J. Puranen

Extensive cerebral white matter abnormality without clinical symptoms: A new hereditary condition?

A. Häkkinen, T. Autti, R. Raininko, 1999, Annals of neurology.

Delayed classic and protracted phenotypes of compound heterozygous juvenile neuronal ceroid lipofuscinosis

P. Munroe, T. Autti, E. Kirveskari, 1999, Neurology.

High‐resolution magic angle spinning and 1H magnetic resonance spectroscopy reveal significantly altered neuronal metabolite profiles in CLN1 but not in CLN3

A. Häkkinen, A. Paetau, T. Bathen, 2004, Journal of neuroscience research.

Neuroradiological Findings (MRS, MRI, SPECT) in Infantile Neuronal Ceroid-Lipofuscinosis (Infantile CLN1) at Different Stages of the Disease

A. Häkkinen, T. Autti, R. Raininko, 2004, Neuropediatrics.

Neuronal Ceroid-Lipofuscinosis

A. Häkkinen, T. Autti, R. Raininko, 2022 .