3 Einträge gefunden

1. TMEM165 Deficiency: Postnatal Changes in Glycosylation

   1. Althoff, S Schulte
   2. Grüneberg, M
   3. Reunert, J
   4. Park, J H
   5. Rust, S
   6. Mühlhausen, C
   7. Wada, Y

   2016 - Forschungsinformationssystem des UKE
2. Decreased plasma concentration of von Willebrand factor antigen (VWF:Ag) in patients with glycogen storage disease type Ia

   1. Mühlhausen, C
   2. Schneppenheim, R
   3. Budde, U
   4. Merkel, M
   5. Muschol, N
   6. Ullrich, K
   7. Santer, R

   2005 - Forschungsinformationssystem des UKE
3. Severe phenotype despite high residual glutaryl-CoA dehydrogenase activity: a novel mutation in a Turkish patient with glutaric aciduria type I.

   1. Mühlhausen, C
   2. Christensen, E
   3. Schwartz, M
   4. Muschol, N
   5. Ullrich, K
   6. Lukacs, Z

   2003 - Forschungsinformationssystem des UKE