Axelman K - Search Results

Year	Number of Results
1992	1
1993	4
1994	2
1995	3
1996	1
1997	3
1998	1
1999	3
2000	1
2001	2
2002	1
2003	4
2005	1
2006	1
2007	1
2008	4
2009	1
2010	1
2011	1
2017	1
2025	0

1

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.

2

Predicting Cognitive Decline across Four Decades in Mutation Carriers and Non-carriers in Autosomal-Dominant Alzheimer's Disease.

Almkvist O, Rodriguez-Vieitez E, Thordardottir S, Amberla K, Axelman K, Basun H, Kinhult-Ståhlbom A, Lilius L, Remes A, Wahlund LO, Viitanen M, Lannfelt L, Graff C. Almkvist O, et al. Among authors: axelman k. J Int Neuropsychol Soc. 2017 Mar;23(3):195-203. doi: 10.1017/S1355617716001028. Epub 2017 Jan 12. J Int Neuropsychol Soc. 2017. PMID: 28079014

3

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 Free article.

4

Glucose metabolism and PIB binding in carriers of a His163Tyr presenilin 1 mutation.

Schöll M, Almkvist O, Axelman K, Stefanova E, Wall A, Westman E, Långström B, Lannfelt L, Graff C, Nordberg A. Schöll M, et al. Among authors: axelman k. Neurobiol Aging. 2011 Aug;32(8):1388-99. doi: 10.1016/j.neurobiolaging.2009.08.016. Epub 2009 Sep 30. Neurobiol Aging. 2011. PMID: 19796846

5

Tau gene polymorphisms and apolipoprotein E epsilon4 may interact to increase risk for Alzheimer's disease.

Lilius L, Froelich Fabre S, Basun H, Forsell C, Axelman K, Mattila K, Andreadis A, Viitanen M, Winblad B, Fratiglioni L, Lannfelt L. Lilius L, et al. Among authors: axelman k. Neurosci Lett. 1999 Dec 17;277(1):29-32. doi: 10.1016/s0304-3940(99)00833-2. Neurosci Lett. 1999. PMID: 10643890

6

Genetic association to the amyloid plaque associated protein gene COL25A1 in Alzheimer's disease.

Forsell C, Björk BF, Lilius L, Axelman K, Fabre SF, Fratiglioni L, Winblad B, Graff C. Forsell C, et al. Among authors: axelman k. Neurobiol Aging. 2010 Mar;31(3):409-15. doi: 10.1016/j.neurobiolaging.2008.04.009. Epub 2008 May 22. Neurobiol Aging. 2010. PMID: 18501477

7

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

8

Progranulin mutation causes frontotemporal dementia in the Swedish Karolinska family.

Chiang HH, Rosvall L, Brohede J, Axelman K, Björk BF, Nennesmo I, Robins T, Graff C. Chiang HH, et al. Among authors: axelman k. Alzheimers Dement. 2008 Nov;4(6):414-20. doi: 10.1016/j.jalz.2008.09.001. Alzheimers Dement. 2008. PMID: 19012866

9

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

10

A unique gene expression signature discriminates familial Alzheimer's disease mutation carriers from their wild-type siblings.

Nagasaka Y, Dillner K, Ebise H, Teramoto R, Nakagawa H, Lilius L, Axelman K, Forsell C, Ito A, Winblad B, Kimura T, Graff C. Nagasaka Y, et al. Among authors: axelman k. Proc Natl Acad Sci U S A. 2005 Oct 11;102(41):14854-9. doi: 10.1073/pnas.0504178102. Epub 2005 Sep 30. Proc Natl Acad Sci U S A. 2005. PMID: 16199521 Free PMC article.

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