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C Forsell

Showing results (11-20 of 26) with videos related to

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American Journal of Medical Genetics|May 31, 1996
Allelic association but only weak evidence for linkage to the apolipoprotein E locus in late-onset Swedish Alzheimer familiesL Liu, C Forsell, L Lilius, et al.
Brain Research|May 29, 1995
Diminished [3H]inositol(1,4,5)P3 but not [3H]inositol(1,3,4,5)P4 binding in Alzheimer's disease brainA Garlind, R F Cowburn, C Forsell, et al.
American Journal of Medical Genetics|July 25, 1997
Mapping of a disease locus for familial rapidly progressive frontotemporal dementia to chromosome 17q12-21S Froelich, H Basun, C Forsell, et al.
Nature Genetics|July 1, 1993
No linkage to chromosome 14 in Swedish Alzheimer's disease familiesL Lannfelt, L Lilius, H Appelgren, et al.
Dementia and Geriatric Cognitive Disorders|November 24, 1999
No detected mutations in the genes for the amyloid precursor protein and presenilins 1 and 2 in a swiss early-onset Alzheimer's disease family with a dominant mode of inheritanceA Savioz, G Leuba, C Forsell, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
Investigations of a CA repeat in the oestrogen receptor beta gene in patients with Alzheimer's diseaseC Forsell, E Enmark, K Axelman, et al.
Folia Neuropathologica|May 25, 1999
A Polish pedigree with Alzheimer's disease determined by a novel mutation in exon 12 of the presenilin 1 gene: clinical and molecular characterizationA Kowalska, C Forsell, J Florczak, et al.
Journal of Internal Medicine|March 1, 1995
Diagnosis of acute intermittent porphyria in northern Sweden: an evaluation of mutation analysis and biochemical methodsC Andersson, S Thunell, Y Floderus, et al.
Molecular Psychiatry|November 17, 2005
Genome scan on Swedish Alzheimer's disease familiesA Sillén, C Forsell, L Lilius, et al.
Experimental Neurology|March 22, 2001
Clinic-based cases with frontotemporal dementia show increased cerebrospinal fluid tau and high apolipoprotein E epsilon4 frequency, but no tau gene mutationsS F Fabre, C Forsell, M Viitanen, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics|May 31, 1996
Allelic association but only weak evidence for linkage to the apolipoprotein E locus in late-onset Swedish Alzheimer familiesL Liu, C Forsell, L Lilius, et al.
Brain Research|May 29, 1995
Diminished [3H]inositol(1,4,5)P3 but not [3H]inositol(1,3,4,5)P4 binding in Alzheimer's disease brainA Garlind, R F Cowburn, C Forsell, et al.
American Journal of Medical Genetics|July 25, 1997
Mapping of a disease locus for familial rapidly progressive frontotemporal dementia to chromosome 17q12-21S Froelich, H Basun, C Forsell, et al.
Nature Genetics|July 1, 1993
No linkage to chromosome 14 in Swedish Alzheimer's disease familiesL Lannfelt, L Lilius, H Appelgren, et al.
Dementia and Geriatric Cognitive Disorders|November 24, 1999
No detected mutations in the genes for the amyloid precursor protein and presenilins 1 and 2 in a swiss early-onset Alzheimer's disease family with a dominant mode of inheritanceA Savioz, G Leuba, C Forsell, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
Investigations of a CA repeat in the oestrogen receptor beta gene in patients with Alzheimer's diseaseC Forsell, E Enmark, K Axelman, et al.
Folia Neuropathologica|May 25, 1999
A Polish pedigree with Alzheimer's disease determined by a novel mutation in exon 12 of the presenilin 1 gene: clinical and molecular characterizationA Kowalska, C Forsell, J Florczak, et al.
Journal of Internal Medicine|March 1, 1995
Diagnosis of acute intermittent porphyria in northern Sweden: an evaluation of mutation analysis and biochemical methodsC Andersson, S Thunell, Y Floderus, et al.
Molecular Psychiatry|November 17, 2005
Genome scan on Swedish Alzheimer's disease familiesA Sillén, C Forsell, L Lilius, et al.
Experimental Neurology|March 22, 2001
Clinic-based cases with frontotemporal dementia show increased cerebrospinal fluid tau and high apolipoprotein E epsilon4 frequency, but no tau gene mutationsS F Fabre, C Forsell, M Viitanen, et al.
Pageof 3