Axelman K - Search Results

1

No linkage to chromosome 14 in Swedish Alzheimer's disease families.

Lannfelt L, Lilius L, Appelgren H, Axelman K, Forsell C, Liu L, Johansson K, Graff C. Lannfelt L, et al. Among authors: axelman k. Nat Genet. 1993 Jul;4(3):218-9. doi: 10.1038/ng0793-218. Nat Genet. 1993. PMID: 8358427 No abstract available.

2

Expanded high-resolution genetic study of 109 Swedish families with Alzheimer's disease.

Sillén A, Andrade J, Lilius L, Forsell C, Axelman K, Odeberg J, Winblad B, Graff C. Sillén A, et al. Among authors: axelman k. Eur J Hum Genet. 2008 Feb;16(2):202-8. doi: 10.1038/sj.ejhg.5201946. Epub 2007 Oct 24. Eur J Hum Genet. 2008. PMID: 17957224

3

A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of beta-amyloid.

Mullan M, Crawford F, Axelman K, Houlden H, Lilius L, Winblad B, Lannfelt L. Mullan M, et al. Among authors: axelman k. Nat Genet. 1992 Aug;1(5):345-7. doi: 10.1038/ng0892-345. Nat Genet. 1992. PMID: 1302033

4

Genetic counseling in a Swedish Alzheimer family with amyloid precursor protein mutation.

Lannfelt L, Axelman K, Lilius L, Basun H. Lannfelt L, et al. Among authors: axelman k. Am J Hum Genet. 1995 Jan;56(1):332-5. Am J Hum Genet. 1995. PMID: 7825596 Free PMC article. No abstract available.

5

Amyloid precursor protein mutation causes Alzheimer's disease in a Swedish family.

Lannfelt L, Bogdanovic N, Appelgren H, Axelman K, Lilius L, Hansson G, Schenk D, Hardy J, Winblad B. Lannfelt L, et al. Among authors: axelman k. Neurosci Lett. 1994 Feb 28;168(1-2):254-6. doi: 10.1016/0304-3940(94)90463-4. Neurosci Lett. 1994. PMID: 8028788

6

Sequencing of exons 16 and 17 of the beta-amyloid precursor protein gene fails to identify new mutations in Swedish Alzheimer's disease patients.

Johnston J, Lilius L, Axelman K, Cowburn R, Johansson K, Viitanen M, Winblad B, Lannfelt L. Johnston J, et al. Among authors: axelman k. Hum Mol Genet. 1993 Jul;2(7):1045-6. doi: 10.1093/hmg/2.7.1045. Hum Mol Genet. 1993. PMID: 8364541 No abstract available.

7

Apolipoprotein epsilon 4 allele in Swedish twins and siblings with Alzheimer disease.

Lannfelt L, Pedersen NL, Lilius L, Axelman K, Johansson K, Viitanen M, Gatz M. Lannfelt L, et al. Among authors: axelman k. Alzheimer Dis Assoc Disord. 1995 Fall;9(3):166-9. Alzheimer Dis Assoc Disord. 1995. PMID: 8534415

8

Allelic association but only weak evidence for linkage to the apolipoprotein E locus in late-onset Swedish Alzheimer families.

Liu L, Forsell C, Lilius L, Axelman K, Corder EH, Lannfelt L. Liu L, et al. Among authors: axelman k. Am J Med Genet. 1996 May 31;67(3):306-11. doi: 10.1002/(SICI)1096-8628(19960531)67:3<306::AID-AJMG7>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8725748

9

Mapping of a disease locus for familial rapidly progressive frontotemporal dementia to chromosome 17q12-21.

Froelich S, Basun H, Forsell C, Lilius L, Axelman K, Andreadis A, Lannfelt L. Froelich S, et al. Among authors: axelman k. Am J Med Genet. 1997 Jul 25;74(4):380-5. doi: 10.1002/(sici)1096-8628(19970725)74:4<380::aid-ajmg8>3.0.co;2-t. Am J Med Genet. 1997. PMID: 9259373

10

Genome scan on Swedish Alzheimer's disease families.

Sillén A, Forsell C, Lilius L, Axelman K, Björk BF, Onkamo P, Kere J, Winblad B, Graff C. Sillén A, et al. Among authors: axelman k. Mol Psychiatry. 2006 Feb;11(2):182-6. doi: 10.1038/sj.mp.4001772. Mol Psychiatry. 2006. PMID: 16288313 Clinical Trial.

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