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Publications by Ulla Feldt- Rasmussen

Receptor-Mediated Endocytosis of Α-Galactosidase a in Human Podocytes in Fabry Disease

Multidisciplinary

English

Related publications

Mannose 6-Phosphate Receptor and Sortilin Mediated Endocytosis of Α-Galactosidase a in Kidney Endothelial Cells

Multidisciplinary

English

Adipocytes Participate in Storage in Α-Galactosidase Deficiency (Fabry Disease)

Journal of Inherited Metabolic Disease

English

Fabry Disease: Twenty Novel Α-Galactosidase a Mutations Causing the Classical Phenotype

Journal of Human Genetics

English

Fabry Disease: Effective Tissue Substrate Depletion Following Enzyme Replacement in Α-Galactosidase a Deficient Mice. • 607

Pediatric Research

English

Fabry Disease: Twenty Novel Α-Galactosidase a Mutations and Genotype-Phenotype Correlations in Classical and Variant Phenotypes

Molecular Medicine

Molecular Medicine

Molecular Biology

English

Novel Α-Galactosidase a Mutation (K391E) in a Young Woman With Severe Cardiac and Renal Manifestations of Fabry Disease

International Heart Journal

Cardiovascular Medicine

English

Replacement of Α-Galactosidase a in Fabry Disease: Effect on Fibroblast Cultures Compared With Biopsied Tissues of Treated Patients

Virchows Archiv

Forensic Medicine

Molecular Biology

English

Receptor-Mediated Endocytosis

English

Alpha-Galactosidase a p.A143T, a Non-Fabry Disease-Causing Variant

Orphanet Journal of Rare Diseases

English