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European Journal of Human Genetics : EJHG|June 15, 2000
Identification of a novel 4.6-kb genomic deletion in presenilin-1 gene which results in exclusion of exon 9 in a Finnish early onset Alzheimer's disease family: an Alu core sequence-stimulated recombination?M Hiltunen, S Helisalmi, A Mannermaa, et al.
Neurology|November 14, 2001
Genome-wide linkage disequilibrium mapping of late-onset Alzheimer's disease in FinlandM Hiltunen, A Mannermaa, D Thompson, et al.
Acta Paediatrica Scandinavica|January 1, 1989
Neonatal septicaemia in Finland 1981-85. Predominance of group B streptococcal infections with very early onsetT Vesikari, E Isolauri, N Tuppurainen, et al.
The Journal of Clinical Investigation|July 1, 1992
The familial hypercholesterolemia (FH)-North Karelia mutation of the low density lipoprotein receptor gene deletes seven nucleotides of exon 6 and is a common cause of FH in FinlandU M Koivisto, H Turtola, K Aalto-Setälä, et al.
International Psychogeriatrics|March 25, 2014
Decreasing sense of coherence and its determinants in spousal caregivers of persons with mild Alzheimer's disease in three year follow-up: ALSOVA studyTarja Välimäki, Janne Martikainen, Kristiina Hongisto, et al.
European Child & Adolescent Psychiatry|February 2, 2000
Emotional and behavioural symptoms in 8-9-year-old children in relation to family structureI Luoma, K Puura, T Tamminen, et al.
European Journal of Neurology|June 25, 2015
Health-related quality of life in patients with idiopathic normal pressure hydrocephalusA Junkkari, H Sintonen, O Nerg, et al.
Dementia and Geriatric Cognitive Disorders Extra|May 23, 2015
The CERAD Neuropsychological Battery in Patients with Frontotemporal Lobar DegenerationRamona M Haanpää, Noora-Maria Suhonen, Päivi Hartikainen, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|October 23, 2001
Genetic determinants of bone mineral content in premature infantsM C Backström, A Mahonen, M Ala-Houhala, et al.
Journal of Periodontal Research|September 27, 2000
Salivary matrix metalloproteinase (MMP-8) levels and gelatinase (MMP-9) activities in patients with type 2 diabetes mellitusH L Collin, T Sorsa, J H Meurman, et al.
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