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

por Finnila, S., Autere, J., Lehtovirta, M., Hartikainen, P., Mannermaa, A., Soininen, H., Majamaa, K.
Publicado em 2001

Longitudinal SPECT study in Alzheimer's disease: relation to apolipoprotein E polymorphism

por Lehtovirta, M, Kuikka, J, Helisalmi, S, Hartikainen, P, Mannermaa, A, Ryynanen, M, Riekkinen, P, Soininen, H
Publicado em 1998

SPECT and MRI analysis in Alzheimer's disease: relation to apolipoprotein E epsilon 4 allele.

por Lehtovirta, M, Soininen, H, Laakso, M P, Partanen, K, Helisalmi, S, Mannermaa, A, Ryynänen, M, Kuikka, J, Hartikainen, P, Riekkinen, P J
Publicado em 1996