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K Fenger

Showing results (41-50 of 63) with videos related to

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European Journal of Neurology|June 26, 2001
Increased intracortical facilitation in patients with autosomal dominant pure spastic paraplegia linked to chromosome 2pJ E Nielsen, P Jennum, K Fenger, et al.
Annals of Hematology|January 18, 2002
Clinically overt hereditary hemochromatosis in Denmark 1948-1985: epidemiology, factors of significance for long-term survival, and causes of death in 179 patientsN Milman, P Pedersen, T á Steig, et al.
Human Molecular Genetics|September 1, 1993
Trinucleotide repeat elongation in the Huntingtin gene in Huntington disease patients from 71 Danish familiesA Nørremølle, O Riess, J T Epplen, et al.
Clinical Genetics|March 3, 2009
4p16.3 haplotype modifying age at onset of Huntington diseaseA Nørremølle, E Budtz-Jørgensen, 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 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.
Journal of Neurology, Neurosurgery, and Psychiatry|September 19, 2001
Motor evoked potentials from the external anal sphincter in patients with autosomal dominant pure spastic paraplegia linked to chromosome 2pP Jennum, L Neerup Jensen, K Fenger, et al.
European Journal of Neurology|June 2, 2007
Double-blind crossover trial of gabapentin in SPG4-linked hereditary spastic paraplegiaK H Scheuer, K Svenstrup, P Jennum, 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.
Human Genetics|July 1, 1990
Family studies of hereditary hemochromatosis in Denmark and the Faroe IslandsN Milman, N Graudal, L S Nielsen, et al.
Pageof 7

Showing results (41-50 of 63) with videos related to

Sort By:
Pageof 7
European Journal of Neurology|June 26, 2001
Increased intracortical facilitation in patients with autosomal dominant pure spastic paraplegia linked to chromosome 2pJ E Nielsen, P Jennum, K Fenger, et al.
Annals of Hematology|January 18, 2002
Clinically overt hereditary hemochromatosis in Denmark 1948-1985: epidemiology, factors of significance for long-term survival, and causes of death in 179 patientsN Milman, P Pedersen, T á Steig, et al.
Human Molecular Genetics|September 1, 1993
Trinucleotide repeat elongation in the Huntingtin gene in Huntington disease patients from 71 Danish familiesA Nørremølle, O Riess, J T Epplen, et al.
Clinical Genetics|March 3, 2009
4p16.3 haplotype modifying age at onset of Huntington diseaseA Nørremølle, E Budtz-Jørgensen, 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 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.
Journal of Neurology, Neurosurgery, and Psychiatry|September 19, 2001
Motor evoked potentials from the external anal sphincter in patients with autosomal dominant pure spastic paraplegia linked to chromosome 2pP Jennum, L Neerup Jensen, K Fenger, et al.
European Journal of Neurology|June 2, 2007
Double-blind crossover trial of gabapentin in SPG4-linked hereditary spastic paraplegiaK H Scheuer, K Svenstrup, P Jennum, 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.
Human Genetics|July 1, 1990
Family studies of hereditary hemochromatosis in Denmark and the Faroe IslandsN Milman, N Graudal, L S Nielsen, et al.
Pageof 7