5 Einträge gefunden

1. Association between polymorphisms of endothelial nitric oxide synthase gene (NOS3) and left posterior wall thickness (LPWT) of the heart in Fabry disease.

   1. Rohard, Imke
   2. Schaefer, E
   3. Kampmann, C
   4. Beck, M
   5. Gal, Andreas

   2008 - Forschungsinformationssystem des UKE
2. [Mutations of the frizzled-4 gene. Their impact on medical care of patients with autosomal dominant exudative vitreoretinopathy]

   1. Müller, M
   2. Kusserow, C
   3. Orth, Ulrike
   4. Klär-Dissars, U
   5. Laqua, H
   6. Gal, Andreas

   2008 - Forschungsinformationssystem des UKE
3. Does proximal myotonic myopathy show anticipation?

   1. Kruse, Bernd
   2. Wöhrle, Doris
   3. Steinbach, Peter
   4. Gal, Andreas

   2008 - Forschungsinformationssystem des UKE
4. The mutation p.Ser298Pro in the sulphamidase gene (SGSH) is associated with a slowly progressive clinical phenotype in mucopolysaccharidosis type IIIA (Sanfilippo A syndrome)

   1. Meyer, Ann
   2. Kossow, Kai
   3. Gal, Andreas
   4. Steglich, Cordula
   5. Mühlhausen, Chris
   6. Ullrich, Kurt
   7. Braulke, Thomas

   2008 - Forschungsinformationssystem des UKE
5. Onset and progression of the Anderson-Fabry disease related cardiomyopathy.

   1. Kampmann, Christoph
   2. Linhart, Ales
   3. Baehner, Frank
   4. Palecek, Tomas
   5. Wiethoff, Christiane M
   6. Miebach, Elke
   7. Whybra, Catharina

   2008 - Forschungsinformationssystem des UKE