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2002
Mark Von Willebrand's disease caused by compound heterozygosity for a substitution mutation (T1156M) in the D3 domain of the von Willebrand factor and a stop mutation (Q2470X).
Lethagen, Stefan ^LU ; Isaksson, Christina ^LU ; Schaedel, Charlotta ^LU and Holmberg, Lars ^LU (2002) In Thrombosis and Haemostasis 88(3). p.421-426
- Contribution to journal › Article
Mark Predictors of deterioration of lung function in cystic fibrosis.
Schaedel, Charlotta ^LU ; de Monestrol, I ; Hjelte, L ; Johannesson, M ; Kornfält, Ragnhild ^LU ; Lindblad, A ; Strandvik, B ; Wahlgren, Lars ^LU and Holmberg, Lars ^LU (2002) In Pediatric Pulmonology 33(6). p.483-491
- Contribution to journal › Article
2001
Mark Clinical and genetical studies in cystic fibrosis and pseudohypoaldosteronism
Schaedel, Charlotta ^LU (2001)
- Thesis › Doctoral thesis (compilation)

your query:: Remove author: Schaedel, Charlotta (LU)