Basun H - Search Results

1

Frontotemporal dementia in a large Swedish family is caused by a progranulin null mutation.

Skoglund L, Brundin R, Olofsson T, Kalimo H, Ingvast S, Blom ES, Giedraitis V, Ingelsson M, Lannfelt L, Basun H, Glaser A. Skoglund L, et al. Among authors: basun h. Neurogenetics. 2009 Feb;10(1):27-34. doi: 10.1007/s10048-008-0155-z. Epub 2008 Oct 15. Neurogenetics. 2009. PMID: 18855025

2

Clinical and molecular aspects of frontotemporal dementia.

Froelich-Fabre S, Skoglund L, Ostojic J, Kilander L, Lindau M, Glaser A, Basun H, Lannfelt L. Froelich-Fabre S, et al. Among authors: basun h. Neurodegener Dis. 2004;1(4-5):218-24. doi: 10.1159/000080989. Neurodegener Dis. 2004. PMID: 16908993 Review.

3

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. Arch Neurol. 2008 Apr;65(4):499-505. doi: 10.1001/archneur.65.4.499. Arch Neurol. 2008. PMID: 18413473 Free PMC article.

4

The Arctic AβPP mutation leads to Alzheimer's disease pathology with highly variable topographic deposition of differentially truncated Aβ.

Kalimo H, Lalowski M, Bogdanovic N, Philipson O, Bird TD, Nochlin D, Schellenberg GD, Brundin R, Olofsson T, Soliymani R, Baumann M, Wirths O, Bayer TA, Nilsson LN, Basun H, Lannfelt L, Ingelsson M. Kalimo H, et al. Among authors: basun h. Acta Neuropathol Commun. 2013 Sep 10;1:60. doi: 10.1186/2051-5960-1-60. Acta Neuropathol Commun. 2013. PMID: 24252272 Free PMC article.

5

Extended investigation of tau and mutation screening of other candidate genes on chromosome 17q21 in a Swedish FTDP-17 family.

Froelich Fabre S, Axelman P, Almkvist A, Basun H, Lannfelt L. Froelich Fabre S, et al. Among authors: basun h. Am J Med Genet B Neuropsychiatr Genet. 2003 Aug 15;121B(1):112-8. doi: 10.1002/ajmg.b.20067. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 12898585

6

[Conformationally altered proteins cause neurodegenerative diseases].

Ingelsson M, Nilsson L, Basun H, Aquilonius SM, Lannfelt L. Ingelsson M, et al. Among authors: basun h. Lakartidningen. 2005 Nov 21-27;102(47):3542-3, 3545-6, 3549 passim. Lakartidningen. 2005. PMID: 16408392 Review. Swedish.

7

High tau levels in cerebrospinal fluid predict nursing home placement and rapid progression in Alzheimer's disease.

Degerman Gunnarsson M, Ingelsson M, Blennow K, Basun H, Lannfelt L, Kilander L. Degerman Gunnarsson M, et al. Among authors: basun h. Alzheimers Res Ther. 2016 Jun 6;8(1):22. doi: 10.1186/s13195-016-0191-0. Alzheimers Res Ther. 2016. PMID: 27263933 Free PMC article.

8

[Alzheimer's disease - the most common cause of dementia].

Bogdanovic N, Hansson O, Zetterberg H, Basun H, Ingelsson M, Lannfelt L, Blennow K. Bogdanovic N, et al. Among authors: basun h. Lakartidningen. 2020 Mar 9;117:FZHM. Lakartidningen. 2020. PMID: 32154904 Free article. Swedish.

9

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. Among authors: basun h. Arch Neurol. 1994 Dec;51(12):1193-7. doi: 10.1001/archneur.1994.00540240037013. Arch Neurol. 1994. PMID: 7986173

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. Among authors: basun h. Arch Neurol. 1998 May;55(5):698-702. doi: 10.1001/archneur.55.5.698. Arch Neurol. 1998. PMID: 9605727 Clinical Trial.

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