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Clinica Chimica Acta; International Journal of Clinical Chemistry|August 15, 1989
ELISA for measuring porphobilinogen deaminase in human erythrocytesL Lannfelt, L Wetterberg, L Lilius, et al.
Journal of Internal Medicine|April 1, 1992
Frequency of low erythrocyte porphobilinogen deaminase activity in FinlandP Mustajoki, R Kauppinen, L Lannfelt, et al.
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|November 1, 1989
Mutations in acute intermittent porphyria detected by ELISA measurement of porphobilinogen deaminaseL Lannfelt, L Wetterberg, P Gellerfors, et al.
Dementia and Geriatric Cognitive Disorders|November 24, 1999
Decreased plasma insulin-like growth factor-I level in familial Alzheimer's disease patients carrying the Swedish APP 670/671 mutationA Mustafa, L Lannfelt, L Lilius, et al.
American Journal of Medical Genetics|May 31, 1996
Allelic association but only weak evidence for linkage to the apolipoprotein E locus in late-onset Swedish Alzheimer familiesL Liu, C Forsell, L Lilius, et al.
American Journal of Medical Genetics|July 25, 1997
Mapping of a disease locus for familial rapidly progressive frontotemporal dementia to chromosome 17q12-21S Froelich, H Basun, C Forsell, et al.
Nature Genetics|August 1, 1992
A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of beta-amyloidM Mullan, F Crawford, K Axelman, et al.
Neuroscience Letters|April 16, 1993
Low frequency of the APP 670/671 mutation in familial Alzheimer's disease in SwedenL Lannfelt, M Viitanen, K Johansson, et al.
Alzheimer Disease and Associated Disorders|January 1, 1995
Apolipoprotein epsilon 4 allele in Swedish twins and siblings with Alzheimer diseaseL Lannfelt, N L Pedersen, L Lilius, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|November 1, 1989
Porphobilinogen deaminase in human erythrocytes: purification of two forms with apparent molecular weights of 40 kDa and 42 kDaL Lannfelt, L Wetterberg, L Lilius, et al.
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