Lindquist SG - Search Results

1

Alzheimer disease-like clinical phenotype in a family with FTDP-17 caused by a MAPT R406W mutation.

Lindquist SG, Holm IE, Schwartz M, Law I, Stokholm J, Batbayli M, Waldemar G, Nielsen JE. Lindquist SG, et al. Eur J Neurol. 2008 Apr;15(4):377-85. doi: 10.1111/j.1468-1331.2008.02069.x. Epub 2008 Feb 16. Eur J Neurol. 2008. PMID: 18284428

2

Meiotic CAG repeat instability in spinocerebellar ataxia type 6: maternally transmitted elongation in a presumed sporadic case.

Lindquist SG, Nørremølle A, Hjermind LE, Hasholt L, Nielsen JE. Lindquist SG, et al. J Neurol Sci. 2006 Feb 15;241(1-2):95-8. doi: 10.1016/j.jns.2005.10.004. Epub 2005 Nov 28. J Neurol Sci. 2006. PMID: 16310805

3

[Dementia--genetic aspects].

Lindquist SG, Waldemar G, Nielsen JE. Lindquist SG, et al. Ugeskr Laeger. 2006 Oct 2;168(40):3405-8. Ugeskr Laeger. 2006. PMID: 17032604 Danish.

4

Atypical early-onset Alzheimer's disease caused by the Iranian APP mutation.

Lindquist SG, Nielsen JE, Stokholm J, Schwartz M, Batbayli M, Ballegaard M, Erdal J, Krabbe K, Waldemar G. Lindquist SG, et al. J Neurol Sci. 2008 May 15;268(1-2):124-30. doi: 10.1016/j.jns.2007.11.021. Epub 2008 Jan 9. J Neurol Sci. 2008. PMID: 18187157

5

Frontotemporal dementia linked to chromosome 3 (FTD-3)--current concepts and the detection of a previously unknown branch of the Danish FTD-3 family.

Lindquist SG, Braedgaard H, Svenstrup K, Isaacs AM, Nielsen JE; FReJA Consortium. Lindquist SG, et al. Eur J Neurol. 2008 Jul;15(7):667-70. doi: 10.1111/j.1468-1331.2008.02144.x. Epub 2008 May 15. Eur J Neurol. 2008. PMID: 18484988

6

A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairment.

Lindquist SG, Hasholt L, Bahl JM, Heegaard NH, Andersen BB, Nørremølle A, Stokholm J, Schwartz M, Batbayli M, Laursen H, Pardossi-Piquard R, Chen F, St George-Hyslop P, Waldemar G, Nielsen JE. Lindquist SG, et al. Eur J Neurol. 2008 Oct;15(10):1135-9. doi: 10.1111/j.1468-1331.2008.02256.x. Epub 2008 Aug 22. Eur J Neurol. 2008. PMID: 18727676

7

Reduced CSF CART in dementia with Lewy bodies.

Schultz K, Wiehager S, Nilsson K, Nielsen JE, Lindquist SG, Hjermind LE, Andersen BB, Wallin A, Nilsson C, Petersén A. Schultz K, et al. Among authors: lindquist sg. Neurosci Lett. 2009 Apr 3;453(2):104-6. doi: 10.1016/j.neulet.2009.02.008. Epub 2009 Feb 10. Neurosci Lett. 2009. PMID: 19356602 Free article.

8

Genetic testing in familial AD and FTD: mutation and phenotype spectrum in a Danish cohort.

Lindquist SG, Schwartz M, Batbayli M, Waldemar G, Nielsen JE. Lindquist SG, et al. Clin Genet. 2009 Aug;76(2):205-9. doi: 10.1111/j.1399-0004.2009.01191.x. Epub 2009 Jul 29. Clin Genet. 2009. PMID: 19659892

9

Transthyretin as a potential CSF biomarker for Alzheimer's disease and dementia with Lewy bodies: effects of treatment with cholinesterase inhibitors.

Schultz K, Nilsson K, Nielsen JE, Lindquist SG, Hjermind LE, Andersen BB, Wallin A, Nilsson C, Petersén A. Schultz K, et al. Among authors: lindquist sg. Eur J Neurol. 2010 Mar;17(3):456-60. doi: 10.1111/j.1468-1331.2009.02841.x. Epub 2009 Nov 17. Eur J Neurol. 2010. PMID: 19922456

10

Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease.

Lindquist SG, Duno M, Batbayli M, Puschmann A, Braendgaard H, Mardosiene S, Svenstrup K, Pinborg LH, Vestergaard K, Hjermind LE, Stokholm J, Andersen BB, Johannsen P, Nielsen JE. Lindquist SG, et al. Clin Genet. 2013 Mar;83(3):279-83. doi: 10.1111/j.1399-0004.2012.01903.x. Epub 2012 Jul 4. Clin Genet. 2013. PMID: 22650353

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

25 results

Search Page

Filters