4 Einträge gefunden

1. Clinical and genetic diagnosis of Marfan syndrome in childhood are Equal- FBN1 mutation should not influence handling of pediatric patients with confirmed Marfansyndrome

   1. Stark, Veronika
   2. Arndt, Florian
   3. Harring, Gesa
   4. Keyser, Britta
   5. von Kodolitsch, Yskert
   6. Kozlik-Feldmann, Rainer
   7. Kutsche, Kerstin

   2016 - Forschungsinformationssystem des UKE
2. Mitral valve prolapse syndrome and MASS phenotype: Stability of aortic dilatation but progression of mitral valve prolapse

   1. Rippe, Moritz
   2. De Backer, Julie
   3. Kutsche, Kerstin
   4. Mosquera, Laura Muiño
   5. Schüler, Helke
   6. Rybczynski, Meike
   7. Bernhardt, Alexander M

   2016 - Forschungsinformationssystem des UKE
3. Comprehensive analysis of dural ectasia in 150 patients with a causative FBN1 mutation

   1. Sheikhzadeh, Sara
   2. Sondermann, Claudia
   3. Rybczynski, Meike
   4. Habermann, Christian R
   5. Brockstädt, Lars
   6. Keyser, Britta
   7. Kaemmerer, Harald

   2014 - Forschungsinformationssystem des UKE
4. Total serum transforming growth factor-β1 is elevated in the entire spectrum of genetic aortic syndromes

   1. Hillebrand, Mathias
   2. Millot, Nathalie
   3. Sheikhzadeh, Sara
   4. Rybczynski, Meike
   5. Gerth, Sabine
   6. Kölbel, Tilo
   7. Keyser, Britta

   2014 - Forschungsinformationssystem des UKE - frei zugänglich