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Human Genetics|December 22, 1998
Mitotic and meiotic instability of the CAG trinucleotide repeat in spinocerebellar ataxia type 1P Koefoed, L Hasholt, K Fenger, et al.
Neuroscience|December 4, 2003
Molecular and behavioral analysis of the R6/1 Huntington's disease transgenic mouseB Naver, C Stub, M Møller, et al.
Human Molecular Genetics|September 25, 1997
CAG repeat expansion in autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24J E Nielsen, P Koefoed, K Abell, et al.
Acta Psychiatrica Scandinavica|March 10, 2001
Platelet serotonin transporters and the transporter gene in control subjects, unipolar patients and bipolar patientsE Mellerup, B Bennike, T Bolwig, et al.
Journal of Neuroendocrinology|November 24, 2007
Impaired glucose tolerance in the R6/1 transgenic mouse model of Huntington's diseaseK Josefsen, M D Nielsen, K H Jørgensen, et al.
Molecular and Cellular Neurosciences|November 22, 2000
Inhibition of Huntington synthesis by antisense oligodeoxynucleotidesC Nellemann, K Abell, A Nørremølle, et al.
Journal of Neuroendocrinology|July 16, 2009
Huntington's disease does not appear to increase the risk of diabetes mellitusT W Boesgaard, T T Nielsen, K Josefsen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 22, 1998
Autosomal dominant pure spastic paraplegia: a clinical, paraclinical, and genetic studyJ E Nielsen, K Krabbe, P Jennum, et al.
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