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The genetics and pathophysiology of Alzheimer's diseaseLANNFELT, L.Journal of internal medicine. 1997, Vol 242, Num 4, pp 281-284, issn 0954-6820Article

Microtubule-associated protein tau in human fibroblasts with the Swedish Alzheimer mutationINGELSON, M; VANMECHELEN, E; LANNFELT, L et al.Neuroscience letters. 1996, Vol 220, Num 1, pp 9-12, issn 0304-3940Article

Wide range of disease onset in a family with Alzheimer disease and a His163Tyr mutation in the presenilin-1 geneAXELMAN, K; BASUN, H; LANNFELT, L et al.Archives of neurology (Chicago). 1998, Vol 55, Num 5, pp 698-702, issn 0003-9942Article

A large Swedish family with Alzheimer's disease with a codon 670/671 amyloid precursor protein mutation : a clinical and genealogical investigationAXELMAN, K; BASUN, H; WINBLAD, B et al.Archives of neurology (Chicago). 1994, Vol 51, Num 12, pp 1193-1197, issn 0003-9942Article

Lack of association between an intronic polymorphism in the presenilin-1 gene and sporadic late-onset Alzheimer disease in polish patientsKOWOLSKA, A; WENDER, M; LANNFELT, L et al.Dementia and geriatric cognitive disorders. 1998, Vol 9, Num 3, pp 137-139, issn 1420-8008Article

Apolipoprotein ε4 allele and disease progression in patients with late-onset Alzheimer's diseaseBASUN, H; GRUT, M; WINBLAD, B et al.Neuroscience letters. 1995, Vol 183, Num 1-2, pp 32-34, issn 0304-3940Article

Increased cerebrospinal fluid tau in patients with Alzheimer's diseaseJENSEN, M; BASUN, H; LANNFELT, L et al.Neuroscience letters. 1995, Vol 186, Num 2-3, pp 189-191, issn 0304-3940Article

Impaired insulin secretion increases the risk ofAlzheimer diseaseRÖNNEMAA, E; ZETHELIUS, B; SUNDELOF, J et al.Neurology. 2008, Vol 71, Num 14, pp 1065-1071, issn 0028-3878, 7 p.Article

Reduction of phosphorylated tau during memantine treatment of Alzheimer's diseaseDEGERMAN GUNNARSSON, M; KILANDER, L; BASUN, H et al.Dementia and geriatric cognitive disorders. 2007, Vol 24, Num 4, pp 247-252, issn 1420-8008, 6 p.Article

New Alzheimer's disease locus on chromosome 8GIEDRAITIS, V; HEDLUND, M; SKOGLUND, L et al.Journal of medical genetics. 2006, Vol 43, Num 12, pp 931-935, issn 0022-2593, 5 p.Article

A follow-up study of the family with the Swedish APP 670/671 Alzheimer's disease mutationWAHLUND, L.-O; BASUN, H; ALMKVIST, O et al.Dementia and geriatric cognitive disorders. 1999, Vol 10, Num 6, pp 526-533, issn 1420-8008Article

Inheritance of the ApoE ε4 allele increases the rate of brain atrophy in dementia patientsWAHLUND, L.-O; JULIN, P; LANNFELT, L et al.Dementia and geriatric cognitive disorders. 1999, Vol 10, Num 4, pp 262-268, issn 1420-8008Article

Predominant deposition of amyloid-β₄₂₍₄₃₎ in plaques in cases of Alzheimer's disease and hereditary cerebral hemorrhage associated with mutations in the amyloid precursor protein geneMANN, D. M. A; IWATSUBO, T; IHARA, Y et al.The American journal of pathology. 1996, Vol 148, Num 4, pp 1257-1266, issn 0002-9440Article

A serine to glycine substitution at position 9 in the extracellular N-terminal part of the dopamine D₃ receptor protein : no role in the genetic predisposition to bipolar affective disorderRIETSCHEL, M; NÖTHEN, M. M; MÖLLER, H.-J et al.Psychiatry research. 1993, Vol 46, Num 3, pp 253-259, issn 0165-1781Article

Genetics of Alzheimer's diseaseLANNFELT, L.Acta neurologica Scandinavica. Supplementum. 1996, Vol 94, Num 168, pp 25-27, issn 0065-1427Conference Paper

A DLST genotype associated with reduced risk for Alzheimer's diseaseSHEU, K.-F. R; BROWN, A. M; KRISTAL, B. S et al.Neurology. 1999, Vol 52, Num 7, pp 1505-1507, issn 0028-3878Article

No detected mutations in the genes for the amyloid precursor protein and presenilins 1 and 2 in a Swiss early-onset Alzheimer's disease family with a dominant mode of inheritanceSAVIOZ, A; LEUBA, G; FORSELL, C et al.Dementia and geriatric cognitive disorders. 1999, Vol 10, Num 6, pp 431-436, issn 1420-8008Article

Brain volumes and regional cerebral blood flow in carriers of the swedish alzheimer amyloid protein mutationJULIN, P; ALMKVIST, O; BASUN, H et al.Alzheimer disease and associated disorders. 1998, Vol 12, Num 1, pp 49-53, issn 0893-0341Article

A methylenetetrahydrofolate reductase gene polymorphism in ischaemic stroke and in carotid artery stenosisKOSTULAS, K; CRISBY, M; HUANG, W.-X et al.European journal of clinical investigation. 1998, Vol 28, Num 4, pp 285-289, issn 0014-2972Article

EEG slowing and cerebrospinal fluid tau levels in patients with cognitive declineJELIC, V; BLOMBERG, M; DIERKS, T et al.Neuroreport (Oxford). 1998, Vol 9, Num 1, pp 157-160, issn 0959-4965Article

α-Ketoglutarate dehydrogenase in Alzheimer brains bearing the APP670/671 mutationGIBSON, G. E; ZHANG, H; SHEU, K. F.-R et al.Annals of neurology. 1998, Vol 44, Num 4, pp 676-681, issn 0364-5134Article

CYP2D6 and CYP2C19 genotypes in an elderly Swedish populationYAMADA, H; DAHL, M.-L; LANNFELT, L et al.European journal of clinical pharmacology. 1998, Vol 54, Num 6, pp 479-481, issn 0031-6970Conference Paper

Nicotinic receptors, muscarinic receptors and choline acetyltransferase activity in the temporal cortex of Alzheimer patients with differing apolipoprotein E genotypesSVENSSON, A.-L; WARPMAN, U; HELLSTROM-LINDAHL, E et al.Neuroscience letters. 1997, Vol 232, Num 1, pp 37-40, issn 0304-3940Article

No difference in cerebral glucose metabolism in patients with Alzheimer disease and differing apolipoprotein E genotypesCORDER, E. H; JELIC, V; BASUN, H et al.Archives of neurology (Chicago). 1997, Vol 54, Num 3, pp 273-277, issn 0003-9942Article