Ulf Ekström
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- 2001
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Mark
Different clinical expressions in two families with Stargardt's macular dystrophy (STGD1)
(
- Contribution to journal › Article
- 2000
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Mark
Expression of an LDL receptor allele with two different mutations (E256K and I402T)
(
- Contribution to journal › Article
- 1999
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Mark
An individual with a healthy phenotype in spite of a pathogenic LDL receptor mutation (C240F)
(
- Contribution to journal › Article
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Mark
Digenic inheritance of a ROM1 gene mutation with a peripherin/RDS or rhodopsin mutation in families with retinitis pigmentosa
(
- Contribution to journal › Article
-
Mark
Mutation Analysis and Hypercholesterolemia: Studies in FH patients and in healthy middle-aged men with high, low, or increasing cholesterol levels during a six-year follow-up (the CRISS study).
1999)(
- Thesis › Doctoral thesis (compilation)
- 1998
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Mark
Mutations in the low-density lipoprotein receptor gene in Swedish familial hypercholesterolaemia patients: clinical expression and treatment response
(
- Contribution to journal › Article
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Mark
Phenotypic expression of autosomal dominant retinitis pigmentosa in a Swedish family expressing a Phe-211-Leu variant of peripherin/RDS
(
- Contribution to journal › Article
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Mark
Detection of alterations in all three exons of the peripherin/RDS gene in Swedish patients with retinitis pigmentosa using an efficient DGGE system
(
- Contribution to journal › Article
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Mark
A Swedish family with a mutation in the peripherin/RDS gene (Arg-172-Trp) associated with a progressive retinal degeneration
(
- Contribution to journal › Article
- 1996
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Mark
Effects of heparin and low molecular weight heparin on lipid transport during parenteral feeding in the rat
(
- Contribution to journal › Article