hydroxylation and prolyl 3-hydroxylase and 4-hydroxylase activities in transformed cells.

av Majamaa, K, Myllylä, R, Alitalo, K, Vaheri, A
Publicerad 1982

Familial aggregation of Parkinson's disease in a Finnish population

av Autere, J., Moilanen, J., Myllyla, V., Majamaa, K.
Publicerad 2000

Partial purification and characterization of chick-embryo prolyl 3-hydroxylase.

av Tryggvason, K, Majamaa, K, Risteli, J, Kivirikko, K I
Publicerad 1979

Increased risk of sensorineural hearing loss and migraine in patients with a rare mitochondrial DNA variant 4336A>G in tRNA(Gln)

av Finnila, S., Autere, J., Lehtovirta, M., Hartikainen, P., Mannermaa, A., Soininen, H., Majamaa, K.
Publicerad 2001

APP locus duplication in a Finnish family with dementia and intracerebral haemorrhage

av Rovelet‐Lecrux, A, Frebourg, T, Tuominen, H, Majamaa, K, Campion, D, Remes, A M
Publicerad 2007

Voxelwise Analysis of Diffusion Tensor Imaging and Structural MR Imaging in Patients with the m.3243A>G Mutation in Mitochondrial DNA

av Virtanen, S.M., Lindroos, M.M., Majamaa, K., Nuutila, P., Borra, R.J., Parkkola, R.
I publikationen AJNR Am J Neuroradiol (2011)

Analysis of mitochondrial DNA sequences in patients with isolated or combined oxidative phosphorylation system deficiency

av Hinttala, R, Smeets, R, Moilanen, J S, Ugalde, C, Uusimaa, J, Smeitink, J A M, Majamaa, K
Publicerad 2006

Genetics of early onset Parkinson’s disease in Finland: exome sequencing and genome-wide association study

av Siitonen, A, Nalls, MA, Hernández, D, Gibbs, JR, Ding, J, Ylikotila, P, Edsall, C, Singleton, A, Majamaa, K
I publikationen Neurobiol Aging (2017)

Differences between collagen hydroxylases and 2-oxoglutarate dehydrogenase in their inhibition by structural analogues of 2-oxoglutarate.

av Majamaa, K, Turpeenniemi-Hujanen, T M, Latipää, P, Günzler, V, Hanauske-Abel, H M, Hassinen, I E, Kivirikko, K I
Publicerad 1985

Epidemiology of the mitochondrial DNA 8344A>G mutation for the myoclonus epilepsy and ragged red fibres (MERRF) syndrome

av Remes, A, Karppa, M, Rusanen, H, Majamaa, K, Hassinen, I, Moilanen, J, Uimonen, S, Sorri, M, Salmela, P, Karvonen, S, Karvonen, S
Publicerad 2003

No association of the mitochondrial DNA A12308G polymorphism with increased risk of stroke in patients with the A3243G mutation

av Deschauer, M, Chinnery, P, Schaefer, A, Turnbull, D, Taylor, R, Zierz, S, Shanske, S, DiMauro, S, Majamaa, K, Wilichowski, E, Thorburn, D
Publicerad 2004

Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.

av Majamaa, K, Moilanen, J S, Uimonen, S, Remes, A M, Salmela, P I, Kärppä, M, Majamaa-Voltti, K A, Rusanen, H, Sorri, M, Peuhkurinen, K J, Hassinen, I E
Publicerad 1998