Axelman K - Search Results

1

The 'Arctic' APP mutation (E693G) causes Alzheimer's disease by enhanced Abeta protofibril formation.

Nilsberth C, Westlind-Danielsson A, Eckman CB, Condron MM, Axelman K, Forsell C, Stenh C, Luthman J, Teplow DB, Younkin SG, Näslund J, Lannfelt L. Nilsberth C, et al. Among authors: axelman k. Nat Neurosci. 2001 Sep;4(9):887-93. doi: 10.1038/nn0901-887. Nat Neurosci. 2001. PMID: 11528419

2

Low frequency of the APP 670/671 mutation in familial Alzheimer's disease in Sweden.

Lannfelt L, Viitanen M, Johansson K, Axelman K, Lilius L, Almqvist E, Winblad B. Lannfelt L, et al. Among authors: axelman k. Neurosci Lett. 1993 Apr 16;153(1):85-7. doi: 10.1016/0304-3940(93)90083-w. Neurosci Lett. 1993. PMID: 8510829

3

No association between polymorphisms in the neprilysin promoter region and Swedish Alzheimer's disease patients.

Lilius L, Forsell C, Axelman K, Winblad B, Graff C, Tjernberg L. Lilius L, et al. Among authors: axelman k. Neurosci Lett. 2003 Feb 6;337(2):111-3. doi: 10.1016/s0304-3940(02)01300-9. Neurosci Lett. 2003. PMID: 12527400

4

Clinical findings in nondemented mutation carriers predisposed to Alzheimer's disease: a model of mild cognitive impairment.

Almkvist O, Axelman K, Basun H, Jensen M, Viitanen M, Wahlund LO, Lannfelt L. Almkvist O, et al. Among authors: axelman k. Acta Neurol Scand Suppl. 2003;179:77-82. doi: 10.1034/j.1600-0404.107.s179.11.x. Acta Neurol Scand Suppl. 2003. PMID: 12603253

5

Clinical and neuropathological features of the arctic APP gene mutation causing early-onset Alzheimer disease.

Basun H, Bogdanovic N, Ingelsson M, Almkvist O, Näslund J, Axelman K, Bird TD, Nochlin D, Schellenberg GD, Wahlund LO, Lannfelt L. Basun H, et al. Among authors: axelman k. Arch Neurol. 2008 Apr;65(4):499-505. doi: 10.1001/archneur.65.4.499. Arch Neurol. 2008. PMID: 18413473 Free PMC article.

6

A large Swedish family with Alzheimer's disease with a codon 670/671 amyloid precursor protein mutation. A clinical and genealogical investigation.

Axelman K, Basun H, Winblad B, Lannfelt L. Axelman K, et al. Arch Neurol. 1994 Dec;51(12):1193-7. doi: 10.1001/archneur.1994.00540240037013. Arch Neurol. 1994. PMID: 7986173

7

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

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

A novel pathogenic mutation (Leu262Phe) found in the presenilin 1 gene in early-onset Alzheimer's disease.

Forsell C, Froelich S, Axelman K, Vestling M, Cowburn RF, Lilius L, Johnston JA, Engvall B, Johansson K, Dahlkild A, Ingelson M, St George-Hyslop PH, Lannfelt L. Forsell C, et al. Among authors: axelman k. Neurosci Lett. 1997 Sep 26;234(1):3-6. doi: 10.1016/s0304-3940(97)00603-4. Neurosci Lett. 1997. PMID: 9347932

10

Wide range of disease onset in a family with Alzheimer disease and a His163Tyr mutation in the presenilin-1 gene.

Axelman K, Basun H, Lannfelt L. Axelman K, et al. Arch Neurol. 1998 May;55(5):698-702. doi: 10.1001/archneur.55.5.698. Arch Neurol. 1998. PMID: 9605727 Clinical Trial.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

34 results

Search Page

Filters