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Ultrastructural Pathology|January 1, 1982
Electron microscopic observations on cultured fibroblasts from Fabry heterozygotes and hemizygotesA Wandall, L Hasholt, S A SørensenClinical Genetics|May 1, 1988
Enzyme replacement in Fabry endothelial cells and fibroblasts: uptake experiments and electron microscopical studiesL Hasholt, A Wandall, S A SørensenJournal of Medical Genetics|May 1, 1990
A Fabry's disease heterozygote with a new mutation: biochemical, ultrastructural, and clinical investigationsL Hasholt, S A Sørensen, A Wandall, et al.Annals of Human Genetics|May 1, 1980
alpha-Galactosidase isozymes in normal individuals, and in Fabry hemizygotes and heterozygotesS A Sørensen, L HasholtHuman Genetics|January 1, 1986
Lysosomal alpha-galactosidase in endothelial cell cultures established from a Fabry hemizygous and normal umbilical veinsL Hasholt, S A SørensenExperimental Cell Research|October 15, 1983
ConA-mediated binding and uptake of purified alpha-galactosidase A in Fabry fibroblastsL Hasholt, S A SørensenClinical Genetics|March 1, 1995
Correlation between magnitude of CAG repeat length alterations and length of the paternal repeat in paternally inherited Huntington's diseaseA Nørremølle, S A Sørensen, K Fenger, et al.Muscle & Nerve|June 1, 1996
Electrophysiological findings in a Danish family with Machado-Joseph diseaseE Colding-Jørgensen, S A Sørensen, L Hasholt, et al.Human Genetics|March 1, 1995
Elongated CAG repeats of the B37 gene in a Danish family with dentato-rubro-pallido-luysian atrophyA Nørremølle, J E Nielsen, S A Sørensen, et al.Pageof 8