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Clinical Genetics|August 8, 2009
Genetic testing in familial AD and FTD: mutation and phenotype spectrum in a Danish cohortS G Lindquist, M Schwartz, M Batbayli, et al.
European Journal of Neurology|May 20, 2008
Frontotemporal dementia linked to chromosome 3 (FTD-3)--current concepts and the detection of a previously unknown branch of the Danish FTD-3 familyS G Lindquist, H Braedgaard, K Svenstrup, et al.
European Journal of Neurology|February 21, 2008
Alzheimer disease-like clinical phenotype in a family with FTDP-17 caused by a MAPT R406W mutationS G Lindquist, I E Holm, M Schwartz, et al.
European Journal of Neurology|November 20, 2009
Transthyretin as a potential CSF biomarker for Alzheimer's disease and dementia with Lewy bodies: effects of treatment with cholinesterase inhibitorsK Schultz, K Nilsson, J E Nielsen, et al.
Clinical Dysmorphology|March 17, 2005
Further delineation of the 22q13 deletion syndromeS G Lindquist, M Kirchhoff, C Lundsteen, et al.
Clinical Genetics|June 2, 2012
Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion diseaseS G Lindquist, M Duno, M Batbayli, et al.
European Journal of Neurology|August 30, 2008
A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairmentS G Lindquist, L Hasholt, J M C Bahl, et al.
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